Biological sex and the risk of cerebral palsy in Victoria, Australia

Aim Males typically outnumber females in cerebral palsy (CP) cohorts. To better understand this ‘male disadvantage’ and provide insight into causal pathways to CP, this study used 1983 to 2009 Australian CP and population birth cohorts to identify associations and trends with respect to biological s...

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Veröffentlicht in:Developmental medicine and child neurology 2016-02, Vol.58 (S2), p.43-49
Hauptverfasser: Reid, Susan M, Meehan, Elaine, Gibson, Catherine S, Scott, Heather, Delacy, Michael J
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container_issue S2
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container_title Developmental medicine and child neurology
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creator Reid, Susan M
Meehan, Elaine
Gibson, Catherine S
Scott, Heather
Delacy, Michael J
description Aim Males typically outnumber females in cerebral palsy (CP) cohorts. To better understand this ‘male disadvantage’ and provide insight into causal pathways to CP, this study used 1983 to 2009 Australian CP and population birth cohorts to identify associations and trends with respect to biological sex and CP. Method Within birth gestation groups, sex ratios were calculated to evaluate any male excess in the CP cohort compared with livebirths, neonatal deaths, neonatal mortality and survival rates, neonatal survivors, and CP rates in survivors. Sex‐ and gestation‐specific trends in neonatal mortality, CP rates, and CP sex ratios were assessed by plotting their annual frequencies and fitting quadratic curves. Results Over‐representation of males in preterm live births partly explained the male excess in the CP cohort after preterm birth, especially at 28 to 31 weeks. Higher CP rates in male neonatal survivors also contributed to the male excess in CP, particularly at
doi_str_mv 10.1111/dmcn.13021
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To better understand this ‘male disadvantage’ and provide insight into causal pathways to CP, this study used 1983 to 2009 Australian CP and population birth cohorts to identify associations and trends with respect to biological sex and CP. Method Within birth gestation groups, sex ratios were calculated to evaluate any male excess in the CP cohort compared with livebirths, neonatal deaths, neonatal mortality and survival rates, neonatal survivors, and CP rates in survivors. Sex‐ and gestation‐specific trends in neonatal mortality, CP rates, and CP sex ratios were assessed by plotting their annual frequencies and fitting quadratic curves. Results Over‐representation of males in preterm live births partly explained the male excess in the CP cohort after preterm birth, especially at 28 to 31 weeks. Higher CP rates in male neonatal survivors also contributed to the male excess in CP, particularly at &lt;28 and 37+ weeks. Higher neonatal mortality rates in males at all gestations had little impact on the CP sex ratio. There was no clearly discernible change over time in the CP sex ratio. Interpretation Gestation‐specific associations between sex and CP provide insight into causal pathways to CP and suggest sex‐specific differences in response to neuroprotective strategies. What this paper adds The male excess in live births was highest at gestations &lt;37 weeks. The increased risk of CP in males was most pronounced in neonatal survivors of birth at &lt;28 and 37+ weeks' gestation. The CP sex ratio remained relatively stable overall, although there were gestation‐specific trends. The possibility of sex‐specific differences in neuroprotective strategies is supported.</description><identifier>ISSN: 0012-1622</identifier><identifier>EISSN: 1469-8749</identifier><identifier>DOI: 10.1111/dmcn.13021</identifier><identifier>PMID: 26762863</identifier><language>eng</language><publisher>England</publisher><subject>Cerebral Palsy - epidemiology ; Cerebral Palsy - etiology ; Female ; Gestational Age ; Humans ; Infant, Newborn ; Male ; Pregnancy ; Premature Birth - epidemiology ; Risk ; Sex Factors ; Survival Rate ; Victoria - epidemiology</subject><ispartof>Developmental medicine and child neurology, 2016-02, Vol.58 (S2), p.43-49</ispartof><rights>2016 The Authors. Developmental Medicine &amp; Child Neurology © 2016 Mac Keith Press</rights><rights>2016 The Authors. 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To better understand this ‘male disadvantage’ and provide insight into causal pathways to CP, this study used 1983 to 2009 Australian CP and population birth cohorts to identify associations and trends with respect to biological sex and CP. Method Within birth gestation groups, sex ratios were calculated to evaluate any male excess in the CP cohort compared with livebirths, neonatal deaths, neonatal mortality and survival rates, neonatal survivors, and CP rates in survivors. Sex‐ and gestation‐specific trends in neonatal mortality, CP rates, and CP sex ratios were assessed by plotting their annual frequencies and fitting quadratic curves. Results Over‐representation of males in preterm live births partly explained the male excess in the CP cohort after preterm birth, especially at 28 to 31 weeks. Higher CP rates in male neonatal survivors also contributed to the male excess in CP, particularly at &lt;28 and 37+ weeks. Higher neonatal mortality rates in males at all gestations had little impact on the CP sex ratio. There was no clearly discernible change over time in the CP sex ratio. Interpretation Gestation‐specific associations between sex and CP provide insight into causal pathways to CP and suggest sex‐specific differences in response to neuroprotective strategies. What this paper adds The male excess in live births was highest at gestations &lt;37 weeks. The increased risk of CP in males was most pronounced in neonatal survivors of birth at &lt;28 and 37+ weeks' gestation. The CP sex ratio remained relatively stable overall, although there were gestation‐specific trends. The possibility of sex‐specific differences in neuroprotective strategies is supported.</description><subject>Cerebral Palsy - epidemiology</subject><subject>Cerebral Palsy - etiology</subject><subject>Female</subject><subject>Gestational Age</subject><subject>Humans</subject><subject>Infant, Newborn</subject><subject>Male</subject><subject>Pregnancy</subject><subject>Premature Birth - epidemiology</subject><subject>Risk</subject><subject>Sex Factors</subject><subject>Survival Rate</subject><subject>Victoria - epidemiology</subject><issn>0012-1622</issn><issn>1469-8749</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kDtPwzAURi0EouWx8AOQR4RI8Y0dJx5Ly0sqsFSskWM7YMij2Img_x6XFEa83OE7OrIOQidAJhDepa5VMwFKYthBY2BcRFnKxC4aEwJxBDyOR-jA-zdCCOUJ20ejmKc8zjgdo_mVbav2xSpZYW--sGw07l4Ndta_47bEyjhTuDCuZOXX2Db42aqudVZe4GnvuzBZeYT2yjCb4-09RMub6-XsLlo83d7PpotIMZpAJAoGcVHy8NNMCJFqk3KmJCt1yaCgQhEjQJZJlmiWqrIoMko4cM14BppqeojOBu3KtR-98V1eW69MVcnGtL3PIei4EEBFQM8HVLnWe2fKfOVsLd06B5JvouWbaPlPtACfbr19URv9h_5WCgAMwKetzPofVT5_mD0O0m9WMXW1</recordid><startdate>201602</startdate><enddate>201602</enddate><creator>Reid, Susan M</creator><creator>Meehan, Elaine</creator><creator>Gibson, Catherine S</creator><creator>Scott, Heather</creator><creator>Delacy, Michael J</creator><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></search><sort><creationdate>201602</creationdate><title>Biological sex and the risk of cerebral palsy in Victoria, Australia</title><author>Reid, Susan M ; Meehan, Elaine ; Gibson, Catherine S ; Scott, Heather ; Delacy, Michael J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4351-9b412bf630289997de764ca4fdf41b39c0e91af585d47cfbb830616d4681d3d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Cerebral Palsy - epidemiology</topic><topic>Cerebral Palsy - etiology</topic><topic>Female</topic><topic>Gestational Age</topic><topic>Humans</topic><topic>Infant, Newborn</topic><topic>Male</topic><topic>Pregnancy</topic><topic>Premature Birth - epidemiology</topic><topic>Risk</topic><topic>Sex Factors</topic><topic>Survival Rate</topic><topic>Victoria - epidemiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Reid, Susan M</creatorcontrib><creatorcontrib>Meehan, Elaine</creatorcontrib><creatorcontrib>Gibson, Catherine S</creatorcontrib><creatorcontrib>Scott, Heather</creatorcontrib><creatorcontrib>Delacy, Michael J</creatorcontrib><creatorcontrib>Australian Cerebral Palsy Register Group</creatorcontrib><creatorcontrib>the Australian Cerebral Palsy Register Group</creatorcontrib><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><jtitle>Developmental medicine and child neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reid, Susan M</au><au>Meehan, Elaine</au><au>Gibson, Catherine S</au><au>Scott, Heather</au><au>Delacy, Michael J</au><aucorp>Australian Cerebral Palsy Register Group</aucorp><aucorp>the Australian Cerebral Palsy Register Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Biological sex and the risk of cerebral palsy in Victoria, Australia</atitle><jtitle>Developmental medicine and child neurology</jtitle><addtitle>Dev Med Child Neurol</addtitle><date>2016-02</date><risdate>2016</risdate><volume>58</volume><issue>S2</issue><spage>43</spage><epage>49</epage><pages>43-49</pages><issn>0012-1622</issn><eissn>1469-8749</eissn><abstract>Aim Males typically outnumber females in cerebral palsy (CP) cohorts. To better understand this ‘male disadvantage’ and provide insight into causal pathways to CP, this study used 1983 to 2009 Australian CP and population birth cohorts to identify associations and trends with respect to biological sex and CP. Method Within birth gestation groups, sex ratios were calculated to evaluate any male excess in the CP cohort compared with livebirths, neonatal deaths, neonatal mortality and survival rates, neonatal survivors, and CP rates in survivors. Sex‐ and gestation‐specific trends in neonatal mortality, CP rates, and CP sex ratios were assessed by plotting their annual frequencies and fitting quadratic curves. Results Over‐representation of males in preterm live births partly explained the male excess in the CP cohort after preterm birth, especially at 28 to 31 weeks. Higher CP rates in male neonatal survivors also contributed to the male excess in CP, particularly at &lt;28 and 37+ weeks. Higher neonatal mortality rates in males at all gestations had little impact on the CP sex ratio. There was no clearly discernible change over time in the CP sex ratio. Interpretation Gestation‐specific associations between sex and CP provide insight into causal pathways to CP and suggest sex‐specific differences in response to neuroprotective strategies. What this paper adds The male excess in live births was highest at gestations &lt;37 weeks. The increased risk of CP in males was most pronounced in neonatal survivors of birth at &lt;28 and 37+ weeks' gestation. The CP sex ratio remained relatively stable overall, although there were gestation‐specific trends. The possibility of sex‐specific differences in neuroprotective strategies is supported.</abstract><cop>England</cop><pmid>26762863</pmid><doi>10.1111/dmcn.13021</doi><tpages>7</tpages><oa>free_for_read</oa></addata></record>
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subjects Cerebral Palsy - epidemiology
Cerebral Palsy - etiology
Female
Gestational Age
Humans
Infant, Newborn
Male
Pregnancy
Premature Birth - epidemiology
Risk
Sex Factors
Survival Rate
Victoria - epidemiology
title Biological sex and the risk of cerebral palsy in Victoria, Australia
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