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Published on: April 26, 2019
Elevated transaminases potentiate the risk for emerging dysglycemia in children with overweight and obesity
Florian Koutny1,2, Robert Stein3,4, Wieland Kiess3,5
1Department of Pediatrics, Paracelsus Medical University, Salzburg, Austria.
Insights
Elevated liver enzymes, indicating nonalcoholic fatty liver disease (NAFLD), predict future dysglycemia in children with obesity. Early NAFLD detection is crucial for preventing type 2 diabetes.
Area of Science:
- Pediatrics
- Hepatology
- Endocrinology
Background:
- Nonalcoholic fatty liver disease (NAFLD) is linked to dysglycemia in children, but longitudinal data are limited.
- Cross-sectional studies suggest a connection, yet the predictive value of NAFLD for future dysglycemia in children requires further investigation.
Purpose of the Study:
- To determine if elevated alanine aminotransferase (ALT) levels, a marker for NAFLD, predict future dysglycemia in children.
- To assess the longitudinal association between NAFLD indicators and dysglycemia development in pediatric populations.
Main Methods:
- Survival analysis was conducted on longitudinal data from 510 children with overweight and obesity.
- Follow-up extended up to 11 years, utilizing data from the Leipzig Childhood Cohort.
- Elevated ALT levels served as a proxy for NAFLD in the analysis.
Main Results:
- Children with overweight/obesity and elevated ALT showed a >2-fold increased risk for future dysglycemia (HR 2.59, P < 0.01).
- This increased risk was independent of age, sex, and BMI-SDS.
- Elevated transaminases emerged as a significant early predictor of glycemic deterioration.
Conclusions:
- Elevated transaminases are an early predictor of glycemic deterioration in children.
- NAFLD should be recognized as a significant risk factor for type 2 diabetes.
- Targeting NAFLD is essential for the early prevention of type 2 diabetes in pediatric populations.
Background:
There is evidence that nonalcoholic fatty liver disease (NAFLD) increases the risk for dysglycemia in children in cross-sectional studies. However, the extent to which NAFLD may confer the risk for dysglycemia in longitudinal studies remains uncertain.
Objectives:
We investigated whether elevated levels of alanine aminotransferase (ALT) as a proxy for NAFLD can serve as a predictor for future dysglycemia among children.
Methods:
We performed survival analysis up to 11 years of follow-up on longitudinal data of 510 children with overweight and obesity from the Leipzig Childhood Cohort.
Results:
Children with overweight/obesity and elevated ALT values had a more than 2-fold increased risk (hazard ratio 2.59, 95% confidence interval 1.49 to 4.50; P < 0.01) for future dysglycemia independent of age, sex and BMI-SDS.
Conclusions:
Elevated transaminases are an early predictor for glycemic deterioration. Hence, NAFLD should further be addressed as a risk factor and therapeutic target for the early prevention of type 2 diabetes.
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