TY - JOUR
T1 - Do ethnoracial differences exist among antiphospholipid antibody-positive patients with no other systemic autoimmune diseases
T2 - results from the APS ACTION registry
AU - Gkrouzman, Elena
AU - Matijasevich, Alicia
AU - Bonilla Richero, Carolina
AU - Barber, Megan R.W.
AU - Tektonidou, Maria G.
AU - Pengo, Vittorio
AU - Sciascia, Savino
AU - Pardos-Gea, Jose
AU - Aguirre-Zamorano, Mª ª.A.
AU - Kello, Nina
AU - Paredes-Ruiz, Diana
AU - Belmont, H. Michael
AU - Fortin, Paul R.
AU - Wahl, Denis
AU - Branch, Ware
AU - Gerosa, Maria
AU - Signorelli, Flavio
AU - Zhang, Zhuoli
AU - Atsumi, Tatsuya
AU - Efthymiou, Maria
AU - Pazzola, Giulia
AU - Nalli, Cecillia
AU - Duarte-García, Alí
AU - Almaraz, Esther Rodriguez
AU - Petri, Michelle
AU - Artim-Esen, Bahar
AU - Pons-Estel, Guillermo
AU - Shi, Hui
AU - Knight, Jason S.
AU - Willis, Rohan
AU - Skeith, Leslie
AU - Clarke, Ann E.
AU - Radin, Massimo
AU - Anunciacion-Llunell, Ariadna
AU - Bertolaccini, Maria Laura
AU - Cohen, Hannah
AU - Cervera, Ricard
AU - de Andrade, Danieli Castro Oliveira
AU - Erkan, Doruk
N1 - Publisher Copyright:
© The Author(s) 2026.
PY - 2026/12
Y1 - 2026/12
N2 - Objective: The APS ACTION Registry was created to study long-term outcomes in persistently antiphospholipid antibody (aPL)-positive patients. The objectives of this study were to examine the ethnoracial differences in clinical and laboratory characteristics of aPL-positive patients with no other systemic autoimmune rheumatic diseases (SARDs). Methods: A web-based data capture system stores patient demographics and aPL-related medical history. Inclusion criteria are positive aPL results, based on the revised Sapporo APS classification criteria, tested at least twice within one year prior to enrollment. For this cross-sectional analysis of the baseline data, demographic, clinical, and laboratory characteristics of registry patients were analyzed based on self-reported ethnorace (White, Latin American Mestizo [LAM], Asian, and Black). Results: 728 patients with no history of other SARD (78% with APS classification) were included in the analysis. The ethnoracial distribution was 516 (78%) White, 82 (12%) LAM, 49 (7%) Asian, and 13 (2%) Black. Based on ethnoracial comparisons: (a) there were less females among White patients; (b) livedo reticularis/racemosa was more frequent in LAM patients; and (c) triple aPL positivity was more frequent in Whites, while isolated lupus anticoagulant positivity was more common in LAM patients. Conclusion: In our international registry of persistently aPL-positive patients with or without APS classification, Blacks were the least frequently (2%) reported ethnoracial group. No major ethnoracial differences were found in the aPL-related clinical manifestations. Our analysis highlights the need for further investigation into the genetic and social determinants impacting the clinical and serologic phenotypes of aPL-positive patients across diverse populations.
AB - Objective: The APS ACTION Registry was created to study long-term outcomes in persistently antiphospholipid antibody (aPL)-positive patients. The objectives of this study were to examine the ethnoracial differences in clinical and laboratory characteristics of aPL-positive patients with no other systemic autoimmune rheumatic diseases (SARDs). Methods: A web-based data capture system stores patient demographics and aPL-related medical history. Inclusion criteria are positive aPL results, based on the revised Sapporo APS classification criteria, tested at least twice within one year prior to enrollment. For this cross-sectional analysis of the baseline data, demographic, clinical, and laboratory characteristics of registry patients were analyzed based on self-reported ethnorace (White, Latin American Mestizo [LAM], Asian, and Black). Results: 728 patients with no history of other SARD (78% with APS classification) were included in the analysis. The ethnoracial distribution was 516 (78%) White, 82 (12%) LAM, 49 (7%) Asian, and 13 (2%) Black. Based on ethnoracial comparisons: (a) there were less females among White patients; (b) livedo reticularis/racemosa was more frequent in LAM patients; and (c) triple aPL positivity was more frequent in Whites, while isolated lupus anticoagulant positivity was more common in LAM patients. Conclusion: In our international registry of persistently aPL-positive patients with or without APS classification, Blacks were the least frequently (2%) reported ethnoracial group. No major ethnoracial differences were found in the aPL-related clinical manifestations. Our analysis highlights the need for further investigation into the genetic and social determinants impacting the clinical and serologic phenotypes of aPL-positive patients across diverse populations.
KW - Anticardiolipin
KW - Antiphospholipid antibodies
KW - Antiphospholipid syndrome
KW - Ethnicity
KW - Race
UR - https://www.scopus.com/pages/publications/105040543889
UR - https://www.scopus.com/pages/publications/105040543889#tab=citedBy
U2 - 10.1186/s42358-026-00536-0
DO - 10.1186/s42358-026-00536-0
M3 - Article
C2 - 41992377
AN - SCOPUS:105040543889
SN - 2523-3106
VL - 66
JO - Advances in Rheumatology
JF - Advances in Rheumatology
IS - 1
M1 - 40
ER -