TY - JOUR
T1 - Loss of y Chromosome in Blood Is Associated with Major Cardiovascular Events during Follow-Up in Men after Carotid Endarterectomy
AU - Haitjema, Saskia
AU - Kofink, Daniel
AU - Van Setten, Jessica
AU - Van Der Laan, Sander W.
AU - Schoneveld, Arjan H.
AU - Eales, James
AU - Tomaszewski, Maciej
AU - De Jager, Saskia C.A.
AU - Pasterkamp, Gerard
AU - Asselbergs, Folkert W.
AU - Den Ruijter, Hester M.
N1 - Funding Information:
Dr Haitjema, D. Kofink, and S.W. van der Laan are supported by the EU’s Seventh Framework Programme project CVgenes@target (HEALTH-F2-2013-601456). S.W. van der Laan is funded through grants from the Netherlands CardioVascular Research Initiative (GENIUS, CVON2011-19) and the Interuniversity Cardiology Institute of the Netherlands (ICIN, 09.001). Dr Asselbergs is supported by a Dekker scholarship-Junior Staff Member 2014T001—Netherlands Heart Foundation and University College London Hospitals National Institute for Health Research Biomedical Research Centre.
Publisher Copyright:
© 2017 American Heart Association, Inc.
PY - 2017/8/1
Y1 - 2017/8/1
N2 - Recent studies found an immune regulatory role for Y chromosome and a relationship between loss of Y chromosome (LOY) in blood cells and a higher risk of cancer and mortality. Given involvement of immune cells in atherosclerosis, we hypothesized that LOY is associated with the severity of atherosclerotic plaque characteristics and outcome in men undergoing carotid endarterectomy. Methods and Results - LOY was quantified in blood and plaque from raw intensity genotyping data in men within the Athero-Express biobank study. Plaques were dissected, and the culprit lesions used for histology and the measurement of inflammatory proteins. We tested LOY for association with (inflammatory) atherosclerotic plaque phenotypes and cytokines and assessed the association of LOY with secondary events during 3-year follow-up. Of 366 patients with carotid endarterectomy, 61 exhibited some degree of LOY in blood. LOY was also present in atherosclerotic plaque lesions (n=8/242, 3%). LOY in blood was negatively associated with age (β=-0.03/10 y; r2=0.07; P=1.6×10-7) but not with cardiovascular disease severity at baseline. LOY in blood was associated with a larger atheroma size (odds ratio, 2.15; 95% confidence interval, 1.06-4.76; P=0.04); however, this association was not significant after correction for multiple testing. LOY was independently associated with secondary major cardiovascular events (hazard ratio=2.28; 95% confidence interval, 1.11-4.67; P=0.02) in blood when corrected for confounders. Conclusions - In this hypothesis-generating study, LOY in blood is independently associated with secondary major cardiovascular events in a severely atherosclerotic population. Our data could indicate that LOY affects secondary outcome via other mechanisms than inflammation in the atherosclerotic plaque.
AB - Recent studies found an immune regulatory role for Y chromosome and a relationship between loss of Y chromosome (LOY) in blood cells and a higher risk of cancer and mortality. Given involvement of immune cells in atherosclerosis, we hypothesized that LOY is associated with the severity of atherosclerotic plaque characteristics and outcome in men undergoing carotid endarterectomy. Methods and Results - LOY was quantified in blood and plaque from raw intensity genotyping data in men within the Athero-Express biobank study. Plaques were dissected, and the culprit lesions used for histology and the measurement of inflammatory proteins. We tested LOY for association with (inflammatory) atherosclerotic plaque phenotypes and cytokines and assessed the association of LOY with secondary events during 3-year follow-up. Of 366 patients with carotid endarterectomy, 61 exhibited some degree of LOY in blood. LOY was also present in atherosclerotic plaque lesions (n=8/242, 3%). LOY in blood was negatively associated with age (β=-0.03/10 y; r2=0.07; P=1.6×10-7) but not with cardiovascular disease severity at baseline. LOY in blood was associated with a larger atheroma size (odds ratio, 2.15; 95% confidence interval, 1.06-4.76; P=0.04); however, this association was not significant after correction for multiple testing. LOY was independently associated with secondary major cardiovascular events (hazard ratio=2.28; 95% confidence interval, 1.11-4.67; P=0.02) in blood when corrected for confounders. Conclusions - In this hypothesis-generating study, LOY in blood is independently associated with secondary major cardiovascular events in a severely atherosclerotic population. Our data could indicate that LOY affects secondary outcome via other mechanisms than inflammation in the atherosclerotic plaque.
KW - atherosclerosis
KW - cardiovascular diseases
KW - cytokines
KW - genetics
KW - inflammation
UR - http://www.scopus.com/inward/record.url?scp=85028923623&partnerID=8YFLogxK
U2 - 10.1161/CIRCGENETICS.116.001544
DO - 10.1161/CIRCGENETICS.116.001544
M3 - Article
C2 - 28768751
AN - SCOPUS:85028923623
SN - 1942-325X
VL - 10
JO - Circulation-Cardiovascular genetics
JF - Circulation-Cardiovascular genetics
IS - 4
M1 - e001544
ER -