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. 2008 Mar 29;336(7646):697-701.
doi: 10.1136/bmj.39478.378241.BE. Epub 2008 Mar 18.

Risk of microalbuminuria and progression to macroalbuminuria in a cohort with childhood onset type 1 diabetes: prospective observational study

Rakesh Amin  1 , Barry Widmer, A Toby Prevost, Phillip Schwarze, Jason Cooper, Julie Edge, Loredana Marcovecchio, Andrew Neil, R Neil Dalton, David B Dunger
Affiliations

Risk of microalbuminuria and progression to macroalbuminuria in a cohort with childhood onset type 1 diabetes: prospective observational study

Rakesh Amin et al. BMJ. .

Abstract

Objectives: To describe independent predictors for the development of microalbuminuria and progression to macroalbuminuria in those with childhood onset type 1 diabetes.

Design: Prospective observational study with follow-up for 9.8 (SD 3.8) years.

Setting: Oxford regional prospective study.

Participants: 527 participants with a diagnosis of type 1 diabetes at mean age 8.8 (SD 4.0) years.

Main outcome measures: Annual measurement of glycated haemoglobin (HbA1c) and assessment of urinary albumin:creatinine ratio.

Results: Cumulative prevalence of microalbuminuria was 25.7% (95% confidence interval 21.3% to 30.1%) after 10 years of diabetes and 50.7% (40.5% to 60.9%) after 19 years of diabetes and 5182 patient years of follow-up. The only modifiable adjusted predictor for microalbuminuria was high HbA1c concentrations (hazard ratio per 1% rise in HbA1c 1.39, 1.27 to 1.52). Blood pressure and history of smoking were not predictors. Microalbuminuria was persistent in 48% of patients. Cumulative prevalence of progression from microalbuminuria to macroalbuminuria was 13.9% (12.9% to 14.9%); progression occurred at a mean age of 18.5 (5.8) years. Although the sample size was small, modifiable predictors of macroalbuminuria were higher HbA(1c) levels and both persistent and intermittent microalbuminuria (hazard ratios 1.42 (1.22 to 1.78), 27.72 (7.99 to 96.12), and 8.76 (2.44 to 31.44), respectively).

Conclusion: In childhood onset type 1 diabetes, the only modifiable predictors were poor glycaemic control for the development of microalbuminuria and poor control and microalbuminuria (both persistent and intermittent) for progression to macroalbuminuria. Risk for macroalbuminuria is similar to that observed in cohorts with adult onset disease but as it occurs in young adult life early intervention in normotensive adolescents might be needed to improve prognosis.

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Conflict of interest statement

Competing interests: None declared.

Figures

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Fig 1 Numbers with microalbuminuria and progression to macroalbuminuria up to September 2005
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Fig 2 Kaplan-Meier survival curves showing cumulative prevalence of developing microalbuminuria (135 events) across age in 527 children with type 1 diabetes, 1986-2005, in relation to quarters of mean lifetime HbA1c concentrations (top) and sex (bottom)
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Fig 3 Kaplan-Meier survival curve showing cumulative prevalence of development of microalbuminuria (135 events) across duration of diabetes in 527 children with type 1 diabetes, 1986-2005, in relation to age at diagnosis of diabetes
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