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The NIDDK Takes on the Complications of Type 1 Diabetes: The Diabetes Control and Complications Trial/Epidemiology of Diabetes Interventions and Complications (DCCT/EDIC) Study

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posted on 2025-04-24, 00:10 authored by Barbara H. Braffett, Ionut Bebu, Gayle M. Lorenzi, Catherine L. Martin, Bruce A. Perkins, Rose Gubitosi-Klug, David M. Nathan

The Diabetes Control and Complications Trial (DCCT, 1983-1993) compared intensive therapy aimed at near-normal glycemia and conventional therapy in 1,441 adolescent and adult participants with type 1 diabetes (T1D) over a mean follow-up of 6.5 years. The primary DCCT results, reported in 1993, demonstrated the benefits of intensive therapy (mean HbA1c ~7%) compared with conventional therapy (HbA1c ~9%) in reducing the risk of development and progression of microvascular complications by 35-76%. HbA1c <7% was adopted worldwide as the therapeutic target for T1D. Subsequently, the Epidemiology of Diabetes Interventions and Complications (EDIC, 1994-present) study was initiated as the observational follow-up of the DCCT cohort. EDIC has shown that the early beneficial effects of intensive vs. conventional therapy on complications persisted for ~10 years after the convergence of HbA1c levels in the two groups during EDIC, a novel concept termed metabolic memory. During EDIC, prior intensive therapy was also shown to reduce the risk of severe microvascular complications, cardiovascular disease, mortality and, recently, age-related outcomes including cognitive impairment, bone loss, and reduced mobility. The DCCT/EDIC cohort is the most extensively studied T1D cohort in history. The participants have been followed and deeply phenotyped for 95% of their diabetes durations and 65% of their lifespans. Throughout its 40+ years, funded by and in close collaboration with the National Institute of Diabetes and Digestive and Kidney Diseases, DCCT/EDIC has generated results that have guided treatment priorities in T1D and led to improved survival and quality-of-life for millions of people with T1D worldwide.

Funding

Support for this DCCT/EDIC collaborative study was provided by grant DP3 DK114812. The DCCT/EDIC has been supported by cooperative agreements (1982-1993, 2012-2017, 2017-2022), and contracts (1982-2012) with the Division of Diabetes, Endocrinology, and Metabolic Diseases of the National Institute of Diabetes and Digestive and Kidney Diseases (current grant numbers U01 DK094176 and U01 DK094157), and through support by the National Eye Institute, the National Institute of Neurologic Disorders and Stroke, the General Clinical Research Centers Program (1993-2007), and Clinical Translational Science Center Program (2006-present), Bethesda, Maryland, USA. The sponsor of this study is represented by the NIDDK Project Scientist who serves as part of the DCCT/EDIC Research Group and plays a part in the study design and conduct as well as the review and approval of manuscripts. The NIDDK Project Scientist was not a member of the writing group of this paper. The opinions expressed are those of the investigators and do not necessarily reflect the views of the funding agencies.

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