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The prevalence and the clinical relevance of anti-Ro52 in Korean patients with primary Sjogren's syndrome

Authors
Song, Jung-SooDo, Jae HyukLee, Sang-Won
Issue Date
Feb-2012
Publisher
SPRINGER HEIDELBERG
Keywords
Anti-Ro52; Clinical manifestations; Primary Sjogren's syndrome
Citation
RHEUMATOLOGY INTERNATIONAL, v.32, no.2, pp 491 - 495
Pages
5
Journal Title
RHEUMATOLOGY INTERNATIONAL
Volume
32
Number
2
Start Page
491
End Page
495
URI
https://scholarworks.bwise.kr/cau/handle/2019.sw.cau/20541
DOI
10.1007/s00296-010-1790-x
ISSN
0172-8172
1437-160X
Abstract
So far, there was no report on the prevalence and clinical relevance of anti-Ro52 in primary Sjogren's syndrome (pSS) patients in Korea. In this study, we investigated the prevalence and the clinical relevance of anti-Ro52 in Korean patients with pSS. We retrospectively reviewed the medical records of 96 patients with pSS. On the first visit clinical manifestations, laboratory features and autoantibodies were assessed. We divided subjects into 4 groups according to the presence of anti-Ro60 or anti-Ro52 and investigated the association between those autoantibodies and clinical manifestations. Anti-Ro52 (66.7%) was the most frequently detected autoantibody, followed by anti-Ro60 (52.1%) and anti-La (49.0%). Patients with anti-Ro52 had higher frequency of liver and muscle involvements than those without, while anti-Ro60 exhibited negative association with liver involvement. Anti-Ro52 showed significant relative risk for liver involvement (OR = 5.987, P = 0.038, 95% CI = 1.109-32.326), while anti-Ro60 showed inverse relative risk for liver involvement (OR = 0.122, P = 0.003, 95% CI = 0.031-0.479). Anti-Ro52 also showed significant OR for muscle involvement (OR = 9.533, P = 0.044, 95% CI = 1.059-85.793). In conclusion, anti-Ro52 was the most frequently detected autoantibody except ANA in patients with pSS in Korea. Anti-Ro52 was significantly associated with liver and muscle involvements, while anti-Ro60 was inversely associated with liver involvement in Korean patients with pSS.
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