Association between adiponectin levels and coronary heart disease and mortality: a systematic review and meta-analysis

被引:96
|
作者
Lee, Eon Sook [1 ]
Park, Sang-shin [2 ]
Kim, Eugene [3 ]
Yoon, Yeong Sook [1 ]
Ahn, Hong-Yup [4 ]
Park, Cheol-Young [5 ]
Yun, Young Ho [6 ]
Oh, Sang Woo [3 ]
机构
[1] Inje Univ, Ilsan Paik Hosp, Dept Family Med, Gyeonggi Do, South Korea
[2] Texas A&M Univ, Coll Vet Med & Biomed Sci, Dept Vet Integrat Biosci, College Stn, TX USA
[3] Dongguk Univ, Coll Med, Ilsan Hosp, Ctr Obes Nutr & Metab,Dept Family Med, Gyeonggi Do, South Korea
[4] Dongguk Univ Seoul, Dept Stat, Seoul, South Korea
[5] Sungkyunkwan Univ, Sch Med, Kangbuk Samsung Hosp, Dept Internal Med, Seoul, South Korea
[6] Seoul Natl Univ, Coll Med, Seoul, South Korea
关键词
Adiponectin; all-cause mortality; cardiovascular mortality; coronary heart disease; MOLECULAR-WEIGHT ADIPONECTIN; MYOCARDIAL-INFARCTION; CARDIOVASCULAR-DISEASE; INSULIN-RESISTANCE; FOLLOW-UP; RISK; MEN; PLASMA; PREDICTOR; EVENTS;
D O I
10.1093/ije/dyt087
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
Background Our aim was to systematically review prospective studies of the association of plasma adiponectin levels with the risk of coronary heart disease (CHD) events, cardiovascular mortality and all-cause mortality. Methods We searched Medline, EMBASE, the Cochrane Library and CINAHL for reports published through October 2011. Search terms included 'adiponectin' AND 'cardiovascular disease' OR 'mortality'. We included prospective studies lasting more than 1 year with plasma adiponectin levels at baseline and all-cause mortality and/or major cardiovascular morbidity and mortality as outcomes. We used a random-effects model to pool the data and conducted additional subgroup meta-analyses according to the pre-existence of CHD. Pooled relative risk (RR) was estimated by a 1-SD increase in the logarithmically transformed circulating adiponectin levels. Results A total of 24 prospective studies were included in the meta-analysis. The pooled RR of adiponectin for CHD events (23 studies) was 1.03 [95% confidence interval (CI): 1.00, 1.06]. In subgroup analyses, the RR of adiponectin was 0.99 (95% CI: 0.94, 1.03) for new-onset CHD (17 studies), but there was an increased risk (RR = 1.12, 95% CI: 1.04, 1.22) for CHD recurrence (seven studies). A 10% increased risk (RR = 1.10, 95% CI: 1.04, 1.16) of all-cause mortality (six studies) and a 14% increased risk (RR = 1.14, 95% CI: 1.05, 1.23) of cardiovascular disease mortality (five studies) were observed. Conclusions No association was observed between adiponectin levels and CHD events. Our results suggest that higher circulating adiponectin levels may be associated with an increased risk of CHD recurrence and all-cause/CVD mortality.
引用
收藏
页码:1029 / 1039
页数:11
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