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      Prevention of cardiovascular disease through reduction of glycaemic exposure in type 2 diabetes: A perspective on glucose-lowering interventions.

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          Abstract

          Type 2 diabetes is a leading cause of cardiovascular disease (CVD). Observational studies have consistently shown an association between glycaemic level and risk of major adverse cardiovascular events (MACE); however, intervention studies have provided limited evidence supporting a reduction in the cardiovascular burden of diabetes through intensive glucose control. In the present review, we aimed to examine the concept of cumulative glycaemic exposure with regard to protection against CVD in diabetes. We address how we can move from a binary approach in trials, to a more quantitative approach based on differences in cumulative glycaemic exposure. We plotted the association between differing glycaemic exposures between study arms and the hazard ratio for MACE in randomized controls trials comparing intensive with conventional glycaemic control in type 2 diabetes. We found a strikingly strong correlation between differential exposure and cardiovascular risk reduction. Similar results were obtained for trials comparing antidiabetes drugs with placebo. The results suggest that a minimum study duration and a minimum gain in glycated haemoglobin (HbA1c) reduction are necessary to drive a relevant risk reduction in CVD risk, and we provide a quantitative perspective in that respect. The present analysis underlines that the duration of the intensification of glycemic control, and the amplitude of the resulting reduction in HbA1c, are important notions for clinical decision-making.

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          Author and article information

          Journal
          Diabetes Obes Metab
          Diabetes, obesity & metabolism
          Wiley
          1463-1326
          1462-8902
          February 2018
          : 20
          : 2
          Affiliations
          [1 ] INSERM, U-1138, Centre de Recherche des Cordeliers, Paris, France.
          [2 ] Sorbonne Paris Cité, UFR de Médecine, Université Paris Diderot, Paris, France.
          [3 ] Assistance Publique Hôpitaux de Paris, Hôpital Bichat, DHU FIRE, Paris, France.
          [4 ] INSERM U-1148, LVTS, French Alliance for Cardiovascular Clinical Trials, Paris, France.
          [5 ] National Heart and Lung Institute, ICMS, Imperial College, Royal Brompton Hospital, London, UK.
          Article
          10.1111/dom.13033
          28597588
          97f5c428-4f3c-470b-a5d2-2f5bc70e634c
          History

          randomised trial,systematic review,antidiabetic drug,cardiovascular disease,clinical trial,glycaemic control

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