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The relationship between microalbuminuria and glomerular filtration rate in young type 1 diabetic subjects: The
Rakesh Amin1, Charles Turner, Sara van Aken
1University Department of Paediatrics, Addenbrookes Hospital, Cambridge, UK.
Insights
Glomerular hyperfiltration in children with type 1 diabetes is linked to puberty and higher HbA1c, predicting future kidney damage. Early intervention to lower GFR may prevent diabetic nephropathy before albuminuria appears.
Area of Science:
- Pediatric Nephrology
- Endocrinology
- Diabetology
Background:
- Diabetic nephropathy is a major complication of type 1 diabetes (T1DM).
- Early detection of kidney damage is crucial for timely intervention.
- Glomerular filtration rate (GFR) and urine albumin excretion are key indicators of kidney health.
Purpose of the Study:
- To investigate the relationship between GFR at 5 years of T1DM duration and subsequent urine albumin excretion.
- To identify predictors of early diabetic kidney disease in children with T1DM.
Main Methods:
- Prospective cohort study of 308 children with T1DM.
- Annual assessments included HbA1c and urine albumin-to-creatinine ratio (ACR).
- GFR was measured at 5 years of diabetes duration.
Main Results:
- Higher GFR and hyperfiltration at 5 years were observed in children who later developed microalbuminuria (MA+).
- Puberty and higher HbA1c levels predicted hyperfiltration.
- Elevated ACR levels after 5 years were associated with hyperfiltration and predicted future MA development, independent of HbA1c.
Conclusions:
- Glomerular hyperfiltration in T1DM is associated with puberty and ACR, and predicts MA independently of glycemic control.
- Factors beyond poor glycemic control may contribute to early diabetic nephropathy.
- Early interventions targeting GFR reduction may benefit children even before MA onset.
Background:
The purpose of this study was to examine the relationship between glomerular filtration rate (GFR) measured at 5 years' diabetes duration and annual urine albumin excretion in a prospective cohort of children with type 1 diabetes (T1DM).
Methods:
Three hundred and eight children were followed from diagnosis of T1DM [aged 9.8 years (range 0.4-15.9) for a median duration of 10.9 years (6.0-17.8) with annual assessments comprising measurement of HbA1(c) and 3 urine samples for albumin:creatinine ratio (ACR). GFR was measured in all children at 5 years' diabetes duration.
Results:
Two hundred forty-three (78.8%) subjects were normoalbuminuric (MA-) for the duration of the study. At 5 years: 35 (11.4%) subjects had MA (MA+) and 30 (9.7%) subjects were normoalbuminuric but developed MA during subsequent follow-up annual assessments (future MA+). In the future MA+ group compared to the MA+ and MA- groups; GFR was higher (167 vs. 134 vs. 139 mL/min/1.73 m(2), P < 0.002); the prevalence of hyperfiltration (GFR >125 mL/min/1.73 m(2)) was greater (97 vs. 57 vs. 64%, P= 0.006) and HbA1c levels were higher (11.4 vs. 10.8 vs. 9.7%, P < 0.001). The probability (Cox Model) of having hyperfiltration at 5 years' duration was related to puberty (a 1.7-fold increased risk with puberty onset) and poor glycemic control (a 10% increased risk for a 1% increase in HbA1c). Comparing subjects with and without hyperfiltration, prior to the first GFR measurement no difference in ACR levels existed; however, after this time median ACR levels were significantly greater [1.2 (0.1-86.4) vs. 0.9 (0.1-71.6) mg/mmol, P= 0.003], independent of age and HbA1c levels. The probability of developing MA between 5 and 10 years' duration was associated with poor glycemic control (a 30% increased risk for a 1% increase in HbA1c) and higher GFR at 5 years (22% increased risk for a 10 mL/min/1.73 m(2) rise in GFR).
Conclusion:
Glomerular hyperfiltration is associated with puberty and increasing ACR levels and is predictive of MA independent of HbA1c. This suggests that factors other than poor glycemic control may be involved in the pathogenesis of early diabetic nephropathy and early intervention with medical therapy to reduce GFR may be beneficial even before onset of MA.
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