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HDL (High-Density Lipoprotein) Subspecies, Prevalent Covert Brain Infarcts, and Incident Overt Ischemic Stroke: Cardiovascular Health Study.

TitleHDL (High-Density Lipoprotein) Subspecies, Prevalent Covert Brain Infarcts, and Incident Overt Ischemic Stroke: Cardiovascular Health Study.
Publication TypeJournal Article
Year of Publication2021
AuthorsKoch, M, Aroner, SA, Fitzpatrick, AL, Longstreth, WT, Furtado, JD, Mukamal, KJ, Jensen, MK
JournalStroke
PaginationSTROKEAHA121034299
Date Published2021 Oct 14
ISSN1524-4628
Abstract<p><b>BACKGROUND AND PURPOSE: </b>Whether HDL (high-density lipoprotein) is associated with risk of vascular brain injury is unclear. HDL is comprised of many apo (apolipoprotein) species, creating distinct subtypes of HDL.</p><p><b>METHODS: </b>We utilized sandwich ELISA to determine HDL subspecies from plasma collected in 1998/1999 from 2001 CHS (Cardiovascular Health Study) participants (mean age, 80 years).</p><p><b>RESULTS: </b>In cross-sectional analyses, participants with higher apoA1 in plasma and lower apoE in HDL were less likely to have prevalent covert magnetic resonance imaging-defined infarcts: odds ratio for apoA1 Q4 versus Q1, 0.68 (95% CI, 0.50-0.93), and odds ratio for apoE Q4 versus Q1, 1.36 (95% CI, 1.01-1.84). Similarly, apoA1 in the subspecies of HDL that lacked apoC3, apoJ, or apoE was inversely related to covert infarcts, and apoE in the subspecies of HDL that lacked apoC3 or apoJ was directly related to covert infarcts in prospective analyses. In contrast, the concentrations of apoA1 and apoE in the complementary subspecies of HDL that contained these apos were unrelated to covert infarcts. Patterns of associations between incident overt ischemic stroke and apoA1, apoE, and apoA1 and apoE in subspecies of HDL were similar to those observed for covert infarcts but less pronounced.</p><p><b>CONCLUSIONS: </b>This study highlights HDL subspecies defined by apo content as relevant biomarkers of covert and overt vascular brain injury.</p>
DOI10.1161/STROKEAHA.121.034299
Alternate JournalStroke
PubMed ID34645286
Grant ListK01 AG066817 / AG / NIA NIH HHS / United States
U01 HL130114 / HL / NHLBI NIH HHS / United States
ePub date: 
21/10