ADAMTS-7 is associated with a high-risk plaque phenotype in human atherosclerosis.

Abstract:

:Several large-scale genome-wide association studies have identified single-nucleotide polymorphisms in the genomic region of A Disintegrin And Metalloproteinase with ThromboSpondin type 1 repeats (ADAMTS)-7 and associations to coronary artery disease. Experimental studies have provided evidence for a functional role of ADAMTS-7 in both injury-induced vascular neointima formation and development of atherosclerotic lesions. However, whether ADAMTS-7 is associated with a specific plaque phenotype in humans has not been investigated. Carotid plaques (n = 206) from patients with and without cerebrovascular symptoms were analyzed for expression of ADAMTS-7 by immunohistochemistry and correlated to components associated with plaque vulnerability. Plaques from symptomatic patients showed increased levels of ADAMTS-7 compared with lesions from asymptomatic patients. High levels of ADAMTS-7 correlated with high levels of CD68-staining and lipid content, but with low smooth muscle cell and collagen content, which together are characteristics of a vulnerable plaque phenotype. ADAMTS-7 levels above median were associated with increased risk for postoperative cardiovascular events. Our data show that ADAMTS-7 is associated with a vulnerable plaque phenotype in human carotid lesions. These data support previous observations of a potential proatherogenic role of ADAMTS-7.

journal_name

Sci Rep

journal_title

Scientific reports

authors

Bengtsson E,Hultman K,Dunér P,Asciutto G,Almgren P,Orho-Melander M,Melander O,Nilsson J,Hultgårdh-Nilsson A,Gonçalves I

doi

10.1038/s41598-017-03573-4

subject

Has Abstract

pub_date

2017-06-16 00:00:00

pages

3753

issue

1

issn

2045-2322

pii

10.1038/s41598-017-03573-4

journal_volume

7

pub_type

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