Objective: To develop and validate new classification criteria for Takayasu arteritis (TAK). Methods: Patients with vasculitis or comparator diseases were recruited into an international cohort. The study proceeded in 6 phases: 1) identification of candidate criteria items, 2) collection of candidate items present at diagnosis, 3) expert panel review of cases, 4) data-driven reduction of candidate items, 5) derivation of a points-based classification score in a development data set, and 6) validation in an independent data set. Results: The development data set consisted of 316 cases of TAK and 323 comparators. The validation data set consisted of an additional 146 cases of TAK and 127 comparators. Age ≤60 years at diagnosis and imaging evidence of large-vessel vasculitis were absolute requirements to classify a patient as having TAK. The final criteria items and weights were as follows: female sex (+1), angina (+2), limb claudication (+2), arterial bruit (+2), reduced upper extremity pulse (+2), reduced pulse or tenderness of a carotid artery (+2), blood pressure difference between arms of ≥20 mm Hg (+1), number of affected arterial territories (+1 to +3), paired artery involvement (+1), and abdominal aorta plus renal or mesenteric involvement (+3). A patient could be classified as having TAK with a cumulative score of ≥5 points. When these criteria were tested in the validation data set, the model area under the curve was 0.97 (95% confidence interval [95% CI] 0.94–0.99) with a sensitivity of 93.8% (95% CI 88.6–97.1%) and specificity of 99.2% (95% CI 96.7–100.0%). Conclusion: The 2022 American College of Rheumatology/EULAR classification criteria for TAK are now validated for use in research.

2022 American College of Rheumatology/EULAR Classification Criteria for Takayasu Arteritis / P.C. Grayson, C. Ponte, R. Suppiah, J.C. Robson, K.B. Gribbons, A. Judge, A. Craven, S. Khalid, A. Hutchings, D. Danda, R.A. Luqmani, R.A. Watts, P.A. Merkel, P. Gatenby, C. Hill, D. Ranganathan, A. Kronbichler, D. Blockmans, L. Barra, S. Carette, C. Pagnoux, N. Dhindsa, A. Fifi-Mah, N. Khalidi, P. Liang, N. Milman, C. Pineau, X. Tian, G. Wang, T. Wang, M.-. Zhao, V. Tesar, B. Baslund, N. Hammam, A. Shahin, L. Pirila, J. Putaala, B. Hellmich, J. Henes, J. Holle, P. Lamprecht, F. Moosig, T. Neumann, W. Schmidt, C. Sunderkoettey, Z. Szekanecz, D. Danda, S. Das, R. Gupta, L. Rajasekhar, A. Sharma, S. Wagh, M. Clarkson, E. Molloy, C. Salvarani, F. Schiavon, E. Tombetti, A. Vaglio, K. Amano, Y. Arimura, H. Dobashi, S. Fujimoto, M. Harigai, F. Hirano, J. Hirahashi, S. Honma, T. Kawakami, S. Kobayashi, H. Kono, H. Makino, K. Matsui, E. Muso, K. Suzuki, K. Ikeda, T. Takeuchi, T. Tsukamoto, S. Uchida, T. Wada, H. Yamada, K. Yamagata, W. Yumura, K.S. Lai, L.F. Flores-Suarez, A. Hinojosa-Azaola, B. Rutgers, P.-. Tak, R. Grainger, V. Quincey, L. Stamp, R. Suppiah, E. Besada, A. Diamantopoulos, J. Sznajd, E. Azevedo, R. Geraldes, M. Rodrigues, E. Santos, Y.-. Song, S. Moiseev, A. Hocevar, M.C. Cid, X.S. Moreno, I. Atukorala, E. Berglin, A. Mohammed, M. Segelmark, T. Daikeler, H. Direskeneli, G. Hatemi, S. Kamali, O. Karadag, S. Pehlevan, M. Adler, N. Basu, I. Bruce, K. Chakravarty, B. Dasgupta, O. Flossmann, N. Gendi, A. Hassan, R. Hoyles, D. Jayne, C. Jones, R. Klocke, P. Lanyon, C. Laversuch, R. Luqmani, J. Robson, M. Magliano, J. Mason, W.W. Maw, I. Mcinnes, J. Mclaren, M. Morgan, A. Morgan, C. Mukhtyar, E. O'Riordan, S. Patel, A. Peall, J. Robson, S. Venkatachalam, E. Vermaak, A. Menon, R. Watts, C.-. Yee, D. Albert, L. Calabrese, S. Chung, L. Forbess, A. Gaffo, O. Gewurz-Singer, P. Grayson, K. Liang, E. Matteson, P.A. Merkel, R. Rhee, J. Springer, A. Sreih. - In: ARTHRITIS & RHEUMATOLOGY. - ISSN 2326-5191. - 74:12(2022), pp. 1872-1880. [10.1002/art.42324]

2022 American College of Rheumatology/EULAR Classification Criteria for Takayasu Arteritis

E. Tombetti
Membro del Collaboration Group
;
2022

Abstract

Objective: To develop and validate new classification criteria for Takayasu arteritis (TAK). Methods: Patients with vasculitis or comparator diseases were recruited into an international cohort. The study proceeded in 6 phases: 1) identification of candidate criteria items, 2) collection of candidate items present at diagnosis, 3) expert panel review of cases, 4) data-driven reduction of candidate items, 5) derivation of a points-based classification score in a development data set, and 6) validation in an independent data set. Results: The development data set consisted of 316 cases of TAK and 323 comparators. The validation data set consisted of an additional 146 cases of TAK and 127 comparators. Age ≤60 years at diagnosis and imaging evidence of large-vessel vasculitis were absolute requirements to classify a patient as having TAK. The final criteria items and weights were as follows: female sex (+1), angina (+2), limb claudication (+2), arterial bruit (+2), reduced upper extremity pulse (+2), reduced pulse or tenderness of a carotid artery (+2), blood pressure difference between arms of ≥20 mm Hg (+1), number of affected arterial territories (+1 to +3), paired artery involvement (+1), and abdominal aorta plus renal or mesenteric involvement (+3). A patient could be classified as having TAK with a cumulative score of ≥5 points. When these criteria were tested in the validation data set, the model area under the curve was 0.97 (95% confidence interval [95% CI] 0.94–0.99) with a sensitivity of 93.8% (95% CI 88.6–97.1%) and specificity of 99.2% (95% CI 96.7–100.0%). Conclusion: The 2022 American College of Rheumatology/EULAR classification criteria for TAK are now validated for use in research.
Autoimmune Diseases; Behcet Syndrome; Cardiovascular Diseases
Settore MEDS-09/C - Reumatologia
Settore MEDS-05/A - Medicina interna
2022
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/1125561
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