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U.K. Prospective Diabetes Study 22: Effect of age at diagnosis on diabetic tissue damage during the first 6 years of NIDDM

  1. Timothy ME Davis, FRACP,
  2. Irene M Stratton, MSC,
  3. Charles J Fox, FRCP,
  4. Rury R Holman, FRCP,
  5. Robert C Turner, MD and
  6. U.K. Prospective Diabetes Study (UKPDS) Group
  1. Radcliffe Infirmary, Oxford; Royal Infirmary Aberdeen General Hospital Birmingham St. George's Hospital and Hammersmith Hospital London City Hospital and Royal Victoria Hospital Belfast North Staffordshire Royal Infirmary Stoke-on-Trent St. Helier Hospital Carshalton Whittington Hospital London Norfolk and Norwich Hospital Norwich Lister Hospital Stevenage Ipswich Hospital Ipswich Ninewells Hospital Dundee
  2. Northampton General Hospital Northampton, U.K.
  1. Address correspondence and reprint requests to the UKPDS Group, Diabetes Research Laboratories, Radcliffe Infirmary, Woodstock Road, Oxford 0X2 6HE, U.K

Abstract

OBJECTIVE To assess the effect of age at diagnosis on the initial prevalence and subsequent risk of the progression of diabetic tissue damage in patients with NIDDM.

RESEARCH DESIGN AND METHODS The prevalence of Q-wave myocardial infarction, absent dorsalis pedis pulses, retinopathy, absent ankle jerks, hypertension, and microalbuminuria were determined at baseline and at 3 and 6 years of follow-up in five consecutive 6-year age-cohorts of 3,027 newly diagnosed white patients aged between 36 and 65 years recruited to the U.K. Prospective Diabetes Study. The effect of age at diagnosis on the initial prevalence and the risk of progression of these complications and associated conditions was analyzed using logistic regression and proportional odds methods, respectively.

RESULTS Q-wave myocardial infarction and hypertension were more prevalent in older patients at presentation, but age at diagnosis did not have a significant effect on the increased risk of either after 6 years of NIDDM. Absent dorsalis pedis pulses and ankle jerks were also more prevalent in the older age-groups at presentation, but age at diagnosis was a significant predictor of the increasing prevalence of both during follow-up. The baseline prevalence of retinopathy and microalbuminuria was not related to age. The subsequent risk of retinopathy, but not microalbuminuria, increased significantly with age at diagnosis.

CONCLUSIONS Age at diagnosis has a variable impact on different types of diabetic tissue damage and may thus be an important variable in epidemiological and intervention studies in NIDDM. Regular ophthalmologic surveillance and examination of the feet increase in importance with increasing age since the diagnosis of NIDDM.

  • Received October 30, 1996.
  • Accepted May 16, 1997.
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This Article

  1. doi: 10.2337/diacare.20.9.1435 Diabetes Care September 1997 vol. 20 no. 9 1435-1441
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