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巨细胞动脉炎中的 HLA-B52 等位基因可能预示着弥漫性大血管血管炎的形成:一项回顾性研究。

HLA-B52 allele in giant cell arteritis may indicate diffuse large-vessel vasculitis formation: a retrospective study.

机构信息

Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Sciences, 3-1-1 Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

Department of Cancer Stem Cell Research, Kyushu University Graduate School of Medical Sciences, Fukuoka, Japan.

出版信息

Arthritis Res Ther. 2021 Sep 13;23(1):238. doi: 10.1186/s13075-021-02618-4.

DOI:10.1186/s13075-021-02618-4
PMID:34517892
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8436550/
Abstract

BACKGROUND

This study aimed to identify new characteristics of elderly onset large-vessel vasculitis (EOLVV) by focusing on human leucocyte antigen (HLA) genotype, polymyalgia rheumatica (PMR), and affected vascular lesions observed on positron emission tomography/computed tomography (PET/CT) imaging.

METHODS

We retrospectively studied 65 consecutive Japanese patients with large-vessel vasculitis (LVV) who had extracranial vasculitis lesions and underwent PET/CT imaging. PET/CT images were assessed using the semi-quantitative PET visual score of each affected vessel, and the PET vascular activity score (PETVAS) and number of affected vessels were calculated. Subjects were subsequently grouped based on age at onset, superficial temporal artery (STA) involvement, and presence of PMR and compared each group according to HLA genotype. Unsupervised hierarchical cluster analysis was used to identify the patients with similar characteristics in terms of affected vascular lesions detected through PET/CT imaging. The clinical characteristics and PET/CT findings of the population newly identified in this study were examined.

RESULTS

Twenty-seven patients with EOLVV did not meet the American College of Rheumatology 1990 criteria for giant cell arteritis (GCA) and Takayasu arteritis and were considered as unclassified EOLVV (UEOLVV). The unsupervised hierarchical cluster analysis revealed that UEOLVV with PMR and large-vessel GCA (LV-GCA) formed a cluster of LVV with GCA features (i.e., PMR and/or STA involvement) when restricted to patients who were HLA-B52-positive. Patients who were HLA-B52-positive with LVV and GCA features had similar clinical characteristics and patterns of affected vessels and presented with diffuse LVV lesions. HLA-B52-positive patients who had LVV with GCA features also presented with higher PETVAS, more affected vessels, and lower rates of biologics usage and relapse compared to HLA-B52-positive patients with TAK.

CONCLUSIONS

Patients who had UEOLVV with PMR had similar characteristics to patients with LV-GCA. Patients who were HLA-B52-positive and had LVV with GCA features presented with diffuse vascular lesions and may comprise a core population of Japanese patients with EOLVV. The findings of HLA-B52 positivity and diffusely affected vessels in patients with EOLVV can be considered as suspicious findings of LV-GCA.

摘要

背景

本研究旨在通过关注人类白细胞抗原(HLA)基因型、巨细胞动脉炎(GCA)和正电子发射断层扫描/计算机断层扫描(PET/CT)成像上观察到的多肌痛,来确定老年发病大血管炎(EOLVV)的新特征。

方法

我们回顾性研究了 65 例连续的日本大血管炎(LVV)患者,这些患者有颅外血管炎病变,并进行了 PET/CT 成像。使用受累血管的半定量 PET 视觉评分评估 PET/CT 图像,并计算 PET 血管活性评分(PETVAS)和受累血管数量。随后根据发病年龄、颞浅动脉(STA)受累和是否存在巨细胞动脉炎(PMR)对受试者进行分组,并根据 HLA 基因型对每组进行比较。使用无监督层次聚类分析来识别在 PET/CT 成像中检测到的受累血管病变具有相似特征的患者。检查了在本研究中新确定的人群的临床特征和 PET/CT 发现。

结果

27 例 EOLVV 患者不符合美国风湿病学会 1990 年巨细胞动脉炎(GCA)和 Takayasu 动脉炎的标准,被认为是未分类的 EOLVV(UEOLVV)。无监督层次聚类分析显示,当局限于 HLA-B52 阳性患者时,PMR 和大血管 GCA(LV-GCA)的 UEOLVV 形成了具有 GCA 特征(即 PMR 和/或 STA 受累)的 LVV 聚类。具有 LVV 和 GCA 特征的 HLA-B52 阳性患者具有相似的临床特征和受累血管模式,并表现为弥漫性 LVV 病变。与 HLA-B52 阳性 TAK 患者相比,具有 GCA 特征的 HLA-B52 阳性患者的 PETVAS 更高、受累血管更多、生物制剂使用率和复发率更低。

结论

具有 PMR 的 UEOLVV 患者具有与 LV-GCA 患者相似的特征。HLA-B52 阳性且具有 GCA 特征的 LVV 患者表现为弥漫性血管病变,可能构成日本 EOLVV 患者的核心人群。在 EOLVV 患者中发现 HLA-B52 阳性和弥漫性受累血管可被视为 LV-GCA 的可疑发现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b02/8436550/24a87fdbea8a/13075_2021_2618_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b02/8436550/bfd9f6923e08/13075_2021_2618_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b02/8436550/bba9393b8075/13075_2021_2618_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b02/8436550/a3bff2d1287c/13075_2021_2618_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b02/8436550/24a87fdbea8a/13075_2021_2618_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b02/8436550/bfd9f6923e08/13075_2021_2618_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b02/8436550/bba9393b8075/13075_2021_2618_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b02/8436550/a3bff2d1287c/13075_2021_2618_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9b02/8436550/24a87fdbea8a/13075_2021_2618_Fig4_HTML.jpg

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