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Assessment of Child Anthropometry in a Large Epidemiologic Study
Published on: February 2, 2017
Microalbuminuria in pediatric obesity: prevalence and relation to other cardiovascular risk factors
T S Burgert1, J Dziura, C Yeckel
1Department of Pediatrics and The General Clinical Research Center, Yale University School of Medicine, New Haven 06520, USA. Tania.Burgert@yale.edu
Background:
Microalbuminuria (MA) has emerged as a strong predictor of cardiovascular (CV) events, even in nondiabetic adults. While the mechanisms behind this association remain to be established, most studies suggest that MA is the result of increased vascular leakage denoting endothelial dysfunction associated with early vasculopathy.
Objective:
To examine if a urine albumin creatinine ratio (UACR) in the microalbuminuric range is related to metabolic markers of CV risk in obese and pre-diabetic youth recruited from an obesity clinic.
Methods:
MA was defined as a UACR between 2.0 and 20 mg/mmol. Subjects with gross proteinuria (UACR>20 mg/mmol) were excluded from the study. Analyses were performed to assess the relationship of MA and markers of CV risk, including body mass index (BMI), % body fat, blood pressure (BP), lipid profile, inflammatory markers, insulin sensitivity indexes and degrees of oral glucose tolerance. MA was also correlated with risk factor constellations unique to the metabolic syndrome, a distinct CV risk entity.
Results:
Postchallenge alterations in glucose metabolism and overall loss in insulin sensitivity were strongly and positively correlated with the presence of MA (P = 0.002 and 0.01, respectively). Neither the metabolic syndrome nor any of the individual CV risk factors examined were associated with MA.
Conclusions:
These data suggest that early glucose toxicity, as reflected by postchallenge elevations in plasma glucose even below the diagnostic cutoff for diabetes mellitus may contribute to the presence of MA. Whether MA is equally as predictive of CV disease in youth, as in adulthood, remains to be investigated.
Insights
Microalbuminuria (MA) in obese, pre-diabetic youth is linked to impaired glucose metabolism and insulin sensitivity. Early glucose toxicity may contribute to MA, a potential cardiovascular risk marker in this population.
Area of Science:
- Pediatric Endocrinology
- Cardiovascular Risk Assessment
- Metabolic Syndrome Research
Background:
- Microalbuminuria (MA) is a significant predictor of cardiovascular (CV) events in adults.
- MA is often associated with endothelial dysfunction and early vasculopathy.
- The link between MA and CV risk in non-diabetic youth requires further investigation.
Purpose of the Study:
- To investigate the relationship between microalbuminuria (MA) and metabolic markers of cardiovascular (CV) risk in obese, pre-diabetic youth.
- To assess if urine albumin-to-creatinine ratio (UACR) in the microalbuminuric range correlates with CV risk factors in this specific demographic.
Main Methods:
- MA was defined as a UACR between 2.0 and 20 mg/mmol; subjects with gross proteinuria were excluded.
- Evaluated associations between MA and markers including BMI, body fat percentage, blood pressure, lipid profiles, inflammatory markers, insulin sensitivity, and oral glucose tolerance.
- Correlated MA with metabolic syndrome risk factors.
Main Results:
- Postchallenge glucose metabolism alterations and reduced insulin sensitivity were significantly correlated with the presence of MA (P = 0.002 and 0.01, respectively).
- No significant association was found between MA and the metabolic syndrome or its individual risk factors.
- These findings highlight early glucose dysregulation as a key factor associated with MA in this cohort.
Conclusions:
- Early glucose toxicity, indicated by elevated postchallenge plasma glucose below diabetes diagnostic thresholds, may contribute to microalbuminuria (MA) in obese, pre-diabetic youth.
- The predictive value of MA for future cardiovascular disease in youth, similar to its role in adults, warrants further research.
- These results underscore the importance of monitoring MA in at-risk pediatric populations.
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