Please use this identifier to cite or link to this item: https://hdl.handle.net/2440/126783
Citations
Scopus Web of Science® Altmetric
?
?
Type: Journal article
Title: A novel genetic marker of decreased inflammation and improved survival after acute myocardial infarction
Author: Coverstone, E.D.
Bach, R.G.
Chen, L.S.
Bierut, L.J.
Li, A.Y.
Lenzini, P.A.
O Neill, H.C.
Spertus, J.A.
Sucharov, C.C.
Stitzel, J.A.
Schilling, J.D.
Cresci, S.
Citation: Basic Research in Cardiology, 2018; 113(5):38-1-38-13
Publisher: Springer
Issue Date: 2018
ISSN: 0300-8428
1435-1803
Statement of
Responsibility: 
Edward D. Coverstone, Richard G. Bach, LiShiun Chen, Laura J. Bierut, Allie Y. Li, Petra A. Lenzini ... et al.
Abstract: The CHRNA5 gene encodes a neurotransmitter receptor subunit involved in multiple processes, including cholinergic autonomic nerve activity and inflammation. Common variants in CHRNA5 have been linked with atherosclerotic cardiovascular disease. Association of variation in CHRNA5 and specific haplotypes with cardiovascular outcomes has not been described. The aim of this study was to examine the association of CHRNA5 haplotypes with gene expression and mortality among patients with acute myocardial infarction (AMI) and explore potential mechanisms of this association. Patients (N = 2054) hospitalized with AMI were genotyped for two common variants in CHRNA5. Proportional hazard models were used to estimate independent association of CHRNA5 haplotype with 1-year mortality. Both individual variants were associated with mortality (p = 0.0096 and 0.0004, respectively) and were in tight LD (D' = 0.99). One haplotype, HAP3, was associated with decreased mortality one year after AMI (adjusted HR = 0.42, 95% CI 0.26, 0.68; p = 0.0004). This association was validated in an independent cohort (N = 637) of post-MI patients (adjusted HR = 0.23, 95% CI 0.07, 0.79; p = 0.019). Differences in CHRNA5 expression by haplotype were investigated in human heart samples (n = 28). Compared with non-carriers, HAP3 carriers had threefold lower cardiac CHRNA5 mRNA expression (p = 0.023). Circulating levels of the inflammatory marker hsCRP were significantly lower in HAP3 carriers versus non-carriers (3.43 ± 4.2 versus 3.91 ± 5.1; p = 0.0379). Activation of the inflammasome, an important inflammatory complex involved in cardiovascular disease that is necessary for release of the pro-inflammatory cytokine IL-1 β, was assessed in bone marrow-derived macrophages (BMDM) from CHRNA5 knockout mice and wild-type controls. In BMDM from CHRNA5 knockout mice, IL-1β secretion was reduced by 50% compared to wild-type controls (p = 0.004). Therefore, a common haplotype of CHRNA5 that results in reduced cardiac expression of CHRNA5 and attenuated macrophage inflammasome activation is associated with lower mortality after AMI. These results implicate CHRNA5 and the cholinergic anti-inflammatory pathway in survival following AMI.
Keywords: Cardiovascular disease; genetic variation; myocardial infarction; mortality; haplotype; inflammation
Rights: © 2018, Springer Nature
DOI: 10.1007/s00395-018-0697-7
Appears in Collections:Aurora harvest 8
Medicine publications

Files in This Item:
There are no files associated with this item.


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.