Journal Article

Clinical, genetic, and structural basis of congenital adrenal hyperplasia due to 11β-hydroxylase deficiency

Rahi, Simran, Kandemir, Nurgun, Khaloul, Najoua, Saad, Ali, Belgorosky, Alicia, Romero, Raquel, Burns, James, Cappa, Marco, Ozon, Alev, Fatima, Saleel, Gribaa, Moez, Dumic, Katja, Nour, Munier A., Azar, Maryam Razzghy, Zaidi, Mone, Dhawan, Samarth, Musa, Noha, Gonc, Nazli, Dumic, Miroslav, de Mendonça, Berenice Bilharinho, Haider, Shozeb, Cheng, Tina, Alam, Dauood, Aisenberg, Javier, Khattab, Ahmed, Charfeddine, Ilhem Ben, Yuen, Tony, Holtzman, Assaf, New, Maria I., Alzahrani, Ali, Pacaud, Daniele, Li, Sun, Li, Di, Hafez, Mona, Kuhnle-Krahl, Ursula, Kumar, Ameet, Alikasifoglu, Ayfer, Estatico, Jessica, Holterhus, Paul-Martin

2017

Overview

Congenital adrenal hyperplasia (CAH), resulting from mutations in CYP11B1, a gene encoding 11β-hydroxylase, represents a rare autosomal recessive Mendelian disorder of aberrant sex steroid production. Unlike CAH caused by 21-hydroxylase deficiency, the disease is far more common in the Middle East and North Africa, where consanguinity is common often resulting in identical mutations. Clinically, affected female newborns are profoundly virilized (Prader score of 4/5), and both genders display significantly advanced bone ages and are oftentimes hypertensive. We find that 11-deoxycortisol, not frequently measured, is the most robust biochemical marker for diagnosing 11β-hydroxylase deficiency. Finally, computational modeling of 25 missense mutations of CYP11B1 revealed that specific modifications in the heme-binding (R374W and R448C) or substrate-binding (W116C) site of 11β-hydroxylase, or alterations in its stability (L299P and G267S), may predict severe disease. Thus, we report clinical, genetic, hormonal, and structural effects of CYP11B1 gene mutations in the largest international cohort of 108 patients with steroid 11β-hydroxylase deficiency CAH.

• Publisher: National Academy of Sciences
• Subject: Adrenal Hyperplasia, Congenital - genetics / Adrenal Hyperplasia, Congenital - pathology / Africa, Northern / Biological Sciences / Consanguinity / Female / Gonadal Steroid Hormones - biosynthesis / Gonadal Steroid Hormones - genetics / Humans / Male / Medical Sciences / Middle East / Mutation, Missense / Pedigree / PNAS Plus / Steroid 11-beta-Hydroxylase - chemistry / Steroid 11-beta-Hydroxylase - genetics