Significant Associations of Neurological Complications of Herpes Zoster With Stroke in Rheumatoid Arthritis Patients

Author:

Liao Tsai‐Ling12,Lin Ching‐Heng13,Chen Hsin‐Hua1425,Chen Yi‐Ming1425,Lin Che‐Chen1,Chen Der‐Yuan6425

Affiliation:

1. Department of Medical Research, Taichung Veterans General Hospital, Taichung, Taiwan

2. Rong Hsing Research Center for Translational Medicine, National Chung Hsing University, Taichung, Taiwan

3. National Taipei University of Nursing and Health Science, Taipei, Taiwan

4. Division of Allergy, Immunology and Rheumatology, Taichung Veterans General Hospital, Taichung, Taiwan

5. Faculty of Medicine, National Yang Ming University, Taipei, Taiwan

6. Department of Internal Medicine and Medical Education, Taichung Veterans General Hospital, Taichung, Taiwan

Abstract

Background Accumulating evidence suggests an increased risk of stroke after herpes zoster ( HZ ). This risk is elevated in immunocompromised patients. The incidence of HZ in Asia is higher than in Western countries. However, the epidemiology of HZ and HZ ‐related stroke among rheumatoid arthritis ( RA ) patients in Asia remains unclear. Methods and Results We conducted a retrospective cohort study using a population‐based database to investigate the epidemiology of HZ in RA patients in Taiwan during the period of 2000‐2011. A total of 27 609 newly diagnosed and eligible RA cases were identified, and 110 436 non‐ RA cases were matched for age and sex at a ratio of 4:1. HZ risk increased by 2.53‐fold ( P <0.0001) in RA patients compared with the general population. Exposure to corticosteroids (adjusted odds ratio=1.73, P <0.0001), adalimumab (adjusted odds ratio=1.61, P =0.002), and rituximab (adjusted odds ratio=2.06, P =0.008) was associated with an increased risk of HZ in RA patients. A significant association between the use of methotrexate or corticosteroids and HZ risk was dose‐dependent ( P trend <0.0001). Elevated risk of stroke was observed in RA patients with HZ (adjusted hazard ratio=1.27, P =0.047), particularly in those with neurological complications (adjusted hazard ratio=1.54, P =0.015). A 2.30‐fold significantly increased risk of stroke within 90 days after HZ occurrence was observed in RA patients compared with those without HZ ( P =0.02). Furthermore, death risk increased in RA patients with HZ (adjusted hazard ratio=1.18, P =0.026). Conclusions The risk of HZ and HZ ‐related stroke has increased in RA patients. Monitoring the occurrence of HZ in RA patients and preventing HZ ‐related stroke or mortality during a specific immunosuppressive therapy are important.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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