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2022 年美国风湿病学会/欧洲风湿病学会联合会嗜酸性肉芽肿伴多血管炎分类标准。

2022 American College of Rheumatology/European Alliance of Associations for Rheumatology Classification Criteria for Eosinophilic Granulomatosis With Polyangiitis.

机构信息

National Institute of Arthritis and Musculoskeletal and Skin Diseases, NIH, Bethesda, Maryland.

Hospital de Santa Maria, Centro Hospitalar Universitário Lisboa Norte, Universidade de Lisboa, and Centro Académico de Medicina de Lisboa, Lisbon, Portugal.

出版信息

Arthritis Rheumatol. 2022 Mar;74(3):386-392. doi: 10.1002/art.41982. Epub 2022 Feb 2.

Abstract

OBJECTIVE

To develop and validate revised classification criteria for eosinophilic granulomatosis with polyangiitis (EGPA).

METHODS

Patients with vasculitis or comparator diseases were recruited into an international cohort. The study proceeded in 5 phases: 1) identification of candidate criteria items using consensus methodology, 2) prospective collection of candidate items present at the time of diagnosis, 3) data-driven reduction of the number of candidate items, 4) expert panel review of cases to define the reference diagnosis, and 5) derivation of a points-based risk score for disease classification in a development set using least absolute shrinkage and selection operator logistic regression, with subsequent validation of performance characteristics in an independent set of cases and comparators.

RESULTS

The development set for EGPA consisted of 107 cases of EGPA and 450 comparators. The validation set consisted of an additional 119 cases of EGPA and 437 comparators. From 91 candidate items, regression analysis identified 11 items for EPGA, 7 of which were retained. The final criteria and their weights were as follows: maximum eosinophil count ≥1 × 10 /liter (+5), obstructive airway disease (+3), nasal polyps (+3), cytoplasmic antineutrophil cytoplasmic antibody (ANCA) or anti-proteinase 3 ANCA positivity (-3), extravascular eosinophilic predominant inflammation (+2), mononeuritis multiplex/motor neuropathy not due to radiculopathy (+1), and hematuria (-1). After excluding mimics of vasculitis, a patient with a diagnosis of small- or medium-vessel vasculitis could be classified as having EGPA if the cumulative score was ≥6 points. When these criteria were tested in the validation data set, the sensitivity was 85% (95% confidence interval [95% CI] 77-91%) and the specificity was 99% (95% CI 98-100%).

CONCLUSION

The 2022 American College of Rheumatology/European Alliance of Associations for Rheumatology classification criteria for EGPA demonstrate strong performance characteristics and are validated for use in research.

摘要

目的

制定并验证嗜酸性肉芽肿性多血管炎(EGPA)修订分类标准。

方法

血管炎或对照疾病患者纳入国际队列。研究分为 5 个阶段:1)使用共识方法确定候选标准项目,2)前瞻性收集诊断时存在的候选项目,3)根据数据减少候选项目数量,4)专家小组审查病例以定义参考诊断,5)使用最小绝对收缩和选择算子逻辑回归在开发集中开发基于分数的疾病分类风险评分,随后在独立病例和对照集中验证性能特征。

结果

EGPA 的开发集包括 107 例 EGPA 和 450 例对照。验证集包括另外 119 例 EGPA 和 437 例对照。从 91 项候选项目中,回归分析确定了 11 项 EGPA 项目,其中 7 项被保留。最终标准及其权重如下:最大嗜酸性粒细胞计数≥1×10 /升(+5),气道阻塞性疾病(+3),鼻息肉(+3),细胞质抗中性粒细胞胞质抗体(ANCA)或抗蛋白酶 3 ANCA 阳性(-3),血管外嗜酸性细胞为主的炎症(+2),多发性单神经病/运动神经病非神经根病所致(+1),血尿(-1)。排除血管炎模拟物后,如果小血管或中血管血管炎患者的累积评分≥6 分,则可诊断为 EGPA。当这些标准在验证数据集中进行测试时,敏感性为 85%(95%置信区间[95%CI]77-91%),特异性为 99%(95%CI 98-100%)。

结论

2022 年美国风湿病学会/欧洲风湿病联盟 EGPA 分类标准表现出良好的性能特征,并经过验证可用于研究。

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