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Production capacity of maximal isometric grip strength in women with rheumatoid arthritis: a pilot study

Abstracts

The aim of this study was to verify the capacity of maximum handgrip strength (HGSmax) in women with rheumatoid arthritis (RA) and its relationship with disease activity. Nine women with RA and ten healthy women were selected. The demographics data were recorded of both groups, and clinical characteristics of women with RA. The level of disease activity was evaluated by the protocol Disease Activity Score (DAS-28) using C-Reactive Protein (CRP). To measure the HGSmax was used an extensometer dynamometer. The results showed a statistically significant difference of HGSmax between the participants (Arthritis and Control: 129.41±52.10 e 192.46±38.98 N). In relation to dominance, women with RA showed no significant difference in HGSmax. The results of HGSmax for the dominant hand showed a strong linear relationship with the CRP (r=0.751). It also noted that was a moderate non-linear relation of HGSmax for the dominant hand and non-dominant with the number of tender and swollen joints. Thus, it is clear that women with RA have reduced ability to produce HGSmax independent of dominance, in addition, this study demonstrated the direct relationship that exists between HGSmax and the level of disease activity.

Arthritis; Rheumatoid; Muscle Strength Dynamometer; C-Reactive Protein


O objetivo deste estudo foi verificar a capacidade de produção de força de preensão manual máxima (FPMmax) em mulheres com artrite reumatoide (AR) e sua relação com a atividade da doença. Foram selecionadas nove mulheres com AR e dez mulheres saudáveis. Foram registrados dados demográficos de ambos os grupos, além de características clínicas das mulheres com AR. A determinação do nível da atividade da doença foi conduzida pelo protocolo Disease Activity Score (DAS-28) por meio da Proteína C-Reativa (PCR). Para aquisição da FPMmax, foi utilizado o dinamômetro do tipo extensômetro. Os resultados demonstraram diferença significativa da FPMmax entre as participantes (Artrite e Controle: 129,41±52,10 e 192,46±38,98 N). Em relação à dominância, as mulheres com AR não apresentaram diferença significativa na FPMmax. Os resultados obtidos da FPMmax para a mão dominante evidenciaram uma forte relação linear com a PCR (r=0,751). Também se constatou uma moderada relação não linear da FPMmax para a mão dominante e não-dominante com o número de articulações dolorosas e edemaciadas. Assim, fica evidente que mulheres com AR apresentam redução na capacidade de produzir a FPMmax ndependente da dominância, além do que este estudo demonstrou a relação direta que existe entre a FPMmax e o nível de atividade da doença.

Artrite Reumatoide; Dinamômetro de Força Muscular; Proteína C-Reativa


Este artículo tuvo como objetivo verificar la capacidad de producción de fuerza de prensión manual máxima (FPMmax) en mujeres con artritis reumatoide (AR) y su relación con la actividad de la enfermedad. Han sido elegidas nueve mujeres con AR y diez saludables. Se han registrado datos demográficos de los dos grupos, además de las características clínicas de las mujeres con AR. La determinación del nivel de actividad de la enfermedad se realizó por el protocolo Disease Activity Score (DAS-28) a través de la Proteína C-Reactiva (PCR). Para la adquisición de la FPMmax se utilizó el dinamómetro de tipo extensómetro. Los resultados muestran una diferencia significativa de la FPMmax entre los participantes (Artritis y Control: 129,41±52,10 e 192,46±38,98 N). Con respeto a la dominación, las mujeres con AR no presentaron diferencias significativas en la FPMmax Se obtuvo resultados para la mano dominante en el cual mostró una fuerte relación lineal con la PCR (r=0,751). También se comprobó una moderada relación no lineal de la FPMmax para la mano dominante y la no dominante con el número de articulaciones dolorosas e inflamadas. De esta manera, resulta evidente que las mujeres con AR presentan reducción en la capacidad de producción de la FPMmax ndependiente de la dominancia, además de mostrar a través de esta investigación la relación directa entre la FPMmax y el nivel de actividad de la enfermedad.

Artritis Reumatoide; Dinamómetro de Fuerza Muscular; Proteína C-Reactiva


INTRODUCTION

Rheumatoid arthritis (RA) is a chronic inflammatory disease, associated with functional disabilities resulting from articular lesions(1). Oken O, Batur G, Gunduz R, Yorgancioglu RZ. Factors associated with functional disability in patients with rheumatoid arthritis. Rheumatol Int. 2008;29(2):163-6. , (2). Eurenius E, Stenström CH. Physical activity, physical fitness, and general health perception among individuals with rheumatoid arthritis. Arthritis Rheum. 2005;53(1):48-55., which mainly affects joints in the hands(3). Watanabe K, Tsubota S, Chin G, Aoki M. Differences in parameters of the explosive grip force test between young and older women. J Gerontol A Biol Sci Med Sci. 2011;66(5):554-8. , (4). Bodur H, Yilmaz O, Keskin D. Hand disability and related variables in patients with rheumatoid arthritis. Rheumatol Int. 2006;26(6):541-4..

A method commonly used in order to assess functionality in patients with RA is the hand grip strength test (HGST)(5). Ferraz MB, Ciconelli RM, Araujo PMP, Oliveira LM, Atra E. The effect of elbow flexion and time of assessment on the measurement of grip strength in rheumatoid-arthritis. J Hand Surg Am. 1992;17A(6):1099-103., which is an effective marker for establishing the level of dysfunction in RA sufferers(6). Thyberg I, Hass UA, Nordenskiöld U, Gerdle B, Skogh T. Activity limitation in rheumatoid arthritis correlates with reduced grip force regardless of sex: the Swedish TIRA project. Arthritis Rheum. 2005;53(6):886-96. , (7). Adams J, Burridge J, Mullee M, Hammond A, Cooper C. Correlation between upper limb functional ability and structural hand impairment in an early rheumatoid population. Clin Rehabil. 2004;18(4):405-13.. Th test provides a quantitative assessment in terms of functionality, which is pertinent because a person's ability to exert pressure with their hands plays an important role in exploring and manipulating objects, as well as contributing to everyday functions related to the upper limbs and torso(8). Hoenig H, Groff G, Pratt K, Goldberg E, Franck W. A randomized controlled trial of home exercise on the rheumatoid hand. J Rheumatol. 1993;20(5):785-9. , (9). Haidar SG, Kumar D, Bassi RS, Deshmukh SC. Average versus maximum grip strength: which is more consistent? J Hand Surg Br. 2004;29(1):82-4.. The HGST has several purposes within the clinical sphere, with it being recommended to provide assistance in the diagnosis, evaluation and comparison of surgical techniques, as well as for recording purposes during the rehabilitation process and in treatment response(10)10 . Rosén B. Recovery of sensory and motor function after nerve repair. A rationale for evaluation. J Hand Ther. 1996;9(4):315-27. , (11)11 . MacDermid JC, Kramer JF, Woodbury MG, McFarlane RM, Roth JH. Interrater reliability of pinch and grip strength measurements in patients with cumulative trauma disorders. J Hand Ther. 1994;7(1):10-4..

Despite some studies having already verified the reduction of hand grip strength (HGS)(12)12 . Hakkinen A, Kautiainen H, Hannonen P, Ylinen J, Makinen H, Sokka T. Muscle strength, pain, and disease activity explain individual subdimensions of the Health Assessment Questionnaire disability index, especially in women with rheumatoid arthritis. Ann Rheum Dis. 2006;65(1):30-4. , (13)13 . Alomari MA, Keewan EF, Shammaa RA, Alawneh K, Khatib SY, Welsch AA. Vascular function and handgrip strength in rheumatoid arthritis patients. Sci World J. 2012;2012., the mechanism that causes this functional loss remains largely misunderstood(14)14 . Rajagopalan A, Burne JA. Stretch reflexes and joint dynamics in rheumatoid arthritis. Exp Brain Res. 2010;201(1):37-45.. The functional restrictions that occur in RA can be related to the progressive and systemic characteristic of the disease, mainly to the effect of the inflammatory process that leads to joint lesions(15)15 . Pollard L, Choy EH, Scott DL. The consequences of rheumatoid arthritis: quality of life measures in the individual patient. Clin Exp Rheumatol. 2005;23(5 Suppl 39):S43-52.. Some studies have verified the relationship between HGS and the level of disease activity by means of the DAS-28(16)16 . Targonska-Stepniak B, Majdan M. Associations between parameters of nutritional status and disease activity in patients with rheumatoid arthritis. Pol Arch Med Wewn. 2011;121(4):122-8. , (17)17 . Dogu B, Kuran B, Yilmaz F, Usen A, Sirzai H. Is hand bone mineral density a marker for hand function in patients with established rheumatoid arthritis? The correlation among bone mineral density of the hand, radiological findings and hand function. Clin Rheumatol. 2013.. In this sense, assessing the level of disease activity provides objective evidence regarding the inflammatory process(18)18 . Fransen J, Van Riel PL. Outcome measures in inflammatory rheumatic diseases. Arthritis Res Ther. 2009;11(5):244., thereby contributing to understanding concerning the influence of the inflammatory process in reducing HGS in individuals with RA.

Given the aforementioned points, the aim of this study was to test the production capacity for maximum hand grip strength (HGSmax) in female RA sufferers and its relationship with the disease's activity.

METHODOLOGY

Study participants

Nine women with RA (arthritis group=AG) and ten healthy women (control group=CG) were selected and paired according to age (±2 years). Th AG was referred by rheumatologists, in accordance with classifi ation criteria from the American College of Rheumatology(19)19 . Arnett FC, Edworthy SM, Bloch DA, McShane DJ, Fries JF, Cooper NS, et al. The American rheumatis association 1987 revised criteria for the classification of rheumatoid arthritis. Arthritis Rheum. 1988;31(3):315-24., with all being active arthritis sufferers (DAS-28≥2.6)(20)20 . Prevoo MLL, Vanthof MA, Kuper HH, Vanleeuwen MA, Vandeputte LBA, Vanriel P. Modified disease-activity scores that include 28-joint counts development and validation in a prospective longitudinal-study of patients with rheumatoid-arthritis. Arthritis Rheum. 1995;38(1):44-8.. All participants with other immune disorders, cognitive deficiencies, sensory or physical of the upper limbs, blindness, estrogen, antibiotic or anticonvulsant users, active smokers and pregnant women were excluded from the study.

Clinical examinations

All participants completed a standardized form in order to record demographic data from both groups, in addition to the clinical characteristics of the women with RA.

The level of disease activity was determined by means of the Disease Activity Score (DAS−28) Protocol, where the number of painful joints (NPJ) and number of swollen joints (NSJ) (shoulders, elbows, wrists, metacarpophalangeals, proximal interphalangeal joints and knees) are bilaterally counted. The patient's own perception regarding their state of health (SOH) was also verified, this was done using a unidimensional scale with a 0-100mm mark(21)21 . Pincus T, Sokka T. Quantitative measures for assessing rheumatoid arthritis in clinical trials and clinical care. Best Pract Res Clin Rheumatol. 2003;17(5):753-81.. Together with the aforementioned parameters, the serum level of the C-reactive protein (CRP) was used in order to perform the final DAS−28(22)22 . Inoue E, Yamanaka H, Hara M, Tomatsu T, Kamatani N. Comparison of Disease Activity Score (DAS)28erythrocyte sedimentation rate and DAS28C-reactive protein threshold values. Ann Rheum Dis. 2007;66(3):407-9. calculation. The final score from the DAS-28 ranged from 0 to 10(23)23 . Fransen J, Van Riel PL. DAS remission cut points. Clin Exp Rheumatol. 2006;24(6 Suppl 43):S-29-32., where the higher the value, the greater the level of disease activity.

The CRP serum concentration was determined by a turbidimetric method, using a CRP-turbilátex kit (Biotécnica) and a Spectrophotometer (BTLyzer 100(r)), at a 540nm wavelength. The values were expressed in mg/L, with values up to 6mg/L being considered as normal.

In order to determine the dominant hand, the Edinburgh Handedness Inventory(24)24 . Brito G, Brito L, Paumgartten F, Lins M. Lateral preferences in brazilian adults: An analysis with the Edinburgh Inventory. CORTEX. 1989;25(3):403-15. , (25)25 . Oldfield RC. The assessment and analysis of handedness: the Edinburgh inventory. Neuropsychologia. 1971;9(1):97-113. was used.

In order to find the HGSmax, an extensometer-type dynamometer was used. The dynamometer component responsible for measuring strength was an S-beam load cell with four strain gauges (Kyowa, Japan). The dynamometer had a load limit of 1000N (Newtons) and an excellent linearity coefficient (r2=0.9999)(26)26 . Borges NGJ, Domenech SC, da Silva ACK, Dias JA. Estudo comparativo da força de preensão isométrica máxima em diferentes modalidades esportivas. Rev Bras Cineantropom Desempenho Hum. 2009;11(3):292-8..

Procedure for collecting the HGSmax

Firstly, hand size was measured in order to individually calculate the dynamometer grip, in accordance with that as described by Ruiz-Ruiz(27)27 . Ruiz-Ruiz J, Mesa JL, Gutiérrez A, Castillo MJ. Hand size influences optimal grip span in women but not in men. J Hand Surg Am. 2002;27(5):897-901.. The guidelines from the American Society of Hand Therapists(28)28 . Fess EE. Grip strenght. In: Casanova JS, editor. Clinical assessment recommendations. Chicago: American Society of Hand Therapists; 1992. p. 41-5. were adopted for the tests. The test's beginning and end were determined through visual feedback, where the participants observed a "press" command on their computer screens and performed a voluntary muscle contraction for a maximum of 10 seconds, in accordance with the Protocol set out by Ronningen and Kjeyen(29)29 . Ronningen A, Kjeyen I. Effect of an intensive hand exercise programme in patients with rheumatoid arthritis. Scand J Occup Ther. 2008;15(3):173-83.. Three repetitions were alternately performed by each hand, beginning with the dominant hand(28)28 . Fess EE. Grip strenght. In: Casanova JS, editor. Clinical assessment recommendations. Chicago: American Society of Hand Therapists; 1992. p. 41-5.. The time interval between the repetitions was 1 minute, based on the protocol from Ikemoto, et al(30)30 . Trossman PB, Li P-W. The effect of the duration of intertrial rest periods on isometric grip strength performance in young adults. Occup Ther J Res. 1989;9(6):362-73..

HGSmax data processing

The data were processed through a specific routine, programmed in Scilab v.4.1.2 Software (INRIA, ENPS, France), which provided the mean from the three maximum strength curves(31)31 . Mathiowetz V, Weber K, Volland G, Kashman N. Reliability and validity of grip and pinch strength evaluations. J Hand Surg Am. 1984;9(2):222-6.. The HSGmax was defined as the highest value from the strength curve vs time(32)32 . Ikemoto Y, Demura S, Yamaji S, Minami M, Nakada M, Uchiama M. Force-time parameters during explosive isometric grip correlate with muscle power. Sport Sci Healt. 2007;2(2):64-70.. The obtained signals were recorded on a hard drive and filtered using a first order low-pass filter with a 25Hz cutoff frequency.

Statistical analysis

AG characterization was achieved through descriptive statistics, using relative frequency distributions for the categorical variables and mean and standard deviation for the continuous variables.

In order to determine the difference of HGSmax between AG and CG, an independent t-test was performed. A paired Student's t-test was conducted in order to identify the differences in the groups depending on dominance. Finally, a Pearson correlation test was performed between the HGSmax vs DAS-28, SOH and CRP. The relationship between the HGSmax, NPJ and NSJ was verified by means of the Spearman test.

The analyses were done using the Statistical Package for the Social Sciences (SPSS−20.0 Version) software, while adopting a 5% significance level.

RESULTS

19 women were evaluated, with an average age of 56.31 years, 9 of these being from the AG, 10 from the CG. Among the clinical characteristics from the AG, all the participants who were found to have active arthritis presented a positive rheumatoid factor with pain being the complaint most made (Table 1).

Table 1
Clinical characteristics of the AG participants (n=9)

While assessing the HGSmax, a statistically significant difference was observed between the AG and CG in both hands. The HGSmax from the AG was 129.41±52.10N, whereas that from the CG was 192.46±38.98N (Chart 1). Regarding dominance, women from the AG did not show any significant difference in the HGSmax However, there was a significant difference found in the CG for the HGSmax, as regards to dominance (Chart 1).

Chart 1
Maximal isometric hand grip strength of the dominant and nondominant hand from the AG and CG.

Based on the correlation tests, in both hands, the HGSmax showed no linear relationship with the total score from the DAS−28. However, the results from the HGSmax for the dominant hand showed a moderately linear relationship with SOH and a strong linear relationship with CRP. Whereas, for the non-dominant hand, there was a strong linear relationship between the HGSmax and the SOH, while there was no significant linear relationship with CRP. A moderate non-linear relationship of the HGSmax was found for the dominant and non-dominant hand with NPJ and NSJ (Table 2).

Table 2
Relationship between the HGSmax of the dominant and non-dominant hand with the parameters for disease activity in the AG

DISCUSSION

The HGSmax results from the tests corroborate with those from published data, thereby reiterating the finding that women with RA have lesser HGSmax when compared with healthy women(33)33 . Nordenskiöld UM, Grimby G. Grip force in patients with rheumatoid arthritis and fibromyalgia and in healthy subjects: a study with the Grippit instrument. Scand J Rheumatol. 1993;22(1):14-9. , (34)34 . Bjork MA, Thyberg ISM, Skogh T, Gerdle BUC. Hand function and activity limitation according to health assessment questionnaire in patients with rheumatoid arthritis and healthy referents: 5-year followup of predictors of activity limitation (the Swedish TIRA project). J Rheumatol. 2007;34(2):296-302. , (35)35 . Brorsson S, Nilsdotter A, Pedersen E, Bremander A, Thorstensson C. Relationship between finger flexion and extension force in healthy women and women with rheumatoid arthritis. J Rehabil Med. 2012;44(7):605-8. , (36)36 . Speed CA, Campbell R. Mechanisms of strength gain in a handgrip exercise programme in rheumatoid arthritis. Rheumatol Int. 2012;32(1):159-63..

Concerning the difference in the HGSmax in relation to dominance, data from the literature are controversial. Fraser, et al.(37)37 . Fraser A, Vallow J, Preston A, Cooper RG. Predicting 'normal' grip strength for rheumatoid arthritis patients. Rheumatology. 1999;38(6):521-8. found that the dominant hand of patients with RA was on average 20% weaker than the contralateral hand. Whereas, in healthy individuals, the dominant hand was stronger than the non-dominant hand. Another study(38)38 . Nordenskiold U, Grimby G. Assessments of disability in women with rheumatoid arthritis in relation to grip force and pain. Disabil Rehabil. 1997;19(1):13-9. found that the dominant hand of individuals with RA presented greater HGSmax. Due to these contradictory findings, it is difficult to draw conclusions regarding the influence of dominance on grip strength(39)39 . Andria G, Attivissimo F, Giaquinto N, Lanzolla AML, Quagliarella L, Sasanelli N. Functional evaluation of handgrip signals for parkinsonian patients. IEEE Trans Instrum Meas. 2006;55(5):1467-73..

In the assessment of the relationship of HGSmax with the disease activity parameter, the HGSmax has been described to present a good association with this variable(40)40 . Myers DB, Grennan DM, Palmer DG. Hand grip function in patients with rheumatoid arthritis. Arch Phys Med Rehabil. 1980;61(8):369-73.. In this sense, Dedeoglu, et al. (41)41 . Dedeoglu M, Gafuroglu U, Yilmaz O, Bodur H. The relationship between hand grip and pinch strengths and disease activity, articular damage, pain, and disability in patients with rheumatoid arthritis. Turk J Rheumatol. 2013;28(2):69-77. found a negative correlation between HGSmax and DAS-28. This relationship was strengthened by West and Wallber- Jonsson(42)42 . West E, Wållberg-Jonsson S. Health-related quality of life in Swedish men and women with early rheumatoid arthritis. Gend Med. 2009;6(4):544-54., during a longitudinal study in which a negative relationship was observed between HGSmax with DAS-28 and CRP. Arvidson, et al.(43)43 . Arvidson NG, Larsson A, Larsen A. Simple function tests, but not the modified HAQ, correlate with radiological joint damage in rheumatoid arthritis. Scand J Rheumatol. 2002;31(3):146-50. , (44)44 . Cesari M, Penninx BW, Pahor M, Lauretani F, Corsi AM, Williams GR, et al. Inflammatory markers and physical performance in older persons: the InCHIANTI study. J Gerontol A Biol Sci Med Sci. 2004;59(3):242-8. also demonstrated a negative association between CRP and HGSmax. Despite no correlation having been verified between HGS and the total DAS−28 score, this study found a negative correlation with NPJ, NSJ and SOH and a positive correlation with CRP.

CRP can serve as a regulatory marker of the inflammatory pathway and other inflammatory markers(45)45 . Stenholm S, Rantanen T, Heliövaara M, Koskinen S. The mediating role of C-reactive protein and handgrip strength between obesity and walking limitation. J Am Geriatr Soc. 2008;56(3):462-9.. Disease activity plays an important role in the mechanism that contributes to physical and functional impairment in patients with RA(46)46 . Stucki G, Brühlmann P, Stucki S, Michel BA. Isometric muscle strength is an indicator of self-reported physical functional disability in patients with rheumatoid arthritis. Br J Rheumatol. 1998;37(6):643-8.. The association between the disease activity parameters and the HGSmax suggests that the inflammatory process can act as catabolic mediators in the muscle(47)47 . Roubenoff R, Roubenoff RA, Ward LM, Holland SM, Hellmann DB. Rheumatoid cachexia: depletion of lean body mass in rheumatoid arthritis. Possible association with tumor necrosis factor. J Rheumatol. 1992;19(10):1505-10..

Häkkinen, et al. (48)48 . Häkkinen A, Hannonen P, Häkkinen K. Muscle strength in healthy people and in patients suffering from recent-onset inflammatory arthritis. Br J Rheumatol. 1995;34(4):355-60. believed that the reduction in strength is related to the inflammatory process, which consequently leads to the affected limb becoming disused, and thereby resulting in functional and structural changes linked to the neuromuscular system, such as the reduction of voluntary neural activation and muscle atrophy. Inflammation is one of the first signs that are related to joint destruction, ligament laxity and an imbalance in muscle function in individuals with RA. The progression of this pathological process can generate serious deformities, which results in significant functional limitations(49)49 . Boutry N, Larde A, Lapegue F, Solau-Gervais E, Flipo RM, Cotten A. Magnetic resonance imaging appearance of the hands and feet in patients with early rheumatoid arthritis. J Rheumatol. 2003;30(4):671-9..

Another mechanism resulting from inflammation that contributes to the loss of motor command, to atrophy and to muscle weakness is pain(50)50 . Riley J, Boulis NM. Molecular mechanisms of pain: a basis for chronic pain and therapeutic approaches based on the cell and the gene. Clin Neurosurg. 2006;53:77-97.. The process that triggers pain in RA sufferers is related to the peripheral sensitization, where the afferent nerves become hypersensitive to movement(51)51 . Coggeshall RE, Hong KA, Langford LA, Schaible HG, Schmidt RF. Discharge characteristics of fine medial articular afferents at rest and during passive movements of inflamed knee joints. Brain Res. 1983;272(1):185-8. , (52)52 . Schaible HG, Schmidt RF. Time course of mechanosensitivity changes in articular afferents during a developing experimental arthritis. J Neurophysiol. 1988;60(6):2180-95.. Considering that pain was the main complaint clinic mentioned by patients, as was verified negative correlation between HGSmax and NPJ, the data from this study reinforce the involvement of the inflammatory process in the reduced HGSmax of individuals with RA.

However, it is important to stress that given the small number of individuals evaluated, where the participants were selected by convenience, as well as the absence of radiological examination in order to determine the state of the disease, there is a limitation inherent to this study, thereby damaging the generalization of the obtained results. Such limitations occurred due to the difficculty of fi patients with RA who were available to go to the laboratory to participate in the study, as well as the lack of funding to perform radiological examinations. Despite their preliminary nature, the data from is study is considered relevant for characterizing the HGS of patients with RA, participants of studies developed in our laboratory. Finally, it is clear that further work must be performed with a larger number of subjects in order to study and characterize the relationship between HGS and the level of disease activity. Th information from this study will contribute in terms of improving the quality of life for these individuals; it also highlighted the importance and relevance of the multidisciplinary treatment, and thereby should lead to better management and treatment of the pathology.

CONCLUSION

The findings showed that women with RA presented a reduction in their ability to produce HGSmax, regardless of the dominant hand. In addition, they demonstrated that there is a direct relationship between HGSmax and the determining parameters for the level of disease activity.

  • 1
    Oken O, Batur G, Gunduz R, Yorgancioglu RZ. Factors associated with functional disability in patients with rheumatoid arthritis. Rheumatol Int. 2008;29(2):163-6.
  • 2
    Eurenius E, Stenström CH. Physical activity, physical fitness, and general health perception among individuals with rheumatoid arthritis. Arthritis Rheum. 2005;53(1):48-55.
  • 3
    Watanabe K, Tsubota S, Chin G, Aoki M. Differences in parameters of the explosive grip force test between young and older women. J Gerontol A Biol Sci Med Sci. 2011;66(5):554-8.
  • 4
    Bodur H, Yilmaz O, Keskin D. Hand disability and related variables in patients with rheumatoid arthritis. Rheumatol Int. 2006;26(6):541-4.
  • 5
    Ferraz MB, Ciconelli RM, Araujo PMP, Oliveira LM, Atra E. The effect of elbow flexion and time of assessment on the measurement of grip strength in rheumatoid-arthritis. J Hand Surg Am. 1992;17A(6):1099-103.
  • 6
    Thyberg I, Hass UA, Nordenskiöld U, Gerdle B, Skogh T. Activity limitation in rheumatoid arthritis correlates with reduced grip force regardless of sex: the Swedish TIRA project. Arthritis Rheum. 2005;53(6):886-96.
  • 7
    Adams J, Burridge J, Mullee M, Hammond A, Cooper C. Correlation between upper limb functional ability and structural hand impairment in an early rheumatoid population. Clin Rehabil. 2004;18(4):405-13.
  • 8
    Hoenig H, Groff G, Pratt K, Goldberg E, Franck W. A randomized controlled trial of home exercise on the rheumatoid hand. J Rheumatol. 1993;20(5):785-9.
  • 9
    Haidar SG, Kumar D, Bassi RS, Deshmukh SC. Average versus maximum grip strength: which is more consistent? J Hand Surg Br. 2004;29(1):82-4.
  • 10
    Rosén B. Recovery of sensory and motor function after nerve repair. A rationale for evaluation. J Hand Ther. 1996;9(4):315-27.
  • 11
    MacDermid JC, Kramer JF, Woodbury MG, McFarlane RM, Roth JH. Interrater reliability of pinch and grip strength measurements in patients with cumulative trauma disorders. J Hand Ther. 1994;7(1):10-4.
  • 12
    Hakkinen A, Kautiainen H, Hannonen P, Ylinen J, Makinen H, Sokka T. Muscle strength, pain, and disease activity explain individual subdimensions of the Health Assessment Questionnaire disability index, especially in women with rheumatoid arthritis. Ann Rheum Dis. 2006;65(1):30-4.
  • 13
    Alomari MA, Keewan EF, Shammaa RA, Alawneh K, Khatib SY, Welsch AA. Vascular function and handgrip strength in rheumatoid arthritis patients. Sci World J. 2012;2012.
  • 14
    Rajagopalan A, Burne JA. Stretch reflexes and joint dynamics in rheumatoid arthritis. Exp Brain Res. 2010;201(1):37-45.
  • 15
    Pollard L, Choy EH, Scott DL. The consequences of rheumatoid arthritis: quality of life measures in the individual patient. Clin Exp Rheumatol. 2005;23(5 Suppl 39):S43-52.
  • 16
    Targonska-Stepniak B, Majdan M. Associations between parameters of nutritional status and disease activity in patients with rheumatoid arthritis. Pol Arch Med Wewn. 2011;121(4):122-8.
  • 17
    Dogu B, Kuran B, Yilmaz F, Usen A, Sirzai H. Is hand bone mineral density a marker for hand function in patients with established rheumatoid arthritis? The correlation among bone mineral density of the hand, radiological findings and hand function. Clin Rheumatol. 2013.
  • 18
    Fransen J, Van Riel PL. Outcome measures in inflammatory rheumatic diseases. Arthritis Res Ther. 2009;11(5):244.
  • 19
    Arnett FC, Edworthy SM, Bloch DA, McShane DJ, Fries JF, Cooper NS, et al. The American rheumatis association 1987 revised criteria for the classification of rheumatoid arthritis. Arthritis Rheum. 1988;31(3):315-24.
  • 20
    Prevoo MLL, Vanthof MA, Kuper HH, Vanleeuwen MA, Vandeputte LBA, Vanriel P. Modified disease-activity scores that include 28-joint counts development and validation in a prospective longitudinal-study of patients with rheumatoid-arthritis. Arthritis Rheum. 1995;38(1):44-8.
  • 21
    Pincus T, Sokka T. Quantitative measures for assessing rheumatoid arthritis in clinical trials and clinical care. Best Pract Res Clin Rheumatol. 2003;17(5):753-81.
  • 22
    Inoue E, Yamanaka H, Hara M, Tomatsu T, Kamatani N. Comparison of Disease Activity Score (DAS)28erythrocyte sedimentation rate and DAS28C-reactive protein threshold values. Ann Rheum Dis. 2007;66(3):407-9.
  • 23
    Fransen J, Van Riel PL. DAS remission cut points. Clin Exp Rheumatol. 2006;24(6 Suppl 43):S-29-32.
  • 24
    Brito G, Brito L, Paumgartten F, Lins M. Lateral preferences in brazilian adults: An analysis with the Edinburgh Inventory. CORTEX. 1989;25(3):403-15.
  • 25
    Oldfield RC. The assessment and analysis of handedness: the Edinburgh inventory. Neuropsychologia. 1971;9(1):97-113.
  • 26
    Borges NGJ, Domenech SC, da Silva ACK, Dias JA. Estudo comparativo da força de preensão isométrica máxima em diferentes modalidades esportivas. Rev Bras Cineantropom Desempenho Hum. 2009;11(3):292-8.
  • 27
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  • Study developed at the Multisector Analysis Laboratory (MULTILAB) of the Health and Sport Sciences Center (CEFID) at the State University of Santa Catarina (UDESC) - Florianópolis, Brazil.
  • Financing source: none

Publication Dates

  • Publication in this collection
    Jan-Mar 2015

History

  • Received
    Sept 2014
  • Accepted
    Dec 2014
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