Abstract 4361466: Association Between Antiphospholipid Antibody and Ischemic Stroke: A Systematic Review and Meta-Analysis

N Nathan Watson (Brigham and Women's Hospital, Boston, Massachusetts, United States) S Syed Bukhari (Johns Hopkins School of Medicine, Baltimore, Maryland, United States) S Sina Rashedi (Thrombosis Research Group, Brigham and Women’s Hospital–Harvard Medical School, Boston) B Brittany Weber (The University of Texas Southwestern Medical Center, Dallas, Texas, United States) C Christopher Anderson (University of Tennessee, Knoxville, Tennessee, United States) M Mitchell Elkind (American Heart Association, Dallas, Texas, United States) M Mariana Pfeferman (Thrombosis Research Group, Brigham and Women’s Hospital–Harvard Medical School, Boston) F Francisco Ujueta (Brigham and Women's Hospital, Boston, Massachusetts, United States) M Mehrdad Zarghami (Jamaica Hospital, New York, New York, United States) Y Yogen Kanthi (NHLBI-National Institutes of Health, Bethesda, Maryland, United States) E Eric Secemsky (Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, United States) J Jean Connors (Brigham and Women's Hospital, Boston, Massachusetts, United States) G Geoffrey Barnes (University of Michigan, Ann Arbor, Michigan, United States) S Samuel Goldhaber (Brigham and Women's Hospital, Boston, Massachusetts, United States) J Jeffrey Weitz (Thrombosis&Atherosclerosis Research Institute, Hamilton, Ontario, Canada) K Karen Costenbader (Brigham and Women's Hospital, Boston, Massachusetts, United States) G Gregory Piazza (Thrombosis Research Group, Brigham and Women’s Hospital, Harvard Medical School, Boston) H Harlan Krumholz (Yale School of Medicine, New Haven, Connecticut, United States) M Mary Cushman B Behnood Bikdeli (Thrombosis Research Group, Brigham and Women’s Hospital–Harvard Medical School, Boston)

Abstract

Background: Emerging evidence suggests that antiphospholipid antibodies (aPL) may be associated with an increased cardiovascular risk beyond the thrombotic antiphospholipid syndrome (APS). Among patients with ischemic stroke, the clinical significance of single positive aPL remains ill-defined. We aimed to assess the prevalence of aPL seropositivity in patients with stroke and the association between aPL seropositivity and stroke risk. Methods: This analysis is part of a larger project with PROSPERO ID CRD420251047305. We conducted a systematic search of PubMed and Embase on 5/13/2025 to identify cohort or case-control studies of unselected adult patients (without APS) investigating the association between aPL seropositivity and acute ischemic stroke compared with non-stroke controls. Positivity for aPL was defined as a single positive measurement for lupus anticoagulant in clot-based assays, IgM/IgG anti-β2-glycoprotein I antibody, or IgM/IgG anticardiolipin antibody at the time of stroke. Random-effects models with inverse weights were utilized to calculate pooled odds ratios (OR) with 95% confidence intervals (CIs). Results: Among 3,241 unique records, 43 studies (39 case-control and 4 cohort studies) were included representing a total of 6,374 patients (mean age 59.0 years, 51.1% men). The pooled prevalence of aPL seropositivity among patients with ischemic stroke was 18.1% (95% CI 17.2%-19.0%) (Figure, Panel A). Patients with ischemic stroke, compared with non-stroke controls, had a higher odds for seropositivity for aPL (OR: 2.94, 95% CI 2.31-3.74, I 2 =69%) (Figure, Panel B). In sensitivity analysis following removal of outlier studies, similar findings were demonstrated with overall improvement in model heterogeneity (OR: 2.58, 95% CI, 2.21-3.02, I 2 =20%). Conclusion: In this analysis, seropositivity for aPL were present in nearly one in five patients with ischemic stroke, significantly more than in the general population, and were associated with an increased odds of stroke. Whether seropositivity for aPL at a single time point is a causal risk factor for stroke warrants further investigation in future prospective studies.

Article Details

Journal Circulation
Volume / Issue Vol. 152, Issue Suppl_3
Published November 04, 2025
ISSN 0009-7322
Publisher Lippincott Williams & Wilkins

Journal Info

Circulation

Lippincott Williams & Wilkins

ISSN: 0009-7322 Health Sciences

Authors (20)

N

Nathan Watson

Brigham and Women's Hospital, Boston, Massachusetts, United States

S

Syed Bukhari

Johns Hopkins School of Medicine, Baltimore, Maryland, United States

S

Sina Rashedi

Thrombosis Research Group, Brigham and Women’s Hospital–Harvard Medical School, Boston

B

Brittany Weber

The University of Texas Southwestern Medical Center, Dallas, Texas, United States

C

Christopher Anderson

University of Tennessee, Knoxville, Tennessee, United States

M

Mitchell Elkind

American Heart Association, Dallas, Texas, United States

M

Mariana Pfeferman

Thrombosis Research Group, Brigham and Women’s Hospital–Harvard Medical School, Boston

F

Francisco Ujueta

Brigham and Women's Hospital, Boston, Massachusetts, United States

M

Mehrdad Zarghami

Jamaica Hospital, New York, New York, United States

Y

Yogen Kanthi

NHLBI-National Institutes of Health, Bethesda, Maryland, United States

E

Eric Secemsky

Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, United States

J

Jean Connors

Brigham and Women's Hospital, Boston, Massachusetts, United States

G

Geoffrey Barnes

University of Michigan, Ann Arbor, Michigan, United States

S

Samuel Goldhaber

Brigham and Women's Hospital, Boston, Massachusetts, United States

J

Jeffrey Weitz

Thrombosis&Atherosclerosis Research Institute, Hamilton, Ontario, Canada

K

Karen Costenbader

Brigham and Women's Hospital, Boston, Massachusetts, United States

G

Gregory Piazza

Thrombosis Research Group, Brigham and Women’s Hospital, Harvard Medical School, Boston

H

Harlan Krumholz

Yale School of Medicine, New Haven, Connecticut, United States

M

Mary Cushman

B

Behnood Bikdeli

Thrombosis Research Group, Brigham and Women’s Hospital–Harvard Medical School, Boston