Relation of Antiphospholipid Antibodies to Postmortem Brain Infarcts in Older People. Issue 2 (13th January 2015)

• Record Type: Journal Article
• Authors: Arvanitakis, Zoe; Brey, Robin L.; Rand, Jacob H.; Schneider, Julie A.; Capuano, Ana W.; Yu, Lei; Leurgans, Sue E.; Bennett, David A.; Levine, Steven R.
• Is Part Of: Circulation. Volume 131:Issue 2(2015)
• Publication Date: 2015-01-13
• Subjects: Blood -- Circulation -- Periodicals; Cardiovascular system -- Periodicals; Cardiology -- Periodicals; Heart -- Diseases -- Periodicals; Blood Circulation; Cardiovascular System; Vascular Diseases; 616.1
• DOI: 10.1161/CIRCULATIONAHA.114.012479
• Languages: English
• ISSNs: 0009-7322

Abstract

<abstract> <title> <x xml:space="preserve">Abstract</x> </title> <sec> <title>Background—</title> <p>There are few data on the relationship of antiphospholipid antibodies (aPLs) to pathologically proven brain infarcts. We tested the hypothesis that aPLs are associated with a higher odds of brain infarcts among older, community-dwelling individuals who came to autopsy.</p> </sec> <sec> <title>Methods and Results—</title> <p>Specimens and clinical and pathological data were derived from 607 deceased subjects (mean age at death, 89 years; 66% women) who were participating in 1 of 2 cohort studies of aging (Rush Memory and Aging Project and Religious Orders Study) and had agreed to brain autopsy. Brain infarcts were identified on gross and microscopic examinations, and severity of cerebral vessel disease (atherosclerosis, arteriolosclerosis) was graded. Four clinically used aPLs were measured longitudinally: 3 in serum (anticardiolipin antibodies, β<sub>2-</sub>glycoprotein I, and anti–phosphatidyl-serine) and 1 in plasma (lupus anticoagulant). A quarter of subjects (142 of 607, 23%) had at least 1 aPL present at baseline (median time interval from baseline to death, 4.6 years), and three quarters of these subjects had persistently positive measures over time. In a logistic regression analysis, baseline aPL positivity did not increase the odds of brain infarcts (odds ratio=1.08; 95% confidence interval, 0.74–1.58; <italic>P</italic>=0.19) or of gross or microscopic infarcts separately. Findings were essentially unchanged when considering number of baseline aPLs, aPLs proximate to death, and persistence of aPLs. Associations did not differ among subjects with increased severity of vessel disease.</p> </sec> <sec> <title>Conclusion—</title> <p>Overall, we did not find evidence that aPLs increase the odds of pathological brain infarcts in older people.</p> </sec> </abstract>