Acessibilidade / Reportar erro

Descriptive epidemiological study on patients with movement disorders, with emphasis on Parkinson’s disease

ABSTRACT

BACKGROUND:

Knowing the epidemiological profile is relevant for improving healthcare practices. Movement disorders are neurological disorders characterized by the presence of involuntary movements. They have a negative impact on patients’ quality of life.

OBJECTIVES:

To outline the frequencies of the different diagnoses seen among patients, along with their demographic characteristics, at a hospital in São Paulo (SP), Brazil, and to highlight the clinical aspects of those with Parkinson’s disease.

DESIGN AND SETTING:

Retrospective descriptive epidemiological analysis at a specialized outpatient clinic in a state public hospital in São Paulo.

METHODS:

Patients treated at this clinic over a four-year period were analyzed. Diagnoses, demographic variables and associations with clinical aspects of Parkinson’s disease were evaluated.

RESULTS:

Out of the 680 medical records analyzed, 58.4% related to females. Most patients were over 60 years of age, white, married and teachers. The most frequent diagnosis was Parkinson’s disease, followed by essential tremor and dystonia. Parkinson’s disease presented in the mixed clinical form; the most common initial symptom was tremor. The akinetic-rigid clinical form occurred in younger individuals and mostly presented with postural instability and freezing of gait in the early years of disease.

CONCLUSIONS:

Parkinson’s disease, essential tremor and dystonia were the most frequent diagnoses. Characteristics like sex, frequency of other pathological conditions and the clinical and demographic aspects of Parkinson’s disease were consistent with the data in the relevant literature.

KEY WORDS (MeSH terms):
Movement disorders; Epidemiology; Parkinson’s disease; Hypokinesia

AUTHORS’ KEY WORDS:
Extrapyramidal symptoms; Parkinsonism; Hyperkinetic syndromes

INTRODUCTION

Epidemiological studies are widely reported in the literature,11. Marques AP, Szwarcwald CL, de Souza-Junior PRB, Malta DC, Montilla DER. Prevalence of arterial hypertension in Brazilian adults and its associated factors and activity limitations: a cross-sectional study. Sao Paulo Med J. 2019;137(4):312-21. PMID: 31691763; https://doi.org/10.1590/1516-3180.2018.0251220719.
https://doi.org/https://doi.org/10.1590/...
,22. Yin J, Ma Y, Vogel U, et al. Methylation status of the PPP1R13L promoter region among lung cancer patients and healthy controls. Analytical cross-sectional study. Sao Paulo Med J. 2019;137(3):255-61. PMID: 31483011; https://doi.org/10.1590/1516-3180.2018.0358230419.
https://doi.org/https://doi.org/10.1590/...
,33. Carmo ÉA, Nery AA, Nascimento Sobrinho CL, Casotti CA. Clinical and epidemiological aspects of scorpionism in the interior of the state of Bahia, Brazil: retrospective epidemiological study. Sao Paulo Med J. 2019;137(2):162-8. PMID: 31314877; https://doi.org/10.1590/1516-3180.2018.0388070219.
https://doi.org/https://doi.org/10.1590/...
,44. Santos EHS, Santos Neto PJD, Santos I S. Carotid intima-media thickness in the Brazilian Longitudinal Study of Adult Health (ELSA-Brasil): a narrative review. Sao Paulo Med J. 2018;136(1):64-72. PMID: 29590246; https://doi.org/10.1590/1516-3180.2017.0272141017.
https://doi.org/https://doi.org/10.1590/...
and are extremely valuable for improving healthcare practices. Epidemiological information is an instrument for healthcare planning that informs guidelines and improvements.55. Ribosa-Nogué R, Gironell A, Pagonabarraga J, et al. Análisis descriptivo de la actividad de una unidad de trastornos del movimiento en un hospital terciario de Cataluña [Descriptive analysis of the activity in a movement disorder unit in a tertiary hospital in Catalonia]. Rev Neurol. 2012;55(6):330-6. PMID: 22972574.,66. Bower JH, Teshome M, Melaku Z, Zenebe G. Frequency of movement disorders in an Ethiopian university practice. Mov Disord. 2005;20(9):1209-13. PMID: 15954128; https://doi.org/10.1002/mds.20567.
https://doi.org/https://doi.org/10.1002/...
,77. Bhidayasiri R, Saksornchai K, Kaewwilai L, Phanthumchinda K. A census of movement disorders at a Thai university hospital. J Neurol Sci. 2011;301(1-2):31-4. PMID: 21131010; https://doi.org/10.1016/j.jns.2010.11.010.
https://doi.org/https://doi.org/10.1016/...
Consequently, analysis on certain factors such as risk, morbidity and mortality, prevalence of certain diseases and assistance provided to patients is required.55. Ribosa-Nogué R, Gironell A, Pagonabarraga J, et al. Análisis descriptivo de la actividad de una unidad de trastornos del movimiento en un hospital terciario de Cataluña [Descriptive analysis of the activity in a movement disorder unit in a tertiary hospital in Catalonia]. Rev Neurol. 2012;55(6):330-6. PMID: 22972574. Such information facilitates identification of a population profile and allows comparison of characteristics with data in other studies that have been consolidated in the literature.66. Bower JH, Teshome M, Melaku Z, Zenebe G. Frequency of movement disorders in an Ethiopian university practice. Mov Disord. 2005;20(9):1209-13. PMID: 15954128; https://doi.org/10.1002/mds.20567.
https://doi.org/https://doi.org/10.1002/...
,77. Bhidayasiri R, Saksornchai K, Kaewwilai L, Phanthumchinda K. A census of movement disorders at a Thai university hospital. J Neurol Sci. 2011;301(1-2):31-4. PMID: 21131010; https://doi.org/10.1016/j.jns.2010.11.010.
https://doi.org/https://doi.org/10.1016/...
,88. Das SK, Ghosh B, Das G, Biswas A, Ray J. Movement disorders: Indian scenario: a clinico-genetic review. Neurol India. 2013;61(5):457-66. PMID: 24262445; https://doi.org/10.4103/0028-3886.121908.
https://doi.org/https://doi.org/10.4103/...

Some studies on neurological diseases have revealed that one of the most recurrent diagnoses consists of movement disorders.99. Wenning GK, Kiechl S, Seppi K, et al. Prevalence of movement disorders in men and women aged 50-89 years (Bruneck Study cohort): a population-based study. Lancet Neurol. 2005;4(12), 815-20. PMID: 16297839; https://doi.org/10.1016/S1474-4422(05)70226-X.
https://doi.org/https://doi.org/10.1016/...
These are neurological disorders resulting from lesions in the basal nuclei, which result in involuntary movements.1010. Vázquez-Alén P, Pérez-Gilabert Y, Mateo D, Giménez-Roldán S. Estudio sobre una base de datos de 2.471 pacientes con enfermedad de Parkinson y trastornos del movimiento en el Área Sanitaria 1 de la Comunidad de Madrid. Cambios demográficos observados a lo largo de ocho años [A study made on a data base of 2,471 patients with Parkinson disease and disorders of movement in Health District 1 of the autonomous region of Madrid. Observed demographic changes over 8 year-period]. Rev Neurol. 2000;30(7):635-40. PMID: 10859741. These disorders are broadly classified into two major groups: hyperkinetic and hypokinetic syndromes. Hyperkinetic syndromes are characterized by hyperactive involuntary and uncontrollable movements, such as ballism, athetosis, dystonia, tremor, tics, myoclonus and others.1111. Siemers E, Reddy V. Profile of patients enrolled in a new movement disorder clinic. Mov Disord. 1991;6(4):336-41. PMID: 1758452; https://doi.org/10.1002/mds.870060412.
https://doi.org/https://doi.org/10.1002/...
,1212. Defazio G, Abbruzzese G, Livrea P, Berardelli A. Epidemiology of primary dystonia. Lancet Neurol. 2004;3(11):673-8. PMID: 15488460; doi: https://doi.org/10.1016/S1474-4422(04)00907-X.
https://doi.org/https://doi.org/10.1016/...
,1313. Defazio G. The epidemiology of primary dystonia: current evidence and perspectives. Eur J Neurol. 2010;17 Suppl 1:9-14. PMID: 20590802; https://doi.org/10.1111/j.1468-1331.2010.03053.x.
https://doi.org/https://doi.org/10.1111/...
Antagonistically, hypokinetic syndromes, for which the prototype is Parkinson’s disease, are characterized by slowness and decreased voluntary movements (bradykinesia/akinesia), in addition to muscle stiffness, resting tremor and postural instability.1111. Siemers E, Reddy V. Profile of patients enrolled in a new movement disorder clinic. Mov Disord. 1991;6(4):336-41. PMID: 1758452; https://doi.org/10.1002/mds.870060412.
https://doi.org/https://doi.org/10.1002/...
,1212. Defazio G, Abbruzzese G, Livrea P, Berardelli A. Epidemiology of primary dystonia. Lancet Neurol. 2004;3(11):673-8. PMID: 15488460; doi: https://doi.org/10.1016/S1474-4422(04)00907-X.
https://doi.org/https://doi.org/10.1016/...
,1313. Defazio G. The epidemiology of primary dystonia: current evidence and perspectives. Eur J Neurol. 2010;17 Suppl 1:9-14. PMID: 20590802; https://doi.org/10.1111/j.1468-1331.2010.03053.x.
https://doi.org/https://doi.org/10.1111/...
This group also includes other parkinsonian syndromes, such as progressive supranuclear palsy (PSP), multiple system atrophy (MSA), corticobasal degeneration and vascular and drug-induced secondary parkinsonism.1414. Fahn S, Jankovic J, Hallett M. Principles and practice of movement disorders. 2nd ed. New York: Saunders; 2011.

Parkinson’s disease is considered to be the second most common degenerative disorder after Alzheimer’s disease.1515. Louis ED, Thawani SP, Andrews HF. Prevalence of essential tremor in a multiethnic, community-based study in northern Manhattan, New York, N.Y. Neuroepidemiology. 2009;32(3):208-14. PMID: 19169043; https://doi.org/10.1159/000195691.
https://doi.org/https://doi.org/10.1159/...
Although its etiology is not yet well defined, it is characterized by degeneration of dopaminergic neurons in the nigrostriatal system of the basal nuclei.1616. Rodríguez-Violante M, Cervantes-Arriaga A, Morales-Briceño H, et al. Prevalencia de parkinsonismos atípicos en la clínica de trastornos del movimiento de un hospital de referencia de la Ciudad de México. Rev Mex Neuroci. 2012;13(6):296-300. Available from: Available from: https://www.medigraphic.com/pdfs/revmexneu/rmn-2012/rmn126b.pdf . Accessed in 2020 (May 14).
https://www.medigraphic.com/pdfs/revmexn...
The prevalence of Parkinson’s disease in the general population has been estimated to be 0.3%,1717. Colosimo C, Morgante L, Antonini A, et al. Non-motor symptoms in atypical and secondary parkinsonism: the PRIAMO study. J Neurol. 2010;257(1):5-14. PMID: 19669613; https://doi.org/10.1007/s00415-009-5255-7.
https://doi.org/https://doi.org/10.1007/...
such that it affects approximately 1% of individuals over 60 years of age1515. Louis ED, Thawani SP, Andrews HF. Prevalence of essential tremor in a multiethnic, community-based study in northern Manhattan, New York, N.Y. Neuroepidemiology. 2009;32(3):208-14. PMID: 19169043; https://doi.org/10.1159/000195691.
https://doi.org/https://doi.org/10.1159/...
,1616. Rodríguez-Violante M, Cervantes-Arriaga A, Morales-Briceño H, et al. Prevalencia de parkinsonismos atípicos en la clínica de trastornos del movimiento de un hospital de referencia de la Ciudad de México. Rev Mex Neuroci. 2012;13(6):296-300. Available from: Available from: https://www.medigraphic.com/pdfs/revmexneu/rmn-2012/rmn126b.pdf . Accessed in 2020 (May 14).
https://www.medigraphic.com/pdfs/revmexn...
,1717. Colosimo C, Morgante L, Antonini A, et al. Non-motor symptoms in atypical and secondary parkinsonism: the PRIAMO study. J Neurol. 2010;257(1):5-14. PMID: 19669613; https://doi.org/10.1007/s00415-009-5255-7.
https://doi.org/https://doi.org/10.1007/...
and 4% to 5% of those over 85 years of age.1515. Louis ED, Thawani SP, Andrews HF. Prevalence of essential tremor in a multiethnic, community-based study in northern Manhattan, New York, N.Y. Neuroepidemiology. 2009;32(3):208-14. PMID: 19169043; https://doi.org/10.1159/000195691.
https://doi.org/https://doi.org/10.1159/...

Progressive supranuclear palsy is considered to be the second most common form within the range of parkinsonian syndromes. Its incidence is approximately 5.3 cases per 100,000 people between 50 and 99 years old, and its prevalence ranges from 4.9 to 6.5/100,000.1818. Benito-León J, Bermejo-Pareja F, Rodríguez J, et al. Prevalence of PD and other types of parkinsonism in three elderly populations of central Spain. Mov Disord. 2003;18(3):267-74. PMID: 12621629; https://doi.org/10.1002/mds.10362.
https://doi.org/https://doi.org/10.1002/...
Another example of parkinsonian syndrome is MSA, with an estimated incidence of 0.6 cases per 100,000 people, and a prevalence of 1.86-4/100,000, although there are few published studies on this.1515. Louis ED, Thawani SP, Andrews HF. Prevalence of essential tremor in a multiethnic, community-based study in northern Manhattan, New York, N.Y. Neuroepidemiology. 2009;32(3):208-14. PMID: 19169043; https://doi.org/10.1159/000195691.
https://doi.org/https://doi.org/10.1159/...
,1919. Savica R, Grossardt BR, Bower JH, et al. Incidence and time trends of drug-induced parkinsonism: A 30-year population-based study. Mov Disord. 2017;32(2):227-34. PMID: 27779780; https://doi.org/10.1002/mds.26839.
https://doi.org/https://doi.org/10.1002/...
Additionally, several other movement disorder-related diagnoses exist, thus highlighting the importance of evaluating their behavior.

These data are necessary for evaluating neurological institutions and services, and are important for identifying risk factors and geographical differences that might influence the development of treatment strategies. Knowledge of the characteristics and prevalence of diagnoses in this environment is required, in order to make comparisons with studies published previously.

OBJECTIVE

The objective of this study was to outline the frequencies of the different diagnoses seen among patients, along with their demographic characteristics, at the movement disorders outpatient clinic of a state public hospital, in São Paulo (SP), Brazil, and to highlight the clinical aspects of those with Parkinson’s disease.

METHODS

This study consisted of a retrospective descriptive epidemiological review of data obtained from the medical records of patients seen at the neurology outpatient clinic specializing in movement disorders in a state public hospital, in São Paulo, Brazil. The medical records were searched based on a survey of patients with scheduled appointments who were seen at the movement disorders outpatient clinic. The analysis period comprised four years, starting from December 2009, when an electronic appointment scheduling system was implemented. The data were collected after the study protocol had been approved by an Internal Review Board (Ethics Committee) on May 13, 2014 (number 668.444/ CAAE: 305294 14.6.0000.5463) and had been authorized by the person in charge of the Medical Archive and Statistics Service (SAME).

Analysis on the medical records was previously authorized and scheduled as a maximum number of 20 medical records per day. The records were analyzed individually in the medical file sector of the state public hospital, by one of the doctors responsible for this research. The study exclusively included patients who had been diagnosed with movement disorders.

The patients’ diagnoses were recorded from the medical records. The clinical evolution of the anamnesis and neurological examination were analyzed based on the diagnostic criteria. This information was described by neurology specialists in the movement disorder department. The entire procedure was supervised by chief neurologists.

The following demographic data were collected: age, sex, skin color, profession and marital status. In addition, correlations of the following relationships were assessed: “clinical diagnosis versus age”; and “clinical diagnosis versus sex”.

Considering that the most frequent etiology would be Parkinson’s disease, the following clinical characteristics were evaluated: initial symptoms, clinical form of the disease, freezing of gait and postural instability within the first five years of the disease. In addition, the following clinical correlations were considered: “clinical form versus age”; and “clinical form versus freezing of gait and postural instability”.

The retrospective nature of this study was characterized as a limitation, considering that there was therefore a possibility of missing information. It is important to highlight that when information was not explicitly reported, these data were classified as not described (ND). Patients who did not have a defined etiological diagnosis due to lack of follow-up at the clinic or insufficient information were classified as “unspecified”.

The data were expressed as absolute and relative frequencies for adequate statistical treatments. The chi-square and Fisher’s exact tests were applied, depending on the distribution of values in the groups. The Stata statistical software, version 13.1, (StataCorp, 2013: Stata Statistical Software, Release 13; College Station, TX, United States) was used in all analyses and the confidence level was set at 95%, i.e. a P-value < 0.05 was considered significant. It is important to note that, when the total number of cases evaluated that were described as “ND” was less than 10%, these were not considered in the study because they were not statistically significant.

RESULTS

Out of the 790 medical records analyzed, 680 were selected because they involved a diagnosis of movement disorders. Of these, 277 records included a diagnosis of Parkinson’s disease. Thus, in order to demonstrate the analysis more clearly, the results are presented in two stages: (1) Parkinson’s disease analysis; and (2) diagnoses of other movement disorders.

Parkinson’s disease

We observed higher occurrence of the mixed clinical form of Parkinson’s disease, which was present in 77.6% of all of these patients. The tremulous (TREM) and akinetic-rigid (AR) forms accounted for 18.4% of the case, and the other 4% of the medical records of Parkinson’s disease did not specify the form. The most common initial symptom reported by the patient was tremor. It is important to emphasize that the diagnoses of postural instability and freezing of gait were not present in the first five years of follow-up, as described in Table 1.

Table 1.
Distribution of patients with Parkinson’s disease treated in the movement disorders outpatient clinic of a state public hospital, São Paulo (SP), 2017

The Parkinson’s disease analysis showed that 66.7% of the patients above 61 years of age were diagnosed with the mixed form, and 71.4% of the patients below 61 years were diagnosed with the AR form. In 46.1 of the patients with the TREM form, the onset was when they were above 71 years old.

Table 2 shows that there was an association between early diagnosis and the AR form. We found that the older the patient was at diagnosis, the greater the probability of occurrence of the mixed and TREM forms was.

Table 2.
Analysis of the association between the clinical form of Parkinson’s disease and age at diagnosis, postural instability and freezing of gait among patients diagnosed with Parkinson’s disease who were treated at the movement disorders outpatient clinic of a state public hospital, São Paulo (SP), 2017

No individual with the TREM form in our sample presented postural instability and freezing of gait within the first five years of the disease. This characteristic was also observed in most patients with the mixed form. Furthermore, there was higher relative frequency of instability and freezing of gait among individuals with the AR form, thus indicating less favorable conditions for those patients.

The results from this analysis were compared with studies in the literature. This demonstrated that similar methodologies had been used to study Parkinson’s disease in different parts of the world. The frequencies of occurrence described in previously published reports55. Ribosa-Nogué R, Gironell A, Pagonabarraga J, et al. Análisis descriptivo de la actividad de una unidad de trastornos del movimiento en un hospital terciario de Cataluña [Descriptive analysis of the activity in a movement disorder unit in a tertiary hospital in Catalonia]. Rev Neurol. 2012;55(6):330-6. PMID: 22972574.,66. Bower JH, Teshome M, Melaku Z, Zenebe G. Frequency of movement disorders in an Ethiopian university practice. Mov Disord. 2005;20(9):1209-13. PMID: 15954128; https://doi.org/10.1002/mds.20567.
https://doi.org/https://doi.org/10.1002/...
,1111. Siemers E, Reddy V. Profile of patients enrolled in a new movement disorder clinic. Mov Disord. 1991;6(4):336-41. PMID: 1758452; https://doi.org/10.1002/mds.870060412.
https://doi.org/https://doi.org/10.1002/...
,1414. Fahn S, Jankovic J, Hallett M. Principles and practice of movement disorders. 2nd ed. New York: Saunders; 2011. suggested that Parkinson’s disease was the most common cause of movement disorders in the entire population studied, which was consistent with the results from our analysis. However, an increasing number of secondary and atypical diagnoses of parkinsonism exist and need to be considered. Consequently, an analysis of other movement disorder diagnoses is presented in the following section, in detail.

Analysis on other movement disorder diagnoses

The results from the analysis on the data collected during the study period showed that the most frequent diagnoses were Parkinson’s disease (40.7%), essential tremor (15.4%) and dystonia (13.1%). The remaining diagnoses accounted for 33.6% of the cases. The frequencies of syndromic and etiological diagnoses of movement disorders are described in Table 3. The pattern shown in Table 3 was also observed in several similar studies conducted in other regions,55. Ribosa-Nogué R, Gironell A, Pagonabarraga J, et al. Análisis descriptivo de la actividad de una unidad de trastornos del movimiento en un hospital terciario de Cataluña [Descriptive analysis of the activity in a movement disorder unit in a tertiary hospital in Catalonia]. Rev Neurol. 2012;55(6):330-6. PMID: 22972574.,66. Bower JH, Teshome M, Melaku Z, Zenebe G. Frequency of movement disorders in an Ethiopian university practice. Mov Disord. 2005;20(9):1209-13. PMID: 15954128; https://doi.org/10.1002/mds.20567.
https://doi.org/https://doi.org/10.1002/...
,1010. Vázquez-Alén P, Pérez-Gilabert Y, Mateo D, Giménez-Roldán S. Estudio sobre una base de datos de 2.471 pacientes con enfermedad de Parkinson y trastornos del movimiento en el Área Sanitaria 1 de la Comunidad de Madrid. Cambios demográficos observados a lo largo de ocho años [A study made on a data base of 2,471 patients with Parkinson disease and disorders of movement in Health District 1 of the autonomous region of Madrid. Observed demographic changes over 8 year-period]. Rev Neurol. 2000;30(7):635-40. PMID: 10859741.,1111. Siemers E, Reddy V. Profile of patients enrolled in a new movement disorder clinic. Mov Disord. 1991;6(4):336-41. PMID: 1758452; https://doi.org/10.1002/mds.870060412.
https://doi.org/https://doi.org/10.1002/...
,1212. Defazio G, Abbruzzese G, Livrea P, Berardelli A. Epidemiology of primary dystonia. Lancet Neurol. 2004;3(11):673-8. PMID: 15488460; doi: https://doi.org/10.1016/S1474-4422(04)00907-X.
https://doi.org/https://doi.org/10.1016/...
,1313. Defazio G. The epidemiology of primary dystonia: current evidence and perspectives. Eur J Neurol. 2010;17 Suppl 1:9-14. PMID: 20590802; https://doi.org/10.1111/j.1468-1331.2010.03053.x.
https://doi.org/https://doi.org/10.1111/...
including the study by Bhidayasiri et al.77. Bhidayasiri R, Saksornchai K, Kaewwilai L, Phanthumchinda K. A census of movement disorders at a Thai university hospital. J Neurol Sci. 2011;301(1-2):31-4. PMID: 21131010; https://doi.org/10.1016/j.jns.2010.11.010.
https://doi.org/https://doi.org/10.1016/...
and a study at the Columbia University Medical Center in conjunction with the Baylor College of Medicine, in which approximately 43,000 patients were analyzed.1414. Fahn S, Jankovic J, Hallett M. Principles and practice of movement disorders. 2nd ed. New York: Saunders; 2011.

Table 3.
Frequencies of diagnoses among patients treated in the movement disorders outpatient clinic of a state public hospital, São Paulo (SP), 2017

In our study, a diagnosis of parkinsonism was described in 336 records, of which 81.7% were attributed to Parkinson’s disease. The other diagnoses included 9.1% with no defined etiology, which was classified as unspecified parkinsonism. Out of that total, 5.6% were diagnosed with drug-induced (n = 11) and vascular (n = 8) secondary parkinsonism. Atypical parkinsonism had an incidence of 3.5%, consisting of Lewy body disease (LBD) (n = 4), multiple system atrophy (n = 4) and progressive supranuclear palsy (n = 4).

The second most frequent pathological condition documented in the present study was 97 cases of essential tremor, which is one of the most common diagnoses in neurology outpatient clinics, often surpassing the number of Parkinson’s disease cases. Its worldwide prevalence is widely variable, with descriptions ranging from one to more than 200 cases per 1,000 individuals.1515. Louis ED, Thawani SP, Andrews HF. Prevalence of essential tremor in a multiethnic, community-based study in northern Manhattan, New York, N.Y. Neuroepidemiology. 2009;32(3):208-14. PMID: 19169043; https://doi.org/10.1159/000195691.
https://doi.org/https://doi.org/10.1159/...
Other etiologies for tremor were found in 31.2% of the cases. These cases included the following types: unspecified (n = 26), drug-induced (n = 4), others represented by a specific writing task (n = 3), Holmes (n = 2), orthostatic (n = 1) and psychogenic (n = 8).

Dystonia, which had the highest incidence, is a frequent condition reported in most studies,55. Ribosa-Nogué R, Gironell A, Pagonabarraga J, et al. Análisis descriptivo de la actividad de una unidad de trastornos del movimiento en un hospital terciario de Cataluña [Descriptive analysis of the activity in a movement disorder unit in a tertiary hospital in Catalonia]. Rev Neurol. 2012;55(6):330-6. PMID: 22972574.,88. Das SK, Ghosh B, Das G, Biswas A, Ray J. Movement disorders: Indian scenario: a clinico-genetic review. Neurol India. 2013;61(5):457-66. PMID: 24262445; https://doi.org/10.4103/0028-3886.121908.
https://doi.org/https://doi.org/10.4103/...
and was diagnosed in 89 cases in our study, all corresponding to primary dystonia. Table 4 shows the classification of primary dystonia according to anatomical location. Out of the total number of cases analyzed, 78 were focal, four were generalized and six were segmental dystonia. The focal dystonia cases accounted for 37.2% and corresponded to the cervical type, followed by 23.1% with writer’s cramps, 17.9% each for upper-limb and blepharospasm cases and 3.8% for oromandibular cases.

Table 4.
Demographic characteristics of patients treated at the movement disorders outpatient clinic of a state public hospital, São Paulo (SP), 2017

The presence of dystonia has also been reported in the literature, at rates ranging from 2-50 cases per million (early onset dystonia) to 30-7,320 cases per million (late onset dystonia). This reflects the need for new epidemiological studies such as the present one.1212. Defazio G, Abbruzzese G, Livrea P, Berardelli A. Epidemiology of primary dystonia. Lancet Neurol. 2004;3(11):673-8. PMID: 15488460; doi: https://doi.org/10.1016/S1474-4422(04)00907-X.
https://doi.org/https://doi.org/10.1016/...
,1313. Defazio G. The epidemiology of primary dystonia: current evidence and perspectives. Eur J Neurol. 2010;17 Suppl 1:9-14. PMID: 20590802; https://doi.org/10.1111/j.1468-1331.2010.03053.x.
https://doi.org/https://doi.org/10.1111/...
According to the published reports, the occurrence rate has not changed over the years. Siemers and Reddy1111. Siemers E, Reddy V. Profile of patients enrolled in a new movement disorder clinic. Mov Disord. 1991;6(4):336-41. PMID: 1758452; https://doi.org/10.1002/mds.870060412.
https://doi.org/https://doi.org/10.1002/...
reported dystonia in 17% of their movement disorder cases, which was a higher prevalence than that of their tremor cases (12%).

In the present study, chorea was present in 2.4% of the cases, Huntington’s disease accounted for 1% of the cases and other forms such as vascular, Huntington-like type 2 and unspecified chorea totaled 1.4%. Ataxia had an occurrence of 1.1%, and the diagnoses of restless leg syndrome, tardive dyskinesia and tics represented 4.1% in our sample.

The demographic data, described in Table 4, showed that 58.4% of the patients were female and 41.6% were male. There was greatest frequency (31.3%) of the 71 to 80-year age group, followed by 61 to 70 years (25.7%) and above 80 years (21.5%). We found that 84.8% of the patient sample self-identified as white, and 64.4% were married. The most frequent professional activity was as a teacher (16.2%), followed by housewife/husband (11.8%) and general service assistant (2.2%). However, 35.9% of the medical records did not have any information on professional activity.

Both sexes exhibited high frequency of parkinsonism, followed by tremor. However, proportionally higher frequencies of restless leg syndrome (76.9%), dystonia (73%) and myoclonus (65.6%) were present in female patients, while tic (60%) and tardive dyskinesia (60 %) were more common in males. Parkinsonism had similar distribution between the male and female groups, as described in Table 5, which shows absolute and relative values.

Table 5.
Distribution of movement disorder patients according to sex and age, São Paulo (SP), 2017

The distribution of the diagnoses according to age group revealed a statistical difference between the groups listed. Parkinsonism was more frequent in the age groups above 60 years, while dystonia showed higher frequency in individuals aged 60 years or less. The other syndromes had uniform distribution, or were highly influenced by low sample sizes in the groups, e.g. the distribution of ataxia. These analyses are described in Table 5.

DISCUSSION

Neuroepidemiology aims to determine the presence of neurological diseases in the population and acts as an instrument for healthcare planning and improvement. This has undergone increasing changes due to increases in life expectancy.

The retrospective use of medical records for data collection (included missing or incomplete data) was a limitation of this study. This can be explained in terms of difficulty in interpreting the documented information and variability in the quality of documentation among professionals. However, the most important information for the purpose of this study was indeed documented, i.e. the final diagnosis and clinical details.

This study demonstrated that high frequency of Parkinson’s disease was present. A previous study conducted in Brazil indicated that the incidence of this pathological condition was 68.9% among a total of 338 patients,2020. Cardoso F, Camargos ST, Silva Júnior GA. Etiology of parkinsonism in a Brazilian movement disorders clinic. Arq Neuropsiquiatr. 1998;56(2):171-5. PMID: 9698723; https://doi.org/10.1590/s0004-282x1998000200001.
https://doi.org/https://doi.org/10.1590/...
a result that was similar to ours. Other studies have indicated high incidence of this diagnosis, in several countries, such as Thailand,77. Bhidayasiri R, Saksornchai K, Kaewwilai L, Phanthumchinda K. A census of movement disorders at a Thai university hospital. J Neurol Sci. 2011;301(1-2):31-4. PMID: 21131010; https://doi.org/10.1016/j.jns.2010.11.010.
https://doi.org/https://doi.org/10.1016/...
Spain,1010. Vázquez-Alén P, Pérez-Gilabert Y, Mateo D, Giménez-Roldán S. Estudio sobre una base de datos de 2.471 pacientes con enfermedad de Parkinson y trastornos del movimiento en el Área Sanitaria 1 de la Comunidad de Madrid. Cambios demográficos observados a lo largo de ocho años [A study made on a data base of 2,471 patients with Parkinson disease and disorders of movement in Health District 1 of the autonomous region of Madrid. Observed demographic changes over 8 year-period]. Rev Neurol. 2000;30(7):635-40. PMID: 10859741.,1818. Benito-León J, Bermejo-Pareja F, Rodríguez J, et al. Prevalence of PD and other types of parkinsonism in three elderly populations of central Spain. Mov Disord. 2003;18(3):267-74. PMID: 12621629; https://doi.org/10.1002/mds.10362.
https://doi.org/https://doi.org/10.1002/...
United States,1111. Siemers E, Reddy V. Profile of patients enrolled in a new movement disorder clinic. Mov Disord. 1991;6(4):336-41. PMID: 1758452; https://doi.org/10.1002/mds.870060412.
https://doi.org/https://doi.org/10.1002/...
Mexico,1616. Rodríguez-Violante M, Cervantes-Arriaga A, Morales-Briceño H, et al. Prevalencia de parkinsonismos atípicos en la clínica de trastornos del movimiento de un hospital de referencia de la Ciudad de México. Rev Mex Neuroci. 2012;13(6):296-300. Available from: Available from: https://www.medigraphic.com/pdfs/revmexneu/rmn-2012/rmn126b.pdf . Accessed in 2020 (May 14).
https://www.medigraphic.com/pdfs/revmexn...
India,88. Das SK, Ghosh B, Das G, Biswas A, Ray J. Movement disorders: Indian scenario: a clinico-genetic review. Neurol India. 2013;61(5):457-66. PMID: 24262445; https://doi.org/10.4103/0028-3886.121908.
https://doi.org/https://doi.org/10.4103/...
Denmark2121. Wermuth L, Lassen CF, Himmerslev L, Olsen J, Ritz B. Validation of hospital register-based diagnosis of Parkinson’s disease. Dan Med J. 2012;59(3):A4391. PMID: 22381086. and Brazil.2020. Cardoso F, Camargos ST, Silva Júnior GA. Etiology of parkinsonism in a Brazilian movement disorders clinic. Arq Neuropsiquiatr. 1998;56(2):171-5. PMID: 9698723; https://doi.org/10.1590/s0004-282x1998000200001.
https://doi.org/https://doi.org/10.1590/...
,2222. Silva EG, Viana MA, Quagliato EMAB. Diagnóstico de síndromes parkinsonianas em uma clínica brasileira de distúrbios do movimento. Rev Neurociências. 2005;13(4):173-7. Available from: Available from: http://www.revistaneurociencias.com.br/edicoes/2005/RN%2013%2004/Pages%20from%20RN%2013%2004.pdf . Accessed in 2020 (May 14).
http://www.revistaneurociencias.com.br/e...
,2323. Barbosa MT, Caramelli P, Maia DP, et al. Parkinsonism and Parkinson’s disease in the elderly: a community-based survey in Brazil (the Bambuí study). Mov Disord. 2006;21(6):800-8. PMID: 16482566; https://doi.org/10.1002/mds.20806.
https://doi.org/https://doi.org/10.1002/...

In contrast, other research showed lower prevalences in Africa,2424. Okubadejo NU, Bower JH, Rocca WA, Maraganore DM. Parkinson’s disease in Africa: A systematic review of epidemiologic and genetic studies. Mov Disord. 2006;21(12):2150-6. PMID: 17044056; https://doi.org/10.1002/mds.21153.
https://doi.org/https://doi.org/10.1002/...
China2525. Ma CL, Su L, Xie JJ, et al. The prevalence and incidence of Parkinson’s disease in China: a systematic review and meta-analysis. J Neural Transm (Vienna). 2014;121(2):123-34. PMID: 24057652; https://doi.org/10.1007/s00702-013-1092-z.
https://doi.org/https://doi.org/10.1007/...
and some countries in Latin America, such as Argentina2626. Melcon MO, Anderson DW, Vergara RH, Rocca WA. Prevalence of Parkinson’s disease in Junín, Buenos Aires Province, Argentina. Mov Disord. 1997;12(2):197-205. PMID: 9087978; https://doi.org/10.1002/mds.870120210.
https://doi.org/https://doi.org/10.1002/...
and Bolivia,2727. Nicoletti A, Sofia V, Bartoloni A, et al. Prevalence of Parkinson’s disease: a door-to-door survey in rural Bolivia. Parkinsonism Relat Disord. 2003;10(1):19-21. PMID: 14499202; https://doi.org/10.1016/s1353-8020(03)00066-x.
https://doi.org/https://doi.org/10.1016/...
compared with developed countries, especially in Europe. The demographic factors in this study showed that there was slight predominance among females, with an F:M ratio of approximately 1.03. On the contrary, other published reports have shown higher prevalence among males.2222. Silva EG, Viana MA, Quagliato EMAB. Diagnóstico de síndromes parkinsonianas em uma clínica brasileira de distúrbios do movimento. Rev Neurociências. 2005;13(4):173-7. Available from: Available from: http://www.revistaneurociencias.com.br/edicoes/2005/RN%2013%2004/Pages%20from%20RN%2013%2004.pdf . Accessed in 2020 (May 14).
http://www.revistaneurociencias.com.br/e...
,2626. Melcon MO, Anderson DW, Vergara RH, Rocca WA. Prevalence of Parkinson’s disease in Junín, Buenos Aires Province, Argentina. Mov Disord. 1997;12(2):197-205. PMID: 9087978; https://doi.org/10.1002/mds.870120210.
https://doi.org/https://doi.org/10.1002/...

Parkinson’s disease may be classified into three clinical forms: tremulous, akinetic-rigid and mixed. As indicated in this study, the mixed form is considered to be most frequent. This conclusion is corroborated by results found in other published studies.1414. Fahn S, Jankovic J, Hallett M. Principles and practice of movement disorders. 2nd ed. New York: Saunders; 2011.,2828. Rajput AH, Voll A, Rajput ML, Robinson CA, Rajput A. Course in Parkinson disease subtypes: A 39-year clinicopathologic study. Neurology. 2009;73(3):206-12. PMID: 19620608; https://doi.org/10.1212/WNL.0b013e3181ae7af1.
https://doi.org/https://doi.org/10.1212/...
,2929. Rajput AH, Rajput ML, Ferguson W, Rajput A. Baseline motor findings and Parkinson disease prognostic subtypes. Neurology. 2017;89(2):138-43. PMID: 28592451; https://doi.org/10.1212/WNL.0000000000004078.
https://doi.org/https://doi.org/10.1212/...
In our study, the clinical forms were correlated with age, and we showed that most patients presenting the tremulous form (84.6%) were over 60 years of age, thus confirming the results of Pagano et al.3030. Pagano G, Ferrara N, Brooks DJ, Pavese N. Age at onset and Parkinson disease phenotype. Neurology. 2016;86(15):1400-7. PMID: 26865518; https://doi.org/10.1212/WNL.0000000000002461.
https://doi.org/https://doi.org/10.1212/...
Approximately 71.4% of the patients with the akinetic-rigid form were diagnosed under the age of 60 years. Previous reports have demonstrated biological differences between the clinical forms of Parkinson’s disease.1414. Fahn S, Jankovic J, Hallett M. Principles and practice of movement disorders. 2nd ed. New York: Saunders; 2011.,3131. Marras C, Chaudhuri KR. Nonmotor features of Parkinson’s disease subtypes. Mov Disord. 2016;31(8):1095-102. PMID: 26861861; https://doi.org/10.1002/mds.26510.
https://doi.org/https://doi.org/10.1002/...

Resting tremor was reported in this study, in 60.3% of the patients at the onset of the disease. It is considered to be the most frequent initial symptom in the mixed and tremulous forms.2929. Rajput AH, Rajput ML, Ferguson W, Rajput A. Baseline motor findings and Parkinson disease prognostic subtypes. Neurology. 2017;89(2):138-43. PMID: 28592451; https://doi.org/10.1212/WNL.0000000000004078.
https://doi.org/https://doi.org/10.1212/...
Delval et al.3232. Delval A, Rambour M, Tard C, et al. Freezing/festination during motor tasks in early-stage Parkinson’s disease: A prospective study. Mov Disord. 2016;31(12):1837-45. PMID: 27618808; https://doi.org/10.1002/mds.26762.
https://doi.org/https://doi.org/10.1002/...
showed that 27% of the patients analyzed in their study presented with a history of freezing of gait at the first evaluation, with a considerable increase observed eight years after the initial diagnosis.3333. Forsaa EB, Larsen JP, Wentzel-Larsen T, Alves G. A 12-year population-based study of freezing of gait in Parkinson’s disease. Parkinsonism Relat Disord. 2015;21(3):254-8. PMID: 25603767; https://doi.org/10.1016/j.parkreldis.2014.12.020.
https://doi.org/https://doi.org/10.1016/...
Other published reports confirmed the results from this study, thus suggesting that freezing of gait occurs with higher frequency in the akinetic-rigid form of the disease.3232. Delval A, Rambour M, Tard C, et al. Freezing/festination during motor tasks in early-stage Parkinson’s disease: A prospective study. Mov Disord. 2016;31(12):1837-45. PMID: 27618808; https://doi.org/10.1002/mds.26762.
https://doi.org/https://doi.org/10.1002/...

As previously stated, the most frequent diagnosis in our study was Parkinson’s disease. However, increasing numbers of cases of secondary and atypical parkinsonism cases are common. This result was found in a previously published study,77. Bhidayasiri R, Saksornchai K, Kaewwilai L, Phanthumchinda K. A census of movement disorders at a Thai university hospital. J Neurol Sci. 2011;301(1-2):31-4. PMID: 21131010; https://doi.org/10.1016/j.jns.2010.11.010.
https://doi.org/https://doi.org/10.1016/...
which showed that vascular parkinsonism was the second most frequent cause (4.9%), and that multiple system atrophy (MSA) and Lewy body disease (LBD) were the most common atypical parkinsonian syndromes (drug-induced parkinsonism was not found). However, studies in other countries have shown different patterns, depending on the region studied. Rodríguez-Violante et al.1616. Rodríguez-Violante M, Cervantes-Arriaga A, Morales-Briceño H, et al. Prevalencia de parkinsonismos atípicos en la clínica de trastornos del movimiento de un hospital de referencia de la Ciudad de México. Rev Mex Neuroci. 2012;13(6):296-300. Available from: Available from: https://www.medigraphic.com/pdfs/revmexneu/rmn-2012/rmn126b.pdf . Accessed in 2020 (May 14).
https://www.medigraphic.com/pdfs/revmexn...
evaluated 647 patients in Mexico, among whom 46 were diagnosed with parkinsonism (atypical and secondary), representing 7.1% of a sample in which the most frequent diagnoses were vascular parkinsonism, progressive supranuclear palsy (PSP) and Lewy body disease.

Colosimo et al.1717. Colosimo C, Morgante L, Antonini A, et al. Non-motor symptoms in atypical and secondary parkinsonism: the PRIAMO study. J Neurol. 2010;257(1):5-14. PMID: 19669613; https://doi.org/10.1007/s00415-009-5255-7.
https://doi.org/https://doi.org/10.1007/...
conducted a longitudinal retrospective analysis on data from the PRIAMO study in Italy, in which 1,307 patients were diagnosed as presenting atypical and secondary parkinsonism. Among these, 6.4% had vascular parkinsonism, 2.6% MSA, 2.3% PSP, 1.1% LBD and 0.8% corticobasal degeneration (a diagnosis not present in the present study). Nevertheless, in a similar study conducted in Spain to evaluate the older population, it was reported that the most frequent etiologies were drug-induced and vascular parkinsonism.1818. Benito-León J, Bermejo-Pareja F, Rodríguez J, et al. Prevalence of PD and other types of parkinsonism in three elderly populations of central Spain. Mov Disord. 2003;18(3):267-74. PMID: 12621629; https://doi.org/10.1002/mds.10362.
https://doi.org/https://doi.org/10.1002/...

Those etiologies were also present in other recent studies. Savica et al.1919. Savica R, Grossardt BR, Bower JH, et al. Incidence and time trends of drug-induced parkinsonism: A 30-year population-based study. Mov Disord. 2017;32(2):227-34. PMID: 27779780; https://doi.org/10.1002/mds.26839.
https://doi.org/https://doi.org/10.1002/...
reported that out of 906 cases of parkinsonism in the United States, 11.9% corresponded to the drug-induced form, a result that differed from the present study. However, a review of previously published surveys conducted in Brazil showed predominance of secondary drug-induced and vascular parkinsonism.2020. Cardoso F, Camargos ST, Silva Júnior GA. Etiology of parkinsonism in a Brazilian movement disorders clinic. Arq Neuropsiquiatr. 1998;56(2):171-5. PMID: 9698723; https://doi.org/10.1590/s0004-282x1998000200001.
https://doi.org/https://doi.org/10.1590/...
,2222. Silva EG, Viana MA, Quagliato EMAB. Diagnóstico de síndromes parkinsonianas em uma clínica brasileira de distúrbios do movimento. Rev Neurociências. 2005;13(4):173-7. Available from: Available from: http://www.revistaneurociencias.com.br/edicoes/2005/RN%2013%2004/Pages%20from%20RN%2013%2004.pdf . Accessed in 2020 (May 14).
http://www.revistaneurociencias.com.br/e...
Notably, some of the studies mentioned above have presented considerable numbers of parkinsonism cases of undetermined etiology, thus emphasizing the need for standardization of clinical evaluations and for possible use of supplementary examinations for better etiological definition.

Hemifacial spasm is characterized by segmental facial myoclonus, which was the fourth most common diagnosis found in the present study. A previously published report by Batla et al.3434. Batla A, Goyal C, Shukla G, et al. Hemifacial spasm: clinical characteristics of 321 Indian patients. J Neurol. 2012;259(8):1561-5. PMID: 22222858; https://doi.org/10.1007/s00415-011-6376-3.
https://doi.org/https://doi.org/10.1007/...
showed that the incidence of this condition was 7% in India. Other surveys conducted in the cities of Barcelona and Madrid indicated that the incidence of hemifacial spasm was 1.8% and 5%, respectively.55. Ribosa-Nogué R, Gironell A, Pagonabarraga J, et al. Análisis descriptivo de la actividad de una unidad de trastornos del movimiento en un hospital terciario de Cataluña [Descriptive analysis of the activity in a movement disorder unit in a tertiary hospital in Catalonia]. Rev Neurol. 2012;55(6):330-6. PMID: 22972574.,1010. Vázquez-Alén P, Pérez-Gilabert Y, Mateo D, Giménez-Roldán S. Estudio sobre una base de datos de 2.471 pacientes con enfermedad de Parkinson y trastornos del movimiento en el Área Sanitaria 1 de la Comunidad de Madrid. Cambios demográficos observados a lo largo de ocho años [A study made on a data base of 2,471 patients with Parkinson disease and disorders of movement in Health District 1 of the autonomous region of Madrid. Observed demographic changes over 8 year-period]. Rev Neurol. 2000;30(7):635-40. PMID: 10859741. Although hemifacial spasm is a common complaint in neurology outpatient clinics, its frequency does not differ significantly from that of other extrapyramidal diseases.55. Ribosa-Nogué R, Gironell A, Pagonabarraga J, et al. Análisis descriptivo de la actividad de una unidad de trastornos del movimiento en un hospital terciario de Cataluña [Descriptive analysis of the activity in a movement disorder unit in a tertiary hospital in Catalonia]. Rev Neurol. 2012;55(6):330-6. PMID: 22972574. This pattern was also observed in a study by Fahn et al.1414. Fahn S, Jankovic J, Hallett M. Principles and practice of movement disorders. 2nd ed. New York: Saunders; 2011. in the United States, which showed the same frequency of this pathological condition as found in the present study.

Our results for ataxia and chorea were similar to those in other published reports.66. Bower JH, Teshome M, Melaku Z, Zenebe G. Frequency of movement disorders in an Ethiopian university practice. Mov Disord. 2005;20(9):1209-13. PMID: 15954128; https://doi.org/10.1002/mds.20567.
https://doi.org/https://doi.org/10.1002/...
,77. Bhidayasiri R, Saksornchai K, Kaewwilai L, Phanthumchinda K. A census of movement disorders at a Thai university hospital. J Neurol Sci. 2011;301(1-2):31-4. PMID: 21131010; https://doi.org/10.1016/j.jns.2010.11.010.
https://doi.org/https://doi.org/10.1016/...
,1010. Vázquez-Alén P, Pérez-Gilabert Y, Mateo D, Giménez-Roldán S. Estudio sobre una base de datos de 2.471 pacientes con enfermedad de Parkinson y trastornos del movimiento en el Área Sanitaria 1 de la Comunidad de Madrid. Cambios demográficos observados a lo largo de ocho años [A study made on a data base of 2,471 patients with Parkinson disease and disorders of movement in Health District 1 of the autonomous region of Madrid. Observed demographic changes over 8 year-period]. Rev Neurol. 2000;30(7):635-40. PMID: 10859741.,1111. Siemers E, Reddy V. Profile of patients enrolled in a new movement disorder clinic. Mov Disord. 1991;6(4):336-41. PMID: 1758452; https://doi.org/10.1002/mds.870060412.
https://doi.org/https://doi.org/10.1002/...
However, one study in Ethiopia reported that the prevalence of ataxia was more than twice that of chorea, even surpassing the rate of diagnosing dystonia.66. Bower JH, Teshome M, Melaku Z, Zenebe G. Frequency of movement disorders in an Ethiopian university practice. Mov Disord. 2005;20(9):1209-13. PMID: 15954128; https://doi.org/10.1002/mds.20567.
https://doi.org/https://doi.org/10.1002/...
These results suggest that there was a lack of uniformity in the data for making this diagnosis.

Huntington’s disease has been described as the primary cause of genetic chorea, which is the most prevalent type of chorea. A study conducted in the city of São Paulo, Brazil, on 119 medical records from patients diagnosed with chorea showed that 79% of the samples corresponded to Sydenham’s chorea, Huntington’s disease and vascular chorea.3535. Mendes MF, de Andrade LA, Ferraz HB. Coréia. Análise clínica de 119 casos [Chorea: clinical correlates of 119 cases]. Arq Neuropsiquiatr. 1996;54(3):419-27. PMID: 9109986; https://doi.org/10.1590/s0004-282x1996000300010.
https://doi.org/https://doi.org/10.1590/...
Another study conducted in Brazil on the genetic causes of chorea showed that the incidence of Huntington’s disease was 89.4%, of which 3.8% were Huntington-like type II cases, which is the second most common cause of chorea.3636. Castilhos RM, Souza AF, Furtado GV, et al. Huntington disease and Huntington disease-like in a case series from Brazil. Clin Genet. 2014;86(4):373-7. PMID: 24102565; https://doi.org/10.1111/cge.12283.
https://doi.org/https://doi.org/10.1111/...
Vascular chorea was the second most common cause of non-genetic chorea in the present study, thus confirming the results of Piccolo et al.,3737. Piccolo I, Defanti CA, Soliveri P, et al. Cause and course in a series of patients with sporadic chorea. J Neurol. 2003;250(4):429-35. PMID: 12700907; https://doi.org/10.1007/s00415-003-1010-7.
https://doi.org/https://doi.org/10.1007/...
who reported that vascular chorea accounted for 41% of their cases in Italy.

The etiological classification of ataxias showed subtle predominance of spinocerebellar ataxia type 6 (SCA6), which has low prevalence in Brazil. This distribution differed from what has been reported in other countries, i.e. 30% prevalence in Australia, 28% in Japan and 15% in the United States.3838. Storey E, du Sart D, Shaw JH, et al. Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia. Am J Med Genet. 2000;95(4):351-7. PMID: 11186889; https://doi.org/10.1002/1096-8628(20001211)95:4<351::aid-ajmg10>3.0.co;2-r.
https://doi.org/https://doi.org/10.1002/...
In our study, SCA2 and SCA3 both had incidences of 12.5%. Despite the low frequency in our study, these etiologies are recognized as the most frequent types.3939. Trott A, Jardim LB, Ludwig HT, et al. Spinocerebellar ataxias in 114 Brazilian families: clinical and molecular findings. Clin Genet. 2006;70(2):173-6. PMID: 16879203; https://doi.org/10.1111/j.1399-0004.2006.00656.x.
https://doi.org/https://doi.org/10.1111/...
Similar results were also found in other studies.3838. Storey E, du Sart D, Shaw JH, et al. Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia. Am J Med Genet. 2000;95(4):351-7. PMID: 11186889; https://doi.org/10.1002/1096-8628(20001211)95:4<351::aid-ajmg10>3.0.co;2-r.
https://doi.org/https://doi.org/10.1002/...
,3939. Trott A, Jardim LB, Ludwig HT, et al. Spinocerebellar ataxias in 114 Brazilian families: clinical and molecular findings. Clin Genet. 2006;70(2):173-6. PMID: 16879203; https://doi.org/10.1111/j.1399-0004.2006.00656.x.
https://doi.org/https://doi.org/10.1111/...
,4040. Teive HA, Munhoz RP, Raskin S, Werneck LC. Spinocerebellar ataxia type 6 in Brazil. Arq Neuropsiquiatr. 2008;66(3B):691-4. PMID: 18949263; https://doi.org/10.1590/s0004-282x2008000500015.
https://doi.org/https://doi.org/10.1590/...

The diagnoses of tics and tardive dyskinesia were infrequent in our study, and also infrequent in other movement disorder outpatient clinics.55. Ribosa-Nogué R, Gironell A, Pagonabarraga J, et al. Análisis descriptivo de la actividad de una unidad de trastornos del movimiento en un hospital terciario de Cataluña [Descriptive analysis of the activity in a movement disorder unit in a tertiary hospital in Catalonia]. Rev Neurol. 2012;55(6):330-6. PMID: 22972574.,66. Bower JH, Teshome M, Melaku Z, Zenebe G. Frequency of movement disorders in an Ethiopian university practice. Mov Disord. 2005;20(9):1209-13. PMID: 15954128; https://doi.org/10.1002/mds.20567.
https://doi.org/https://doi.org/10.1002/...
,1111. Siemers E, Reddy V. Profile of patients enrolled in a new movement disorder clinic. Mov Disord. 1991;6(4):336-41. PMID: 1758452; https://doi.org/10.1002/mds.870060412.
https://doi.org/https://doi.org/10.1002/...
Fahn et al.1414. Fahn S, Jankovic J, Hallett M. Principles and practice of movement disorders. 2nd ed. New York: Saunders; 2011. reported that tics and Tourette’s syndrome together accounted for the diagnoses of 6.4% out of a total of 2,753 patients in the United States. Similar results were also found in another study conducted in Brazil.4141. Cardoso F, Veado CC, Oliveira JT. A Brazilian cohort of patients with Tourette’s syndrome. J Neurol Neurosurg Psychiatry. 1996;60(2):209-12. PMID: 8708658; https://doi.org/10.1136/jnnp.60.2.209.
https://doi.org/https://doi.org/10.1136/...

Lastly, the demographic characteristics reported in the present study corroborated what was observed in most studies in the literature. Females predominated among the diagnoses of ataxia,3939. Trott A, Jardim LB, Ludwig HT, et al. Spinocerebellar ataxias in 114 Brazilian families: clinical and molecular findings. Clin Genet. 2006;70(2):173-6. PMID: 16879203; https://doi.org/10.1111/j.1399-0004.2006.00656.x.
https://doi.org/https://doi.org/10.1111/...
chorea,3535. Mendes MF, de Andrade LA, Ferraz HB. Coréia. Análise clínica de 119 casos [Chorea: clinical correlates of 119 cases]. Arq Neuropsiquiatr. 1996;54(3):419-27. PMID: 9109986; https://doi.org/10.1590/s0004-282x1996000300010.
https://doi.org/https://doi.org/10.1590/...
,3737. Piccolo I, Defanti CA, Soliveri P, et al. Cause and course in a series of patients with sporadic chorea. J Neurol. 2003;250(4):429-35. PMID: 12700907; https://doi.org/10.1007/s00415-003-1010-7.
https://doi.org/https://doi.org/10.1007/...
myoclonus, parkinsonism,2323. Barbosa MT, Caramelli P, Maia DP, et al. Parkinsonism and Parkinson’s disease in the elderly: a community-based survey in Brazil (the Bambuí study). Mov Disord. 2006;21(6):800-8. PMID: 16482566; https://doi.org/10.1002/mds.20806.
https://doi.org/https://doi.org/10.1002/...
dystonia1212. Defazio G, Abbruzzese G, Livrea P, Berardelli A. Epidemiology of primary dystonia. Lancet Neurol. 2004;3(11):673-8. PMID: 15488460; doi: https://doi.org/10.1016/S1474-4422(04)00907-X.
https://doi.org/https://doi.org/10.1016/...
and tremor,55. Ribosa-Nogué R, Gironell A, Pagonabarraga J, et al. Análisis descriptivo de la actividad de una unidad de trastornos del movimiento en un hospital terciario de Cataluña [Descriptive analysis of the activity in a movement disorder unit in a tertiary hospital in Catalonia]. Rev Neurol. 2012;55(6):330-6. PMID: 22972574.,1515. Louis ED, Thawani SP, Andrews HF. Prevalence of essential tremor in a multiethnic, community-based study in northern Manhattan, New York, N.Y. Neuroepidemiology. 2009;32(3):208-14. PMID: 19169043; https://doi.org/10.1159/000195691.
https://doi.org/https://doi.org/10.1159/...
while males predominated in the other cases. Movement disorders predominated among adult and older patients. The younger diagnostic groups were represented by ataxia, tics and dystonia.55. Ribosa-Nogué R, Gironell A, Pagonabarraga J, et al. Análisis descriptivo de la actividad de una unidad de trastornos del movimiento en un hospital terciario de Cataluña [Descriptive analysis of the activity in a movement disorder unit in a tertiary hospital in Catalonia]. Rev Neurol. 2012;55(6):330-6. PMID: 22972574.,66. Bower JH, Teshome M, Melaku Z, Zenebe G. Frequency of movement disorders in an Ethiopian university practice. Mov Disord. 2005;20(9):1209-13. PMID: 15954128; https://doi.org/10.1002/mds.20567.
https://doi.org/https://doi.org/10.1002/...
,88. Das SK, Ghosh B, Das G, Biswas A, Ray J. Movement disorders: Indian scenario: a clinico-genetic review. Neurol India. 2013;61(5):457-66. PMID: 24262445; https://doi.org/10.4103/0028-3886.121908.
https://doi.org/https://doi.org/10.4103/...

CONCLUSIONS

Knowledge of the characteristics of movement disorder patients helps to model and promote better diagnostic and treatment strategies for this population. This study showed higher frequencies of diagnoses of Parkinson’s disease, essential tremor and dystonia, and the patients were predominantly white, female, aged between 71 and 80 years, teachers and married. The mixed clinical form of Parkinson’s disease with an initial symptom of resting tremor was found in higher numbers of patients. The akinetic-rigid (AR) clinical form of Parkinson’s disease tended to occur in younger individuals, with symptoms of postural instability and freezing of gait that developed earlier. On the other hand, the mixed and tremulous forms of Parkinson’s disease had greater likelihood of late onset. The present study showed that there is a need for more complete medical records, to enable better healthcare practices and epidemiological follow-up for patients. This would result in better diagnoses and strategies for analyzing the profile of patients with movement disorders.

REFERENCES

  • 1
    Marques AP, Szwarcwald CL, de Souza-Junior PRB, Malta DC, Montilla DER. Prevalence of arterial hypertension in Brazilian adults and its associated factors and activity limitations: a cross-sectional study. Sao Paulo Med J. 2019;137(4):312-21. PMID: 31691763; https://doi.org/10.1590/1516-3180.2018.0251220719.
    » https://doi.org/https://doi.org/10.1590/1516-3180.2018.0251220719
  • 2
    Yin J, Ma Y, Vogel U, et al. Methylation status of the PPP1R13L promoter region among lung cancer patients and healthy controls. Analytical cross-sectional study. Sao Paulo Med J. 2019;137(3):255-61. PMID: 31483011; https://doi.org/10.1590/1516-3180.2018.0358230419.
    » https://doi.org/https://doi.org/10.1590/1516-3180.2018.0358230419
  • 3
    Carmo ÉA, Nery AA, Nascimento Sobrinho CL, Casotti CA. Clinical and epidemiological aspects of scorpionism in the interior of the state of Bahia, Brazil: retrospective epidemiological study. Sao Paulo Med J. 2019;137(2):162-8. PMID: 31314877; https://doi.org/10.1590/1516-3180.2018.0388070219.
    » https://doi.org/https://doi.org/10.1590/1516-3180.2018.0388070219
  • 4
    Santos EHS, Santos Neto PJD, Santos I S. Carotid intima-media thickness in the Brazilian Longitudinal Study of Adult Health (ELSA-Brasil): a narrative review. Sao Paulo Med J. 2018;136(1):64-72. PMID: 29590246; https://doi.org/10.1590/1516-3180.2017.0272141017.
    » https://doi.org/https://doi.org/10.1590/1516-3180.2017.0272141017
  • 5
    Ribosa-Nogué R, Gironell A, Pagonabarraga J, et al. Análisis descriptivo de la actividad de una unidad de trastornos del movimiento en un hospital terciario de Cataluña [Descriptive analysis of the activity in a movement disorder unit in a tertiary hospital in Catalonia]. Rev Neurol. 2012;55(6):330-6. PMID: 22972574.
  • 6
    Bower JH, Teshome M, Melaku Z, Zenebe G. Frequency of movement disorders in an Ethiopian university practice. Mov Disord. 2005;20(9):1209-13. PMID: 15954128; https://doi.org/10.1002/mds.20567.
    » https://doi.org/https://doi.org/10.1002/mds.20567
  • 7
    Bhidayasiri R, Saksornchai K, Kaewwilai L, Phanthumchinda K. A census of movement disorders at a Thai university hospital. J Neurol Sci. 2011;301(1-2):31-4. PMID: 21131010; https://doi.org/10.1016/j.jns.2010.11.010.
    » https://doi.org/https://doi.org/10.1016/j.jns.2010.11.010
  • 8
    Das SK, Ghosh B, Das G, Biswas A, Ray J. Movement disorders: Indian scenario: a clinico-genetic review. Neurol India. 2013;61(5):457-66. PMID: 24262445; https://doi.org/10.4103/0028-3886.121908.
    » https://doi.org/https://doi.org/10.4103/0028-3886.121908
  • 9
    Wenning GK, Kiechl S, Seppi K, et al. Prevalence of movement disorders in men and women aged 50-89 years (Bruneck Study cohort): a population-based study. Lancet Neurol. 2005;4(12), 815-20. PMID: 16297839; https://doi.org/10.1016/S1474-4422(05)70226-X.
    » https://doi.org/https://doi.org/10.1016/S1474-4422(05)70226-X
  • 10
    Vázquez-Alén P, Pérez-Gilabert Y, Mateo D, Giménez-Roldán S. Estudio sobre una base de datos de 2.471 pacientes con enfermedad de Parkinson y trastornos del movimiento en el Área Sanitaria 1 de la Comunidad de Madrid. Cambios demográficos observados a lo largo de ocho años [A study made on a data base of 2,471 patients with Parkinson disease and disorders of movement in Health District 1 of the autonomous region of Madrid. Observed demographic changes over 8 year-period]. Rev Neurol. 2000;30(7):635-40. PMID: 10859741.
  • 11
    Siemers E, Reddy V. Profile of patients enrolled in a new movement disorder clinic. Mov Disord. 1991;6(4):336-41. PMID: 1758452; https://doi.org/10.1002/mds.870060412.
    » https://doi.org/https://doi.org/10.1002/mds.870060412
  • 12
    Defazio G, Abbruzzese G, Livrea P, Berardelli A. Epidemiology of primary dystonia. Lancet Neurol. 2004;3(11):673-8. PMID: 15488460; doi: https://doi.org/10.1016/S1474-4422(04)00907-X.
    » https://doi.org/https://doi.org/10.1016/S1474-4422(04)00907-X
  • 13
    Defazio G. The epidemiology of primary dystonia: current evidence and perspectives. Eur J Neurol. 2010;17 Suppl 1:9-14. PMID: 20590802; https://doi.org/10.1111/j.1468-1331.2010.03053.x.
    » https://doi.org/https://doi.org/10.1111/j.1468-1331.2010.03053.x
  • 14
    Fahn S, Jankovic J, Hallett M. Principles and practice of movement disorders. 2nd ed. New York: Saunders; 2011.
  • 15
    Louis ED, Thawani SP, Andrews HF. Prevalence of essential tremor in a multiethnic, community-based study in northern Manhattan, New York, N.Y. Neuroepidemiology. 2009;32(3):208-14. PMID: 19169043; https://doi.org/10.1159/000195691.
    » https://doi.org/https://doi.org/10.1159/000195691
  • 16
    Rodríguez-Violante M, Cervantes-Arriaga A, Morales-Briceño H, et al. Prevalencia de parkinsonismos atípicos en la clínica de trastornos del movimiento de un hospital de referencia de la Ciudad de México. Rev Mex Neuroci. 2012;13(6):296-300. Available from: Available from: https://www.medigraphic.com/pdfs/revmexneu/rmn-2012/rmn126b.pdf Accessed in 2020 (May 14).
    » https://www.medigraphic.com/pdfs/revmexneu/rmn-2012/rmn126b.pdf
  • 17
    Colosimo C, Morgante L, Antonini A, et al. Non-motor symptoms in atypical and secondary parkinsonism: the PRIAMO study. J Neurol. 2010;257(1):5-14. PMID: 19669613; https://doi.org/10.1007/s00415-009-5255-7.
    » https://doi.org/https://doi.org/10.1007/s00415-009-5255-7
  • 18
    Benito-León J, Bermejo-Pareja F, Rodríguez J, et al. Prevalence of PD and other types of parkinsonism in three elderly populations of central Spain. Mov Disord. 2003;18(3):267-74. PMID: 12621629; https://doi.org/10.1002/mds.10362.
    » https://doi.org/https://doi.org/10.1002/mds.10362
  • 19
    Savica R, Grossardt BR, Bower JH, et al. Incidence and time trends of drug-induced parkinsonism: A 30-year population-based study. Mov Disord. 2017;32(2):227-34. PMID: 27779780; https://doi.org/10.1002/mds.26839.
    » https://doi.org/https://doi.org/10.1002/mds.26839
  • 20
    Cardoso F, Camargos ST, Silva Júnior GA. Etiology of parkinsonism in a Brazilian movement disorders clinic. Arq Neuropsiquiatr. 1998;56(2):171-5. PMID: 9698723; https://doi.org/10.1590/s0004-282x1998000200001.
    » https://doi.org/https://doi.org/10.1590/s0004-282x1998000200001
  • 21
    Wermuth L, Lassen CF, Himmerslev L, Olsen J, Ritz B. Validation of hospital register-based diagnosis of Parkinson’s disease. Dan Med J. 2012;59(3):A4391. PMID: 22381086.
  • 22
    Silva EG, Viana MA, Quagliato EMAB. Diagnóstico de síndromes parkinsonianas em uma clínica brasileira de distúrbios do movimento. Rev Neurociências. 2005;13(4):173-7. Available from: Available from: http://www.revistaneurociencias.com.br/edicoes/2005/RN%2013%2004/Pages%20from%20RN%2013%2004.pdf Accessed in 2020 (May 14).
    » http://www.revistaneurociencias.com.br/edicoes/2005/RN%2013%2004/Pages%20from%20RN%2013%2004.pdf
  • 23
    Barbosa MT, Caramelli P, Maia DP, et al. Parkinsonism and Parkinson’s disease in the elderly: a community-based survey in Brazil (the Bambuí study). Mov Disord. 2006;21(6):800-8. PMID: 16482566; https://doi.org/10.1002/mds.20806.
    » https://doi.org/https://doi.org/10.1002/mds.20806
  • 24
    Okubadejo NU, Bower JH, Rocca WA, Maraganore DM. Parkinson’s disease in Africa: A systematic review of epidemiologic and genetic studies. Mov Disord. 2006;21(12):2150-6. PMID: 17044056; https://doi.org/10.1002/mds.21153.
    » https://doi.org/https://doi.org/10.1002/mds.21153
  • 25
    Ma CL, Su L, Xie JJ, et al. The prevalence and incidence of Parkinson’s disease in China: a systematic review and meta-analysis. J Neural Transm (Vienna). 2014;121(2):123-34. PMID: 24057652; https://doi.org/10.1007/s00702-013-1092-z.
    » https://doi.org/https://doi.org/10.1007/s00702-013-1092-z
  • 26
    Melcon MO, Anderson DW, Vergara RH, Rocca WA. Prevalence of Parkinson’s disease in Junín, Buenos Aires Province, Argentina. Mov Disord. 1997;12(2):197-205. PMID: 9087978; https://doi.org/10.1002/mds.870120210.
    » https://doi.org/https://doi.org/10.1002/mds.870120210
  • 27
    Nicoletti A, Sofia V, Bartoloni A, et al. Prevalence of Parkinson’s disease: a door-to-door survey in rural Bolivia. Parkinsonism Relat Disord. 2003;10(1):19-21. PMID: 14499202; https://doi.org/10.1016/s1353-8020(03)00066-x.
    » https://doi.org/https://doi.org/10.1016/s1353-8020(03)00066-x
  • 28
    Rajput AH, Voll A, Rajput ML, Robinson CA, Rajput A. Course in Parkinson disease subtypes: A 39-year clinicopathologic study. Neurology. 2009;73(3):206-12. PMID: 19620608; https://doi.org/10.1212/WNL.0b013e3181ae7af1.
    » https://doi.org/https://doi.org/10.1212/WNL.0b013e3181ae7af1
  • 29
    Rajput AH, Rajput ML, Ferguson W, Rajput A. Baseline motor findings and Parkinson disease prognostic subtypes. Neurology. 2017;89(2):138-43. PMID: 28592451; https://doi.org/10.1212/WNL.0000000000004078.
    » https://doi.org/https://doi.org/10.1212/WNL.0000000000004078
  • 30
    Pagano G, Ferrara N, Brooks DJ, Pavese N. Age at onset and Parkinson disease phenotype. Neurology. 2016;86(15):1400-7. PMID: 26865518; https://doi.org/10.1212/WNL.0000000000002461.
    » https://doi.org/https://doi.org/10.1212/WNL.0000000000002461
  • 31
    Marras C, Chaudhuri KR. Nonmotor features of Parkinson’s disease subtypes. Mov Disord. 2016;31(8):1095-102. PMID: 26861861; https://doi.org/10.1002/mds.26510.
    » https://doi.org/https://doi.org/10.1002/mds.26510
  • 32
    Delval A, Rambour M, Tard C, et al. Freezing/festination during motor tasks in early-stage Parkinson’s disease: A prospective study. Mov Disord. 2016;31(12):1837-45. PMID: 27618808; https://doi.org/10.1002/mds.26762.
    » https://doi.org/https://doi.org/10.1002/mds.26762
  • 33
    Forsaa EB, Larsen JP, Wentzel-Larsen T, Alves G. A 12-year population-based study of freezing of gait in Parkinson’s disease. Parkinsonism Relat Disord. 2015;21(3):254-8. PMID: 25603767; https://doi.org/10.1016/j.parkreldis.2014.12.020.
    » https://doi.org/https://doi.org/10.1016/j.parkreldis.2014.12.020
  • 34
    Batla A, Goyal C, Shukla G, et al. Hemifacial spasm: clinical characteristics of 321 Indian patients. J Neurol. 2012;259(8):1561-5. PMID: 22222858; https://doi.org/10.1007/s00415-011-6376-3.
    » https://doi.org/https://doi.org/10.1007/s00415-011-6376-3
  • 35
    Mendes MF, de Andrade LA, Ferraz HB. Coréia. Análise clínica de 119 casos [Chorea: clinical correlates of 119 cases]. Arq Neuropsiquiatr. 1996;54(3):419-27. PMID: 9109986; https://doi.org/10.1590/s0004-282x1996000300010.
    » https://doi.org/https://doi.org/10.1590/s0004-282x1996000300010
  • 36
    Castilhos RM, Souza AF, Furtado GV, et al. Huntington disease and Huntington disease-like in a case series from Brazil. Clin Genet. 2014;86(4):373-7. PMID: 24102565; https://doi.org/10.1111/cge.12283.
    » https://doi.org/https://doi.org/10.1111/cge.12283
  • 37
    Piccolo I, Defanti CA, Soliveri P, et al. Cause and course in a series of patients with sporadic chorea. J Neurol. 2003;250(4):429-35. PMID: 12700907; https://doi.org/10.1007/s00415-003-1010-7.
    » https://doi.org/https://doi.org/10.1007/s00415-003-1010-7
  • 38
    Storey E, du Sart D, Shaw JH, et al. Frequency of spinocerebellar ataxia types 1, 2, 3, 6, and 7 in Australian patients with spinocerebellar ataxia. Am J Med Genet. 2000;95(4):351-7. PMID: 11186889; https://doi.org/10.1002/1096-8628(20001211)95:4<351::aid-ajmg10>3.0.co;2-r.
    » https://doi.org/https://doi.org/10.1002/1096-8628(20001211)95:4<351::aid-ajmg10>3.0.co;2-r
  • 39
    Trott A, Jardim LB, Ludwig HT, et al. Spinocerebellar ataxias in 114 Brazilian families: clinical and molecular findings. Clin Genet. 2006;70(2):173-6. PMID: 16879203; https://doi.org/10.1111/j.1399-0004.2006.00656.x.
    » https://doi.org/https://doi.org/10.1111/j.1399-0004.2006.00656.x
  • 40
    Teive HA, Munhoz RP, Raskin S, Werneck LC. Spinocerebellar ataxia type 6 in Brazil. Arq Neuropsiquiatr. 2008;66(3B):691-4. PMID: 18949263; https://doi.org/10.1590/s0004-282x2008000500015.
    » https://doi.org/https://doi.org/10.1590/s0004-282x2008000500015
  • 41
    Cardoso F, Veado CC, Oliveira JT. A Brazilian cohort of patients with Tourette’s syndrome. J Neurol Neurosurg Psychiatry. 1996;60(2):209-12. PMID: 8708658; https://doi.org/10.1136/jnnp.60.2.209.
    » https://doi.org/https://doi.org/10.1136/jnnp.60.2.209
  • 1
    Instituto de Assistência Médica ao Servidor Público Estadual, Hospital do Servidor Público Estadual (IAMSPE/HSPE), São Paulo (SP), Brazil
  • Sources of funding: None

Publication Dates

  • Publication in this collection
    08 Jan 2021
  • Date of issue
    Jan-Feb 2021

History

  • Reviewed
    04 June 2020
  • Received
    24 Sept 2020
  • Accepted
    30 Oct 2020
Associação Paulista de Medicina - APM APM / Publicações Científicas, Av. Brigadeiro Luís Antonio, 278 - 7º and., 01318-901 São Paulo SP - Brazil, Tel.: +55 11 3188-4310 / 3188-4311, Fax: +55 11 3188-4255 - São Paulo - SP - Brazil
E-mail: revistas@apm.org.br