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阿拉斯加原住民和阿拉斯加印第安人的血管炎患病率及临床特征

Prevalence and Clinical Characteristics of Vasculitis in the Alaska Native and American Indian Peoples of Alaska.

作者信息

Henderson Ben A, Mehta Vivek R, Holck Peter, Choromanski Tammy L, Wilson Amy, Lee Flora, Ferucci Elizabeth D

机构信息

Alaska Native Tribal Health Consortium, Anchorage, Alaska.

出版信息

Arthritis Care Res (Hoboken). 2025 Jul;77(7):873-880. doi: 10.1002/acr.25506. Epub 2025 Mar 5.

DOI:10.1002/acr.25506
PMID:39936239
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12213184/
Abstract

OBJECTIVE

Our objective was to determine the prevalence and clinical characteristics of vasculitis in Alaska Native and American Indian (AN/AI) peoples of Alaska.

METHODS

We queried the electronic health records of participating tribal health organizations within the Alaska Tribal Health System (ATHS) to identify adults with diagnostic codes related to vasculitis. Medical record abstraction was performed for all adults with potential vasculitis to confirm fulfillment of inclusion criteria, subtype, and clinical characteristics. The denominator for prevalence was the 2019 ATHS user population ≥ 18 (except giant cell arteritis [GCA], defined for persons ≥ 50).

RESULTS

The age-adjusted prevalence per 1,000,000 AN/AI adults was 752 (95% confidence interval [CI] 581-959) for all vasculitis, with systemic vasculitis being the most common at 518 (95% CI 379-695). The most prevalent types of systemic vasculitis were antineutrophil cytoplasmic antibody-associated vasculitis (AAV) at 340 per million adults (95% CI 230-488) and GCA at 28 per 100,000 ≥ 50 (95% CI 12-56). The most prevalent subtype of AAV was granulomatosis with polyangiitis (GPA) at 244 per million adults (95% CI 148-380). AAV was diagnosed at a mean age of 54.2 years (SD 17), often with high markers of inflammation and renal involvement. GCA was diagnosed at a mean age of 69.6 years (SD 9.2).

CONCLUSION

The prevalence of AAV (especially GPA) in AN/AI peoples is high. GCA prevalence is lower than White populations, but higher than many other populations. AN/AI peoples with AAV and GCA may present at younger ages with more severe disease than other populations.

摘要

目的

我们的目的是确定阿拉斯加原住民和阿拉斯加美洲印第安人(AN/AI)中血管炎的患病率及临床特征。

方法

我们查询了阿拉斯加部落卫生系统(ATHS)内参与的部落卫生组织的电子健康记录,以识别具有与血管炎相关诊断代码的成年人。对所有可能患有血管炎的成年人进行病历摘要,以确认是否符合纳入标准、亚型和临床特征。患病率的分母为2019年ATHS中年龄≥18岁的用户人群(巨细胞动脉炎[GCA]除外,其定义为年龄≥50岁的人群)。

结果

所有血管炎在每100万AN/AI成年人中的年龄调整患病率为752(95%置信区间[CI]581 - 959),其中系统性血管炎最为常见,为518(95%CI 379 - 695)。系统性血管炎最常见的类型是抗中性粒细胞胞浆抗体相关性血管炎(AAV),每百万成年人中有340例(95%CI 230 - 488),GCA在年龄≥50岁的人群中每10万人中有28例(95%CI 12 - 56)。AAV最常见的亚型是肉芽肿性多血管炎(GPA),每百万成年人中有244例(95%CI 148 - 380)。AAV的诊断平均年龄为54.2岁(标准差17),通常伴有高炎症指标和肾脏受累。GCA的诊断平均年龄为69.6岁(标准差9.2)。

结论

AN/AI人群中AAV(尤其是GPA)的患病率较高。GCA的患病率低于白人人群,但高于许多其他人群。患有AAV和GCA的AN/AI人群可能比其他人群发病年龄更小,疾病更严重。

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