Glycated Hemoglobin and All-Cause and Cause-Specific Mortality among Adults with and Without Diabetes

Fu Rong Li, Xi Ru Zhang, Wen Fang Zhong, Zhi Hao Li, Xiang Gao, Virginia Byers Kraus, Yue Bin Lv, Meng Chen Zou, Guo Chong Chen, Pei Liang Chen, Min Yi Zhang, Akech Kuol Akech Kur, Xiao Ming Shi, Xian Bo Wu, Chen Mao

Research output: Contribution to journalArticlepeer-review

28 Scopus citations

Abstract

Context The patterns of associations between glycated Hb (HbA 1c) and mortality are still unclear. Objective To explore the extent to which ranges of HbA 1c levels are associated with the risk of mortality among participants with and without diabetes. Design, Setting, and Patients This was a nationwide, community-based prospective cohort study. Included were 15,869 participants (median age 64 years) of the Health and Retirement Study, with available HbA 1c data and without a history of cancer. Cox proportional hazards regression models were used to estimate hazard ratios with 95% CIs for mortality. Results A total of 2133 participants died during a median follow-up of 5.8 years. In participants with diabetes, those with an HbA 1c level of 6.5% were at the lowest risk of all-cause mortality. When HbA 1c level was <5.6% or >7.4%, the increased all-cause mortality risk became statistically significant as compared with an HbA 1c level of 6.5%. As for participants without diabetes, those with an HbA 1c level of 5.4% were at the lowest risk of all-cause mortality. When the HbA 1c level was <5.0%, the increased all-cause mortality risk became statistically significant as compared with an HbA 1c level of 5.4%. However, we did not observe a statistically significant elevated risk of all-cause mortality above an HbA 1c level of 5.4%. Conclusions A U-shaped and reverse J-shaped association for all-cause mortality was found among participants with and without diabetes. The corresponding optimal ranges for overall survival are predicted to be 5.6% and 7.4% and 5.0% and 6.5%, respectively.

Original languageEnglish (US)
Pages (from-to)3345-3354
Number of pages10
JournalJournal of Clinical Endocrinology and Metabolism
Volume104
Issue number8
DOIs
StatePublished - Jun 19 2019

All Science Journal Classification (ASJC) codes

  • Endocrinology, Diabetes and Metabolism
  • Biochemistry
  • Endocrinology
  • Clinical Biochemistry
  • Biochemistry, medical

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