3.8 Review

Genetic obesity: an update with emerging therapeutic approaches

Journal

ANNALS OF PEDIATRIC ENDOCRINOLOGY & METABOLISM
Volume 27, Issue 3, Pages 169-175

Publisher

KOREAN SOC PEDIATRIC ENDOCRINOLOGY
DOI: 10.6065/apem.2244188.094

Keywords

Genetic obesity; Leptin-melanocortin pathway; Melanocortin 4 receptor agonist

Ask authors/readers for more resources

Childhood obesity can be classified into three groups based on genetic contribution: common polygenic obesity, syndromic obesity, and monogenic obesity. Genetic testing advancements have led to the identification of more causes of obesity. Early genetic evaluation is critical in identifying treatable obesity and providing personalized management for favorable outcomes.
Based on the genetic contribution, childhood obesity can be classified into 3 groups: common polygenic obesity, syndromic obesity, and monogenic obesity. More genetic causes of obesity are being identified along with the advances in the genetic testing. Genetic obesities including syndromic and monogenic obesity should be suspected and evaluated in children with early- onset morbid obesity and hyperphagia under 5 years of age. Patients with syndromic obesity have early- onset severe obesity associated specific genetic syndromes including Prader-Willi syndrome, Bardet-Biedle syndrome, and Alstrom syndrome. Syndromic obesity is often accompanied with neurodevelopmental delay or dysmorphic features. Nonsyndromic monogenic obesity is caused by variants in single gene which are usually involved in the regulation of hunger and satiety associated with the hypothalamic leptin-melanocortin pathway in central nervous system. Unlike syndromic obesity, patients with monogenic obesity usually show normal neurodevelopment. They would be presented with hyperphagia and early-onset severe obesity with additional clinical symptoms including short stature, red hair, adrenal insufficiency, hypothyroidism, hypogonadism, pituitary insufficiencies, diabetes insipidus, increased predisposition to infection or intractable recurrent diarrhea. Identifying patients with genetic obesity is critical as new innovative therapies including melanocortin 4 receptor agonist have become available. Early genetic evaluation enables to identify treatable obesity and provide timely intervention which may eventually achieve favorable outcome by establishing personalized management.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

3.8
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available