Loading…

Idiopathic impaired spermatogenesis: genetic epidemiology is unlikely to provide a short-cut to better understanding

The aetiology of impaired spermatogenesis is unknown in the majority of subfertile men. From several studies of concordance for involuntary childlessness among men, we can conclude that there is a substantial familial component in male subfertility and that shared loci segregating through families c...

Full description

Saved in:
Bibliographic Details
Published in:Human reproduction update 2004-11, Vol.10 (6), p.533-539
Main Authors: Gianotten, Judith, Lombardi, M.Paola, Zwinderman, A.H., Lilford, Richard J., van der Veen, Fulco
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c490t-7084f2ec1511fd65aaf98ecb46b7245c16ed0346f8fcfeb17ab771636161a8bc3
cites cdi_FETCH-LOGICAL-c490t-7084f2ec1511fd65aaf98ecb46b7245c16ed0346f8fcfeb17ab771636161a8bc3
container_end_page 539
container_issue 6
container_start_page 533
container_title Human reproduction update
container_volume 10
creator Gianotten, Judith
Lombardi, M.Paola
Zwinderman, A.H.
Lilford, Richard J.
van der Veen, Fulco
description The aetiology of impaired spermatogenesis is unknown in the majority of subfertile men. From several studies of concordance for involuntary childlessness among men, we can conclude that there is a substantial familial component in male subfertility and that shared loci segregating through families can be assumed. We now know that deletions on the Y chromosome, which do not penetrate fully, account for some of these cases. There are good reasons to suspect that other cases result from mutations in genes located elsewhere in the genome. In this article, we discuss different approaches to unravelling the molecular basis of impaired spermatogenesis originating from genetic abnormalities in chromosomes other than the Y chromosome. Genetic mapping studies are in general a good approach to detect disease-causing genes that are segregating through a population; they can provide a shortcut to unravelling the biochemistry of a disease. In this paper, we explain our reasons for arguing that linkage and association studies are no promising means to identify the genes causing impaired spermatogenesis. We conclude that direct screening of candidate genes for mutations will be necessary to detect genes involved in impaired spermatogenesis. However, this approach requires studies of the biochemical pathways of normal and abnormal spermatogenesis. Since we have a poor understanding of these pathways, more research is needed into the biochemistry of spermatogenesis.
doi_str_mv 10.1093/humupd/dmh045
format article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67025049</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>21229268</sourcerecordid><originalsourceid>FETCH-LOGICAL-c490t-7084f2ec1511fd65aaf98ecb46b7245c16ed0346f8fcfeb17ab771636161a8bc3</originalsourceid><addsrcrecordid>eNqFkc1v1DAQxS0EoqVw5IoiDtxC_e2EG6qgLa3UQ4tAvViOPdl1m8Sp7aDuf49Xu2olLpxmNO-np3l6CL0n-DPBLTteL-Myu2M3rjEXL9Ah4RLXlMn2ZdmZEDVXjTxAb1K6w5hI0qjX6IAILkXD5CHK586H2eS1t5UfZ-MjuCrNEEeTwwomSD59qbZLLgTM3sHowxBWm8qnapkGfw_DpsqhmmP4U9TKVGkdYq7tkrfnDnKGWEgHMWUzOT-t3qJXvRkSvNvPI_Tz-7ebk7P68ur0_OTrZW15i3OtcMN7CpYIQnonhTF924DtuOwU5cISCQ4zLvumtz10RJlOKSKZLDFN01l2hD7tfMtvDwukrEefLAyDmSAsSUuFqcC8_S9ICaUtlU0BP_4D3oUlTiVEYQjFjFJeoHoH2RhSitDrOfrRxI0mWG9L07vS9K60wn_Ymy7dCO6Z3rf0bOhThscn3cT7EoEpoc9-3-rrC_GL3_yg-pb9BUh1plw</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>211203224</pqid></control><display><type>article</type><title>Idiopathic impaired spermatogenesis: genetic epidemiology is unlikely to provide a short-cut to better understanding</title><source>Oxford Journals Online</source><creator>Gianotten, Judith ; Lombardi, M.Paola ; Zwinderman, A.H. ; Lilford, Richard J. ; van der Veen, Fulco</creator><creatorcontrib>Gianotten, Judith ; Lombardi, M.Paola ; Zwinderman, A.H. ; Lilford, Richard J. ; van der Veen, Fulco</creatorcontrib><description>The aetiology of impaired spermatogenesis is unknown in the majority of subfertile men. From several studies of concordance for involuntary childlessness among men, we can conclude that there is a substantial familial component in male subfertility and that shared loci segregating through families can be assumed. We now know that deletions on the Y chromosome, which do not penetrate fully, account for some of these cases. There are good reasons to suspect that other cases result from mutations in genes located elsewhere in the genome. In this article, we discuss different approaches to unravelling the molecular basis of impaired spermatogenesis originating from genetic abnormalities in chromosomes other than the Y chromosome. Genetic mapping studies are in general a good approach to detect disease-causing genes that are segregating through a population; they can provide a shortcut to unravelling the biochemistry of a disease. In this paper, we explain our reasons for arguing that linkage and association studies are no promising means to identify the genes causing impaired spermatogenesis. We conclude that direct screening of candidate genes for mutations will be necessary to detect genes involved in impaired spermatogenesis. However, this approach requires studies of the biochemical pathways of normal and abnormal spermatogenesis. Since we have a poor understanding of these pathways, more research is needed into the biochemistry of spermatogenesis.</description><identifier>ISSN: 1355-4786</identifier><identifier>EISSN: 1460-2369</identifier><identifier>DOI: 10.1093/humupd/dmh045</identifier><identifier>PMID: 15465836</identifier><identifier>CODEN: HRUPF8</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Chromosomes, Human, Y ; Environment ; gene mutations ; genetic epidemiology ; Genetic Linkage ; Humans ; Infertility, Male - genetics ; Male ; male infertility ; Models, Genetic ; Mutation ; spermatogenesis ; Spermatogenesis - genetics ; Y chromosome</subject><ispartof>Human reproduction update, 2004-11, Vol.10 (6), p.533-539</ispartof><rights>Copyright Oxford University Press(England) Nov 2004</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c490t-7084f2ec1511fd65aaf98ecb46b7245c16ed0346f8fcfeb17ab771636161a8bc3</citedby><cites>FETCH-LOGICAL-c490t-7084f2ec1511fd65aaf98ecb46b7245c16ed0346f8fcfeb17ab771636161a8bc3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15465836$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Gianotten, Judith</creatorcontrib><creatorcontrib>Lombardi, M.Paola</creatorcontrib><creatorcontrib>Zwinderman, A.H.</creatorcontrib><creatorcontrib>Lilford, Richard J.</creatorcontrib><creatorcontrib>van der Veen, Fulco</creatorcontrib><title>Idiopathic impaired spermatogenesis: genetic epidemiology is unlikely to provide a short-cut to better understanding</title><title>Human reproduction update</title><addtitle>Hum. Reprod. Update</addtitle><description>The aetiology of impaired spermatogenesis is unknown in the majority of subfertile men. From several studies of concordance for involuntary childlessness among men, we can conclude that there is a substantial familial component in male subfertility and that shared loci segregating through families can be assumed. We now know that deletions on the Y chromosome, which do not penetrate fully, account for some of these cases. There are good reasons to suspect that other cases result from mutations in genes located elsewhere in the genome. In this article, we discuss different approaches to unravelling the molecular basis of impaired spermatogenesis originating from genetic abnormalities in chromosomes other than the Y chromosome. Genetic mapping studies are in general a good approach to detect disease-causing genes that are segregating through a population; they can provide a shortcut to unravelling the biochemistry of a disease. In this paper, we explain our reasons for arguing that linkage and association studies are no promising means to identify the genes causing impaired spermatogenesis. We conclude that direct screening of candidate genes for mutations will be necessary to detect genes involved in impaired spermatogenesis. However, this approach requires studies of the biochemical pathways of normal and abnormal spermatogenesis. Since we have a poor understanding of these pathways, more research is needed into the biochemistry of spermatogenesis.</description><subject>Chromosomes, Human, Y</subject><subject>Environment</subject><subject>gene mutations</subject><subject>genetic epidemiology</subject><subject>Genetic Linkage</subject><subject>Humans</subject><subject>Infertility, Male - genetics</subject><subject>Male</subject><subject>male infertility</subject><subject>Models, Genetic</subject><subject>Mutation</subject><subject>spermatogenesis</subject><subject>Spermatogenesis - genetics</subject><subject>Y chromosome</subject><issn>1355-4786</issn><issn>1460-2369</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2004</creationdate><recordtype>article</recordtype><recordid>eNqFkc1v1DAQxS0EoqVw5IoiDtxC_e2EG6qgLa3UQ4tAvViOPdl1m8Sp7aDuf49Xu2olLpxmNO-np3l6CL0n-DPBLTteL-Myu2M3rjEXL9Ah4RLXlMn2ZdmZEDVXjTxAb1K6w5hI0qjX6IAILkXD5CHK586H2eS1t5UfZ-MjuCrNEEeTwwomSD59qbZLLgTM3sHowxBWm8qnapkGfw_DpsqhmmP4U9TKVGkdYq7tkrfnDnKGWEgHMWUzOT-t3qJXvRkSvNvPI_Tz-7ebk7P68ur0_OTrZW15i3OtcMN7CpYIQnonhTF924DtuOwU5cISCQ4zLvumtz10RJlOKSKZLDFN01l2hD7tfMtvDwukrEefLAyDmSAsSUuFqcC8_S9ICaUtlU0BP_4D3oUlTiVEYQjFjFJeoHoH2RhSitDrOfrRxI0mWG9L07vS9K60wn_Ymy7dCO6Z3rf0bOhThscn3cT7EoEpoc9-3-rrC_GL3_yg-pb9BUh1plw</recordid><startdate>20041101</startdate><enddate>20041101</enddate><creator>Gianotten, Judith</creator><creator>Lombardi, M.Paola</creator><creator>Zwinderman, A.H.</creator><creator>Lilford, Richard J.</creator><creator>van der Veen, Fulco</creator><general>Oxford University Press</general><general>Oxford Publishing Limited (England)</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>7QP</scope><scope>K9.</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope></search><sort><creationdate>20041101</creationdate><title>Idiopathic impaired spermatogenesis: genetic epidemiology is unlikely to provide a short-cut to better understanding</title><author>Gianotten, Judith ; Lombardi, M.Paola ; Zwinderman, A.H. ; Lilford, Richard J. ; van der Veen, Fulco</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c490t-7084f2ec1511fd65aaf98ecb46b7245c16ed0346f8fcfeb17ab771636161a8bc3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2004</creationdate><topic>Chromosomes, Human, Y</topic><topic>Environment</topic><topic>gene mutations</topic><topic>genetic epidemiology</topic><topic>Genetic Linkage</topic><topic>Humans</topic><topic>Infertility, Male - genetics</topic><topic>Male</topic><topic>male infertility</topic><topic>Models, Genetic</topic><topic>Mutation</topic><topic>spermatogenesis</topic><topic>Spermatogenesis - genetics</topic><topic>Y chromosome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gianotten, Judith</creatorcontrib><creatorcontrib>Lombardi, M.Paola</creatorcontrib><creatorcontrib>Zwinderman, A.H.</creatorcontrib><creatorcontrib>Lilford, Richard J.</creatorcontrib><creatorcontrib>van der Veen, Fulco</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>Calcium &amp; Calcified Tissue Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Human reproduction update</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gianotten, Judith</au><au>Lombardi, M.Paola</au><au>Zwinderman, A.H.</au><au>Lilford, Richard J.</au><au>van der Veen, Fulco</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Idiopathic impaired spermatogenesis: genetic epidemiology is unlikely to provide a short-cut to better understanding</atitle><jtitle>Human reproduction update</jtitle><addtitle>Hum. Reprod. Update</addtitle><date>2004-11-01</date><risdate>2004</risdate><volume>10</volume><issue>6</issue><spage>533</spage><epage>539</epage><pages>533-539</pages><issn>1355-4786</issn><eissn>1460-2369</eissn><coden>HRUPF8</coden><abstract>The aetiology of impaired spermatogenesis is unknown in the majority of subfertile men. From several studies of concordance for involuntary childlessness among men, we can conclude that there is a substantial familial component in male subfertility and that shared loci segregating through families can be assumed. We now know that deletions on the Y chromosome, which do not penetrate fully, account for some of these cases. There are good reasons to suspect that other cases result from mutations in genes located elsewhere in the genome. In this article, we discuss different approaches to unravelling the molecular basis of impaired spermatogenesis originating from genetic abnormalities in chromosomes other than the Y chromosome. Genetic mapping studies are in general a good approach to detect disease-causing genes that are segregating through a population; they can provide a shortcut to unravelling the biochemistry of a disease. In this paper, we explain our reasons for arguing that linkage and association studies are no promising means to identify the genes causing impaired spermatogenesis. We conclude that direct screening of candidate genes for mutations will be necessary to detect genes involved in impaired spermatogenesis. However, this approach requires studies of the biochemical pathways of normal and abnormal spermatogenesis. Since we have a poor understanding of these pathways, more research is needed into the biochemistry of spermatogenesis.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>15465836</pmid><doi>10.1093/humupd/dmh045</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1355-4786
ispartof Human reproduction update, 2004-11, Vol.10 (6), p.533-539
issn 1355-4786
1460-2369
language eng
recordid cdi_proquest_miscellaneous_67025049
source Oxford Journals Online
subjects Chromosomes, Human, Y
Environment
gene mutations
genetic epidemiology
Genetic Linkage
Humans
Infertility, Male - genetics
Male
male infertility
Models, Genetic
Mutation
spermatogenesis
Spermatogenesis - genetics
Y chromosome
title Idiopathic impaired spermatogenesis: genetic epidemiology is unlikely to provide a short-cut to better understanding
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T00%3A15%3A12IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Idiopathic%20impaired%20spermatogenesis:%20genetic%20epidemiology%20is%20unlikely%20to%20provide%20a%20short-cut%20to%20better%20understanding&rft.jtitle=Human%20reproduction%20update&rft.au=Gianotten,%20Judith&rft.date=2004-11-01&rft.volume=10&rft.issue=6&rft.spage=533&rft.epage=539&rft.pages=533-539&rft.issn=1355-4786&rft.eissn=1460-2369&rft.coden=HRUPF8&rft_id=info:doi/10.1093/humupd/dmh045&rft_dat=%3Cproquest_cross%3E21229268%3C/proquest_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c490t-7084f2ec1511fd65aaf98ecb46b7245c16ed0346f8fcfeb17ab771636161a8bc3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=211203224&rft_id=info:pmid/15465836&rfr_iscdi=true