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Differences of adrenal‐derived androgens in 5α‐reductase deficiency versus androgen insensitivity syndrome
Steroid 5α‐reductase type 2 deficiency (5α‐RD2) and androgen insensitivity syndrome (AIS) are difficult to distinguish clinically and biochemically, and adrenal‐derived androgens have not been investigated in these conditions using modern methods. The objective of the study was to compare Chinese pa...
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Published in: | Clinical and translational science 2022-03, Vol.15 (3), p.658-666 |
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description | Steroid 5α‐reductase type 2 deficiency (5α‐RD2) and androgen insensitivity syndrome (AIS) are difficult to distinguish clinically and biochemically, and adrenal‐derived androgens have not been investigated in these conditions using modern methods. The objective of the study was to compare Chinese patients with 5α‐RD2, AIS, and healthy men. Sixteen patients with 5α‐RD2, 10 patients with AIS, and 39 healthy men were included. Serum androgen profiles were compared in these subjects using liquid chromatography/tandem mass spectrometry (LC‐MS/MS). Based on clinical features and laboratory tests, 5α‐RD2 and AIS were diagnosed and confirmed by genotyping. Dihydrotestosterone (DHT) and testosterone (T) were both significantly lower in patients with 5α‐RD2 than AIS (p < 0.0001). The T/DHT ratio was higher in 5α‐RD2 (4.5–88.6) than AIS (13.4–26.7) or healthy men (7.6–40.5). Using LC‐MS/MS, a cutoff T/DHT value of 27.3 correctly diagnosed 5α‐RD2 versus AIS with sensitivity 93.8% and specificity 100%. Among the adrenal‐derived 11‐oxygenated androgens, 11β‐hydroxyandrostenedione (11OHA4) and 11‐ketoandrostenedione (11KA4) were also lower in patients with 5α‐RD2 than those of patients with AIS. In contrast, 11β‐hydroxytestosterone (11OHT) was higher in 5α‐RD2 than AIS. Furthermore, a 11OHT/11OHA4 cutoff value of 0.048 could also distinguish 5α‐RD2 from AIS. Thus, both elevated T/DHT values above 27.3 and the unexpected 11‐oxygenated androgen profile, with a 11OHT/11OHA4 ratio greater than 0.048, distinguished 5α‐RD2 from AIS. These data suggest that the metabolism of both gonadal and adrenal‐derived androgens is altered in 5α‐RD2. |
doi_str_mv | 10.1111/cts.13184 |
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The objective of the study was to compare Chinese patients with 5α‐RD2, AIS, and healthy men. Sixteen patients with 5α‐RD2, 10 patients with AIS, and 39 healthy men were included. Serum androgen profiles were compared in these subjects using liquid chromatography/tandem mass spectrometry (LC‐MS/MS). Based on clinical features and laboratory tests, 5α‐RD2 and AIS were diagnosed and confirmed by genotyping. Dihydrotestosterone (DHT) and testosterone (T) were both significantly lower in patients with 5α‐RD2 than AIS (p < 0.0001). The T/DHT ratio was higher in 5α‐RD2 (4.5–88.6) than AIS (13.4–26.7) or healthy men (7.6–40.5). Using LC‐MS/MS, a cutoff T/DHT value of 27.3 correctly diagnosed 5α‐RD2 versus AIS with sensitivity 93.8% and specificity 100%. Among the adrenal‐derived 11‐oxygenated androgens, 11β‐hydroxyandrostenedione (11OHA4) and 11‐ketoandrostenedione (11KA4) were also lower in patients with 5α‐RD2 than those of patients with AIS. In contrast, 11β‐hydroxytestosterone (11OHT) was higher in 5α‐RD2 than AIS. Furthermore, a 11OHT/11OHA4 cutoff value of 0.048 could also distinguish 5α‐RD2 from AIS. Thus, both elevated T/DHT values above 27.3 and the unexpected 11‐oxygenated androgen profile, with a 11OHT/11OHA4 ratio greater than 0.048, distinguished 5α‐RD2 from AIS. These data suggest that the metabolism of both gonadal and adrenal‐derived androgens is altered in 5α‐RD2.</description><identifier>ISSN: 1752-8054</identifier><identifier>EISSN: 1752-8062</identifier><identifier>DOI: 10.1111/cts.13184</identifier><identifier>PMID: 34755921</identifier><language>eng</language><publisher>United States: John Wiley & Sons, Inc</publisher><subject>3-Oxo-5-alpha-Steroid 4-Dehydrogenase - deficiency ; Androgen-Insensitivity Syndrome - diagnosis ; Androgens ; Androgens - metabolism ; Chromatography ; Chromatography, Liquid ; Cryptorchidism ; Dihydrotestosterone ; Disorder of Sex Development, 46,XY ; Female ; Genotyping ; Humans ; Hypospadias ; Laboratories ; Liquid chromatography ; Male ; Mass spectrometry ; Mass spectroscopy ; Mutation ; Nitrogen ; Patients ; Polycystic ovary syndrome ; Puberty ; Scientific imaging ; Steroid Metabolism, Inborn Errors ; Steroids ; Tandem Mass Spectrometry ; Testosterone ; Variance analysis</subject><ispartof>Clinical and translational science, 2022-03, Vol.15 (3), p.658-666</ispartof><rights>2021 The Authors. published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.</rights><rights>2021 The Authors. Clinical and Translational Science published by Wiley Periodicals LLC on behalf of American Society for Clinical Pharmacology and Therapeutics.</rights><rights>2022. This work is published under http://creativecommons.org/licenses/by-nc/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5094-c32df079ed774f855e5ddae1158d8562c3ba9995d81f22a7b5493ead1f115cb13</citedby><cites>FETCH-LOGICAL-c5094-c32df079ed774f855e5ddae1158d8562c3ba9995d81f22a7b5493ead1f115cb13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2640383442/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2640383442?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,11562,25753,27924,27925,37012,37013,44590,46052,46476,53791,53793,75126</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34755921$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Han, Bing</creatorcontrib><creatorcontrib>Zhu, Hui</creatorcontrib><creatorcontrib>Yao, Haijun</creatorcontrib><creatorcontrib>Ren, Jianwei</creatorcontrib><creatorcontrib>O’Day, Patrick</creatorcontrib><creatorcontrib>Wang, Hao</creatorcontrib><creatorcontrib>Zhu, Wenjiao</creatorcontrib><creatorcontrib>Cheng, Tong</creatorcontrib><creatorcontrib>Auchus, Richard J.</creatorcontrib><creatorcontrib>Qiao, Jie</creatorcontrib><title>Differences of adrenal‐derived androgens in 5α‐reductase deficiency versus androgen insensitivity syndrome</title><title>Clinical and translational science</title><addtitle>Clin Transl Sci</addtitle><description>Steroid 5α‐reductase type 2 deficiency (5α‐RD2) and androgen insensitivity syndrome (AIS) are difficult to distinguish clinically and biochemically, and adrenal‐derived androgens have not been investigated in these conditions using modern methods. The objective of the study was to compare Chinese patients with 5α‐RD2, AIS, and healthy men. Sixteen patients with 5α‐RD2, 10 patients with AIS, and 39 healthy men were included. Serum androgen profiles were compared in these subjects using liquid chromatography/tandem mass spectrometry (LC‐MS/MS). Based on clinical features and laboratory tests, 5α‐RD2 and AIS were diagnosed and confirmed by genotyping. Dihydrotestosterone (DHT) and testosterone (T) were both significantly lower in patients with 5α‐RD2 than AIS (p < 0.0001). The T/DHT ratio was higher in 5α‐RD2 (4.5–88.6) than AIS (13.4–26.7) or healthy men (7.6–40.5). Using LC‐MS/MS, a cutoff T/DHT value of 27.3 correctly diagnosed 5α‐RD2 versus AIS with sensitivity 93.8% and specificity 100%. Among the adrenal‐derived 11‐oxygenated androgens, 11β‐hydroxyandrostenedione (11OHA4) and 11‐ketoandrostenedione (11KA4) were also lower in patients with 5α‐RD2 than those of patients with AIS. In contrast, 11β‐hydroxytestosterone (11OHT) was higher in 5α‐RD2 than AIS. Furthermore, a 11OHT/11OHA4 cutoff value of 0.048 could also distinguish 5α‐RD2 from AIS. Thus, both elevated T/DHT values above 27.3 and the unexpected 11‐oxygenated androgen profile, with a 11OHT/11OHA4 ratio greater than 0.048, distinguished 5α‐RD2 from AIS. These data suggest that the metabolism of both gonadal and adrenal‐derived androgens is altered in 5α‐RD2.</description><subject>3-Oxo-5-alpha-Steroid 4-Dehydrogenase - deficiency</subject><subject>Androgen-Insensitivity Syndrome - diagnosis</subject><subject>Androgens</subject><subject>Androgens - metabolism</subject><subject>Chromatography</subject><subject>Chromatography, Liquid</subject><subject>Cryptorchidism</subject><subject>Dihydrotestosterone</subject><subject>Disorder of Sex Development, 46,XY</subject><subject>Female</subject><subject>Genotyping</subject><subject>Humans</subject><subject>Hypospadias</subject><subject>Laboratories</subject><subject>Liquid chromatography</subject><subject>Male</subject><subject>Mass spectrometry</subject><subject>Mass spectroscopy</subject><subject>Mutation</subject><subject>Nitrogen</subject><subject>Patients</subject><subject>Polycystic ovary syndrome</subject><subject>Puberty</subject><subject>Scientific imaging</subject><subject>Steroid Metabolism, Inborn Errors</subject><subject>Steroids</subject><subject>Tandem Mass Spectrometry</subject><subject>Testosterone</subject><subject>Variance analysis</subject><issn>1752-8054</issn><issn>1752-8062</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp1kktuFDEQQC0EIiGw4AKoJTawmMTftr1BioZfpEgsCGvLY5cHj3rawe4e1DuOwFW4CIfgJHjSYUSQqI1LVa-eSnIh9JTgU1LjzA3llDCi-D10TKSgC4Vbev-QC36EHpWywbhlrRIP0RHjUghNyTFKr2MIkKF3UJoUGutrbrtf3757yHEHvrG9z2kNfWli34ifP2orgx_dYAs0HkJ0sU5PzQ5yGcsBr3SpQ3GIuzhMTZn29S08Rg-C7Qo8uX1P0Ke3b66W7xeXH95dLM8vF05gzReOUR-w1OCl5EEJAcJ7C4QI5ZVoqWMrq7UWXpFAqZUrwTUD60moiFsRdoIuZq9PdmOuc9zaPJlko7kppLw2Ng_RdWBkK2tQb0UrOcW8mh0nNnDZYlDYVder2XU9rrbgHfRDtt0d6d1OHz-bddoZpRlVdL_Mi1tBTl9GKIPZxuKg62wPaSyGCt1iorlkFX3-D7pJY64_UqmWY6YY57RSL2fK5VRKhnBYhmCzPwlTT8LcnERln_29_YH8cwMVOJuBr7GD6f8ms7z6OCt_AxV1xOI</recordid><startdate>202203</startdate><enddate>202203</enddate><creator>Han, Bing</creator><creator>Zhu, Hui</creator><creator>Yao, Haijun</creator><creator>Ren, Jianwei</creator><creator>O’Day, Patrick</creator><creator>Wang, Hao</creator><creator>Zhu, Wenjiao</creator><creator>Cheng, Tong</creator><creator>Auchus, Richard J.</creator><creator>Qiao, Jie</creator><general>John Wiley & Sons, Inc</general><general>John Wiley and Sons Inc</general><general>Wiley</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QP</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>202203</creationdate><title>Differences of adrenal‐derived androgens in 5α‐reductase deficiency versus androgen insensitivity syndrome</title><author>Han, Bing ; Zhu, Hui ; Yao, Haijun ; Ren, Jianwei ; O’Day, Patrick ; Wang, Hao ; Zhu, Wenjiao ; Cheng, Tong ; Auchus, Richard J. ; Qiao, Jie</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5094-c32df079ed774f855e5ddae1158d8562c3ba9995d81f22a7b5493ead1f115cb13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>3-Oxo-5-alpha-Steroid 4-Dehydrogenase - deficiency</topic><topic>Androgen-Insensitivity Syndrome - diagnosis</topic><topic>Androgens</topic><topic>Androgens - metabolism</topic><topic>Chromatography</topic><topic>Chromatography, Liquid</topic><topic>Cryptorchidism</topic><topic>Dihydrotestosterone</topic><topic>Disorder of Sex Development, 46,XY</topic><topic>Female</topic><topic>Genotyping</topic><topic>Humans</topic><topic>Hypospadias</topic><topic>Laboratories</topic><topic>Liquid chromatography</topic><topic>Male</topic><topic>Mass spectrometry</topic><topic>Mass spectroscopy</topic><topic>Mutation</topic><topic>Nitrogen</topic><topic>Patients</topic><topic>Polycystic ovary syndrome</topic><topic>Puberty</topic><topic>Scientific imaging</topic><topic>Steroid Metabolism, Inborn Errors</topic><topic>Steroids</topic><topic>Tandem Mass Spectrometry</topic><topic>Testosterone</topic><topic>Variance analysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Han, Bing</creatorcontrib><creatorcontrib>Zhu, Hui</creatorcontrib><creatorcontrib>Yao, Haijun</creatorcontrib><creatorcontrib>Ren, Jianwei</creatorcontrib><creatorcontrib>O’Day, Patrick</creatorcontrib><creatorcontrib>Wang, Hao</creatorcontrib><creatorcontrib>Zhu, Wenjiao</creatorcontrib><creatorcontrib>Cheng, Tong</creatorcontrib><creatorcontrib>Auchus, Richard J.</creatorcontrib><creatorcontrib>Qiao, Jie</creatorcontrib><collection>Wiley_OA刊</collection><collection>Wiley-Blackwell Open Access Backfiles</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Health & Medical Collection (Proquest)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biological Science Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest - 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The objective of the study was to compare Chinese patients with 5α‐RD2, AIS, and healthy men. Sixteen patients with 5α‐RD2, 10 patients with AIS, and 39 healthy men were included. Serum androgen profiles were compared in these subjects using liquid chromatography/tandem mass spectrometry (LC‐MS/MS). Based on clinical features and laboratory tests, 5α‐RD2 and AIS were diagnosed and confirmed by genotyping. Dihydrotestosterone (DHT) and testosterone (T) were both significantly lower in patients with 5α‐RD2 than AIS (p < 0.0001). The T/DHT ratio was higher in 5α‐RD2 (4.5–88.6) than AIS (13.4–26.7) or healthy men (7.6–40.5). Using LC‐MS/MS, a cutoff T/DHT value of 27.3 correctly diagnosed 5α‐RD2 versus AIS with sensitivity 93.8% and specificity 100%. Among the adrenal‐derived 11‐oxygenated androgens, 11β‐hydroxyandrostenedione (11OHA4) and 11‐ketoandrostenedione (11KA4) were also lower in patients with 5α‐RD2 than those of patients with AIS. In contrast, 11β‐hydroxytestosterone (11OHT) was higher in 5α‐RD2 than AIS. Furthermore, a 11OHT/11OHA4 cutoff value of 0.048 could also distinguish 5α‐RD2 from AIS. Thus, both elevated T/DHT values above 27.3 and the unexpected 11‐oxygenated androgen profile, with a 11OHT/11OHA4 ratio greater than 0.048, distinguished 5α‐RD2 from AIS. These data suggest that the metabolism of both gonadal and adrenal‐derived androgens is altered in 5α‐RD2.</abstract><cop>United States</cop><pub>John Wiley & Sons, Inc</pub><pmid>34755921</pmid><doi>10.1111/cts.13184</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | 3-Oxo-5-alpha-Steroid 4-Dehydrogenase - deficiency Androgen-Insensitivity Syndrome - diagnosis Androgens Androgens - metabolism Chromatography Chromatography, Liquid Cryptorchidism Dihydrotestosterone Disorder of Sex Development, 46,XY Female Genotyping Humans Hypospadias Laboratories Liquid chromatography Male Mass spectrometry Mass spectroscopy Mutation Nitrogen Patients Polycystic ovary syndrome Puberty Scientific imaging Steroid Metabolism, Inborn Errors Steroids Tandem Mass Spectrometry Testosterone Variance analysis |
title | Differences of adrenal‐derived androgens in 5α‐reductase deficiency versus androgen insensitivity syndrome |
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