Systemic lupus erythematosus is associated with increased risk of Parkinson’s disease

IF 3.4 2区 医学 Q2 RHEUMATOLOGY
I. Kim, Y. Eun, Jaejoon Lee, K. Han, Da Hye Kim, J. Min, H. Cha, E. Koh, D. Shin, Hyungjin Kim
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Abstract

A small number of studies have suggested an association between systemic lupus erythematosus (SLE) and Parkinson’s disease (PD). This study aimed to determine the risk of incident PD among Korean patients with SLE. A nationwide retrospective cohort study using the claims database of the National Health Insurance Service of Korea was conducted. Patients above 40 years of age diagnosed with SLE between 2010 and 2015 were included in the study. The primary outcome of the study was incident PD, defined by registration in the rare intractable diseases program for PD and an ICD-10 code of G20. Subjects were followed until PD diagnosis or the end of 2017. We estimated the cumulative incidence of PD among the SLE cohort and compared this to that in a 1:5 age- and sex-matched control group. Totals of 11,615 SLE cases and 58,075 matched controls were identified. The cumulative incidence rate of PD was 0.7 per 1000 person-years in the SLE cohort. The crude hazard ratio (HR) of incident PD was 1.71 (95% CI: 1.25–2.36) among the SLE cohort compared to the control group. The HR was 1.59 (95% CI: 1.15–2.20) after adjustment for age, sex, income, and baseline comorbidities. This study demonstrated that patients with SLE had an increased risk of incident PD compared to non-SLE controls. Further research is required to determine the mechanism underlying this and to elucidate the precise role of systemic inflammation in the development of PD in patients with SLE.
系统性红斑狼疮与帕金森病的风险增加有关
少数研究表明系统性红斑狼疮(SLE)与帕金森病(PD)之间存在关联。本研究旨在确定韩国SLE患者发生PD的风险。使用韩国国民健康保险服务的索赔数据库进行了一项全国性的回顾性队列研究。2010年至2015年间诊断为SLE的40岁以上患者纳入研究。该研究的主要结局是偶发性帕金森病,通过在罕见难治性帕金森病项目和G20的ICD-10代码中注册来定义。受试者被跟踪到PD诊断或2017年底。我们估计了SLE队列中PD的累积发病率,并将其与1:5年龄和性别匹配的对照组进行了比较。总共确定了11,615例SLE病例和58,075例匹配对照。在SLE队列中,PD的累积发病率为0.7 / 1000人年。与对照组相比,SLE队列中PD发生的粗风险比(HR)为1.71 (95% CI: 1.25-2.36)。调整年龄、性别、收入和基线合并症后,HR为1.59 (95% CI: 1.15-2.20)。该研究表明,与非SLE对照相比,SLE患者发生PD的风险增加。需要进一步的研究来确定其潜在的机制,并阐明全身性炎症在SLE患者PD发展中的确切作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.80
自引率
4.80%
发文量
132
审稿时长
18 weeks
期刊介绍: Therapeutic Advances in Musculoskeletal Disease delivers the highest quality peer-reviewed articles, reviews, and scholarly comment on pioneering efforts and innovative studies across all areas of musculoskeletal disease.
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