Association of Monocyte Chemoattractant Protein‐1 (MCP‐1)‐2518A>G Polymorphism with Susceptibility to Coronary Artery Disease: A Meta‐Analysis. (27th February 2015)
- Record Type:
- Journal Article
- Title:
- Association of Monocyte Chemoattractant Protein‐1 (MCP‐1)‐2518A>G Polymorphism with Susceptibility to Coronary Artery Disease: A Meta‐Analysis. (27th February 2015)
- Main Title:
- Association of Monocyte Chemoattractant Protein‐1 (MCP‐1)‐2518A>G Polymorphism with Susceptibility to Coronary Artery Disease: A Meta‐Analysis
- Authors:
- Bai, Xiao‐Yan
Li, Shujing
Wang, Miao
Qu, Xinjian
Hu, Gaolei
Xu, Zhaowei
Chen, Min
He, Guo‐Wei
Wu, Huijian - Abstract:
- <abstract abstract-type="main"> <title>Summary</title> <p>We attempted to systematically elucidate the association between monocyte chemoattractant protein‐1 (<italic>MCP‐1</italic>) ‐2518A&gt;G polymorphism and risk of coronary artery disease (CAD). Eligible studies were identified through PubMed, EBSCO, and Web of Science Databases. The magnitude of <italic>MCP‐1</italic> polymorphism effect and its possible mode of action on CAD were estimated. The odds ratio (OR) with 95% confidence intervals (CI) were pooled in a specific genetic model to assess the association. A total of 21 studies were involved. There was significant gene effect on CAD risk in the overall population (likelihood ratio test: <italic>p</italic> &lt; 0.0001). Patients with GG and AG genotypes had 1.435 (95% CI: 1.183–1.740) and 1.087 (95% CI: 1.008–1.172) times higher risk of CAD than those with AA genotype. These gene effects suggested a recessive model to be appropriate. The pooled OR was 1.362 (95% CI: 1.137–1.631; <italic>p</italic><sub>uncorrected</sub> = 0.001, <italic>p</italic><sub>FDR</sub> = 0.005) in the recessive model. In the ethnicity‐stratified analysis, significant association was observed in the Caucasian population (OR = 1.492; 95% CI: 1.106–2.014; <italic>p</italic><sub>uncorrected</sub> = 0.009, <italic>p</italic><sub>FDR</sub> = 0.015), whereas no statistical significant association was detected in the Asian population (adjusted <italic>p</italic> = 0.124). The results suggested that<abstract abstract-type="main"> <title>Summary</title> <p>We attempted to systematically elucidate the association between monocyte chemoattractant protein‐1 (<italic>MCP‐1</italic>) ‐2518A&gt;G polymorphism and risk of coronary artery disease (CAD). Eligible studies were identified through PubMed, EBSCO, and Web of Science Databases. The magnitude of <italic>MCP‐1</italic> polymorphism effect and its possible mode of action on CAD were estimated. The odds ratio (OR) with 95% confidence intervals (CI) were pooled in a specific genetic model to assess the association. A total of 21 studies were involved. There was significant gene effect on CAD risk in the overall population (likelihood ratio test: <italic>p</italic> &lt; 0.0001). Patients with GG and AG genotypes had 1.435 (95% CI: 1.183–1.740) and 1.087 (95% CI: 1.008–1.172) times higher risk of CAD than those with AA genotype. These gene effects suggested a recessive model to be appropriate. The pooled OR was 1.362 (95% CI: 1.137–1.631; <italic>p</italic><sub>uncorrected</sub> = 0.001, <italic>p</italic><sub>FDR</sub> = 0.005) in the recessive model. In the ethnicity‐stratified analysis, significant association was observed in the Caucasian population (OR = 1.492; 95% CI: 1.106–2.014; <italic>p</italic><sub>uncorrected</sub> = 0.009, <italic>p</italic><sub>FDR</sub> = 0.015), whereas no statistical significant association was detected in the Asian population (adjusted <italic>p</italic> = 0.124). The results suggested that <italic>MCP‐1</italic> ‐2518A&gt;G polymorphism may be associated with susceptibility to CAD, especially in Caucasians.</p> </abstract> … (more)
- Is Part Of:
- Annals of human genetics. Volume 79:Number 3(2015:May)
- Journal:
- Annals of human genetics
- Issue:
- Volume 79:Number 3(2015:May)
- Issue Display:
- Volume 79, Issue 3 (2015)
- Year:
- 2015
- Volume:
- 79
- Issue:
- 3
- Issue Sort Value:
- 2015-0079-0003-0000
- Page Start:
- 173
- Page End:
- 187
- Publication Date:
- 2015-02-27
- Subjects:
- Human genetics -- Periodicals
599.935 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1469-1809/issues ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/ahg.12105 ↗
- Languages:
- English
- ISSNs:
- 0003-4800
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 1041.000000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 4272.xml