Case Studies

Tumor necrosis factor-alpha blockade with etanercept improves autonomic dysfunction in rheumatoid arthritis

Ashit Syngle1*, Inderjeet Verma2, Pawan Krishan2, Simran Chahal2, Vijaita Syngle3

 

Author Affiliations

1Cardio Rheuma & Healing Touch City Clinic, Chandigarh, Physician & Rheumatologist Fortis Multi Specialty Hospital, Mohali, India.

2Department of Pharmaceutical Sciences & Drug Research, Punjabi University, Patiala, India.

3Healing Touch City Clinic, Chandigarh, India

 

IJRCI. 2016;4(1):CS5

 

Submitted: 8 June 2016, Accepted: 13 July 2016, Published: 14 September 2016

 

© IJRCI

 

Abstract

Rheumatoid arthritis (RA) is an autoimmune and chronic inflammatory disease associated with autonomic neuropathy. There is no specific treatment recommendation for autonomic neuropathy (AN) in rheumatic diseases. In addition, there is no study demonstrating therapeutic efficacy of TNF-inhibitor (TNFi) etanercept on autonomic neuropathy in RA. This is the first reported observation of improvement in AN with blockade of TNFi-etanercept in RA. We report a case of a 46-year-old female with severe disease activity treated with subcutaneous etanercept 50mg once a week along with methotrexate 15 mg/week.  A significant improvement in cardiovascular autonomic neuropathy and sudomotor function was noted after 6 weeks of treatment.

 

Keywords: Rheumatoid arthritis, etanercept, autonomic dysfunction, cardiovascular autonomic neuropathy, sudomotor dysfunction.

 

Introduction

Autonomic neuropathy, a well-recognized extra-articular manifestation of rheumatoid arthritis (RA), is first reported by Bennett and Scott in 1965.1 It has been shown to be one of the most important predictors of cardiovascular risk.2 However, despite the completion of half a century after the first reporting of the condition, there is no specific therapeutic strategy for autonomic dysfunction in rheumatic diseases. Therapeutic effect of disease-modifying anti-rheumatic drugs (DMARDs) and biologic DMARDs (infliximab, tociluzimab, rituximab) on autonomic neuropathy has been demonstrated in RA and ankylosing spondylitis (AS) patients.3-5 However, there is no specific treatment recommendation for autonomic neuropathy in RA. Treatment with TNF-inhibitor (TNFi) etanercept has revolutionized the treatment of RA, however, its impact on autonomic neuropathy has not been reported. The present case study describes the improvement of autonomic neuropathy with etanercept in RA.

 

Case report

A 46-year-old normotensive, non-diabetic female with 20 years of seropositive RA with inadequate response to combination of synthetic DMARDs (methotrexate 15 mg/week, hydrochloroquine 400 mg/day and sulphasalazine 3 gm/day) was initiated with subcutaneous etanercept 50 mg once a week along with methotrexate 15 mg/week.

 

In addition to active RA, the patient had light headedness and bloating after eating a small meal. These symptoms were suggestive of autonomic dysfunction. High erythrocyte sedimentation rate (ESR) of 35 mm/1st hr and high c-reactive protein (CRP) of 21 mg/dl were noted, and DAS-28 (Disease Activity Score in 28 joints) score was 8.35 (Table 1). Cardiovascular autonomic function tests were assessed using a battery of non-invasive tests and sudomotor function- peripheral sympathetic autonomic function (Sudoscan-Impeto Medical Device, EZS 01750010193, Paris-France). Autonomic function tests showed marked abnormalities of sympathetic, parasympathetic and sudomotor function (Table 1, Fig.1). No other cause for neuropathy was apparent from clinical history, physical examination and biochemical screening.

 

Table 1: Clinical and autonomic function characteristics

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Fig. 1: Sudomotor function before and after 6 weeks of treatment with etanercept

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Vitamin D, vitamin B12, and thyroid, renal and liver functions were normal. No abnormalities were reported in detailed neurological examination. Autonomic function tests were repeated after 6 weeks of etanercept exposure. After 6 weeks of therapeutic etanercept, there was a rapid improvement in heart rate response to standing and valsalva reflecting parasympathetic autonomic activity, and blood pressure response to handgrip reflecting sympathetic autonomic activity (Table 1). There was also a significant improvement in sudomotor function after 6 weeks of therapy (Table 1). ESR, CRP and DAS-28 scores were reduced (Table 1) and autonomic symptoms disappeared after 6 weeks of etanercept administration.

 

Discussion

This is the first case study to demonstrate the therapeutic impact of TNFi etanercept on autonomic neuropathy in RA. The early diagnosis and appropriate treatment of autonomic neuropathy is important because of patients being at higher risk of cardiovascular morbidity and mortality.6 Cardiovascular autonomic neuropathy is a significant risk predictor for sudden cardiac death in autoimmune rheumatic diseases.7

 

The improvement of autonomic dysfunction by TNFi etanercept therapy could be explained by the following theoretical evidence. Primarily, it has been proposed that the drug action might be through the inhibition of inflammatory cytokines. In a recent study it has been suggested that increased disease severity, ESR, TNF-α and IL-6 predicts the autonomic dysfunction in RA, and TNF-α and IL-6 blockade could potentially be beneficial for the treatment of autonomic dysfunction.8 This hypothesis is supported by the observation that RR interval variability (heart rate variability) is a marker of vagus nerve tone and is inversely related to levels of inflammatory markers (IL-6 and CRP) in the Coronary Artery Risk Development in Young Adults(CARDIA) study.9 A study by Malave and colleagues has demonstrated that circulating level of TNF has been described as an independent predictor of depressed heart rate variability.10 Furthermore, a similar study has shown that heart rate variability predicts anti-TNF therapy response in RA patients.11 Secondly, the patients with increased ESR, CRP and disease activity also have disturbances in the balance of the autonomic nervous system. Finally, there is numerous evidence for the contribution of the nervous system to inflammation. A review (2008) of thirteen studies on heart rate variability, inflammation, and cardiovascular function by Haensel et al. has stated a strong relationship between heart rate variability and inflammatory markers in cardiovascular diseases.12

 

Conclusion

To the best of our knowledge this is first reported observation of improvement in autonomic neuropathy with etanercept, in RA. In conclusion, the present case highlights that abnormal cardiovascular autonomic function and peripheral sympathetic neuropathy appeared to be rapidly improved after treatment with etanercept. Further clinical studies are warranted to confirm these observations and explore the role of etanercept in large population.

 

Competing interests

The authors declare that they have no competing interests.

 

Declaration of Interest

None

 

References

1.     Bennett PH, Scott JT. Autonomic neuropathy in rheumatoid arthritis: Ann Rheum Dis 1965;24:161-168.

2.     Vinik AI, Nevoret ML, Casellini C. The new age of sudomotor function testing: a sensitive and specific biomarker for diagnosis, estimation of severity, monitoring progression, and regression in response to intervention. Front. Endocrinol. 2015;6:94. doi: 10.3389/fendo.2015.00094.

3.     Syngle A, Verma I, Krishan P, Garg N, Syngle V. Disease-modifying anti-rheumatic drugs improve autonomic neuropathy in arthritis: DIANA study. Clin Rheumatol. 2014.34:1233-41. 

4.     Syngle A, Verma I, Krishan P. Interleukin-6 blockade Improves Autonomic Dysfunction in Rheumatoid Arthritis. Acta Reumato Port. 2015; 40:85-8.

5.     Syngle A, Verma I, Krishan P, Garg N. Tumor necrosis factor inhibition may improve autonomic dysfunction in rheumatoid arthritis. IJRCI. 2013; 1:CS7.

6.     Boulton, AJ., Freeman, R., Vinik, AI. Diabetic neuropathies: a statement by the American diabetes association. Diabetes Care. 2005;28:956-962.

7.     Milovanović B, Stojanović L, Milićevik N, Vasić K, Bjelaković B, Krotin M. Cardiac Autonomic Dysfunction in Patients with Systemic Lupus, Rheumatoid Arthritis and Sudden Death Risk. Srp Arh Celok Lek. 2010;138:26-32.

8.     Syngle A, Verma I, Garg N, Krishan P. Mediators of Autonomic Neuropathy in Rheumatoid Arthritis. Annals of rheum dis. 2014;73 (Suppl2):633-34.

9.     Sloan RP1, McCreath H, Tracey KJ, Sidney S, Liu K, Seeman T. RR interval variability is inversely related to inflammatory markers: the CARDIA study: Mol Med 2007;13:178-84.

10.   Malave HA, Taylor AA, Nattama J, Deswal A, Mann DL. Circulating levels of tumor necrosis factor correlate with indexes of depressed heart rate variability: a study in patients with mild-to moderate heart failure. Chest. 2003;123:716-24.

11.   Holman, AJ. And Ng, E. Heart rate variability predicts anti-tumor necrosis factor therapy response for inflammatory arthritis. Auton Neurosci. 2008;143:58-67.

12.   Haensel A, Mills PJ, Nelesen RA, Ziegler MG, Dimsdale JE. The relationship between heart rate variability and inflammatory markers in cardiovascular disease. Psycho neuro endocrionology. 2008;33:1305-12.