Yagmur Bayindir, Peter C Grayson, Katherine B Gribbons, Selcan Demir, Alexandra Audemard-Verger, Cristina Ponte, Joanna C Robson, Ravi Suppiah, Cemal Bes, Bugu Bulat, Fatih Yildirim, Omer Karadag, Raashid Ahmed Luqmani, Richard A Watts, Peter A Merkel, Seza Ozen
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After the initial assessment of the performance of the criteria, possible revisions to increase the performance were tested. The revised criteria were then assessed in an independent validation cohort within a multicentre Turkish vasculitis registry.</p><p><strong>Results: </strong>The dataset consisted of 178 IgAV cases and 1705 comparators. The Ankara 2008 criteria require skin involvement plus one of the following four criteria: abdominal pain, a biopsy showing IgA deposition, arthritis or arthralgia, or renal involvement (any haematuria and/or proteinuria). The specificity of the criteria improved when a positive test for anti-neutrophil cytoplasmic autoantibody or blood cryoglobulins was considered an exclusion criterion. The revised criteria had a sensitivity of 76.4% (95% CI 69.8% to 82.2%) and a specificity of 94.5% (95.0% CI 93.4% to 95.1%). In the validation set, the sensitivity and specificity of the revised criteria were 97.8% (95% CI 94.0% to 99.0%) and 85.0% (95.0% CI 78.0% to 90.0%), respectively.</p><p><strong>Conclusion: </strong>The revised EULAR/PReS-endorsed Ankara 2008 IgAV classification criteria perform well in adults with IgAV and are appropriate for use in clinical research.</p>","PeriodicalId":21396,"journal":{"name":"RMD Open","volume":"11 3","pages":""},"PeriodicalIF":4.7000,"publicationDate":"2025-07-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12281324/pdf/","citationCount":"0","resultStr":"{\"title\":\"Performance in adults of the EULAR/PRINTO/PRES (Ankara 2008) classification criteria for IgA vasculitis.\",\"authors\":\"Yagmur Bayindir, Peter C Grayson, Katherine B Gribbons, Selcan Demir, Alexandra Audemard-Verger, Cristina Ponte, Joanna C Robson, Ravi Suppiah, Cemal Bes, Bugu Bulat, Fatih Yildirim, Omer Karadag, Raashid Ahmed Luqmani, Richard A Watts, Peter A Merkel, Seza Ozen\",\"doi\":\"10.1136/rmdopen-2025-005728\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objective: </strong>To examine the performance in adults of the European Alliance of Associations for Rheumatology (EULAR)/Pediatric Rheumatology European Society (PReS)-endorsed Ankara 2008 classification criteria for IgA vasculitis (IgAV).</p><p><strong>Methods: </strong>The EULAR/PReS/Ankara 2008 classification criteria for IgAV were applied to patients enrolled in an international observational cohort which included patients with IgAV and comparators with other forms of small-vessel and medium-vessel vasculitis. After the initial assessment of the performance of the criteria, possible revisions to increase the performance were tested. The revised criteria were then assessed in an independent validation cohort within a multicentre Turkish vasculitis registry.</p><p><strong>Results: </strong>The dataset consisted of 178 IgAV cases and 1705 comparators. The Ankara 2008 criteria require skin involvement plus one of the following four criteria: abdominal pain, a biopsy showing IgA deposition, arthritis or arthralgia, or renal involvement (any haematuria and/or proteinuria). The specificity of the criteria improved when a positive test for anti-neutrophil cytoplasmic autoantibody or blood cryoglobulins was considered an exclusion criterion. The revised criteria had a sensitivity of 76.4% (95% CI 69.8% to 82.2%) and a specificity of 94.5% (95.0% CI 93.4% to 95.1%). 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引用次数: 0
摘要
目的:研究欧洲风湿病协会联盟(EULAR)/欧洲儿科风湿病学会(PReS)认可的IgA血管炎(IgAV)安卡拉2008分类标准在成人中的表现。方法:将EULAR/PReS/Ankara 2008 IgAV分类标准应用于纳入国际观察队列的患者,该队列包括IgAV患者和其他形式的小血管和中血管炎比较者。在对标准的性能进行初步评估之后,测试了可能的改进以提高性能。修订后的标准随后在土耳其多中心血管炎登记的独立验证队列中进行评估。结果:该数据集包括178例IgAV病例和1705例比较者。安卡拉2008标准要求皮肤受累加上以下四个标准中的一个:腹痛,活检显示IgA沉积,关节炎或关节痛,或肾脏受累(任何血尿和/或蛋白尿)。当抗中性粒细胞胞浆自身抗体或血冷球蛋白阳性试验被视为排除标准时,标准的特异性得到改善。修订后的标准的敏感性为76.4% (95% CI 69.8%至82.2%),特异性为94.5% (95.0% CI 93.4%至95.1%)。在验证集中,修订后标准的敏感性和特异性分别为97.8% (95% CI 94.0% ~ 99.0%)和85.0% (95.0% CI 78.0% ~ 90.0%)。结论:修订后的EULAR/ press认可的Ankara 2008 IgAV分类标准在成人IgAV患者中表现良好,适合用于临床研究。
Performance in adults of the EULAR/PRINTO/PRES (Ankara 2008) classification criteria for IgA vasculitis.
Objective: To examine the performance in adults of the European Alliance of Associations for Rheumatology (EULAR)/Pediatric Rheumatology European Society (PReS)-endorsed Ankara 2008 classification criteria for IgA vasculitis (IgAV).
Methods: The EULAR/PReS/Ankara 2008 classification criteria for IgAV were applied to patients enrolled in an international observational cohort which included patients with IgAV and comparators with other forms of small-vessel and medium-vessel vasculitis. After the initial assessment of the performance of the criteria, possible revisions to increase the performance were tested. The revised criteria were then assessed in an independent validation cohort within a multicentre Turkish vasculitis registry.
Results: The dataset consisted of 178 IgAV cases and 1705 comparators. The Ankara 2008 criteria require skin involvement plus one of the following four criteria: abdominal pain, a biopsy showing IgA deposition, arthritis or arthralgia, or renal involvement (any haematuria and/or proteinuria). The specificity of the criteria improved when a positive test for anti-neutrophil cytoplasmic autoantibody or blood cryoglobulins was considered an exclusion criterion. The revised criteria had a sensitivity of 76.4% (95% CI 69.8% to 82.2%) and a specificity of 94.5% (95.0% CI 93.4% to 95.1%). In the validation set, the sensitivity and specificity of the revised criteria were 97.8% (95% CI 94.0% to 99.0%) and 85.0% (95.0% CI 78.0% to 90.0%), respectively.
Conclusion: The revised EULAR/PReS-endorsed Ankara 2008 IgAV classification criteria perform well in adults with IgAV and are appropriate for use in clinical research.
期刊介绍:
RMD Open publishes high quality peer-reviewed original research covering the full spectrum of musculoskeletal disorders, rheumatism and connective tissue diseases, including osteoporosis, spine and rehabilitation. Clinical and epidemiological research, basic and translational medicine, interesting clinical cases, and smaller studies that add to the literature are all considered.