HbA1c below 7 % as the goal of glucose control fails to maximize the cardiovascular benefits: A meta-analysis

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Abstract

Objective: Whether lowering glycosylated haemoglobin (HbA1c) level below 7.0 % improves macro-vascular outcomes in diabetes remains unclear. Here, we aimed to assess the effect of relatively tight glucose control resulting in a follow-up HbA1c level of less or more than 7.0 % on cardiovascular outcomes in diabetic patients. Research design and methods: We systematically searched Medline, Web of science and Cochrane Library for prospective randomized controlled trials published between Jan 1, 1996 and July 1, 2015 that recorded cardiovascular outcome trials of glucose-lowering drugs or strategies in patients with type 2 diabetes mellitus. Results: Data from 15 studies involving 88,266 diabetic patients with 4142 events of non-fatal myocardial infarction, 6997 of major cardiovascular events, 3517 of heart failure, 6849 of all-cause mortality, 2084 of non-fatal stroke, 3816 of cardiovascular death were included. A 7 % reduction of major cardiovascular events was observed only when relatively tight glucose control resulted in a follow-up HbA1c level above 7.0 % (OR 0.93, 95 % CI 0.88-0.98; I 2 = 33 %), however, the patients can benefit from reduction incidence of non-fatal myocardial infarction only when the follow-up HbA1c value below 7.0 % (OR 0.85, 95 % CI 0.74-0.96). Apart from the HbA1c value above 7.0 % (OR 1.22, 95 % CI 1.06-1.40), the application of thiazolidinediones (OR 1.39, 95 % CI 1.14-1.69) also increased the risk of heart failure, while the gliptins shows neutral effects to heart failure (OR 1.14, 95 % CI 0.97-1.34). Conclusions: Relatively tight glucose control has some cardiovascular benefits. HbA1c below 7.0 % as the goal to maximize the cardiovascular benefits remains suspended.

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Wang, P., Huang, R., Lu, S., Xia, W., Sun, H., Sun, J., … Wang, S. (2015). HbA1c below 7 % as the goal of glucose control fails to maximize the cardiovascular benefits: A meta-analysis. Cardiovascular Diabetology, 14(1). https://doi.org/10.1186/s12933-015-0285-1

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