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Arquivos de Neuro-Psiquiatria

Print version ISSN 0004-282XOn-line version ISSN 1678-4227

Arq. Neuro-Psiquiatr. vol.75 no.8 São Paulo Aug. 2017

http://dx.doi.org/10.1590/0004-282x20170091 

ARTICLES

Quality of life in Parkinson’s disease patients: progression markers of mild to moderate stages

Qualidade de vida de indivíduos com doença de Parkinson: marcadores da progressão da fase leve para moderada

Raissa Carla Moreira1 

Marise Bueno Zonta2 

Ana Paula Serra de Araújo3 

Vera Lúcia Israel4 

Hélio A. G. Teive5 

1Universidade Federal do Paraná, Curitiba PR, Brasil;

2Universidade Federal do Paraná, Hospital de Clínicas, Departamento de Reabilitação, Curitiba PR, Brasil;

3Secretaria Municipal de Saúde, Prefeitura Municipal de Guarapuava, Guarapuava PR, Brasil;

4Universidade Federal do Paraná, Departamento de Fisioterapia, Curitiba PR, Brasil;

5Universidade Federal do Paraná, Departamento de Medicina, Curitiba PR, Brasil.

ABSTRACT

Objective

To investigate which factors are associated with the quality of life decline in Parkinson’s disease patients from mild to moderate stages.

Methods

The Unified Parkinson’s Disease Rating Scale and Parkinson’s Disease Questionnaire-39 were used to evaluate clinical/functional data and the quality of life.

Results

The markers of clinical/functional worsening were drooling (p < 0.004), need for assistance with hygiene (p = 0.02), greater freezing frequency (p = 0.042), bradykinesia (p = 0.031), greater intensity of the resting tremor (p = 0.035) and “pill rolling” (p = 0.001). The decline in quality of life was related to stigma (p = 0.043), greater impairment in cognition (p = 0.002), mobility (p = 0.013) and for daily living activities (p = 0.05), and was considered more significant in men, married, older individuals, and those with a longer time of disease.

Conclusions

The quality of life worsening markers at the moderate stage were related to stigma, worsening of cognition, and to greater impairment in mobility and daily living activities.

Key words: Parkinson disease; quality of life; surveys and questionnaires

RESUMO

Objetivo

Verificar os fatores relacionados ao declínio clínico/funcional e de Qualidade de Vida de indivíduos com Doença de Parkinson, da fase leve para moderada.

Métodos

Foram utilizadas as escalas Unified Parkinson’s Disease Rating Scale and Parkinson’s Disease Questionnaire-39 (UPDRS e PDQ-39) para avaliação clínico/funcional e de qualidade de vida

Resultados

Os marcadores de piora clínico/funcional na fase moderada foram: sialorréia (p < 0,004), necessidade de ajuda para higiene (p = 0,02), maior frequência do “freezing” (p = 0,042), bradicinesia (p = 0,031) e maior intensidade do tremor de repouso (p = 0,035) e bater dos dedos (p = 0,001). O declínio da qualidade de vida esteve relacionado ao estigma (p = 0,043), ao maior comprometimento da cognição (p = 0,002), da mobilidade (p = 0,013) e da independência para realizar as atividade de vida diária (AVD’s) (p = 0,05), sendo mais importante nos homens, nos casados, nos indivíduos com maior idade e naqueles com maior tempo de evolução da doença.

Conclusão

Os marcadores de piora da qualidade de vida na fase moderada estiveram relacionados ao estigma, à piora da cognição, ao maior comprometimento para mobilidade e AVD’s.

Palavras-Chave: doença de Parkinson; qualidade de vida; inquéritos e questionários

Parkinson’s disease (PD) is a chronic degenerative disease of the central nervous system that evolves slowly and progressively and is characterized by bradykinesia, muscle rigidity and resting tremor among other motor signs and symptoms1,2. Quality of life is significantly impaired not only by motor symptoms, but also by non-motor symptoms such as depression, anxiety, pain, constipation, hyposmia and sleep disturbances3,4.

There are few studies on the incidence and prevalence of PD in Brazil; however, the most recent study shows that the disease affects 3.3% of Brazilians over the age of 60 years4. One of the concerns when treating PD patients is to improve their quality of life. This includes their physical, functional and emotional well-being, their degree of independence and their family relationships, as well as social, economic and political aspects of their lives5,6.

A decline in quality of life in individuals with PD has been associated with worsening motor symptoms and the combination of neurodegenerative phenomena, psychological suffering and stigma associated with the disease7. However, in-depth studies are required to differentiate between the impact of PD at different stages of the disease6,7.

The objective of this study was to investigate which factors are associated with clinical/functional decline and a decline in quality of life in individuals with mild and moderate PD.

METHODS

The study was a cross-sectional one, and data on individuals who had been diagnosed with PD, and were registered at the Paraná Association for Individuals with Parkinson’s Disease (APPP), were collected from January to May 2012 in the city of Curitiba, in the state of Paraná, Brazil. The convenience sample comprised 100 individuals of both sexes between the ages of 60 and 80 years with impairment rated between 1 and 3 on the Hoehn and Yahr (HY) scale. The group with mild PD (MIG), consisting of 50 individuals classified as HY 1-2, was compared with the group with moderate PD (MOG), which consisted of 50 individuals classified as HY 38,9. The demographic data are shown in Table 1.

Table 1 Comparison of mild Parkinson’s disease and moderate Parkinson’s disease groups in terms of gender, age, race, marital status and level of education. 

Variable Mild Moderate p-value*


n (%) n (%)
Gender
Female 28 (56) 22 (44)
Male 22 (44) 28 (56) 0.317
Age (years)
60-65 11 (22) 13 (26)
66-70 16 (32) 8 (16)
71-75 10 (20) 17 (34)
76-80 13 (26) 12 (24) 0.196
Race
White 45 (90) 46 (92)
Yellow/Black 5 (10) 4 (8) 1
Marital status
Married 32 (64) 38 (76)
Separated/widow(er)/single 18 (36) 12 (24) 0.275
Level of education
Primary education (incomplete) 9 (18) 11 (22)
Primary education (complete) 27 (54) 19 (38)
High school (complete or incomplete) 5 (10) 8 (16)
Third-level education (complete or incomplete) 9 (18) 12 (24) 0.438

p* < 0.05.

Individuals were only included in the study if they agreed to take part, signed a voluntary informed-consent form and were present on the days when the data were collected. Individuals with dementia or any other concomitant neurodegenerative disease were excluded. The study started after it had been approved by the Human Research Ethics Committee of the Hospital de Clínicas, Federal University of Paraná (ref. no. 2654.261/2011-11).

The evaluation protocol covered clinical history and demographic, clinical, functional and quality-of-life data. The demographic data were collected in the interview, and the clinical history was obtained from the patients’ medical records. Clinical/functional data were obtained by applying the Unified Parkinson’s Disease Rating Scale (UPDRS) (activities of daily living [ADL] and motor examination sections)9. Quality-of-life data were collected with the Parkinson’s Disease Questionnaire (PDQ-39)10. The UPDRS and PDQ-39 were filled out by the researcher.

The UPDRS evaluates an individual’s signs, symptoms and activities based on self-reports and clinical observation and consists of 42 questions in four sections. The ADL and motor examination sections were analyzed.

The PDQ-39 is an easily-applied, widely-used questionnaire on quality of life in individuals with PD, which evaluates the individual’s health in the previous month. The 39 multiple choice questions cover eight domains and have five possible answers: never, occasionally, sometimes, often and always11,12. The questionnaire is normally filled out by the individual. However, it was decided to complete it with the help of the researcher during a one-to-one interview because of the possibility of some of the respondents having a limited education or difficulty writing due to the motor symptoms of the disease.

Information on HY staging was obtained from the patients’ medical records at APPP. The influences of age, gender, education, marital status and disease duration on quality of life and ADL and motor examination scores were also examined.

Statistics

Quantitative variables were described in terms of their mean, median, minimum, maximum and standard deviation, and qualitative variables in terms of frequency and percentage. The non-parametric Mann-Whitney test was used to compare the two groups (MIG and MOG) based on the UPDRS and PDQ-39 scores.

Spearman’s coefficient was used to evaluate the correlation between the UPDRS and PDQ-39 scores and HY staging and between the UPDRS and the PDQ-39 scores. The significance level was set at p < 0.05. The data were analyzed with Statistica 8.0.

RESULTS

The mean disease duration in the MIG was 3.4 (± 2.2) years and 8.1 (± 4.7) in the MOG. The MOG had greater impairment in the ADL domain (UPDRS). This finding had borderline significance and was particularly noticeable in the increased drooling (p < 0.004), greater need for assistance with personal hygiene (p = 0.02) and increased frequency of freezing (p = 0.042) in this group. Although greater impairment was observed in motor examination items in the MOG, this was not statistically significant (p = 0.220). Nevertheless, when each item in this domain was considered individually, significant differences were observed in resting tremor (p < 0.035), pill-rolling (p < 0.001) and bradykinesia (p < 0.031) (Table 2).

Table 2 Comparison of the mild Parkinson’s disease group with the moderate Parkinson’s disease group in the activities of daily living and motor-examination sections of the UPDRS items with a statistically significant difference. 

UPDRS – ADLs Stage Number of individuals and % for each answer p-value*

0 1 2 3 or 4
Drooling Mild 24 (48) 15 (30) 11 (22) 0 (0)
Moderate 9 (18) 18 (36) 19 (38) 4 (8) 0.004*
Personal hygiene Mild 5 (10) 34 (68) 10 (20) 1 (2)
Moderate 0 (0) 38 (76) 6 (12) 6 (12) 0.020*
Freezing Mild 7 (14) 23 (46) 12 (24) 8 (16)
Moderate 8 (16) 11 (22) 13 (26) 18 (36) 0.042*
UPDRS - Motor examination
Resting tremor Mild 5 (10) 30 (60) 12 (24) 3 (6)
Moderate 1 (2) 33 (66) 6 (12) 10 (20) 0.035*
Pill-rolling Mild 25 (50) 23 (46) 2 (4) 0 (0)
Moderate 7 (14) 39 (78) 3 (6) 1 (2) 0.001**
Bradykinesia Mild 3 (6) 21 (42) 1 (2) 25 (50)
Moderate 1 (2) 32 (64) 4 (8) 13 (26) 0.031*

UPDRS: Unified Parkinson’s Disease Rating Scale. ADLs: Activities of Daily living. Categories 2, 3 and 4 were combined for the statistical analysis. Motor Examination: Categories 3 and 4 were combined for the statistical analysis. *Chi-square test, p < 0.05.

In the evaluation of quality of life as measured by the PDQ-39, the means of seven of the eight items analyzed were greater in the MOG than in the MIG. These differences were statistically significant in the mobility (p < 0.013), stigma (p < 0.043) and cognition (p < 0.002) domains (Table 3). The difference in the bodily discomfort domain between the groups was not statistically significant, but individual analysis of the items showed that painful muscle cramps and spasms caused significantly more impairment of quality of life in the MOG group (p = 0.04). The answers to the PDQ-39 for which there was a statistically significant difference between the two groups are shown in Table 4.

Table 3 Comparison of quality-of-life scores in the Parkinson’s Disease Questionnaire-39 domains for the mild, and moderate Parkinson’s disease groups. 

Domain Stage n Mean Median Minimum Maximum Standard deviation p-value*
Mobility Mild 50 19.2 20.0 1.0 37.0 7.5
Moderate 50 23.4 23.0 10.0 38.0 7.1 0.013*
ADLs Mild 50 9.4 9.0 0.0 19.0 4.6
Moderate 50 11.6 11.0 2.0 24.0 4.8 0.050
Well-being Mild 50 10.0 12.0 0.0 26.0 5.1
Moderate 50 10.5 11.0 1.0 18.0 4.4 0.724
Stigma Mild 50 2.7 1.5 0.0 12.0 3.1
Moderate 50 3.9 2.0 0.0 18.0 3.8 0.043*
Support Mild 50 6.7 8.0 1.0 12.0 2.3
Moderate 50 7.4 8.0 2.0 11.0 2.1 0.089
Cognition Mild 50 5.8 7.0 0.0 12.0 2.6
Moderate 49 7.3 8.0 2.0 12.0 2.4 0.002*
Communication Mild 50 3.3 3.5 0.0 8.0 2.6
Moderate 50 3.6 4.0 0.0 8.0 2.4 0.614
Bodily discomfort Mild 50 6.3 7.0 0.0 11.0 2.3
Moderate 50 6.2 6.0 2.0 10.0 1.8 0.525

ADLs: Activities of Daily living; *Statistically significant difference in the non-parametric Mann-Whitney test at a significance level of p < 0.05.

Table 4 Answers in the PDQ-39 domains with statistically significant, or borderline statistically significant differences between the mild, and moderate Parkinson’s disease groups. 

PDQ-39 domains Difference between the MIG and MOG groups
Mobility
Q1. Have you had difficulty doing the leisure activities you like? p = 0.041
Q10. Have you been confined to the house more than you would like? p = 0.052
ADLs domain
Q5. Have you had difficulty cutting up your food? p = 0.048
Q6. Have you had difficulty holding a drink without spilling it? p = 0.043
Emotional well-being domain
Q5. Have you felt anxious? p = 0.01
Q6. Have you felt worried about your future? (p=0.054) p = 0.054
Stigma domain
Q2. Have you avoided situations which involve eating or drinking in public? p = 0.045
Cognition domain
Q2. Have you had problems with your concentration? p = 0.018
Q3. Have you felt your memory was bad? p = 0.027
Bodily discomfort domain
Q1. Have you had painful muscle cramps or spasms? p = 0.04

MIG: group with mild PD; MOG: group with moderate PD; PDQ-39: Parkinson’s disease questionnaire-39.

There was no correlation between gender and clinical/functional status or quality of life in individuals in the MIG. In the MOG, a decline in quality of life was associated with a lack of support from friends and family members (p = 0.01).

Among married individuals, a decline in quality of life was associated with stigma (p = 0.02) in the MOG and with a lack of support from friends and family members in both groups (p < 0.001).

There was no correlation between age and clinical/functional status or quality of life in individuals in the MIG. In the MOG, increasing age was associated with greater dependence in ADLs (p = 0.02) and greater cognitive impairment (concentration and memory, p = 0.01).

Greater disease duration was associated with a decline in quality of life in the ADL (MIG, p = 0.03) and emotional well-being (MOG, p = 0.01) domains (Table 5).

Table 5 Relation between UPDRS and PDQ-39 domains and disease duration in the mild, and moderate Parkinson’s disease groups. 

Variable Mild Moderate


r p-value r p-value
ADLs 0.14 0.328 0.17 0.230
UPDRS
Motor examination -0.03 0.811 0.17 0.232
Mobility -0.05 0.742 0.19 0.188
ADLs 0.30 0.035* 0.11 0.459
Well-being 0.01 0.948 0.34 0.017*
PDQ-39
Stigma 0.12 0.414 -0.05 0.729
Support -0.13 0.387 0.01 0.972
Cognition 0.15 0.311 0.27 0.060
Communication 0.06 0.681 0.24 0.087
Bodily discomfort 0.16 0.275 0.07 0.629

ADLs: activities of daily living; UPDRS: unified Parkinson’s disease rating scale. PDQ-39: Parkinson’s disease questionnaire-39.

DISCUSSION

The domain that evaluates independence in ADLs was significantly more affected in patients with moderate PD. This finding corroborates the results reported in the literature, in which mild PD is characterized by complete functionality and moderate PD by functional impairment due to the more severe signs and symptoms, which act as precursors of disability13,14.

Detailed analysis of the responses in this domain showed that the need for assistance with personal hygiene together with drooling and more frequent freezing were markers of loss of independence and difficulty living with embarrassment and limited social interaction. Drooling is associated with muscle rigidity and bradykinesia, symptoms that also lead to a greater need for assistance with personal hygiene15. For Khoo et al.16, non-motor signs such as drooling were common in the early stages of PD and may adversely affect patients’ functional status and well-being.

A sudden loss of the ability to start or sustain a specific motor activity (freezing) can also adversely affect performance in ADLs and subject the individual to more frequent falls17.

While there was no significant difference between the mild and moderate PD groups in the motor examination section of the UPDRS as a whole, analysis of each item showed that there was a significant difference in resting tremor, pill-rolling and bradykinesia between the groups. Bradykinesia, or slowness of movement, directly affects performance of activities such as turning in bed, standing up, getting dressed and walking2,15. It can be inferred from the results of the ADL section that the ability to perform activities related to personal hygiene is also affected.

Resting tremor, which is usually the first sign reported by individuals with PD15,16,17,18, was identified as the sign most closely associated with perceived worsening of the patient’s health. Santos, Menezes and Souza19 reported that individuals in their series experienced embarrassment, particularly in connection with tremor because of its association with alcoholism. In addition to embarrassment, symptoms such as tremor and pill-rolling evolve in parallel with prejudice and reduced self-esteem and self-image, as they lead to shame, anxiety, a risk of depression, shyness in public spaces and social isolation19.

Akinetic-rigid syndrome generally manifests when there has already been a 60% to 80% loss in dopaminergic neurons in the substantia nigra. Here, these symptoms were more important in individuals in the MOG, who had a mean disease duration of eight years, compared with three years in the MIG17,20.

The greatest impairment in terms of quality of life in the MOG was observed in the domains of mobility, stigma, cognition and ADLs, corroborating the findings of studies by Navarro-Peternella et al.,9 Pinheiro et al.,13 Navarro-Peternella and Marcon14, and Quintella et al.21

In the mobility domain, having difficulty doing pleasurable leisure activities was one factor that adversely affected quality of life, a finding also reported in studies by Mandira22 and Tavares et al.23. Normal mobility is required to perform ADLs and leisure activities; reduced mobility compromises performance of these activities, limits the activities that can be performed and increases the time required to perform them. Individuals in the MOG also reported that they were confined to the home more than they would like, indicating that they are increasingly less able to perform activities outside their homes. Increasing physical impairment associated with the main symptoms of the disease causes individuals with PD to become isolated, while at the same time making them more dependent on others to perform activities that previously gave them a sense of personal satisfaction, in turn further reducing their quality of life13,24.

A greater dependence on others to carry out daily activities such as cutting food and drinking without spilling was a further factor in the decline in quality of life in these patients, particularly when the disease was in the moderate stage. Rigidity, bradykinesia and tremor impose limitations on these activities15, which in turn leads to irritability, anxiety, insecurity and pessimism as the individual is faced with the prospect of increasing dependence on others24.

Anxiety and concern about the future were significantly more important in the MOG, corroborating the study by Correia et al.20, showing that depressive symptoms, including anxiety, contribute to a decline in quality of life in these individuals. Navarro-Peternella and Marcon14 studied individuals with PD and found that fear and insecurity about dependence on others, about loss of independence at work and in ADLs and about the future in general, help to aggravate the condition. The individuals in their study reported that understanding the unstable nature of the disease and the fact that it was incurable is something that sadly they have to face for the rest of their lives and that will be part of their relationships and day-to-day activities.

More individuals in the MOG than the MIG reported avoiding situations that involved eating or drinking in public. This difference was statistically significant. Stigma in the MOG was an important social factor that adversely affected quality of life in the individuals assessed. Werle et al.25 investigated quality of life in individuals with cervical dystonia, a chronic disease that is also associated with stigma. They found that the need to hide the disease, insecurity in the presence of new people, problems with friends and family members, fear about the disease and sadness and irritation were factors that reduced their quality of life.

In our sample, problems related to concentration and poor memory were more significant in the MOG and progressively impaired quality of life, corroborating the study by Rodríguez-Violante et al.26 Motor symptoms are no longer considered the only important determinants of quality of life in individuals with PD, and the importance of non-motor symptoms, such as depression, apathy, fatigue, pain and cognitive deterioration, have been increasingly recognized9,17.

Here, the groups were similar in terms of gender, and the decline in quality of life among men was related to lack of support from friends and family members, corroborating the study by Navarro-Peternella and Marcon9. In a study by Tavares et al.,23 the domain that evaluated social relations was a predictor of decline in quality of life in men with PD.

Quality of life among married individuals in our series was worse in the social support domain in both the mild and moderate stages. Among married individuals with moderate PD, greater impairment of quality of life was also associated with stigma. This finding is unexpected as married individuals are normally considered to have greater support and acceptance. On the other hand, this finding may be explained by the fact that a chronic disease that causes increasing dependence can be a source of conflict and strengthen or weaken affective ties and family bonds14,27.

While in the present study older age among individuals in the moderate stage was related to worse scores for ADLs and cognition in the PDQ-39, in a study by Tedrus et al.,28 the greatest impairment was observed for the ADL and mobility domains. Longer disease duration was associated with greater impairment of quality of life in the ADL and emotional well-being domains in the PDQ-39, a finding also reported in other studies26,29. In the study by Tedrus et al.,28 a decline in quality of life in individuals with PD was associated not only with disease duration but also with advanced age and age of onset.

In conclusion, markers of decline in quality of life in the moderate stage of PD were related to stigma, worsening cognition, greater mobility impairment and reduced independence in ADLs. Drooling, a greater need for assistance with personal hygiene and a greater frequency of freezing caused significant quality-of-life impairment in individuals in the moderate stage of the disease together with resting tremor, pill-rolling and bradykinesia.

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Received: November 25, 2016; Revised: March 31, 2017; Accepted: May 11, 2017

Correspondence: Raissa Carla Moreira; Rua XV de Novembro, 1299; 80060-000 Curitiba PR, Brasil; E-mail: fisioraissa@hotmail.com

Conflict of interest: There is no conflict of interest to declare.

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