Baldness, acne and testicular germ cell tumours
Summary Androgen levels during critical periods of testicular development may be involved in the aetiology of testicular germ cell tumours (TGCT). We evaluated the roles of adolescent and early adult life correlates of androgen exposure and TGCT in a hospital‐based case–control study. TGCT cases (n ...
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description | Summary
Androgen levels during critical periods of testicular development may be involved in the aetiology of testicular germ cell tumours (TGCT). We evaluated the roles of adolescent and early adult life correlates of androgen exposure and TGCT in a hospital‐based case–control study. TGCT cases (n = 187) and controls (n = 148), matched on age, race and state of residence, participated in the study. Unconditional logistic regression was used to estimate associations between TGCT and male pattern baldness, severe acne, markers of puberty onset and body size. Cases were significantly less likely to report hair loss than controls [odds ratio (OR): 0.6; 95% confidence interval (CI): 0.4, 1.0]. Amount of hair loss, increasing age at onset and increasing rate of loss were all inversely associated with TGCT (rate of hair loss: p‐trend = 0.03; age at onset: p‐trend = 0.03; amount of hair loss: p‐trend = 0.01). History of severe acne was inversely associated with TGCT (OR: 0.5; 95% CI: 0.3, 0.9) and height was positively associated with TGCT (p‐trend = 0.02). Increased endogenous androgen levels during puberty and early adulthood may be associated with a decreased risk of TGCT. Additional studies of endogenous hormone levels during puberty and early adult life are warranted, especially studies evaluating the role of androgen synthesis, metabolism and uptake. |
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Androgen levels during critical periods of testicular development may be involved in the aetiology of testicular germ cell tumours (TGCT). We evaluated the roles of adolescent and early adult life correlates of androgen exposure and TGCT in a hospital‐based case–control study. TGCT cases (n = 187) and controls (n = 148), matched on age, race and state of residence, participated in the study. Unconditional logistic regression was used to estimate associations between TGCT and male pattern baldness, severe acne, markers of puberty onset and body size. Cases were significantly less likely to report hair loss than controls [odds ratio (OR): 0.6; 95% confidence interval (CI): 0.4, 1.0]. Amount of hair loss, increasing age at onset and increasing rate of loss were all inversely associated with TGCT (rate of hair loss: p‐trend = 0.03; age at onset: p‐trend = 0.03; amount of hair loss: p‐trend = 0.01). History of severe acne was inversely associated with TGCT (OR: 0.5; 95% CI: 0.3, 0.9) and height was positively associated with TGCT (p‐trend = 0.02). Increased endogenous androgen levels during puberty and early adulthood may be associated with a decreased risk of TGCT. Additional studies of endogenous hormone levels during puberty and early adult life are warranted, especially studies evaluating the role of androgen synthesis, metabolism and uptake.</description><identifier>ISSN: 0105-6263</identifier><identifier>EISSN: 1365-2605</identifier><identifier>DOI: 10.1111/j.1365-2605.2010.01125.x</identifier><identifier>PMID: 21128977</identifier><language>eng</language><publisher>Oxford, UK: Blackwell Publishing Ltd</publisher><subject>acne ; Acne Vulgaris - epidemiology ; Adolescent ; Adult ; Age of Onset ; Alopecia - epidemiology ; Androgens - blood ; baldness ; case-control ; Case-Control Studies ; hospital-based ; Humans ; Male ; Middle Aged ; Neoplasms, Germ Cell and Embryonal - epidemiology ; Risk Factors ; testicular germ cell tumours ; Testicular Neoplasms - epidemiology ; Testis - embryology ; Testis - pathology</subject><ispartof>International journal of andrology, 2011-08, Vol.34 (4pt2), p.e59-e67</ispartof><rights>No claim to original US government works. International Journal of Andrology © 2011 European Academy of Andrology</rights><rights>No claim to original US government works. International Journal of Andrology © 2011 European Academy of Andrology.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5125-47ebad7f5bd00617a8121f90d50ba1b77953c4f204763574a9ef03adeef31b963</citedby><cites>FETCH-LOGICAL-c5125-47ebad7f5bd00617a8121f90d50ba1b77953c4f204763574a9ef03adeef31b963</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2605.2010.01125.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2605.2010.01125.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>230,314,780,784,885,1416,1432,27923,27924,45573,45574,46408,46832</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21128977$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Trabert, B.</creatorcontrib><creatorcontrib>Sigurdson, A. J.</creatorcontrib><creatorcontrib>Sweeney, A. M.</creatorcontrib><creatorcontrib>Amato, R. J.</creatorcontrib><creatorcontrib>Strom, S. S.</creatorcontrib><creatorcontrib>McGlynn, K. A.</creatorcontrib><title>Baldness, acne and testicular germ cell tumours</title><title>International journal of andrology</title><addtitle>Int J Androl</addtitle><description>Summary
Androgen levels during critical periods of testicular development may be involved in the aetiology of testicular germ cell tumours (TGCT). We evaluated the roles of adolescent and early adult life correlates of androgen exposure and TGCT in a hospital‐based case–control study. TGCT cases (n = 187) and controls (n = 148), matched on age, race and state of residence, participated in the study. Unconditional logistic regression was used to estimate associations between TGCT and male pattern baldness, severe acne, markers of puberty onset and body size. Cases were significantly less likely to report hair loss than controls [odds ratio (OR): 0.6; 95% confidence interval (CI): 0.4, 1.0]. Amount of hair loss, increasing age at onset and increasing rate of loss were all inversely associated with TGCT (rate of hair loss: p‐trend = 0.03; age at onset: p‐trend = 0.03; amount of hair loss: p‐trend = 0.01). History of severe acne was inversely associated with TGCT (OR: 0.5; 95% CI: 0.3, 0.9) and height was positively associated with TGCT (p‐trend = 0.02). Increased endogenous androgen levels during puberty and early adulthood may be associated with a decreased risk of TGCT. Additional studies of endogenous hormone levels during puberty and early adult life are warranted, especially studies evaluating the role of androgen synthesis, metabolism and uptake.</description><subject>acne</subject><subject>Acne Vulgaris - epidemiology</subject><subject>Adolescent</subject><subject>Adult</subject><subject>Age of Onset</subject><subject>Alopecia - epidemiology</subject><subject>Androgens - blood</subject><subject>baldness</subject><subject>case-control</subject><subject>Case-Control Studies</subject><subject>hospital-based</subject><subject>Humans</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Neoplasms, Germ Cell and Embryonal - epidemiology</subject><subject>Risk Factors</subject><subject>testicular germ cell tumours</subject><subject>Testicular Neoplasms - epidemiology</subject><subject>Testis - embryology</subject><subject>Testis - pathology</subject><issn>0105-6263</issn><issn>1365-2605</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMtOwzAQRS0EglL4BZQdG9LacfzIBgkqnq1AIBDLkZM4kJJHsRNo_x6HlgI7vLHluXNm7kXII3hA3BlOB4Ry5gccs0GA3S8mJGCD-QbqrQubqOcqzOcBpzto19opxphKSrbRTuDkMhKih4anqkgrbe2Rp5JKe6pKvUbbJk_aQhnvWZvSS3RReE1b1q2xe2grU4XV-6u7jx7Pzx5Gl_7k9uJqdDLxE-Y28UOhY5WKjMUpxpwIJUlAsginDMeKxEJEjCZhFuBQcMpEqCKdYapSrTNK4ojTPjpecmdtXOo00VVjVAEzk5fKLKBWOfytVPkLPNfvQDnu4A5wuAKY-q11jqDMbedEVbpuLUgpaUikYE4pl8rE1NYana2nEAxd3DCFLlXoUoUubviKG-au9eD3luvG73x_bHzkhV78GwxX1yc33dMB_CUgt42erwHKvAIXVDB4urkAMb4fU3Y3crRPoS-dIA</recordid><startdate>201108</startdate><enddate>201108</enddate><creator>Trabert, B.</creator><creator>Sigurdson, A. J.</creator><creator>Sweeney, A. M.</creator><creator>Amato, R. J.</creator><creator>Strom, S. S.</creator><creator>McGlynn, K. A.</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</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>7X8</scope><scope>5PM</scope></search><sort><creationdate>201108</creationdate><title>Baldness, acne and testicular germ cell tumours</title><author>Trabert, B. ; Sigurdson, A. J. ; Sweeney, A. M. ; Amato, R. J. ; Strom, S. S. ; McGlynn, K. A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5125-47ebad7f5bd00617a8121f90d50ba1b77953c4f204763574a9ef03adeef31b963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>acne</topic><topic>Acne Vulgaris - epidemiology</topic><topic>Adolescent</topic><topic>Adult</topic><topic>Age of Onset</topic><topic>Alopecia - epidemiology</topic><topic>Androgens - blood</topic><topic>baldness</topic><topic>case-control</topic><topic>Case-Control Studies</topic><topic>hospital-based</topic><topic>Humans</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Neoplasms, Germ Cell and Embryonal - epidemiology</topic><topic>Risk Factors</topic><topic>testicular germ cell tumours</topic><topic>Testicular Neoplasms - epidemiology</topic><topic>Testis - embryology</topic><topic>Testis - pathology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Trabert, B.</creatorcontrib><creatorcontrib>Sigurdson, A. J.</creatorcontrib><creatorcontrib>Sweeney, A. M.</creatorcontrib><creatorcontrib>Amato, R. J.</creatorcontrib><creatorcontrib>Strom, S. S.</creatorcontrib><creatorcontrib>McGlynn, K. A.</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of andrology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Trabert, B.</au><au>Sigurdson, A. J.</au><au>Sweeney, A. M.</au><au>Amato, R. J.</au><au>Strom, S. S.</au><au>McGlynn, K. A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Baldness, acne and testicular germ cell tumours</atitle><jtitle>International journal of andrology</jtitle><addtitle>Int J Androl</addtitle><date>2011-08</date><risdate>2011</risdate><volume>34</volume><issue>4pt2</issue><spage>e59</spage><epage>e67</epage><pages>e59-e67</pages><issn>0105-6263</issn><eissn>1365-2605</eissn><abstract>Summary
Androgen levels during critical periods of testicular development may be involved in the aetiology of testicular germ cell tumours (TGCT). We evaluated the roles of adolescent and early adult life correlates of androgen exposure and TGCT in a hospital‐based case–control study. TGCT cases (n = 187) and controls (n = 148), matched on age, race and state of residence, participated in the study. Unconditional logistic regression was used to estimate associations between TGCT and male pattern baldness, severe acne, markers of puberty onset and body size. Cases were significantly less likely to report hair loss than controls [odds ratio (OR): 0.6; 95% confidence interval (CI): 0.4, 1.0]. Amount of hair loss, increasing age at onset and increasing rate of loss were all inversely associated with TGCT (rate of hair loss: p‐trend = 0.03; age at onset: p‐trend = 0.03; amount of hair loss: p‐trend = 0.01). History of severe acne was inversely associated with TGCT (OR: 0.5; 95% CI: 0.3, 0.9) and height was positively associated with TGCT (p‐trend = 0.02). Increased endogenous androgen levels during puberty and early adulthood may be associated with a decreased risk of TGCT. Additional studies of endogenous hormone levels during puberty and early adult life are warranted, especially studies evaluating the role of androgen synthesis, metabolism and uptake.</abstract><cop>Oxford, UK</cop><pub>Blackwell Publishing Ltd</pub><pmid>21128977</pmid><doi>10.1111/j.1365-2605.2010.01125.x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
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subjects | acne Acne Vulgaris - epidemiology Adolescent Adult Age of Onset Alopecia - epidemiology Androgens - blood baldness case-control Case-Control Studies hospital-based Humans Male Middle Aged Neoplasms, Germ Cell and Embryonal - epidemiology Risk Factors testicular germ cell tumours Testicular Neoplasms - epidemiology Testis - embryology Testis - pathology |
title | Baldness, acne and testicular germ cell tumours |
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