Epidemiological characteristics of hepatitis B and C in patients with inflammatory arthritis: Implications from treasure database.

HBV HCV TReasure rheumatic diseases rheumatoid arthritis spondyloarthritis viral hepatitis viral reactivation.

Journal

Archives of rheumatology
ISSN: 2618-6500
Titre abrégé: Arch Rheumatol
Pays: Turkey
ID NLM: 101639000

Informations de publication

Date de publication:
Sep 2023
Historique:
received: 04 02 2022
accepted: 19 08 2022
medline: 4 12 2023
pubmed: 4 12 2023
entrez: 4 12 2023
Statut: epublish

Résumé

This study aimed to evaluate the hepatitis B (HBV) and C (HCV) frequency and clinical characteristics among patients with rheumatoid arthritis (RA) or spondyloarthritis (SpA) who receive biological treatments. The observational study was conducted with patients from the TReasure database, a web-based prospective observational registry collecting data from 17 centers across Türkiye, between December 2017 and June 2021. From this database, 3,147 RA patients (2,502 males, 645 females; median age 56 years; range, 44 to 64 years) and 6,071 SpA patients (2,709 males, 3,362 females; median age 43 years; range, 36 to 52 years) were analyzed in terms of viral hepatitis, patient characteristics, and treatments used. The screening rate for HBV was 97% in RA and 94.2% in SpA patients. Hepatitis B surface antigen (HBsAg) positivity rates were 2.6% and 2%, hepatitis B surface antibody positivity rates were 32.3% and 34%, hepatitis B core antibody positivity rates were 20.3% and 12.5%, HBV DNA (deoxyribonucleic acid) positivity rates were 3.5% and 12.5%, and antibody against HCV positivity rates were 0.8% and 0.3% in RA and SpA patients, respectively. The HBsAg-positive patients were older and had more comorbidities, including hypertension, diabetes, and coronary artery disease. In addition, rheumatoid factor (RF) positivity was more common in HBsAg-positive cases. The most frequently prescribed biologic disease-modifying antirheumatic drugs were adalimumab (28.5%), etanercept (27%), tofacitinib (23.4%), and tocilizumab (21.5%) in the RA group and adalimumab (48.1%), etanercept (31.4%), infliximab (22.6%), and certolizumab (21.1%) in the SpA group. Hepatitis B reactivation was observed in one RA patient during treatment, who received rituximab and prophylaxis with tenofovir. The epidemiological characteristics of patients with rheumatic diseases and viral hepatitis are essential for effective patient management. This study provided the most recent epidemiological characteristics from the prospective TReasure database, one of the comprehensive registries in rheumatology practice.

Identifiants

pubmed: 38046251
doi: 10.46497/ArchRheumatol.2023.9504
pmc: PMC10689007
doi:

Types de publication

Journal Article

Langues

eng

Pagination

347-357

Informations de copyright

Copyright © 2023, Turkish League Against Rheumatism.

Déclaration de conflit d'intérêts

Conflict of Interest: The authors declared no conflicts of interest with respect to the authorship and/or publication of this article.

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Auteurs

Emine Duygu Ersözlü (ED)

Department of Internal Medicine, Division of Rheumatology, Adana City Training and Research Hospital, Adana, Türkiye.

Mustafa Ekici (M)

Department of Internal Medicine, Division of Rheumatology, Hacettepe University, Ankara, Türkiy.

Belkis Nihan Coşkun (BN)

Department of Internal Medicine, Division of Rheumatology, Uludağ University, Bursa, Türkiye.

Suade Özlem Badak (SÖ)

Department of Internal Medicine, Division of Rheumatology, Adana City Training and Research Hospital, Adana, Türkiye.

Emre Bilgin (E)

Department of Internal Medicine, Division of Rheumatology, Hacettepe University, Ankara, Türkiy.

Umut Kalyoncu (U)

Department of Internal Medicine, Division of Rheumatology, Hacettepe University, Ankara, Türkiy.

Burcu Yağız (B)

Department of Internal Medicine, Division of Rheumatology, Afyonkarahisar Hospital, Afyonkarahisar, Türkiye.

Yavuz Pehlivan (Y)

Department of Internal Medicine, Division of Rheumatology, Uludağ University, Bursa, Türkiye.

Orhan Küçükşahin (O)

Department of Internal Medicine, Division of Rheumatology, Ankara Yıldırım Beyazıt Üniversitesi, Ankara, Türkiye.

Abdulsamet Erden (A)

Department of Internal Medicine, Division of Rheumatology, Ankara City Hospital, Ankara, Türkiye.

Dilek Solmaz (D)

Department of Internal Medicine, Division of Rheumatology, Katip Çelebi University, Atatürk Eğitim ve Araştırma Hospital, Izmir, Türkiye.

Pamir Atagündüz (P)

Department of Internal Medicine, Division of Rheumatology, Marmara University, Istanbul, Türkiye.

Gezmiş Kimyon (G)

Department of Internal Medicine, Division of Rheumatology, Mustafa Kemal University, Hatay, Türkiye.

Cemal Beş (C)

Department of Internal Medicine, Division of Rheumatology, University of Health Sciences, Istanbul Başakşehir Cam and Sakura City Hospital, Istanbul, Türkiye.

Seda Çolak (S)

Department of Internal Medicine, Division of Rheumatology, University of Health Sciences, Gülhane Faculty of Medicine, Ankara, Türkiye.

Rıdvan Mercan (R)

Department of Internal Medicine, Division of Rheumatology, Namık Kemal University, Tekirdağ, Türkiye.

Timuçin Kaşifoğlu (T)

Department of Internal Medicine, Division of Rheumatology, Osmangazi University, Eskişehir, Türkiye.

Hakan Emmungil (H)

Department of Internal Medicine, Division of Rheumatology, Trakya University, Edirne, Türkiye.

Nilüfer Alpay Kanıtez (N)

Department of Internal Medicine, Division of Rheumatology, Koç University, Istanbul, Türkiye.

Aşkın Ateş (A)

Department of Internal Medicine, Division of Rheumatology, Ankara University, Ankara, Türkiye.

Süleyman Serdar Koca (SS)

Department of Internal Medicine, Division of Rheumatology, Fırat University, Elazığ, Türkiye.

Sedat Kiraz (S)

Department of Internal Medicine, Division of Rheumatology, Hacettepe University, Ankara, Türkiy.

İhsan Ertenli (İ)

Department of Internal Medicine, Division of Rheumatology, Hacettepe University, Ankara, Türkiy.

Classifications MeSH