Abstract | BACKGROUND: METHODS: PubMed, Embase, and the Cochrane Library databases were searched for prospective cohort studies published prior to June 2016. Multivariate-adjusted hazard ratios (HRs) with 95% confidence intervals (CIs) for CHD and IS risks according to Lp-PLA2 activity or mass were extracted, pooled, and weighted using random-effects modeling. RESULTS: Twelve studies examining Lp-PLA2 activity or mass and long-term risks of CHD and IS were included. Combined HRs for CHD and IS risks for the highest category referring to lowest category of Lp-PLA2 were 1.46 (95% CI: 1.20-1.78, P<0.001) and 1.58 (95% CI: 1.21-2.07, P=0.001), respectively. The same patterns were observed for both mass and activity, with the exception of those for CHD. For every 1-standard deviation (SD) increase in Lp-PLA2 activity, CHD risk increased by 12% (HR: 1.12, 95% CI: 1.05-1.22, P=0.002); no association between 1-SD increases in Lp-PLA2 activity and IS was observed. Lp-PLA2 mass was associated with CHD risk (HR: 1.02-1.24, 95% CI: 1.02-1.24, P=0.021). Lp-PLA2 mass per 1-SD increase was not associated with IS risk. CONCLUSIONS: Greater Lp-PLA2 activity or mass was associated with an increased risk of CHD and IS; however, additional well-designed trials are warranted to confirm this association.
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Authors | Dongze Li, Wei Wei, Xun Ran, Jing Yu, Hui Li, Lizhi Zhao, Honglian Zeng, Yu Cao, Zhi Zeng, Zhi Wan |
Journal | Clinica chimica acta; international journal of clinical chemistry
(Clin Chim Acta)
Vol. 471
Pg. 38-45
(Aug 2017)
ISSN: 1873-3492 [Electronic] Netherlands |
PMID | 28514697
(Publication Type: Journal Article, Meta-Analysis, Review, Systematic Review)
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Copyright | Copyright © 2017 Elsevier B.V. All rights reserved. |
Chemical References |
- 1-Alkyl-2-acetylglycerophosphocholine Esterase
|
Topics |
- 1-Alkyl-2-acetylglycerophosphocholine Esterase
(metabolism)
- Brain Ischemia
(complications)
- Coronary Disease
(enzymology, epidemiology)
- Humans
- Risk
- Stroke
(complications, enzymology, epidemiology)
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