Obesity in Classic Congenital Adrenal Hyperplasia: Mechanisms, Complications and Management
Year: 2026
Type: article
Abstract: Classic congenital adrenal hyperplasia (CCAH) is an autosomal recessive genetic disorder primarily caused by 21-hydroxylase deficiency. Although the survival rate of patients has significantly improved with glucocorticoid replacement therapy, long-term use of supraphysiological doses and multiple factors inherent to the disease itself have led to obesity becoming a common metabolic complication in CCAH patients. The mechanism of obesity in CCAH patients is complex and involves multiple factors related to both treatment and the disease itself. This article provides a narrative review of the incidence, influencing factors, related complications and treatment management strategies of obesity in CCAH patients, with the aim of offering comprehensive management recommendations for clinical practice.
Source: Clinical Endocrinology
DOI: 10.1111/cen.70155
Authors: Jialin Mu, Yue Li, Meng Sun, Yulin Li, Panpan Li, Hui Zou
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $4,250
OpenAlex ID: W7160848896
