Subclinical hyperthyroidism and the risk of cardiovascular events and all-cause mortality: an updated meta-analysis of cohort studies

被引:55
|
作者
Yang, Li-bo [1 ,3 ]
Jiang, Dong-qing [2 ]
Qi, Wen-bo [3 ]
Zhang, Tie [3 ]
Feng, You-lun [3 ]
Gao, Ling [4 ]
Zhao, Jiajun [1 ]
机构
[1] Shandong Univ, Prov Hosp, Dept Endocrinol, Jinan 250021, Peoples R China
[2] Shandong Univ, Hosp 2, Dept Endocrinol, Jinan 250021, Peoples R China
[3] Taian City Cent Hosp, Dept Endocrinol, Tai An, Shandong, Peoples R China
[4] Shandong Univ, Prov Hosp, Dept Cent Lab, Jinan 250021, Peoples R China
基金
中国国家自然科学基金;
关键词
CORONARY-HEART-DISEASE; THYROID-DYSFUNCTION; SERUM TSH; COGNITIVE FUNCTION; ELDERLY-PEOPLE; BLOOD-PRESSURE; FOLLOW-UP; ASSOCIATION; HYPOTHYROIDISM; TRIIODOTHYRONINE;
D O I
10.1530/EJE-12-0015
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Whether subclinical hyperthyroidism (SCH) results in poor prognosis remains controversial. Our aim was to evaluate the association between SCH and the risk of cardiovascular disease (CVD), cardiovascular mortality, and all-cause mortality by conducting a meta-analysis of cohort studies. Methods: The PubMed and Embase databases were searched through November 2011 to identify studies that met pre-stated inclusion criteria. Relevant information for analysis was extracted. Either a fixed or a random effects model was used to calculate the overall combined risk estimates. Results: Seventeen cohort studies were included in this meta-analysis. The overall combined relative risks for individuals with SCH compared with the reference group were 1.19 (95% confidence interval (CI): 1.10 to 1.28) for CVD, 1.52 (95% CI: 1.08 to 2.13) for cardiovascular mortality, and 1.25 (95% CI: 1.00 to 1.55) for all-cause mortality. Subgroup analysis by sample source (community or convenience sample) showed that the significant association for cardiovascular and all-cause mortality only existed when pooling studies from convenience samples. Heterogeneity was observed when pooling studies on the association between SCH and cardiovascular and all-cause mortality. Sensitivity analysis showed omission of each individual study did not significantly change the pooled effects. No evidence of publication bias was observed. Conclusions: Our findings demonstrated that SCH significantly increased the risk of CVD for the general population and the risk of cardiovascular and all-cause mortality for the individuals with other morbidities.
引用
收藏
页码:75 / 84
页数:10
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