Lessons from 17β-HSD3 deficiency: Clinical spectrum and complex molecular basis in Chinese patients.

Abstract

17β-Hydroxysteroid dehydrogenase type 3 (17β-HSD3) deficiency is rarely reported in Chinese patients with 46, XY disorders of sexual development (DSD). Seven subjects with 17β-HSD3 deficiency were identified from 206 Chinese 46, XY DSD patients using targeted next-generation sequencing (NGS). Serum AD and T levels were measured by liquid chromatography-tandem mass spectrometry (LC-MS/MS). In silico and functional studies were performed to evaluate the enzymatic activity impairment of HSD17B3 variants. A minigene assay was performed in an exonic splicing variant. Our results showed that four novel and five reported HSD17B3 variants were identified in 7 unrelated patients. The patients showed cryptic presentation during childhood and classical virilization after puberty with T/AD ratio< 0.4. A heterozygous large deletion from the 5'UTR to exon 1 was identified in a patient with a monoallelic variant of p.N130S. Although predicted to be 'likely pathogenic', only p. S232P and p. S160F drastically reduced the enzymatic activity of 17β-HSD3. A previously reported 'missense' variant c 0.277 G>A (p. E93K) was revealed to have no impact on enzyme activity but resulted in aberrant splicing of exon 3 and was reclassified as an exonic splicing variant. In our study, one nonsense, one exonic splicing, one deletion, one large deletion and five missense variants were detected in patients with 17β-HSD3 deficiency, expanding the clinical and molecular profile of this disorder. In silico analysis should be cautiously interpreted when the heredity pattern and functional study are inconsistent.

• Authors: Hui Zhu, Haijun Yao, Xuemeng Liu, Yue Xu, Yang Liu, Qingqiong Luo, Yan Chen, Yuanping Shi, Fuxiang Chen, Shuangxia Zhao, Huaidong Song, Bing Han, Jie Qiao
• Journal: The Journal of steroid biochemistry and molecular biology (J Steroid Biochem Mol Biol) Vol. 225 Pg. 106191 (01 2023) ISSN: 1879-1220 [Electronic] England
• PMID: 36154887 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
• Copyright: Copyright © 2022 Elsevier Ltd. All rights reserved.

Chemical References

• 17beta-hydroxysteroid dehydrogenase type 3
• 17-Hydroxysteroid Dehydrogenases

Topics

• Female
• Humans
• Disorder of Sex Development, 46,XY (genetics)
• Chromatography, Liquid
• Tandem Mass Spectrometry
• 17-Hydroxysteroid Dehydrogenases (chemistry)
• China