Insulin Secretion Defect in Children and Adolescents with Obesity: Clinical and Molecular Genetic Characterization.
Helena Enders-SeidlitzKlemens RaileMaolian GongAngela GallerPeter KühnenSusanna WiegandPublished in: Journal of diabetes research (2024)
Using surrogate parameters of beta-cell function and insulin resistance can help identify patients with insulin secretion disorder. A prevalence of 40% mutations of known diabetes genes in the subgroup with low insulin secretion suggests that at least 1.7% of patients with adolescent obesity have monogenic diabetes. A successful molecular genetic diagnosis can help to improve individual therapy.
Keyphrases
- insulin resistance
- type diabetes
- glycemic control
- high fat diet induced
- metabolic syndrome
- cardiovascular disease
- adipose tissue
- high fat diet
- weight loss
- genome wide
- skeletal muscle
- polycystic ovary syndrome
- young adults
- mental health
- risk factors
- weight gain
- single molecule
- clinical trial
- cell therapy
- dna methylation
- randomized controlled trial
- phase iii
- mesenchymal stem cells
- genome wide identification
- double blind
- smoking cessation