Prevalence of vasculitis, systemic lupus erythematosus, rheumatoid arthritis, systemic sclerosis, idiopathic inflammatory myopathies and spondyloarthritis in Australia: a systematic review and meta-analysis.

IF 1.5 4区 医学 Q2 MEDICINE, GENERAL & INTERNAL
L Roper, E Cameron, T Yu, N Li, M Parker, N Nassar, M Nikpour
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引用次数: 0

Abstract

Background: Systemic autoimmune rheumatic diseases (SARDs), including vasculitis, systemic lupus erythematosus (SLE), rheumatoid arthritis (RA), systemic sclerosis (SSc), idiopathic inflammatory myopathies (IIM), spondyloarthritis (SpA), Sjogrens disease (SjD) and mixed connective tissue disease (MCTD), are rare but associated with substantial morbidity and healthcare burden. Their clinical heterogeneity and diagnostic complexity pose challenges for epidemiological study.

Objective: To summarise Australian data on the incidence or prevalence of the SARDs listed above.

Methods: Scientific databases were searched in July 2024. Studies reporting SARD incidence or prevalence in the general Australian population were included. Where three or more studies of the same disease existed within a comparable population, which were not at high risk of bias (Hoy Tool), a random effects model was fitted.

Results: From 1357 publications, 58 were included, on: vasculitis (16), SLE (14), RA (10), SSc (nine), IIM (six) and SpA (three), with none on SjD or MCTD identified. Meta-analysis was possible in ANCA-associated vasculitis (AAV) (incidence 10.80 per million person-years), SLE (prevalence 57.86 per 100 000), lupus nephritis (prevalence 11.20 per 100 000, incidence 1.02 per 100 000 person-years), SSc (prevalence 25.58 per 100 000), IIM (incidence 9.96 per million person-years) and inclusion body myositis (prevalence 27.73 per million). Data were limited for paediatric populations and specific at-risk groups (e.g. Australians of Asian heritage).

Conclusion: Australia may have above-average prevalence of SLE and SSc and geographic variation in SSc and AAV. Key research gaps include: (1) sparse data for non-AAV vasculitis, RA, SpA, SjD, MCTD and children; (2) limited validated algorithms to identify SARDs in administrative health data; and (3) a need for large-scale spatial studies to detect disease clusters.

澳大利亚血管炎、系统性红斑狼疮、类风湿性关节炎、系统性硬化症、特发性炎性肌病和脊椎关节炎的患病率:一项系统综述和荟萃分析
背景:系统性自身免疫性风湿性疾病(SARDs),包括血管炎、系统性红斑狼疮(SLE)、类风湿性关节炎(RA)、系统性硬化症(SSc)、特发性炎症性肌病(IIM)、脊柱关节炎(SpA)、Sjogrens病(SjD)和混合性结缔组织病(MCTD),是罕见的,但与大量发病率和医疗负担相关。其临床异质性和诊断复杂性给流行病学研究带来了挑战。目的:总结澳大利亚关于上述SARDs发病率或患病率的数据。方法:于2024年7月检索科学数据库。研究报告了SARD在澳大利亚普通人群中的发病率或流行程度。如果在可比较的人群中存在三个或更多关于同一疾病的研究,且不存在高偏倚风险(霍伊工具),则拟合随机效应模型。结果:在1357篇文献中,58篇文献被纳入,涉及血管炎(16篇)、SLE(14篇)、RA(10篇)、SSc(9篇)、IIM(6篇)和SpA(3篇),未发现SjD或MCTD。对anca相关血管炎(AAV)(发病率10.80 /百万人年)、SLE(患病率57.86 / 10万人年)、狼疮性肾炎(患病率11.20 / 10万人年,发病率1.02 / 10万人年)、SSc(患病率25.58 / 10万人年)、IIM(发病率9.96 /百万人年)和包涵体肌炎(患病率27.73 /百万人)进行meta分析。儿科人群和特定高危人群(如亚洲血统的澳大利亚人)的数据有限。结论:澳大利亚SLE和SSc的患病率可能高于平均水平,SSc和AAV的地理差异。主要研究缺口包括:(1)非aav血管炎、RA、SpA、SjD、MCTD和儿童数据稀疏;(2)在行政卫生数据中识别sard的有效算法有限;(3)需要大规模的空间研究来发现疾病聚集。
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
Internal Medicine Journal
Internal Medicine Journal 医学-医学:内科
CiteScore
3.50
自引率
4.80%
发文量
600
审稿时长
3-6 weeks
期刊介绍: The Internal Medicine Journal is the official journal of the Adult Medicine Division of The Royal Australasian College of Physicians (RACP). Its purpose is to publish high-quality internationally competitive peer-reviewed original medical research, both laboratory and clinical, relating to the study and research of human disease. Papers will be considered from all areas of medical practice and science. The Journal also has a major role in continuing medical education and publishes review articles relevant to physician education.
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