| Literature DB >> 31620864 |
Koichi Murata1,2, Motomu Hashimoto3,4, Wataru Yamamoto3,5, Yonsu Son6, Hideki Amuro6, Koji Nagai7, Tohru Takeuchi7, Masaki Katayama8, Yuichi Maeda9, Kosuke Ebina10, Ryota Hara11, Sadao Jinno12, Akira Onishi12, Kosaku Murakami4, Masao Tanaka3,4, Hiromu Ito13, Tsuneyo Mimori4,14, Shuichi Matsuda13.
Abstract
A family history of rheumatoid arthritis (RA) is a strong risk factor for developing RA, affecting both genetically and environmentally. However, whether family history provides clinically relevant information in the modern classification and treatment remains largely unknown. This study aimed to determine whether a family history of RA is associated with a different clinical presentation of RA and treatment response. We retrospectively evaluated the demographic data and disease activity of newly diagnosed RA patients at baseline, 1 year, and 2 years after onset, using the ANSWER (Kansai consortium for the well-being of rheumatic disease patients) cohort data. Thirty-one patients (11.9%) among 260 newly diagnosed RA patients had a family history of RA up to second degree. There was no significant difference in the age at onset, time from onset to first visit, sex, positivity or value of rheumatoid factor or anti-cyclic citrullinated peptide antibody (ACPA), or disease activity between patients with and without a family history of RA. However, patients who had a family history of RA and were ACPA positive showed significantly lower erythrocyte sedimentation rate, and C-reactive protein. Disease activity in patients with a family history was not worse at baseline, after 1 year or 2 years of treatment. The Larsen score 2 years after onset was equivalent between the patients with and without a family history of RA in ACPA-positive patients. Family history of RA in ACPA-positive patients is not associated with high disease activity at baseline and is not a predictor of poor outcome 2 years after onset.Entities:
Keywords: Anti-citrullinated protein antibody; Family history taking; Rheumatoid arthritis
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Year: 2019 PMID: 31620864 DOI: 10.1007/s00296-019-04464-9
Source DB: PubMed Journal: Rheumatol Int ISSN: 0172-8172 Impact factor: 2.631