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Fertility and ageing
The late 20th century trend to delay birth of the first child until the age at which female fecundity or reproductive capacity is lower has increased the incidence of age-related infertility. The trend and its consequences have also stimulated interest in the possible factors in the female and the m...
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Published in: | Human reproduction update 2005-05, Vol.11 (3), p.261-276 |
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creator | Baird, D T Collins, J Egozcue, J Evers, L H Gianaroli, L Leridon, H Sunde, A Templeton, A Van Steirteghem, A Cohen, J Crosignani, P G Devroey, P Diedrich, K Fauser, B C J M Fraser, L Glasier, A Liebaers, I Mautone, G Penney, G Tarlatzis, B |
description | The late 20th century trend to delay birth of the first child until the age at which female fecundity or reproductive capacity is lower has increased the incidence of age-related infertility. The trend and its consequences have also stimulated interest in the possible factors in the female and the male that may contribute to the decline in fecundity with age; in the means that exist to predict fecundity; and in the consequences for pregnancy and childbirth. In the female, the number of oocytes decreases with age until the menopause. Oocyte quality also diminishes, due in part to increased aneuploidy because of factors such as changes in spindle integrity. Although older male age affects the likelihood of conception, abnormalities in sperm chromosomes and in some components of the semen analysis are less important than the frequency of intercourse. Age is as accurate as any other predictor of conception with assisted reproductive technology. The decline in fecundity becomes clinically relevant when women reach their mid-30s, when even assisted reproduction treatment cannot compensate for the decline in fecundity associated with delaying attempts at conceiving. Pregnancies among women aged >40 years are associated with more non-severe complications, more premature births, more congenital malformations and more interventions at birth. |
doi_str_mv | 10.1093/humupd/dmi006 |
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The trend and its consequences have also stimulated interest in the possible factors in the female and the male that may contribute to the decline in fecundity with age; in the means that exist to predict fecundity; and in the consequences for pregnancy and childbirth. In the female, the number of oocytes decreases with age until the menopause. Oocyte quality also diminishes, due in part to increased aneuploidy because of factors such as changes in spindle integrity. Although older male age affects the likelihood of conception, abnormalities in sperm chromosomes and in some components of the semen analysis are less important than the frequency of intercourse. Age is as accurate as any other predictor of conception with assisted reproductive technology. The decline in fecundity becomes clinically relevant when women reach their mid-30s, when even assisted reproduction treatment cannot compensate for the decline in fecundity associated with delaying attempts at conceiving. Pregnancies among women aged >40 years are associated with more non-severe complications, more premature births, more congenital malformations and more interventions at birth.</description><identifier>ISSN: 1355-4786</identifier><identifier>EISSN: 1460-2369</identifier><identifier>DOI: 10.1093/humupd/dmi006</identifier><identifier>PMID: 15831503</identifier><identifier>CODEN: HRUPF8</identifier><language>eng</language><publisher>England: Oxford University Press</publisher><subject>Adult ; ageing ; Aging - physiology ; demographics ; Demography ; fecundity ; Female ; fertility ; Fertility - physiology ; Humans ; infertility ; Male ; Middle Aged ; Oocytes - physiology ; Pregnancy ; Reproductive Techniques, Assisted - standards ; Sex Factors ; Spermatozoa - physiology</subject><ispartof>Human reproduction update, 2005-05, Vol.11 (3), p.261-276</ispartof><rights>Copyright Oxford University Press(England) May 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c356t-d538258d6bfc4225339109ab2bf39dfee73687e3939072571db271f9258e2fe23</citedby></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/15831503$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Baird, D T</creatorcontrib><creatorcontrib>Collins, J</creatorcontrib><creatorcontrib>Egozcue, J</creatorcontrib><creatorcontrib>Evers, L H</creatorcontrib><creatorcontrib>Gianaroli, L</creatorcontrib><creatorcontrib>Leridon, H</creatorcontrib><creatorcontrib>Sunde, A</creatorcontrib><creatorcontrib>Templeton, A</creatorcontrib><creatorcontrib>Van Steirteghem, A</creatorcontrib><creatorcontrib>Cohen, J</creatorcontrib><creatorcontrib>Crosignani, P G</creatorcontrib><creatorcontrib>Devroey, P</creatorcontrib><creatorcontrib>Diedrich, K</creatorcontrib><creatorcontrib>Fauser, B C J M</creatorcontrib><creatorcontrib>Fraser, L</creatorcontrib><creatorcontrib>Glasier, A</creatorcontrib><creatorcontrib>Liebaers, I</creatorcontrib><creatorcontrib>Mautone, G</creatorcontrib><creatorcontrib>Penney, G</creatorcontrib><creatorcontrib>Tarlatzis, B</creatorcontrib><creatorcontrib>ESHRE Capri Workshop Group</creatorcontrib><creatorcontrib>ESHRE Capri Workshop Group</creatorcontrib><title>Fertility and ageing</title><title>Human reproduction update</title><addtitle>Hum. Reprod. Update</addtitle><description>The late 20th century trend to delay birth of the first child until the age at which female fecundity or reproductive capacity is lower has increased the incidence of age-related infertility. The trend and its consequences have also stimulated interest in the possible factors in the female and the male that may contribute to the decline in fecundity with age; in the means that exist to predict fecundity; and in the consequences for pregnancy and childbirth. In the female, the number of oocytes decreases with age until the menopause. Oocyte quality also diminishes, due in part to increased aneuploidy because of factors such as changes in spindle integrity. Although older male age affects the likelihood of conception, abnormalities in sperm chromosomes and in some components of the semen analysis are less important than the frequency of intercourse. Age is as accurate as any other predictor of conception with assisted reproductive technology. The decline in fecundity becomes clinically relevant when women reach their mid-30s, when even assisted reproduction treatment cannot compensate for the decline in fecundity associated with delaying attempts at conceiving. Pregnancies among women aged >40 years are associated with more non-severe complications, more premature births, more congenital malformations and more interventions at birth.</description><subject>Adult</subject><subject>ageing</subject><subject>Aging - physiology</subject><subject>demographics</subject><subject>Demography</subject><subject>fecundity</subject><subject>Female</subject><subject>fertility</subject><subject>Fertility - physiology</subject><subject>Humans</subject><subject>infertility</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Oocytes - physiology</subject><subject>Pregnancy</subject><subject>Reproductive Techniques, Assisted - standards</subject><subject>Sex Factors</subject><subject>Spermatozoa - physiology</subject><issn>1355-4786</issn><issn>1460-2369</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><recordid>eNpdkE1Lw0AQhhdRbK3e9CrFg7fY3Z3sR45SbSNUBVGQXpYku6mp-ai7Cdh_70qKBU8zMM-8vDwIXRB8Q3AEk4-u6jZ6oqsCY36AhiTkOKDAo0O_A2NBKCQfoBPn1hgTTqQ4RgPCJBCGYYjOZ8a2RVm023FS63GyMkW9OkVHeVI6c7abI_Q2u3-dxsHief4wvV0EGTDeBpqBpExqnuZZSCkDiHylJKVpDpHOjRHApTAQQYQFZYLolAqSR_7H0NxQGKHrPndjm6_OuFZVhctMWSa1aTqnuBCc4RB78OofuG46W_tuihJCpZCUeyjoocw2zlmTq40tqsRuFcHq15XqXanelecvd6FdWhm9p3dy9oGFa8333z2xn74ZCKbi96WKn8Ll3ct8rh7hB767ctk</recordid><startdate>20050501</startdate><enddate>20050501</enddate><creator>Baird, D T</creator><creator>Collins, J</creator><creator>Egozcue, J</creator><creator>Evers, L H</creator><creator>Gianaroli, L</creator><creator>Leridon, H</creator><creator>Sunde, A</creator><creator>Templeton, A</creator><creator>Van Steirteghem, A</creator><creator>Cohen, J</creator><creator>Crosignani, P G</creator><creator>Devroey, P</creator><creator>Diedrich, K</creator><creator>Fauser, B C J M</creator><creator>Fraser, L</creator><creator>Glasier, A</creator><creator>Liebaers, I</creator><creator>Mautone, G</creator><creator>Penney, G</creator><creator>Tarlatzis, B</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>7X8</scope></search><sort><creationdate>20050501</creationdate><title>Fertility and ageing</title><author>Baird, D T ; Collins, J ; Egozcue, J ; Evers, L H ; Gianaroli, L ; Leridon, H ; Sunde, A ; Templeton, A ; Van Steirteghem, A ; Cohen, J ; Crosignani, P G ; Devroey, P ; Diedrich, K ; Fauser, B C J M ; Fraser, L ; Glasier, A ; Liebaers, I ; Mautone, G ; Penney, G ; Tarlatzis, B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c356t-d538258d6bfc4225339109ab2bf39dfee73687e3939072571db271f9258e2fe23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Adult</topic><topic>ageing</topic><topic>Aging - physiology</topic><topic>demographics</topic><topic>Demography</topic><topic>fecundity</topic><topic>Female</topic><topic>fertility</topic><topic>Fertility - physiology</topic><topic>Humans</topic><topic>infertility</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Oocytes - physiology</topic><topic>Pregnancy</topic><topic>Reproductive Techniques, Assisted - standards</topic><topic>Sex Factors</topic><topic>Spermatozoa - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Baird, D T</creatorcontrib><creatorcontrib>Collins, J</creatorcontrib><creatorcontrib>Egozcue, J</creatorcontrib><creatorcontrib>Evers, L H</creatorcontrib><creatorcontrib>Gianaroli, L</creatorcontrib><creatorcontrib>Leridon, H</creatorcontrib><creatorcontrib>Sunde, A</creatorcontrib><creatorcontrib>Templeton, A</creatorcontrib><creatorcontrib>Van Steirteghem, A</creatorcontrib><creatorcontrib>Cohen, J</creatorcontrib><creatorcontrib>Crosignani, P G</creatorcontrib><creatorcontrib>Devroey, P</creatorcontrib><creatorcontrib>Diedrich, K</creatorcontrib><creatorcontrib>Fauser, B C J M</creatorcontrib><creatorcontrib>Fraser, L</creatorcontrib><creatorcontrib>Glasier, A</creatorcontrib><creatorcontrib>Liebaers, I</creatorcontrib><creatorcontrib>Mautone, G</creatorcontrib><creatorcontrib>Penney, G</creatorcontrib><creatorcontrib>Tarlatzis, B</creatorcontrib><creatorcontrib>ESHRE Capri Workshop Group</creatorcontrib><creatorcontrib>ESHRE Capri Workshop Group</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 & Calcified Tissue Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Human reproduction update</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Baird, D T</au><au>Collins, J</au><au>Egozcue, J</au><au>Evers, L H</au><au>Gianaroli, L</au><au>Leridon, H</au><au>Sunde, A</au><au>Templeton, A</au><au>Van Steirteghem, A</au><au>Cohen, J</au><au>Crosignani, P G</au><au>Devroey, P</au><au>Diedrich, K</au><au>Fauser, B C J M</au><au>Fraser, L</au><au>Glasier, A</au><au>Liebaers, I</au><au>Mautone, G</au><au>Penney, G</au><au>Tarlatzis, B</au><aucorp>ESHRE Capri Workshop Group</aucorp><aucorp>ESHRE Capri Workshop Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fertility and ageing</atitle><jtitle>Human reproduction update</jtitle><addtitle>Hum. 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Although older male age affects the likelihood of conception, abnormalities in sperm chromosomes and in some components of the semen analysis are less important than the frequency of intercourse. Age is as accurate as any other predictor of conception with assisted reproductive technology. The decline in fecundity becomes clinically relevant when women reach their mid-30s, when even assisted reproduction treatment cannot compensate for the decline in fecundity associated with delaying attempts at conceiving. Pregnancies among women aged >40 years are associated with more non-severe complications, more premature births, more congenital malformations and more interventions at birth.</abstract><cop>England</cop><pub>Oxford University Press</pub><pmid>15831503</pmid><doi>10.1093/humupd/dmi006</doi><tpages>16</tpages></addata></record> |
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subjects | Adult ageing Aging - physiology demographics Demography fecundity Female fertility Fertility - physiology Humans infertility Male Middle Aged Oocytes - physiology Pregnancy Reproductive Techniques, Assisted - standards Sex Factors Spermatozoa - physiology |
title | Fertility and ageing |
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