Abstract 4361451: Prevalence and Outcomes of Antiphospholipid Antibodies in Patients with Peripheral Artery Disease

N Nathan Watson (Brigham and Women's Hospital, Boston, Massachusetts, United States) S Saman Asad Siddiqui (Harvard Medical School, Boston, Massachusetts, United States) S Sina Rashedi (Thrombosis Research Group, Brigham and Women’s Hospital–Harvard Medical School, Boston) M Mariana Pfeferman (Thrombosis Research Group, Brigham and Women’s Hospital–Harvard Medical School, Boston) D David Jiménez M Manuel Monreal (Department of Internal Medicine, Institut de Recerca Germans Trias i Pujol, Hospital Universitari Germans Trias i Pujol, Badalona, Spain) G Geoffrey Barnes (University of Michigan, Ann Arbor, Michigan, United States) M Mattia Galli (Sapienza University of Rome, Rome, Italy) B Brittany Weber (The University of Texas Southwestern Medical Center, Dallas, Texas, United States) S Samuel Goldhaber (Brigham and Women's Hospital, Boston, Massachusetts, United States) J Jean Connors (Brigham and Women's Hospital, Boston, Massachusetts, United States) S Sacha Uljon (Massachusetts General Hospital, Boston, Massachusetts, United States) E Eric Secemsky (Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, Massachusetts, United States) G Gregory Lip H Harlan Krumholz (Yale School of Medicine, New Haven, Connecticut, United States) J Jason Knight (University of Michigan, Ann Arbor, Michigan, United States) M Mary Cushman 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) B Behnood Bikdeli (Thrombosis Research Group, Brigham and Women’s Hospital–Harvard Medical School, Boston)

Abstract

Background: Although antiphospholipid antibodies (aPL) are classically associated with excess risk of thrombosis in antiphospholipid syndrome (APS), emerging data suggest that aPLs may confer a prognostic role in patients with cardiovascular conditions who do not fulfill traditional research criteria for APS. We aimed to investigate the prevalence of aPL seropositivity among patients with peripheral artery disease (PAD) and to assess outcomes among those with and without aPL. Methods: In this study, as part of a larger project (PROSPERO ID CRD420251047305), we systematically searched PubMed and Embase through 3/11/2025 to determine the pooled prevalence of aPL seropositivity among patients with PAD. Despite variation in PAD severity across studies, aPL testing occurred in unselected individuals (rather than by clinical suspicion). aPL positivity was defined as at least one single positive measurement for either anticardiolipin, anti-β2 glycoprotein, or lupus anticoagulant. For studies with longitudinal data available, we assessed a composite outcome of subsequent arterial thrombosis, revascularization failure, amputations, and death stratified by aPL seropositivity. Random-effects models with inverse weights were used to calculate pooled odds ratios (ORs). Results: Among 2,890 records, we identified 31 studies assessing aPL prevalence and 11 evaluating clinical outcomes (3,364 total patients, mean age 58.6 years, 62.3% men). Seropositivity for at least one aPL was observed in 21.1% of patients with PAD (95% CI, 19.7%-22.5%). aPL seropositivity was associated with a significantly higher odds of the primary outcome (OR: 2.49, 95% CI 1.48-4.18) (Figure). Among patients who underwent revascularization, aPL seropositivity was associated with a higher odds of a failed revascularization procedure (OR: 2.72, 95% CI 1.49-4.98). Conclusion: aPL seropositivity is present in approximately one-in-five patients with PAD and correlates with a subsequent risk of adverse clinical events. Whether early testing can help inform management strategies and improve outcomes requires further investigation.

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

Saman Asad Siddiqui

Harvard Medical School, Boston, Massachusetts, United States

S

Sina Rashedi

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

M

Mariana Pfeferman

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

D

David Jiménez

M

Manuel Monreal

Department of Internal Medicine, Institut de Recerca Germans Trias i Pujol, Hospital Universitari Germans Trias i Pujol, Badalona, Spain

G

Geoffrey Barnes

University of Michigan, Ann Arbor, Michigan, United States

M

Mattia Galli

Sapienza University of Rome, Rome, Italy

B

Brittany Weber

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

S

Samuel Goldhaber

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

J

Jean Connors

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

S

Sacha Uljon

Massachusetts General Hospital, Boston, Massachusetts, United States

E

Eric Secemsky

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

G

Gregory Lip

H

Harlan Krumholz

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

J

Jason Knight

University of Michigan, Ann Arbor, Michigan, United States

M

Mary Cushman

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

B

Behnood Bikdeli

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