Performance of the modified 2022 ACR/EULAR giant cell arteritis classification criteria without age restriction for discriminating from Takayasu arteritis

IF 4.6 2区 医学 Q1 Medicine Arthritis Research & Therapy Pub Date : 2025-01-31 DOI:10.1186/s13075-025-03486-y
Takahiko Sugihara, Masayoshi Harigai, Haruhito A. Uchida, Hajime Yoshifuji, Yasuhiro Maejima, Jun Ishizaki, Yoshiko Watanabe, Hiroaki Dobashi, Yoshinori Komagata, Naoto Tamura, Yoshikazu Nakaoka
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Abstract

To evaluate the ability to discriminate giant cell arteritis (GCA) from Takayasu arteritis (TAK) according to the modified 2022 American College of Rheumatology/European Alliance of Associations for Rheumatology (ACR/EULAR) GCA classification criteria. Patients enrolled in the Japanese nationwide retrospective registry were evaluated using the criteria with partial modification; wall thickening of descending thoracic-abdominal aorta were mainly diagnosed by contrast-enhanced computed tomography (CT) or magnetic resonance imaging instead of evaluating with positron emission tomography (PET)-CT. The discriminability of the criteria was evaluated using C-statistic (> 0.7: good ability). Newly diagnosed patients with GCA (n = 139) and TAK (n = 129) were assessed, and 23.3% of TAK were aged 50 years or older at onset. The sensitivity of the modified 2022 ACR/EULAR GCA classification criteria with a score ≥ 6 was 82.0%, 68.5%, and 32.1% in all GCA, GCA with large-vessel involvement, and GCA without cranial arteritis, respectively. The specificity of the modified criteria was 96.1% for the 129 TAK as controls. Five patients with late-onset TAK met the modified criteria, and four had cranial signs and symptoms, two had bilateral axillary artery involvement, and four had descending thoracic-abdominal aorta involvement. The discriminability of the criteria was good (C-statistic: 0.986, 95% confidence interval [CI]: 0.976–0.996) and remained good after excluding age (C-statistic: 0.927, 95% CI: 0.894–0.961). The discriminability of a set of large-vessel lesions (bilateral axillary artery and descending thoracic-abdominal aorta) and inflammatory markers was markedly decreased with poor C-statistic value (C-statistic: 0.598, 95% CI: 0.530–0.667). Discriminability was improved after adding polymyalgia rheumatica (PMR) (C-statistic: 0.757, 95% CI: 0.700–0.813) or age (C-statistic: 0.913, 95%CI: 0.874–0.951) to the set of large-vessel lesions. In GCA patients with a score ≤ 5, 52% had bilateral subclavian and/or axillary artery involvement. The modified 2022 ACR/EULAR GCA classification criteria well performed in classifying GCA and TAK without PET-CT in routine clinical practice. A set of items included in the modified GCA classification criteria had good discriminative ability for GCA and TAK, even when age was excluded. However, age restriction or PMR was required to distinguish GCA without cranial lesions from TAK.
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修改后的无年龄限制的2022年ACR/EULAR巨细胞动脉炎分类标准在鉴别高松动脉炎中的表现
根据修订后的2022年美国风湿病学会/欧洲风湿病协会联盟(ACR/EULAR) GCA分类标准,评估巨细胞动脉炎(GCA)和高须动脉炎(TAK)的鉴别能力。纳入日本全国回顾性登记的患者使用部分修改的标准进行评估;胸腹降主动脉壁增厚主要通过CT或磁共振成像诊断,而非正电子发射断层扫描(PET)-CT评价。采用c -统计量评价标准的可辨别性(> .7:能力好)。新诊断的GCA (n = 139)和TAK (n = 129)患者中,23.3%的TAK患者发病年龄在50岁及以上。评分≥6分的改进的2022 ACR/EULAR GCA分类标准对所有GCA、伴大血管累及的GCA和无颅动脉炎的GCA的敏感性分别为82.0%、68.5%和32.1%。129例TAK作为对照,修改标准的特异性为96.1%。5例迟发性TAK患者符合修改后的标准,其中4例有颅脑体征和症状,2例累及双侧腋窝动脉,4例累及胸腹降主动脉。标准的可判别性良好(c -统计量:0.986,95%可信区间[CI]: 0.976 ~ 0.996),排除年龄后仍保持良好(c -统计量:0.927,95% CI: 0.894 ~ 0.961)。一组大血管病变(双侧腋窝动脉和胸腹降主动脉)和炎症标志物的可辨别性明显降低,c统计值较差(c统计值:0.598,95% CI: 0.530-0.667)。在大血管病变组中加入风湿性多肌痛(PMR) (C-statistic: 0.757, 95%CI: 0.700 ~ 0.813)或年龄(C-statistic: 0.913, 95%CI: 0.874 ~ 0.951)后,可提高辨别性。在评分≤5的GCA患者中,52%有双侧锁骨下和/或腋窝动脉受累。修订后的2022 ACR/EULAR GCA分类标准在常规临床实践中对GCA和TAK无PET-CT的分类效果良好。修改后的GCA分类标准中包含的一组项目即使在排除年龄的情况下,对GCA和TAK也有较好的判别能力。然而,需要年龄限制或PMR来区分无颅脑病变的GCA和TAK。
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来源期刊
CiteScore
8.60
自引率
2.00%
发文量
261
审稿时长
14 weeks
期刊介绍: Established in 1999, Arthritis Research and Therapy is an international, open access, peer-reviewed journal, publishing original articles in the area of musculoskeletal research and therapy as well as, reviews, commentaries and reports. A major focus of the journal is on the immunologic processes leading to inflammation, damage and repair as they relate to autoimmune rheumatic and musculoskeletal conditions, and which inform the translation of this knowledge into advances in clinical care. Original basic, translational and clinical research is considered for publication along with results of early and late phase therapeutic trials, especially as they pertain to the underpinning science that informs clinical observations in interventional studies.
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