4.7 Article

Age at type 2 diabetes onset and glycaemic control: results from the National Health and Nutrition Examination Survey (NHANES) 2005-2010

期刊

DIABETOLOGIA
卷 56, 期 12, 页码 2593-2600

出版社

SPRINGER
DOI: 10.1007/s00125-013-3036-4

关键词

Ageing; Diabetes mellitus; Epidemiology; Prevention and control

资金

  1. institutional National Research Service Award [T32HP10251]
  2. Ryoichi Sasakawa Fellowship Fund
  3. General Medicine Division at Massachusetts General Hospital
  4. National Institutes of Health [R03DK090196]
  5. [K24 DK080140]

向作者/读者索取更多资源

We tested the hypothesis that age younger than 65 years at type 2 diabetes diagnosis is associated with worse subsequent glycaemic control. A cross-sectional analysis of data from participants in the 2005-2010 National Health and Nutrition Examination Survey was performed. For adults with self-reported diabetes, we dichotomised age at diabetes diagnosis as younger (< 65 years) vs older (a parts per thousand yen65 years). The primary outcome of interest was HbA(1c) > 9.0% (75 mmol/mol). Secondary outcomes were HbA(1c) > 8.0% (64 mmol/mol) and > 7.0% (53 mmol/mol). We used multivariable logistic regression for analysis. Among 1,438 adults with diabetes, a higher proportion of those < 65 years at diagnosis compared with those a parts per thousand yen65 at diagnosis had an HbA(1c) > 9.0% (14.4% vs 2.5%, p < 0.001). After adjustment for sex, race/ethnicity, education, income, insurance, usual source of care, hyperglycaemia medication, duration of diabetes, family history, BMI and waist circumference, age < 65 years at diagnosis remained significantly associated with greater odds of HbA(1c) > 9.0% (OR 3.22, 95% CI 1.54, 6.72), HbA(1c) > 8.0% (OR 2.72, 95% CI 1.43, 5.16) and HbA(1c) > 7.0% (OR 1.92, 95% CI 1.18, 3.11). The younger group reported fewer comorbidities, but were less likely to report good health (OR 0.54, 95% CI 0.36, 0.83). Younger age at type 2 diabetes diagnosis is significantly associated with worse subsequent glycaemic control. Because patients who are younger at diagnosis have fewer competing comorbidities and complications, safe, aggressive, individualised treatment could benefit this higher-risk group.

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