Fatness at birth predicts adult susceptibility to ovarian suppression: An empirical test of the Predictive Adaptive Response hypothesis
Poor fetal environments are thought to produce adaptive changes in human developmental trajectories according to the Predictive Adaptive Response hypothesis. Although many studies have demonstrated correlations between indicators of fetal environment and negative adult health outcomes, the adaptive...
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Veröffentlicht in: | Proceedings of the National Academy of Sciences - PNAS 2006-08, Vol.103 (34), p.12759-12762 |
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description | Poor fetal environments are thought to produce adaptive changes in human developmental trajectories according to the Predictive Adaptive Response hypothesis. Although many studies have demonstrated correlations between indicators of fetal environment and negative adult health outcomes, the adaptive significance of these outcomes is unclear. Our study explicitly tests the adaptive nature of fetal programming in humans. We show that differences in nutritional status at birth are associated with adaptive differences in the sensitivity of adult ovarian function to energetic stress. Women who were born as relatively fat babies do not exhibit ovarian suppression in response to moderate levels of physical activity at adulthood, in contrast to women who were born as skinnier babies. The levels of estradiol in women born in the highest tertile of ponderal index (an indicator of neonatal nutritional status) were 37% and 46% higher, respectively, than levels of estradiol in women born in the low and middle ponderal index tertiles. These findings suggest that fetal programming of reproductive function results in developmentally plastic, but essentially adaptive, shifts in set points of ovarian response to energetic stress, such that women who were gestated under conditions of energetic constraint show greater sensitivity to energetic stress in adulthood. Our results have practical implications in terms of behavioral strategies for reducing the risk of breast cancer. We suggest that the amount of activity necessary to reduce levels of estrogen, which may in turn reduce cancer risk, can depend on a woman's nutritional status at birth. |
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Although many studies have demonstrated correlations between indicators of fetal environment and negative adult health outcomes, the adaptive significance of these outcomes is unclear. Our study explicitly tests the adaptive nature of fetal programming in humans. We show that differences in nutritional status at birth are associated with adaptive differences in the sensitivity of adult ovarian function to energetic stress. Women who were born as relatively fat babies do not exhibit ovarian suppression in response to moderate levels of physical activity at adulthood, in contrast to women who were born as skinnier babies. The levels of estradiol in women born in the highest tertile of ponderal index (an indicator of neonatal nutritional status) were 37% and 46% higher, respectively, than levels of estradiol in women born in the low and middle ponderal index tertiles. These findings suggest that fetal programming of reproductive function results in developmentally plastic, but essentially adaptive, shifts in set points of ovarian response to energetic stress, such that women who were gestated under conditions of energetic constraint show greater sensitivity to energetic stress in adulthood. Our results have practical implications in terms of behavioral strategies for reducing the risk of breast cancer. We suggest that the amount of activity necessary to reduce levels of estrogen, which may in turn reduce cancer risk, can depend on a woman's nutritional status at birth.</description><identifier>ISSN: 0027-8424</identifier><identifier>EISSN: 1091-6490</identifier><identifier>DOI: 10.1073/pnas.0605488103</identifier><identifier>PMID: 16908839</identifier><language>eng</language><publisher>United States: National Academy of Sciences</publisher><subject>Adaptation, Physiological ; Adult ; Adulthood ; Adults ; Biological Sciences ; Birth weight ; Birth Weight - physiology ; Breast cancer ; Disease Susceptibility ; Empirical Research ; estradiol ; Estradiol - metabolism ; Estrogens ; Exercise ; Female ; Fetal development ; fetal programming ; hormone secretion ; Humans ; maternal nutrition ; Menstrual cycle ; Metabolic equivalent ; Models, Biological ; neonates ; neoplasms ; Nutritional status ; Nutritional Status - physiology ; Ovarian Diseases - physiopathology ; ovarian function ; ovaries ; Overweight - physiology ; Pathology ; physical activity ; Physical fitness ; ponderal index ; Predictive Adaptive Response hypothesis ; Prenatal development ; risk assessment ; Saliva - metabolism ; Social Sciences ; Steroids ; Women</subject><ispartof>Proceedings of the National Academy of Sciences - PNAS, 2006-08, Vol.103 (34), p.12759-12762</ispartof><rights>Copyright 2006 National Academy of Sciences of the United States of America</rights><rights>Copyright National Academy of Sciences Aug 22, 2006</rights><rights>2006 by The National Academy of Sciences of the USA 2006</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c589t-87e819f37b9a0d60de7b22516271fe7edc6ba86501d07262bc7ea22d9643303f3</citedby><cites>FETCH-LOGICAL-c589t-87e819f37b9a0d60de7b22516271fe7edc6ba86501d07262bc7ea22d9643303f3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://www.pnas.org/content/103/34.cover.gif</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/30051082$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/30051082$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,727,780,784,803,885,27922,27923,53789,53791,58015,58248</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/16908839$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jasienska, G</creatorcontrib><creatorcontrib>Thune, I</creatorcontrib><creatorcontrib>Ellison, P.T</creatorcontrib><title>Fatness at birth predicts adult susceptibility to ovarian suppression: An empirical test of the Predictive Adaptive Response hypothesis</title><title>Proceedings of the National Academy of Sciences - PNAS</title><addtitle>Proc Natl Acad Sci U S A</addtitle><description>Poor fetal environments are thought to produce adaptive changes in human developmental trajectories according to the Predictive Adaptive Response hypothesis. Although many studies have demonstrated correlations between indicators of fetal environment and negative adult health outcomes, the adaptive significance of these outcomes is unclear. Our study explicitly tests the adaptive nature of fetal programming in humans. We show that differences in nutritional status at birth are associated with adaptive differences in the sensitivity of adult ovarian function to energetic stress. Women who were born as relatively fat babies do not exhibit ovarian suppression in response to moderate levels of physical activity at adulthood, in contrast to women who were born as skinnier babies. The levels of estradiol in women born in the highest tertile of ponderal index (an indicator of neonatal nutritional status) were 37% and 46% higher, respectively, than levels of estradiol in women born in the low and middle ponderal index tertiles. These findings suggest that fetal programming of reproductive function results in developmentally plastic, but essentially adaptive, shifts in set points of ovarian response to energetic stress, such that women who were gestated under conditions of energetic constraint show greater sensitivity to energetic stress in adulthood. Our results have practical implications in terms of behavioral strategies for reducing the risk of breast cancer. We suggest that the amount of activity necessary to reduce levels of estrogen, which may in turn reduce cancer risk, can depend on a woman's nutritional status at birth.</description><subject>Adaptation, Physiological</subject><subject>Adult</subject><subject>Adulthood</subject><subject>Adults</subject><subject>Biological Sciences</subject><subject>Birth weight</subject><subject>Birth Weight - physiology</subject><subject>Breast cancer</subject><subject>Disease Susceptibility</subject><subject>Empirical Research</subject><subject>estradiol</subject><subject>Estradiol - metabolism</subject><subject>Estrogens</subject><subject>Exercise</subject><subject>Female</subject><subject>Fetal development</subject><subject>fetal programming</subject><subject>hormone secretion</subject><subject>Humans</subject><subject>maternal nutrition</subject><subject>Menstrual cycle</subject><subject>Metabolic equivalent</subject><subject>Models, Biological</subject><subject>neonates</subject><subject>neoplasms</subject><subject>Nutritional status</subject><subject>Nutritional Status - physiology</subject><subject>Ovarian Diseases - physiopathology</subject><subject>ovarian function</subject><subject>ovaries</subject><subject>Overweight - physiology</subject><subject>Pathology</subject><subject>physical activity</subject><subject>Physical fitness</subject><subject>ponderal index</subject><subject>Predictive Adaptive Response hypothesis</subject><subject>Prenatal development</subject><subject>risk assessment</subject><subject>Saliva - metabolism</subject><subject>Social Sciences</subject><subject>Steroids</subject><subject>Women</subject><issn>0027-8424</issn><issn>1091-6490</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2006</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1u1DAUhS0EokNhzQqwWCCxmPbaTvzDAmlUUUCqBAK6tpzE6XiUiVPbGTFPwGvjNKMOsGFly-e7R_f4IPScwBkBwc6H3sQz4FAWUhJgD9CCgCJLXih4iBYAVCxlQYsT9CTGDQCoUsJjdEK4AimZWqBflyb1NkZsEq5cSGs8BNu4OuWXZuwSjmOs7ZBc5TqX9jh57HcmONNnZchsjM737_Cqx3Y7uOBq0-FkY8K-xWlt8dfZzu0sXjVmuLt8s3HwfbR4vR98hqKLT9Gj1nTRPjucp-j68sOPi0_Lqy8fP1-srpZ1KVVaSmElUS0TlTLQcGisqCgtCaeCtFbYpuaVkbwE0oCgnFa1sIbSRvGCMWAtO0XvZ99hrLYZt30KptNDcFsT9tobp_9WerfWN36nScmloiQbvDkYBH875qB66_IPdZ3prR-j5rmIgkiawdf_gBs_hj6H0xRI3qYoRYbOZ6gOPsZg2_tNCOipYT01rI8N54mXfwY48odKM4APwDR5tGOaFZpQUU7I2_8guh27LtmfKbMvZnYTkw_3MAMoCdzFfDXrrfHa3AQX9fX3KSCA4EQSzn4DmqrQtg</recordid><startdate>20060822</startdate><enddate>20060822</enddate><creator>Jasienska, G</creator><creator>Thune, I</creator><creator>Ellison, P.T</creator><general>National Academy of Sciences</general><general>National Acad Sciences</general><scope>FBQ</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>7QG</scope><scope>7QL</scope><scope>7QP</scope><scope>7QR</scope><scope>7SN</scope><scope>7SS</scope><scope>7T5</scope><scope>7TK</scope><scope>7TM</scope><scope>7TO</scope><scope>7U9</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>H94</scope><scope>M7N</scope><scope>P64</scope><scope>RC3</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20060822</creationdate><title>Fatness at birth predicts adult susceptibility to ovarian suppression: An empirical test of the Predictive Adaptive Response hypothesis</title><author>Jasienska, G ; Thune, I ; Ellison, P.T</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c589t-87e819f37b9a0d60de7b22516271fe7edc6ba86501d07262bc7ea22d9643303f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2006</creationdate><topic>Adaptation, Physiological</topic><topic>Adult</topic><topic>Adulthood</topic><topic>Adults</topic><topic>Biological Sciences</topic><topic>Birth weight</topic><topic>Birth Weight - physiology</topic><topic>Breast cancer</topic><topic>Disease Susceptibility</topic><topic>Empirical Research</topic><topic>estradiol</topic><topic>Estradiol - metabolism</topic><topic>Estrogens</topic><topic>Exercise</topic><topic>Female</topic><topic>Fetal development</topic><topic>fetal programming</topic><topic>hormone secretion</topic><topic>Humans</topic><topic>maternal nutrition</topic><topic>Menstrual cycle</topic><topic>Metabolic equivalent</topic><topic>Models, Biological</topic><topic>neonates</topic><topic>neoplasms</topic><topic>Nutritional status</topic><topic>Nutritional Status - physiology</topic><topic>Ovarian Diseases - physiopathology</topic><topic>ovarian function</topic><topic>ovaries</topic><topic>Overweight - physiology</topic><topic>Pathology</topic><topic>physical activity</topic><topic>Physical fitness</topic><topic>ponderal index</topic><topic>Predictive Adaptive Response hypothesis</topic><topic>Prenatal development</topic><topic>risk assessment</topic><topic>Saliva - metabolism</topic><topic>Social Sciences</topic><topic>Steroids</topic><topic>Women</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jasienska, G</creatorcontrib><creatorcontrib>Thune, I</creatorcontrib><creatorcontrib>Ellison, P.T</creatorcontrib><collection>AGRIS</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Animal Behavior Abstracts</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Calcium & Calcified Tissue Abstracts</collection><collection>Chemoreception Abstracts</collection><collection>Ecology Abstracts</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Immunology Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Oncogenes and Growth Factors Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>Genetics Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jasienska, G</au><au>Thune, I</au><au>Ellison, P.T</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fatness at birth predicts adult susceptibility to ovarian suppression: An empirical test of the Predictive Adaptive Response hypothesis</atitle><jtitle>Proceedings of the National Academy of Sciences - PNAS</jtitle><addtitle>Proc Natl Acad Sci U S A</addtitle><date>2006-08-22</date><risdate>2006</risdate><volume>103</volume><issue>34</issue><spage>12759</spage><epage>12762</epage><pages>12759-12762</pages><issn>0027-8424</issn><eissn>1091-6490</eissn><abstract>Poor fetal environments are thought to produce adaptive changes in human developmental trajectories according to the Predictive Adaptive Response hypothesis. Although many studies have demonstrated correlations between indicators of fetal environment and negative adult health outcomes, the adaptive significance of these outcomes is unclear. Our study explicitly tests the adaptive nature of fetal programming in humans. We show that differences in nutritional status at birth are associated with adaptive differences in the sensitivity of adult ovarian function to energetic stress. Women who were born as relatively fat babies do not exhibit ovarian suppression in response to moderate levels of physical activity at adulthood, in contrast to women who were born as skinnier babies. The levels of estradiol in women born in the highest tertile of ponderal index (an indicator of neonatal nutritional status) were 37% and 46% higher, respectively, than levels of estradiol in women born in the low and middle ponderal index tertiles. These findings suggest that fetal programming of reproductive function results in developmentally plastic, but essentially adaptive, shifts in set points of ovarian response to energetic stress, such that women who were gestated under conditions of energetic constraint show greater sensitivity to energetic stress in adulthood. Our results have practical implications in terms of behavioral strategies for reducing the risk of breast cancer. We suggest that the amount of activity necessary to reduce levels of estrogen, which may in turn reduce cancer risk, can depend on a woman's nutritional status at birth.</abstract><cop>United States</cop><pub>National Academy of Sciences</pub><pmid>16908839</pmid><doi>10.1073/pnas.0605488103</doi><tpages>4</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adaptation, Physiological Adult Adulthood Adults Biological Sciences Birth weight Birth Weight - physiology Breast cancer Disease Susceptibility Empirical Research estradiol Estradiol - metabolism Estrogens Exercise Female Fetal development fetal programming hormone secretion Humans maternal nutrition Menstrual cycle Metabolic equivalent Models, Biological neonates neoplasms Nutritional status Nutritional Status - physiology Ovarian Diseases - physiopathology ovarian function ovaries Overweight - physiology Pathology physical activity Physical fitness ponderal index Predictive Adaptive Response hypothesis Prenatal development risk assessment Saliva - metabolism Social Sciences Steroids Women |
title | Fatness at birth predicts adult susceptibility to ovarian suppression: An empirical test of the Predictive Adaptive Response hypothesis |
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