Glycated Hemoglobin and All-Cause and Cause-Specific Mortality in Singaporean Chinese Without Diagnosed Diabetes: The Singapore Chinese Health Study

被引:15
|
作者
Bancks, Michael P. [1 ]
Odegaard, Andrew O. [1 ]
Pankow, James S. [1 ]
Koh, Woon-Puay [2 ,3 ]
Yuan, Jian-Min [4 ,5 ]
Gross, Myron D. [1 ]
Pereira, Mark A. [1 ]
机构
[1] Univ Minnesota, Sch Publ Hlth, Div Epidemiol & Community Hlth, Minneapolis, MN 55455 USA
[2] Duke NUS Grad Med Sch Singapore, Singapore, Singapore
[3] Natl Univ Singapore, Saw Swee Hock Sch Publ Hlth, Singapore 117548, Singapore
[4] Univ Pittsburgh, Inst Canc, Div Canc Control & Populat Sci, Pittsburgh, PA USA
[5] Univ Pittsburgh, Grad Sch Publ Hlth, Dept Epidemiol, Pittsburgh, PA USA
基金
美国国家卫生研究院;
关键词
FACTOR BINDING PROTEIN-1; GROWTH-FACTOR-I; COLORECTAL-CANCER; US ADULTS; C-PEPTIDE; RISK; INSULIN; ASSOCIATION; HYPERGLYCEMIA; EPIDEMIOLOGY;
D O I
10.2337/dc14-0390
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
OBJECTIVE Glycated hemoglobin (HbA(1c)) is a robust biomarker of the preceding 2 to 3months average blood glucose level. The aim of this study was to examine the association between HbA(1c) and mortality in a cohort of Southeast Asians. RESEARCH DESIGN AND METHODS Analysis of 7,388men andwomen, mean age 62 years, fromthe Singapore Chinese Health Studywho provided a blood sample at the follow-up I visit (1999-2004) and reported no history of diabetes, previous adverse cardiovascular events, or cancer. A total of 888 deaths were identified through 31 December 2011 via registry linkage. Participants represented a random study sample of potential control subjects for a nested case-control genome-wide association study of type 2 diabetes in the population. Hazard ratios (HRs) for all-cause and cause-specific mortality by six categories of HbA(1c) were estimated with Cox regression models. RESULTS Relative to participantswith an HbA(1c) of 5.4-5.6%(36-38mmol/mol), participants with HbA(1c) >= 6.5% (>= 48 mmol/mol) had an increased risk of all-cause, cardiovascular, and cancermortality during an average of 10.1 years of follow-up; HRs (95% CIs) were 1.96 (1.56-2.46), 2.63 (1.77-3.90), and 1.51 (1.04-2.18), respectively. No level of HbA(1c) was associated with increased risk of respiratory mortality. Levels < 6.5% HbA(1c) were not associated with mortality during follow-up. The results did not materially change after excluding observation of first 3 years post-blood draw. CONCLUSIONS HbA(1c) levels consistent with undiagnosed type 2 diabetes (>= 6.5%) are associated with an increased risk of all-cause and cause-specificmortality in Chinesemen and women.
引用
收藏
页码:3180 / 3187
页数:8
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