The Risk of Herpes Zoster Events in Patients with Spondyloarthritis and the Effect of BNT162b2 mRNA COVID-19 Vaccine

Author:

Gazitt Tal12ORCID,Hayat Noa3,Stein Nili4,Haddad Amir1,Feldhamer Ilan5,Cohen Arnon Dov56,Saliba Walid47,Zisman Devy17

Affiliation:

1. Rheumatology Unit, Carmel Medical Center, Haifa 3436212, Israel

2. Division of Rheumatology, University of Washington Medical Center, Seattle, WA 98195-6428, USA

3. Department of Internal Medicine, Carmel Medical Center, Haifa 3436212, Israel

4. Department of Community Medicine and Epidemiology, Carmel Medical Center, Haifa 3436212, Israel

5. Chief Physician’s Office, Central Headquarters, Clalit Health Services, Tel Aviv 67754, Israel

6. Siaal Research Center for Family Medicine and Primary Care, Faculty of Health Sciences, Ben-Gurion University of the Negev, Beer-Sheva 84105, Israel

7. The Ruth and Bruce Rappaport Faculty of Medicine, Technion, Haifa 31096, Israel

Abstract

The data on the risk of herpes zoster (HZ) in spondyloarthropathy (SpA) patients are sparse, especially regarding its association with the novel mRNA COVID-19 vaccines and immunosuppressants. We aimed to evaluate whether SpA diagnosis and/or immunosuppressant use affect HZ risk and the influence of mRNA COVID-19 vaccination. We assessed the association between SpA (psoriatic arthritis (PsA) and ankylosing spondylitis (AS)) diagnoses and HZ in a large population database with patients matched by age and sex to controls. We also assessed the association between the COVID-19 vaccine and new-onset HZ using two nested case–control studies, identifying all new HZ cases diagnosed from 1 January–31 December 2021 within the SpA and general population cohorts, matched randomly by sex, age and HZ index date to controls without HZ. Exposure to mRNA COVID-19 vaccination was ascertained in the 6 weeks prior to the index date both in cases and controls. In our results, the incidence rate of HZ was higher in PsA patients vs. the general population, at 1.03 vs. 0.64 per 100 person-years, respectively (adjusted HR = 1.55; 95%CI, 1.19–2.02). Within the SpA group, Jak-I treatment was associated with a higher risk of developing new-onset HZ (adjusted OR = 3.79; 1.15–12.5). Multivariable conditional logistic regression models we used showed no association between COVID-19 vaccination and new-onset HZ among the SpA patients (OR = 1.46; 0.68–3.14).

Publisher

MDPI AG

Subject

Pharmacology (medical),Infectious Diseases,Drug Discovery,Pharmacology,Immunology

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