Abstract

Aims/hypothesisSeveral pathophysiological mechanisms would suggest a causal link between hypoglycaemia and cardiovascular death; conversely, current knowledge would not support a causal relationship with other causes of death. To clarify the nature and the magnitude of the association between hypoglycaemia and death, we investigated the 5 year mortality risks for cardiovascular disease, cancer and other causes in individuals with type 2 diabetes admitted to hospital for a severe hypoglycaemic episode.MethodsWe defined in the UK Clinical Practice Research Datalink database a prevalent cohort of adults with type 2 diabetes diagnosed between 1 January 1998 and 1 January 2011 (index date), with available linkage to the Office for National Statistics (ONS) and the Hospital Episode Statistics (HES). A hospital admission reporting hypoglycaemia as the underlying cause was identified before the index date in the HES; date and underlying cause of death were obtained from the ONS. We quantified the 5 year risk of cause-specific death in people with and without admission to hospital for severe hypoglycaemia, adjusting for potential confounders and accounting for competing risk.ResultsOf the 74,610 subjects included in the cohort, 388 (0.5%) were admitted at least once for a severe hypoglycaemic episode; subjects admitted were older, with higher HbA1c and a greater prevalence of multimorbidity. During a median follow-up of 7.1 years, 236 (60.8%) and 18,539 (25.0%) deaths occurred in subjects with and without a previous severe hypoglycaemia, respectively. Non-cardiovascular causes accounted for 71% of all deaths in both subjects with and without hypoglycaemia. In a 60-year-old person with severe hypoglycaemia, the 5 year absolute risk of death, adjusted for age, sex, ethnicity, systolic blood pressure, total cholesterol, HbA1c, BMI, eGFR, smoking status, alcohol consumption and deprivation (Townsend score), was 6.6%, 1.1% and 13.1% for cardiovascular, cancer and other causes, respectively, while the 5 year absolute risk difference compared with a subject without severe hypoglycaemia was 4.7% (95% CI 1.0, 8.3) for cardiovascular, −1.4% (−4.1, 1.4) for cancer and 11.1% (6.1, 16.1) for other causes of death. Results were consistent in models further adjusted for medications and comorbidities (myocardial infarction, stroke, peripheral artery disease, heart failure, atrial fibrillation, cancer), with sulfonylurea and insulin associated with increased mortality rates (from cause-specific hazard ratio of 1.06 [95% CI 0.99, 1.14] for cancer death with use of sulfonylurea to 1.42 [1.29, 1.56] for cardiovascular death with use of insulin). Results were robust to missing data.Conclusions/interpretationThe results of this study indicate severe hypoglycaemia as a marker of, rather than causally linked to, an increased risk of long-term mortality. Regardless of the nature of the association, a severe hypoglycaemic episode represents a strong negative prognostic factor in patients with type 2 diabetes.Graphical abstract

Highlights

  • One of the proposed hypotheses to explain the results of the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial, which showed a 22% higher relative risk of death in individuals with type 2 diabetes randomised to intensive glucose control, was the higher rate of hypoglycaemic events in participants intensively treated compared to those randomised to conventional glucose control [1]

  • Cohort definition and subject characteristics Of the 87,660 subjects with type 2 diabetes included in the cohort, 1461 had implausible values of covariates and 11,589 had missing data for at least one covariate, leaving a final cohort of 74,610 subjects with complete data for the main analysis (Fig. 1)

  • Further differences between the two groups were observed for medications and comorbidities: insulin therapy was more frequent in people with a severe hypoglycaemic episode, as well as a medical history of cancer, myocardial infarction (5.7%), peripheral artery disease (9.1%), atrial fibrillation (12.9%), heart failure (14.5%) or stroke (15.1%)

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Summary

Introduction

One of the proposed hypotheses to explain the results of the Action to Control Cardiovascular Risk in Diabetes (ACCORD) trial, which showed a 22% higher relative risk of death in individuals with type 2 diabetes randomised to intensive glucose control, was the higher rate of hypoglycaemic events in participants intensively treated compared to those randomised to conventional glucose control [1]. A post hoc analysis of the Action in Diabetes and Vascular Disease: Preterax and Diamicron Controlled Evaluation (ADVANCE) trial indicated that participants with type 2 diabetes reporting hypoglycaemic episodes requiring assistance had an increased risk of cancer and skin, respiratory or digestive diseases [6]. These analyses would suggest severe hypoglycaemia as a marker of other medical conditions that are causally associated with a higher risk of CVD and death. Numerous observational studies have shown an increased CVD and non-CVD risk after controlling for multiple potential confounders [2]

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