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17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature

CONTEXT: There are more than 100 pathogenic variants in CYP17A1 that have been identified in patients with 17α-hydroxylase/17,20-lyase deficiency (17OHD). OBJECTIVE: We aimed to describe 46,XY patients with 17OHD from our center and review the literature. METHODS: We retrospectively analyzed genetic...

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Autores principales: Maheshwari, Madhur, Arya, Sneha, Lila, Anurag Ranjan, Sarathi, Vijaya, Barnabas, Rohit, Rai, Khushnandan, Bhandare, Vishwambhar Vishnu, Memon, Saba Samad, Karlekar, Manjiri Pramod, Patil, Virendra, Shah, Nalini S, Kunwar, Ambarish, Bandgar, Tushar
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8845120/
https://www.ncbi.nlm.nih.gov/pubmed/35178494
http://dx.doi.org/10.1210/jendso/bvac011
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author Maheshwari, Madhur
Arya, Sneha
Lila, Anurag Ranjan
Sarathi, Vijaya
Barnabas, Rohit
Rai, Khushnandan
Bhandare, Vishwambhar Vishnu
Memon, Saba Samad
Karlekar, Manjiri Pramod
Patil, Virendra
Shah, Nalini S
Kunwar, Ambarish
Bandgar, Tushar
author_facet Maheshwari, Madhur
Arya, Sneha
Lila, Anurag Ranjan
Sarathi, Vijaya
Barnabas, Rohit
Rai, Khushnandan
Bhandare, Vishwambhar Vishnu
Memon, Saba Samad
Karlekar, Manjiri Pramod
Patil, Virendra
Shah, Nalini S
Kunwar, Ambarish
Bandgar, Tushar
author_sort Maheshwari, Madhur
collection PubMed
description CONTEXT: There are more than 100 pathogenic variants in CYP17A1 that have been identified in patients with 17α-hydroxylase/17,20-lyase deficiency (17OHD). OBJECTIVE: We aimed to describe 46,XY patients with 17OHD from our center and review the literature. METHODS: We retrospectively analyzed genetically proven index cases of 17OHD from our 46,XY disorders of sex development cohort and reviewed similar cases from the literature (n = 150). Based on the phenotype, 17OHD probands were classified into combined severe deficiency (n = 128) and combined partial deficiency (n = 16). Additionally, patients with the apparent isolated 17,20-lyase deficiency (n = 7, from 6 families) were noted. Residual enzyme activities with the observed mutant enzymes were divided in 2 categories as < 1% and ≥ 1%, each for hydroxylase and lyase. RESULTS: We present 4 index cases of 46,XY 17OHD with a complete spectrum of undervirilization and 2 novel variants in CYP17A1. In the review, the combined severe deficiency was the most common form, with more frequent female sex of rearing, hypertension, hypokalemia, suppressed renin, higher plasma corticotropin, lower serum cortisol, and androgens. Immunoassay-measured serum aldosterone was frequently (68.2%) unsuppressed (>5 ng/dL). Elevated serum progesterone had high sensitivity for diagnosis of combined 17OHD, even in combined partial deficiency (83.3%). Among patients with clinical phenotype of combined severe deficiency, 11.5% had partial 17α-hydroxylase and complete 17,20-lyase deficiency (>1%/<1%) and had significantly higher serum cortisol than those with < 1%/<1% activity. CONCLUSION: We report the first monocentric case series of Asian Indian 46,XY patients with 17OHD. We propose that a phenotype of severe undervirilization with milder cortisol deficiency may represent a distinct subtype of combined severe 17OHD with residual 17α-hydroxylase activity but severe 17,20-lyase deficiency (>1%/<1%), which needs further validation.
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spelling pubmed-88451202022-02-16 17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature Maheshwari, Madhur Arya, Sneha Lila, Anurag Ranjan Sarathi, Vijaya Barnabas, Rohit Rai, Khushnandan Bhandare, Vishwambhar Vishnu Memon, Saba Samad Karlekar, Manjiri Pramod Patil, Virendra Shah, Nalini S Kunwar, Ambarish Bandgar, Tushar J Endocr Soc Clinical Research Article CONTEXT: There are more than 100 pathogenic variants in CYP17A1 that have been identified in patients with 17α-hydroxylase/17,20-lyase deficiency (17OHD). OBJECTIVE: We aimed to describe 46,XY patients with 17OHD from our center and review the literature. METHODS: We retrospectively analyzed genetically proven index cases of 17OHD from our 46,XY disorders of sex development cohort and reviewed similar cases from the literature (n = 150). Based on the phenotype, 17OHD probands were classified into combined severe deficiency (n = 128) and combined partial deficiency (n = 16). Additionally, patients with the apparent isolated 17,20-lyase deficiency (n = 7, from 6 families) were noted. Residual enzyme activities with the observed mutant enzymes were divided in 2 categories as < 1% and ≥ 1%, each for hydroxylase and lyase. RESULTS: We present 4 index cases of 46,XY 17OHD with a complete spectrum of undervirilization and 2 novel variants in CYP17A1. In the review, the combined severe deficiency was the most common form, with more frequent female sex of rearing, hypertension, hypokalemia, suppressed renin, higher plasma corticotropin, lower serum cortisol, and androgens. Immunoassay-measured serum aldosterone was frequently (68.2%) unsuppressed (>5 ng/dL). Elevated serum progesterone had high sensitivity for diagnosis of combined 17OHD, even in combined partial deficiency (83.3%). Among patients with clinical phenotype of combined severe deficiency, 11.5% had partial 17α-hydroxylase and complete 17,20-lyase deficiency (>1%/<1%) and had significantly higher serum cortisol than those with < 1%/<1% activity. CONCLUSION: We report the first monocentric case series of Asian Indian 46,XY patients with 17OHD. We propose that a phenotype of severe undervirilization with milder cortisol deficiency may represent a distinct subtype of combined severe 17OHD with residual 17α-hydroxylase activity but severe 17,20-lyase deficiency (>1%/<1%), which needs further validation. Oxford University Press 2022-01-29 /pmc/articles/PMC8845120/ /pubmed/35178494 http://dx.doi.org/10.1210/jendso/bvac011 Text en © The Author(s) 2022. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (https://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Clinical Research Article
Maheshwari, Madhur
Arya, Sneha
Lila, Anurag Ranjan
Sarathi, Vijaya
Barnabas, Rohit
Rai, Khushnandan
Bhandare, Vishwambhar Vishnu
Memon, Saba Samad
Karlekar, Manjiri Pramod
Patil, Virendra
Shah, Nalini S
Kunwar, Ambarish
Bandgar, Tushar
17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature
title 17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature
title_full 17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature
title_fullStr 17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature
title_full_unstemmed 17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature
title_short 17α-Hydroxylase/17,20-Lyase Deficiency in 46,XY: Our Experience and Review of Literature
title_sort 17α-hydroxylase/17,20-lyase deficiency in 46,xy: our experience and review of literature
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8845120/
https://www.ncbi.nlm.nih.gov/pubmed/35178494
http://dx.doi.org/10.1210/jendso/bvac011
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