[HTML][HTML] Child and adolescent obesity

NB Lister, LA Baur, JF Felix, AJ Hill, C Marcus… - Nature Reviews …, 2023 - nature.com
The prevalence of child and adolescent obesity has plateaued at high levels in most high-
income countries and is increasing in many low-income and middle-income countries …

Tissue-specific effects of leptin on glucose and lipid metabolism

S Pereira, DL Cline, MM Glavas, SD Covey… - Endocrine …, 2021 - academic.oup.com
The discovery of leptin was intrinsically associated with its ability to regulate body weight.
However, the effects of leptin are more far-reaching and include profound glucose-lowering …

The role of hypoleptinemia in the psychological and behavioral adaptation to starvation: Implications for anorexia nervosa

J Hebebrand, T Hildebrandt, H Schlögl, J Seitz… - Neuroscience & …, 2022 - Elsevier
This narrative review aims to pinpoint mental and behavioral effects of starvation, which may
be triggered by hypoleptinemia and as such may be amenable to treatment with leptin …

Leptin receptor deficiency: a systematic literature review and prevalence estimation based on population genetics

L Kleinendorst, O Abawi… - European journal of …, 2020 - academic.oup.com
Abstract Objective Leptin receptor (LepR) deficiency is an autosomal-recessive endocrine
disorder causing early-onset severe obesity, hyperphagia and pituitary hormone …

[HTML][HTML] The promise of new anti-obesity therapies arising from knowledge of genetic obesity traits

A Hinney, A Körner, P Fischer-Posovszky - Nature Reviews …, 2022 - nature.com
Obesity is a multifactorial and complex disease that often manifests in early childhood with a
lifelong burden. Polygenic and monogenic obesity are driven by the interaction between …

Natural history of obesity due to POMC, PCSK1, and LEPR deficiency and the impact of setmelanotide

M Wabitsch, S Farooqi, CE Flück… - Journal of the …, 2022 - academic.oup.com
Context Rare homozygous or biallelic variants in POMC, PCSK1, and LEPR can disrupt
signaling through the melanocortin-4 receptor (MC4R) pathway, resulting in hyperphagia …

Rare genetic forms of obesity: from gene to therapy

K Clément, H Mosbah, C Poitou - Physiology & behavior, 2020 - Elsevier
Monogenic non-syndromic obesity is characterized by severe early-onset obesity with
abnormal eating behaviour and endocrine disorders. Genes contributing to these rare forms …

Mechanisms in endocrinology: update on treatments for patients with genetic obesity

C Poitou, H Mosbah, K Clément - European Journal of …, 2020 - academic.oup.com
Obesity, defined by an excess of body fat impacting on health, is a complex disease
resulting from the interaction between many genetic/epigenetic factors and environmental …

[HTML][HTML] Association and interaction of the MC4R rs17782313 polymorphism with plasma ghrelin, GLP-1, cortisol, food intake and eating behaviors in overweight …

S Rahati, M Qorbani, A Naghavi, H Pishva - BMC Endocrine Disorders, 2022 - Springer
Background Recent studies have shown that obesity is largely influenced by heredity and
created by the interactions between several genes and environmental and behavioral …

[HTML][HTML] Identifying underlying medical causes of pediatric obesity: results of a systematic diagnostic approach in a pediatric obesity center

L Kleinendorst, O Abawi, B van der Voorn… - PLoS …, 2020 - journals.plos.org
Background Underlying medical causes of obesity (endocrine disorders, genetic obesity
disorders, cerebral or medication-induced obesities) are thought to be rare. Even in …