|Year : 2019 | Volume
| Issue : 1 | Page : 22-26
Prevalence and patterns of peripheral neuropathy in patients of rheumatoid arthritis
Nidhi Kaeley1, Sohaib Ahmad2, Monika Pathania3, Rajesh Kakkar3
1 Department of Emergency Medicine, AIIMS, Rishikesh, Uttarakhand, India
2 Department of General Medicine, HIHT, Jolly Grant, Dehradun, Uttarakhand, India
3 Department of General Medicine, AIIMS, Rishikesh, Uttarakhand, India
|Date of Web Publication||31-Jan-2019|
Dr. Nidhi Kaeley
Department of Emergency Medicine, AIIMS, Rishikesh, Uttarakhand
Source of Support: None, Conflict of Interest: None
Background: Rheumatoid arthritis (RA) is an autoimmune disorder characterized by involvement of multiple small and large joints with multisystem extra-articular manifestations. Peripheral neuropathy is known extra-articular manifestation of RA with the incidence of around 39.19% as per previous studies. Early diagnosis and treatment of peripheral neuropathy has been shown to improve both physical and functional disabilities of patients with RA. Objectives: The primary objective was to study prevalence and patterns of peripheral neuropathy in patients with RA. The secondary objective was to study demographic, clinical parameters, disease severity, and extra- articular manifestations in patients with RA with and without peripheral neuropathy. Materials and Methods: Consecutive patients of RA were recruited. Detailed clinical examination and electrophysiological tests were done to diagnose peripheral neuropathy. The demographic and clinical parameters were noted and tabulated. Student's t-test was used to analyze continuous variable, whereas Chi-square test was used for analysis of categorical variables. Results: Of 89 patients with RA, 75.28% (n = 67) patients had peripheral neuropathy electrophysiologically, whereas 20.89% (14 patients of 67) had superficial touch sensory loss on examination. Subclinical neuropathy was present in 50.74% (n = 34) of patients. Statistically significant association between the presence of neuropathy and age of the patients, disease duration, use of disease-modifying antirheumatoid drugs, disease severity (disease activity score-28), and presence of subcutaneous nodules (P < 0.05). Conclusion: Patients with RA, especially elderly patients, should undergo electrophysiological testing to rule out peripheral neuropathy. Electrophysiological study is a diagnostic and gold standard tool to diagnose subclinical neuropathy in patients with RA. Presence of peripheral neuropathy in these patients has been found to be significantly associated with deteriorating health status, pain scores, and presence of extra-articular manifestations.
Keywords: Axonal, neuropathy, sensorimotor, subcutaneous nodules
|How to cite this article:|
Kaeley N, Ahmad S, Pathania M, Kakkar R. Prevalence and patterns of peripheral neuropathy in patients of rheumatoid arthritis. J Family Med Prim Care 2019;8:22-6
|How to cite this URL:|
Kaeley N, Ahmad S, Pathania M, Kakkar R. Prevalence and patterns of peripheral neuropathy in patients of rheumatoid arthritis. J Family Med Prim Care [serial online] 2019 [cited 2021 Apr 17];8:22-6. Available from: https://www.jfmpc.com/text.asp?2019/8/1/22/251152
| Introduction|| |
Rheumatoid arthritis (RA) is a chronic inflammatory autoimmune multisystem disorder with symmetrical involvement of small and large joints. It has multiple extra-articular manifestations such as interstitial lung disease, peripheral neuropathy, and ocular involvement such as episcleritis, scleritis, and vasculitis. The prevalence of clinical neuropathy varies from 0.5% to 85% in patients with RA. Presence of peripheral neuropathy exacerbates to functional disability in patients with RA. A previous study by Hart and Goldin was the first case series of patients wit RA with peripheral neuropathy. The types of peripheral neuropathy in patients with RA are pure sensory, distal axonal sensory motor, mono-neuritis multiplex, and entrapment neuropathy. Patients with peripheral neuropathy present with diverse signs and symptoms such as pain, numbness, pins and needle sensation, and muscle weakness., Thus, it is difficult to differentiate between signs and symptoms of peripheral neuropathy and that of arthritis. RA leads to joint and cartilage destruction. The etiology of peripheral neuropathy is poorly understood. Previous studies have attributed nerve entrapment, drug toxicity, vasculitis, amyloidosis, and autoimmune phenomenon as possible causes of peripheral neuropathy in patients with RA.,, It is responsible for deteriorating quality of life and life expectancy rates., The purpose of this study was to determine the prevalence, types, and clinical determinants of peripheral neuropathy in patients with RA.
| Materials and Methods|| |
This study was conducted at a tertiary care hospital of Uttrakhand. Eighty-nine newly diagnosed patients with RA age more than 18 years attending medicine clinic were recruited from May 2017 to December 2017 over a period of 6 months. The patients were diagnosed as per American Rheumatology Association (ARA) criteria, 2010. Detailed demographic, clinical, and drug history was obtained from all patients. Detailed history of sensory symptoms such as pins and needle sensation, burning, numbness, and motor symptoms such as weakness of distal extremities was compiled in the form of structured questionnaire. Detailed sensory examination in the form of testing for loss of superficial touch sensation, pain, temperature, vibration sense, and two-point discrimination was done.
For testing superficial touch sensation, a 5.07 Semmes Weinstein monofilament was used. Pain sensation was tested using the blunt end of the needle. A 256-Hz turning fork was used to test vibration sense. Disease activity score (DAS)-28 was used to assess the severity of RA. Score more than 3.2 was considered to be active disease. Patients who were unconscious or had presented in altered sensorium were excluded from the study. Also, patients suffering from diabetes mellitus, hypothyroidism, hyperthyroidism, malignancy, and with alcohol or toxic exposure were excluded from the study.
Sensory nerve conduction study was done for bilateral sural nerves at mid- calf level. Similarly, sensory neuropathy was checked on bilateral median and ulnar nerves at wrist levels.
Motor nerve conduction studies were done for bilateral median and ulnar nerves at wrist and elbow levels and also for bilateral peroneal and tibial nerve at ankle and knee level. F waves were calculated for bilateral tibial and peroneal nerves. The polyneuropathy was pathophysiologically differentiated as axonal or demyelinating type. Detailed physical examination was done to look for extra-articular manifestations such as subcutaneous nodules, interstitial lung disease, and features suggestive of vasculitis in the form of palpable purpura and digital infarcts. Routine investigations in the form of liver function tests, renal function tests, and inflammatory markers in the form of erythrocyte sedimentation rate (ESR), and C-reactive protein were done in all the patients with RA.
Past and current treatment history including prior use of steroids and disease-modifying antirheumatoid drugs (DMARDS) was noted. X-rays of bilateral hands were done in all the patients to detect joint erosions. Pulmonary function tests and HRCT thorax were done in 17 patients with RA who had symptoms and signs suggesting interstitial lung disease. Quantitative assessment of rheumatoid factor was done using latex agglutination test. Stanford Health Assessment Questionnaire Disability Index (HAQ-D1) was used to assess functional disability of patients with RA. It is a set of eight questions based on daily physical activities. Tinsel's sign was elicited to detect possible tibial and peroneal neuropathies. Phalen's sign was elicited to detect median neuropathy. Pain assessment was done using visual analog scale (VAS). Ethical clearance was taken from institutional ethics committee. Written informed consent was taken from all the patients participating in this study.
| Results|| |
Eighty-nine patients with RA were included in the study. Sixty-seven (75.28%) patients showed peripheral neuropathy detected electrophysiologically. Out of 67 patients with RA with peripheral neuropathy, only 20.89% had clinical loss of superficial touch sensation, 14.42% had loss of temperature sensation, and only 4.1% patients had loss of joint position and vibration sense [Table 1]. Phalen's sign was positive in 8 (8.9%), whereas Tinsel's sign was positive in 24 (26.9%). Six (8.95%) patients with RA with peripheral neuropathy had motor abnormalities. Subclinical neuropathy was present in 34 (50.74%). The mean age of the patients with RA with peripheral neuropathy was 54.34 ± 11.64 years which was significantly higher than those without peripheral neuropathy. The mean duration of illness of patients with neuropathy was significantly (15 ± 7.29 years) longer than that without neuropathy (5.32 ± 5.51) [Table 2].
|Table 1: Demographic, clinical, and extra-articular manifestation of patients of rheumatoid arthritis|
Click here to view
|Table 2: Comparison of parameters of patients with RA with and without neuropathy|
Click here to view
Five (7.46%) patients out of 67 patients had foot deformities, 3 (4.47%) had hammer toes, 2 (2.98%) had claw toes, whereas only one (1.49%) patient had hallus valgus deformity. Four (5.97%) patients had Achilles tendonitis and two (2.98%) had plantar fasciitis. The majority (n = 30, 22.38%) of the patients with RA had asymmetrical sensorimotor axonal neuropathy followed by pure motor neuropathy (n = 15, 22.38%), 6 (8.95%) patients had sensory neuropathy, 8 (11.94%) had entrapment neuropathy, and 8 (11.94%) had mononeuritis multiplex on nerve conduction study. Out of eight patients with entrapment neuropathy, two had bilateral median nerve involvement, four had unilateral median nerve, whereas only two had unilateral ulnar nerve entrapment. The majority of the patients with RA with peripheral neuropathy were receiving DMARDS (methotrexate 94.02%, hydoxychloroquine 80.59, sulfasalazine 70.14%. leflunamide 38.80%) when compared with the other group. The mean DAS-28 score was higher (6.63% ± 0.544%) in the group of patients with peripheral neuropathy. The values of phase reactants (ESR, CRP) were also higher in the group with peripheral neuropathy (ESR = 75.16 ± 18.33) compared with the other group (50.54 ± 2.50).
However, no significant correlation was found between presence neuropathy, interstitial lung disease, or prior use of steroids with the presence of neuropathy. Health assessment score (HAQ-D1) and VAS were significantly higher in patients with RA with neuropathy. [Table 3] shows comparisons of peripheral neuropathy patterns between present and past studies.
|Table 3: Comparisons of peripheral neuropathy patterns between present and past studies|
Click here to view
| Discussion|| |
This study focuses on prevalence and types of peripheral neuropathy in patients with RA. It highlights the differences of various demographic, clinical, and extra-articular manifestations between patients with RA with and without peripheral neuropathy. We also assessed the effect of peripheral neuropathy on general well-being as well as pain scores of patients with RA.
The presence of peripheral neuropathy in our study was (75.28%) slightly higher than previous studies conducted by Sim et al. (33%) and Biswas et al. (39.19%). This difference could be explained by the fact that our study included all the old and newly diagnosed cases of RA. Previous studies have included either newly diagnosed cases of RA or only patients with signs and symptoms of peripheral neuropathy. Biswas et al. included 74 patients with RA, whereas Sim et al. included only 30 patients with RA who had symptoms of peripheral neuropathy.,
Interestingly, only 49.25% (n = 33) of patients with peripheral neuropathy detected electrophysiologically had sensory signs and symptoms of neuropathy. Around 50% patients were asymptomatic and had subclinical neuropathy. The most common diagnosis was loss of superficial fine touch followed by loss of ankle reflex. We used standard questionnaire to elicit symptoms of peripheral neuropathy and specific tests to diagnose peripheral neuropathy clinically. Despite using a standard protocol of examination, we could only diagnose less than 50% cases of neuropathy clinically. The remaining cases were asymptomatic. Hence, it is difficult to diagnose peripheral neuropathy only by physical examination. Electrophysiological studies and further nerve biopsy studies are gold standard techniques. Aneja et al. observed that 24.2% of patients had sensory signs of peripheral neuropathy and 9.09% patients had motor signs. In our study, the majority of the patients had asymmetrical sensory motor axonal neuropathy followed by pure motor neuropathy.
Nadkar et al. and Lanzillo et al. also found that sensorimotor axonal neuropathy was the most common type of peripheral neuropathy in patients with RA., However, Biswas et al. and Albani et al. reported that pure sensory type was the most common type of peripheral neuropathy in the patients with RA.,
Females outnumbered males (7.3:1.1) in our study. This could be due to the fact that RA is a female-dominant disease. This association of gender and presence of peripheral neuropathy was not in accordance with the studies conducted by Sivri et al. Interestingly, Albani et al. reported that male gender was significantly associated with the presence of peripheral neuropathy. Our study described a significant association of increasing age and presence of peripheral neuropathy. Thus, one of the secondary causes of peripheral neuropathy in geriatric population is RA. Peripheral neuropathy in geriatric population is often underdiagnosed. Apart from the secondary causes, there are physiological deterioration in the anatomy and function of peripheral nerves with increasing age. These patients are more prone to falls. This could significantly limit their daily activities and functional decline in old age.,, Bharadwaj et al. and Agarwal et al. reported this association to be significant., On the contrary, certain studies in the past did not find this association to be significant. This could be attributed to smaller sample size in these studies.
Rheumatoid factor positivity was found to be significantly associated with presence of peripheral neuropathy. A similar result was reported by Albani et al. and Biswas et al., However, multiple studies in the past have refuted this correlation.,
Studies conducted by Bhardwaj et al. and Hamed et al. have found a positive association between presence of neuropathy and disease duration., Our study also showed a similar result. A significant association was found between inflammatory markers of disease activity (ESR, CRP) and peripheral neuropathy in our study. Similarly, significant association was found between DAS-28 and presence of peripheral neuropathy. This was also observed by Rajesh et al. There was no significant association between presence of subcutaneous nodules and peripheral neuropathy in our study. Similar results were reported by previous studies.,
Significantly large number of patients with peripheral neuropathy in our study had radiological evidence of joint erosion of bilateral hands. Such an association was reported to be insignificant by Biswas et al., Sivri et al., and Nadkar et al. Smaller sample size could be the reason for this. No significant association was found between presence of neuropathy and prior use of steroids, and interstitial lung disease in our study. This was in accordance with previous studies.,, Previous studies have found a significant correlation between presence of functional incapacity in patients with RA with neuropathy and disease activity. Also, pain score (VAS) was higher in patients with RA with neuropathy. Our study also had higher HAQ-D1 score in patients with RA with neuropathy. Hence, overall well-being of the patient with RA can be correlated with presence of neuropathy especially in geriatric population.
The treatment of peripheral neuropathy involves a multispecialty approach. Hence, the role of family medicine physician is pivotal in not only treating these patients but also improving their quality of life.
| Conclusion|| |
Peripheral neuropathy in RA is associated with increasing age, duration of Disease, and increased disease severity. This adds to the functional disabilities especially in geriatric population. Overt neuropathic symptoms can be detected clinically, whereas subclinical neuropathy can only be detected electrophysiologically. Hence, nerve conduction studies should be carried out in all the patients with RA. This will help in better management of these patients.
Financial support and sponsorship
Conflicts of interest
There are no conflicts of interest.
| References|| |
Agarwal V, Singh R, Wiclaf, Chauhan S, Tahlan A, Ahuja CK, et al
. A clinical, electrophysiological, and pathological study of neuropathy in rheumatoid arthritis. Clin Rheumatol 2008;27:841-4.
Hart FD, Goldin JR. Rheumatoid neuropathy. Br Med J 1960;1:1594-600.
Bharadwaj A, Haroon N. Interstitial lung disease and neuropathy as predominant exta-articular manifestation in patients with rheumatoid arthritis. Med Sci Monit 2005;11:CR498-502.
Golding DN. Rheumatoid neuropathy. Br Med J 1971;2:169.
Pouget J. Vascular neuropathies. Rev Prat 2000;50:749-52.
Salih AM, Nixon NB, Gagan RM, Heath P, Hawkins CP, Dawes PT, et al
. Anti-ganglioside antibodies in patients with rheumatoid arthritis complicated by peripheral neuropathy. Br J Rheumatol 1996;35:725-31.
Bayrak AO, Durmus D, Durmaz Y, Demir I, Canturk F, Onar MK. Electrophysiological assessment of polyneuropathic involvement in rheumatoid arthritis: Relationships among demographic, clinical and laboratory findings. Neurol Res 2010;32:711-4.
Kawaguchi Y, Matsuno H, Kanamori M, Ishihara H, Ohmori K, Kimura T. Radiologic findings of the lumbar spine in patients with rheumatoid arthritis, and a review of pathologic mechanisms. J Spinal Disord Tech 2003;16:38-43.
Kay J, Katherine S. Upchurch. ACR/EULAR 2010 rheumatoid arthritis classification criteria. Rheumatology 2012;51:vi5-9.
Haefeli M, Elfering A. Pain assessment. Eur Spine J 2006;15(Suppl. 1):S17-24.
Sim MK, Kim DY, Yoon J, Park DH, Kim YG. Assessment of peripheral neuropathy in patients with rheumatoid arthritis who complain of neurologic symptoms. Ann Rehabil Med 2014;38:249-55.
Biswas M, Chatterjee A, Ghosh SK, Dasgupta S, Ghosh K, Ganguly PK. Prevalence, types, clinical associations, and determinants of peripheral neuropathy in rheumatoid patients. Ann Indian Acad Neurol 2011;14:194-7.
] [Full text]
Aneja R, Singh MB, Shankar S, Dhir V, Grover R, Gupta R, et al
. Prevalence of peripheral neuropathy in patients with newly diagnosed rheumatoid arthritis. Indian J Rheumatol 2007;2:47-50. [Full text]
Nadkar MY, Agarwal R, Samant RS, Chhugani SS, Idgunji SS, Iyer S, et al
. Neuropathy in rheumatoid arthritis. J Assoc Pysicians India 2001;49:217-20.
Lanzillo B, Pappone N, Crisci CDI, Girolamo C, Massini R, Caruso G. Subclinical peripheral nerve involvement in patients with rheumatoid arthritis. Arthritis Rheum 1998;41:1196-202.
Albani G, Ravaglia S, Cavagna L, Caporali R, Montecucco C, Mauro A. Clinical and electrophysiological evaluation of peripheral neuropathy in rheumatoid arthritis. J Peripher Nerv Syst 2006;11:174-5.
Sivri A, Guler-Uysal F. The electroneurophysiological findings in rheumatoid arthritis patients. Electromyogr Clin Neurophysiol 1999;39:387-91.
Dorfman LJ, Bosley TM. Age-related changes in peripheral and central nerve conduction in man. Neurology 1979;29:38-44.
Bouche P, Cattelin F, Saint-Jean O, Léger JM, Queslati S, Guez D, et al
. Clinical and electrophysiological study of the peripheral nervous system in the elderly. J Neurol 1993;240:263-8.
Taylor PK. Non-linear effects of age on nerve conduction in adults. J Neurol Sci 1984;66:223-34.
Lang AH, Kalliomäki JL, Puusa A, Halonen JP. Sensory neuropathy in rheumatoid arthritis: An electroneurographic study. Scand J Rheumatol 1981;10:81-4.
Woo JH, Lee KH, Park YW, Lee HS, Uhm WS, Kim TH, et al
. Clinical manifestation of mononeuritis multiplex in patients with rheumatoid arthritis. J Korean Rheum Assoc 2004;11:90-5.
Hamed SA, Hamed EA, Elattar AM, Rahman MS, Amine NF. Cranial and peripheral neuropathy in rheumatoid arthritis with special emphasis to II, V, VII and XI cranial nerves. Aplar J Rheum 2006;9:216-26.
Rajesh K, Pradhan RN, Bhagatula S. Peripheral neuropathy in rheumatoid arthritis: A hospital based study. 2016;4.
El-Hewala AE, Soliman SG, Labeeb AA, Zytoon AA, El-Shanawany AT. Foot neuropathy in rheumatoid arthritis patients: Clinical, electrophysiological, and ultrasound studies. Ear 2016;43:85-94.
Mold J, Vesely S, Keyl B, Schenk J, Roberts M. The prevalence, predictors, and consequences of peripheral sensory neuropathy in older patients. J Am Board Fam Med 2004;17:309-18.
[Table 1], [Table 2], [Table 3]
|This article has been cited by|
||Rheumatologisch bedingte neurologische Erkrankungen
| ||Matthias Maschke,Stefan Weiner |
| ||DNP - Der Neurologe & Psychiater. 2021; 22(1): 40 |
|[Pubmed] | [DOI]|
||Advances in imaging technologies for the assessment of peripheral neuropathies in rheumatoid arthritis
| ||Josefina Gutiérrez,Hugo Sandoval,Iván Pérez-Neri,Antonio Arauz,Juan Carlos López-Hernández,Carlos Pineda |
| ||Rheumatology International. 2021; |
|[Pubmed] | [DOI]|
||Screen the Effective Components of Lycopodii herba on Rheumatoid Arthritis with the Aid of Spectrum-Effect Relationship and Uncover its Potential Mechanism
| ||Zhen Yang,Qingsheng Yin,Jing Ma,Changshuo Yang,Yuanyuan Sheng,Lili Song,Tan Pang,Pengwei Zhuang,Hong Guo,Yanjun Zhang |
| ||Inflammation. 2020; |
|[Pubmed] | [DOI]|
||Amyloid Proteins and Peripheral Neuropathy
| ||Mohammed M. H. Asiri,Sjoukje Engelsman,Niels Eijkelkamp,Jo W. M. Höppener |
| ||Cells. 2020; 9(6): 1553 |
|[Pubmed] | [DOI]|
||What can hand sonography and nerve conduction velocity disclose regarding hand dysfunction in rheumatoid arthritis patients?
| ||E. A. Abda,M. M. Hassanien,E. Abdelrazek,S. A. Mahran |
| ||Zeitschrift für Rheumatologie. 2020; |
|[Pubmed] | [DOI]|