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Longitudinal Association of Telomere Dynamics with Obesity and Metabolic Disorders in Young Children
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In adults, short leukocyte telomere length (LTL) is associated with metabolic disorders, such as obesity and diabetes mellitus type 2. These associations could stem from early life interactions between LTL and metabolic disorders. To test this hypothesis, we explored the associations between LTL and metabolic parameters as well as their evolution over time in children with or without obesity at baseline. Seventy-three (n = 73) children attending our Outpatient Clinic for the Prevention and Management of Overweight and Obesity in Childhood and Adolescence, aged 2–10 years (mean ± SD: 7.6 ± 2.0 years), were followed for 2 to 4 years. Anthropometric, clinical, and biological (including LTL by Southern blot) measurements were performed annually. Baseline LTL correlated negatively with BMI (p = 0.02), fat percentage (p = 0.01), and blood glucose (p = 0.0007). These associations persisted after adjustments for age and sex. No associations were found between LTL attrition during the follow-up period and any of the metabolic parameters. In young children, obesity and metabolic disturbances were associated with shorter telomeres but were not associated with more pronounced LTL attrition. These results suggest that short telomeres contribute to the development of obesity and metabolic disorders very early in life, which can have a major impact on health.
Title: Longitudinal Association of Telomere Dynamics with Obesity and Metabolic Disorders in Young Children
Description:
In adults, short leukocyte telomere length (LTL) is associated with metabolic disorders, such as obesity and diabetes mellitus type 2.
These associations could stem from early life interactions between LTL and metabolic disorders.
To test this hypothesis, we explored the associations between LTL and metabolic parameters as well as their evolution over time in children with or without obesity at baseline.
Seventy-three (n = 73) children attending our Outpatient Clinic for the Prevention and Management of Overweight and Obesity in Childhood and Adolescence, aged 2–10 years (mean ± SD: 7.
6 ± 2.
0 years), were followed for 2 to 4 years.
Anthropometric, clinical, and biological (including LTL by Southern blot) measurements were performed annually.
Baseline LTL correlated negatively with BMI (p = 0.
02), fat percentage (p = 0.
01), and blood glucose (p = 0.
0007).
These associations persisted after adjustments for age and sex.
No associations were found between LTL attrition during the follow-up period and any of the metabolic parameters.
In young children, obesity and metabolic disturbances were associated with shorter telomeres but were not associated with more pronounced LTL attrition.
These results suggest that short telomeres contribute to the development of obesity and metabolic disorders very early in life, which can have a major impact on health.
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