4.8 Article

Screening for type 2 diabetes and population mortality over 10 years (ADDITION-Cambridge): a cluster-randomised controlled trial

Journal

LANCET
Volume 380, Issue 9855, Pages 1741-1748

Publisher

ELSEVIER SCIENCE INC
DOI: 10.1016/S0140-6736(12)61422-6

Keywords

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Funding

  1. Wellcome Trust [G061895]
  2. UK Medical Research Council
  3. National Health Service
  4. UK National Institute for Health Research
  5. University of Aarhus, Denmark
  6. Bio-Rad
  7. Ely Lilly
  8. Novo Nordisk
  9. Medical Research Council [G0001164]
  10. National Institute for Health Research
  11. Gates Cambridge Trust
  12. NIHR Research funds
  13. Department of Health NIHR Programme [RP-PG-0606-1259]
  14. NIHR Biomedical Research Centre
  15. NIHR [RP-PG-0606-1259]
  16. Medical Research Council [MC_U106179474, G0200391, G0001164, MC_U106179471] Funding Source: researchfish
  17. National Institute for Health Research [RP-PG-0606-1259, 08/116/300] Funding Source: researchfish
  18. MRC [MC_U106179474, G0001164, G0200391] Funding Source: UKRI

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Background The increasing prevalence of type 2 diabetes poses a major public health challenge. Population-based screening and early treatment for type 2 diabetes could reduce this growing burden. However, uncertainty persists around the benefits of screening for type 2 diabetes. We assessed the effect of a population-based stepwise screening programme on mortality. Methods In a pragmatic parallel group, cluster-randomised trial, 33 general practices in eastern England were randomly assigned by the method of minimisation in an unbalanced design to: screening followed by intensive multifactorial treatment for people diagnosed with diabetes (n=15); screening plus routine care of diabetes according to national guidelines (n=13); and a no-screening control group (n=5). The study population consisted of 20 184 individuals aged 40-69 years (mean 58 years), at high risk of prevalent undiagnosed diabetes, on the basis of a previously validated risk score. In screening practices, individuals were invited to a stepwise programme including random capillary blood glucose and glycated haemoglobin (HbA(1c)) tests, a fasting capillary blood glucose test, and a confirmatory oral glucose tolerance test. The primary outcome was all-cause mortality. All participants were flagged for mortality surveillance by the England and Wales Office of National Statistics. Analysis was by intention-to-screen and compared all-cause mortality rates between screening and control groups. This study is registered, number ISRCTN86769081. Findings Of 16 047 high-risk individuals in screening practices, 15 089 (94%) were invited for screening during 2001-06, 11 737 (73%) attended, and 466 (3%) were diagnosed with diabetes. 4137 control individuals were followed up. During 184 057 person-years of follow up (median duration 9.6 years [IQR 8.9-9.9]), there were 1532 deaths in the screening practices and 377 in control practices (mortality hazard ratio [HR] 1.06, 95% CI 0.90-1.25). We noted no significant reduction in cardiovascular (HR 1.02, 95% CI 0.75-1.38), cancer (1.08, 0.90-1.30), or diabetes-related mortality (1.26, 0.75-2.10) associated with invitation to screening. Interpretation In this large UK sample, screening for type 2 diabetes in patients at increased risk was not associated with a reduction in all-cause, cardiovascular, or diabetes-related mortality within 10 years. The benefits of screening might be smaller than expected and restricted to individuals with detectable disease.

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