14-Year risk of all-cause mortality according to hypoglycaemic drug exposure in a general population

PLoS One. 2014 Apr 21;9(4):e95671. doi: 10.1371/journal.pone.0095671. eCollection 2014.

Abstract

Purpose: Guidelines for management of patients with type 2 diabetes mellitus recommend the use of hypoglycaemic drugs when lifestyle interventions remain insufficient for glycaemic control. Recent trials have provided worrying safety data on certain hypoglycaemic drugs. The aim of this study was to assess 14-year risk of all-cause mortality according to hypoglycaemic drug exposure at baseline, in a general population.

Methods: Our analysis was based on the observational Third French MONICA survey on cardiovascular risk factors (1995-1997). Vital status was obtained 14 years after inclusion, and assessment of determinants of mortality was based on multivariable Cox modelling.

Results: There were 3336 participants and 248 deaths over the 14-year period. At baseline, there were 3162 (95%) non-diabetic, 46 (1%) untreated type 2 diabetic and 128 (4%) type 2 diabetic subjects with hypoglycaemic drug treatment (metformin alone (31%), sulfonylureas alone or in combination (49%), insulin alone or in combination (10%), or other treatments (9%)). After adjustment for duration of diabetes, history of diabetes complications, area of residence (centre), age, gender, educational level, alcohol consumption, smoking, blood pressure, LDL and HDL cholesterol, which all were significant and independent determinants of mortality, the hazard ratio for all-cause mortality was 3.22 [95% confidence interval: 0.87-11.9] for untreated diabetic subjects, 2.28 [0.98-5.26] for diabetics treated with metformin alone, 1.70 [0.92-3.16] for diabetics with sulfonylureas and 4.92 [1.70-14.3] for diabetic with insulin versus non-diabetic subjects.

Conclusions: Our results support the conclusion that until more evidence is provided from randomized trials, a prudent approach should be to restrain use of insulin to situations in which combinations of non-insulin agents have failed to appropriately achieve glycemic control, as it is recommended in the current guidelines for the management of type 2 diabetes.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Diabetes Mellitus, Type 2 / drug therapy*
  • Diabetes Mellitus, Type 2 / mortality*
  • Female
  • Humans
  • Hypoglycemic Agents / adverse effects*
  • Hypoglycemic Agents / therapeutic use*
  • Male
  • Middle Aged
  • Risk Factors
  • Survival Analysis

Substances

  • Hypoglycemic Agents

Grants and funding

The authors would like to thank the “Institut National de la Santé et de la Recherche Médicale” (INSERM), the “Direction Générale de la Santé (DGS),” the “Institut Pasteur de Lille,” the “University Hospital of Lille,” the “Fonds d'intervention en Santé Publique,” the “Mutuelle Générale de l'Education Nationale,” “ONIVINS,” the “Fondation de France,” the “CPAM of Selestat,” the “Fédération Française de Cardiologie,” the “Conseil Régional du Nord-Pas de Calais,” Parke-Davis and Bayer pharmaceuticals, and CERIN for their financial support enabling this work. The sponsors did not take part or interfere in data analysis or editing of the manuscript.