Are Lower Fasting Plasma Glucose Levels at Diagnosis of Type 2 Diabetes Associated With Improved Outcomes?

U.K. Prospective Diabetes Study 61

  1. Stephen Colagiuri, FRACP1,
  2. Carole A. Cull, PHD2,
  3. Rury R. Holman, FRCP2 and
  4. For the UKPDS Group
  1. 1Diabetes Center, Prince of Wales Hospital, Randwick, Australia
  2. 2Diabetes Trials Unit, Oxford Center for Diabetes, Endocrinology and Metabolism, University of Oxford, Oxford, U.K

    Abstract

    OBJECTIVE—Type 2 diabetes may be present for several years before diagnosis, by which time many patients have already developed diabetic complications. Earlier detection and treatment may reduce this burden, but evidence to support this approach is lacking.

    RESEARCH DESIGN AND METHODS—Glycemic control and clinical and surrogate outcomes were compared for 5,088 of 5,102 U.K. Diabetes Prospective Study participants according to whether they had low (<140 mg/dl [<7.8 mmol/l]), intermediate (140 to <180 mg/dl [7.8 to <10.0 mmol/l]), or high (≥180 mg/dl [≥10 mmol/l]) fasting plasma glucose (FPG) levels at diagnosis. Individuals who presented with and without diabetic symptoms were also compared.

    RESULTS—Fewer people with FPG in the lowest category had retinopathy, abnormal biothesiometer measurements, or reported erectile dysfunction. The rate of increase in FPG and HbA1c during the study was identical in all three groups, although absolute differences persisted. Individuals in the low FPG group had a significantly reduced risk for each predefined clinical outcome except stroke, whereas those in the intermediate group had significantly reduced risk for each outcome except stroke and myocardial infarction. The low and intermediate FPG groups had a significantly reduced risk for progression of retinopathy, reduction in vibration sensory threshold, or development of microalbuminuria.

    CONCLUSIONS—People presenting with type 2 diabetes with lower initial glycemia who may be earlier in the course of their disease had fewer adverse clinical outcomes despite similar glycemic progression. Since most such people are asymptomatic at diagnosis, active case detection programs would be required to identify them.

    Footnotes

    • Address correspondence and reprint requests to Prof. S. Colagiuri, Diabetes Center, Prince Wales Hospital, Randwick, 2031 NSW, Australia. E-mail: colagiuris{at}sesahs.nsw.gov.au.

      Received for publication 7 December 2001 and accepted in revised form 29 April 2002.

      A table elsewhere in this issue shows conventional and Système International (SI) units and conversion factors for many substances.

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