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Normal weight metabolically unhealthy phenotype in youth: Do definitions matter?
Mélanie Henderson1,2, Andraea Van Hulst2,3, Julia E von Oettingen4
1Division of Endocrinology, Department of Pediatrics, Centre Hospitalier Universitaire Sainte-Justine and Université de Montréal, Montreal, Quebec, Canada.
Insights
Normal weight metabolically unhealthy children have lower insulin sensitivity over time. Even with normal weight, metabolic syndrome components predict reduced insulin sensitivity in youth.
Area of Science:
- Pediatric Endocrinology
- Metabolic Health
- Cardiometabolic Risk
Background:
- Normal weight metabolically unhealthy (NWMU) adults face increased cardiometabolic disease risk.
- Limited data exists on NWMU status in children and its long-term health implications.
Purpose of the Study:
- To investigate associations between NWMU definitions in children (8-10 years) and subsequent insulin sensitivity and secretion.
- To evaluate the predictive value of metabolic syndrome components in normal-weight youth.
Main Methods:
- Utilized data from the QUALITY cohort (n=630, Caucasian youth aged 8-10 years).
- Classified 322 normal-weight children as NWMU using four definitions.
- Assessed insulin sensitivity (Matsuda index) and secretion (AUC insulin/glucose ratio) at ages 10-12 years via oral glucose tolerance tests.
- Employed multiple linear regression models.
Main Results:
- NWMU children exhibited lower baseline insulin sensitivity compared to metabolically healthy peers.
- After two years, insulin sensitivity was significantly reduced in NWMU children with one or more metabolic risk factors (14.4-29.7% lower).
- Insulin secretion was not predicted by metabolic syndrome components.
Conclusions:
- Established NWMU definitions effectively predict insulin sensitivity changes in youth entering puberty.
- Normal-weight children with metabolic syndrome components demonstrate persistently lower insulin sensitivity.
Background:
Normal weight metabolically unhealthy (NWMU) adults are at increased risk of cardiometabolic disease, however, little is known regarding NWMU children.
Objectives:
We examined the associations between existing definitions of NWMU in children aged 8 to 10 years and insulin sensitivity (IS) and secretion 2 years later.
Methods:
Data stem from the Quebec Adipose and Lifestyle InvesTigation in Youth (QUALITY) cohort of 630 Caucasian youth, 8 to 10 years old at baseline, with at least one obese biological parent. Of these, 322 normal weight children were classified as NWMU using four definitions. At 10 to 12 years, IS was measured with the Matsuda-insulin sensitivity index; insulin secretion was measured with the ratio of the area under the curve (AUC) of insulin to the AUC of glucose over a 2-hour oral glucose tolerance test. Multiple linear regression models were used.
Results:
Because few children met the existing definitions of metabolic syndrome, associations were examined for less stringent definitions (eg, having two vs no risk factors). At baseline, IS was lower in NWMU children compared to children with no risk factors (virtually all definitions). Moreover, after 2 years, IS was 14.4-19.3% lower in NWMU children with one or more risk factors, and up to 29.7% lower in those with two or more risk factors compared to those with none. Insulin secretion was not predicted by components of the metabolic syndrome.
Conclusion:
Existing definitions of NWMU youth performed relatively similarly in predicting IS as youth entered puberty. Children with one or more components of metabolic syndrome-even when of normal weight-have significantly lower IS over time.
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