Disrupted Prenatal Maternal Cortisol, Maternal Obesity, and Childhood Wheeze: Insights into Prenatal Programming
Exploring prenatal factors influencing childhood wheeze may inform programming mechanisms. We examined associations among prenatal maternal cortisol profiles, maternal obesity, and repeated wheeze up to age 2 years (n = 261). Salivary cortisol was collected five times per day over 3 days at 29.0 ± 4...
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description | Exploring prenatal factors influencing childhood wheeze may inform programming mechanisms.
We examined associations among prenatal maternal cortisol profiles, maternal obesity, and repeated wheeze up to age 2 years (n = 261).
Salivary cortisol was collected five times per day over 3 days at 29.0 ± 4.9 weeks gestation. Mothers were categorized as obese (body mass index ≥ 30 kg/m(2)) versus nonobese (body mass index < 30 kg/m(2)). Using logistic regression, we examined the influence of log-transformed cortisol metrics (level at each time point, morning rise, diurnal and afternoon slopes) and obesity on wheeze adjusting for covariates. Linear mixed models were implemented to examine associations between cortisol trajectories and wheezing. Interactions between maternal cortisol and obesity were considered.
Mothers were primarily minority (56.5% Hispanic, 24.1% African American), 61% had less than or equal to 12 years of education, 34% were obese, and 8.4% of children had repeated wheeze. An interquartile range increase in mean log cortisol at bedtime (odds ratio, 2.2; 95% confidence interval, 1.09-4.09) and maternal obesity (odds ratio, 3.43; 95% confidence interval, 1.26-9.35) were independently associated with wheeze. Linear mixed models revealed an association between a flatter afternoon slope (slower decline in log cortisol per hour) and repeated wheeze in children of obese mothers (children with [-0.017 change] and without [-0.061 change] wheeze [P = 0.009 for time × wheeze interaction]), but not in children of nonobese mothers (with [-0.050 change] and without [-0.061 change] wheeze [P = 0.51]).
Maternal prenatal cortisol disruption and obesity were independently associated with children's wheeze. Obese women with adverse cortisol profiles were most likely to have children with repeated wheeze. |
doi_str_mv | 10.1164/rccm.201208-1530OC |
format | Article |
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We examined associations among prenatal maternal cortisol profiles, maternal obesity, and repeated wheeze up to age 2 years (n = 261).
Salivary cortisol was collected five times per day over 3 days at 29.0 ± 4.9 weeks gestation. Mothers were categorized as obese (body mass index ≥ 30 kg/m(2)) versus nonobese (body mass index < 30 kg/m(2)). Using logistic regression, we examined the influence of log-transformed cortisol metrics (level at each time point, morning rise, diurnal and afternoon slopes) and obesity on wheeze adjusting for covariates. Linear mixed models were implemented to examine associations between cortisol trajectories and wheezing. Interactions between maternal cortisol and obesity were considered.
Mothers were primarily minority (56.5% Hispanic, 24.1% African American), 61% had less than or equal to 12 years of education, 34% were obese, and 8.4% of children had repeated wheeze. An interquartile range increase in mean log cortisol at bedtime (odds ratio, 2.2; 95% confidence interval, 1.09-4.09) and maternal obesity (odds ratio, 3.43; 95% confidence interval, 1.26-9.35) were independently associated with wheeze. Linear mixed models revealed an association between a flatter afternoon slope (slower decline in log cortisol per hour) and repeated wheeze in children of obese mothers (children with [-0.017 change] and without [-0.061 change] wheeze [P = 0.009 for time × wheeze interaction]), but not in children of nonobese mothers (with [-0.050 change] and without [-0.061 change] wheeze [P = 0.51]).
Maternal prenatal cortisol disruption and obesity were independently associated with children's wheeze. Obese women with adverse cortisol profiles were most likely to have children with repeated wheeze.</description><identifier>ISSN: 1073-449X</identifier><identifier>EISSN: 1535-4970</identifier><identifier>DOI: 10.1164/rccm.201208-1530OC</identifier><identifier>PMID: 23590260</identifier><language>eng</language><publisher>New York, NY: American Thoracic Society</publisher><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy ; Asthma ; Biological and medical sciences ; Body Mass Index ; Children & youth ; Childrens health ; Chronic obstructive pulmonary disease, asthma ; Confidence intervals ; Female ; Hormones ; Humans ; Hydrocortisone - biosynthesis ; Incidence ; Influence ; Intensive care medicine ; Maternal Exposure - adverse effects ; Medical sciences ; Metabolic diseases ; Obesity ; Obesity - complications ; Obesity - epidemiology ; Obesity - metabolism ; Pneumology ; Pregnancy ; Prenatal Care - methods ; Prenatal Exposure Delayed Effects - epidemiology ; Prenatal Exposure Delayed Effects - etiology ; Prenatal Exposure Delayed Effects - metabolism ; Prospective Studies ; Respiratory Sounds - etiology ; Risk Factors ; Saliva - chemistry ; United States - epidemiology ; Womens health</subject><ispartof>American journal of respiratory and critical care medicine, 2013-06, Vol.187 (11), p.1186-1193</ispartof><rights>2014 INIST-CNRS</rights><rights>Copyright American Thoracic Society Jun 1, 2013</rights><rights>Copyright © 2013 by the American Thoracic Society 2013</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c460t-6469dfa848c80239db98cebf7ca595a99d81fb0afab324b9025fb0aa0b8924733</citedby><cites>FETCH-LOGICAL-c460t-6469dfa848c80239db98cebf7ca595a99d81fb0afab324b9025fb0aa0b8924733</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,4011,27901,27902</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=27476680$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23590260$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>WRIGHT, Rosalind J</creatorcontrib><creatorcontrib>FISHER, Kate</creatorcontrib><creatorcontrib>CHIU, Yueh-Hsiu Mathilda</creatorcontrib><creatorcontrib>WRIGHT, Robert O</creatorcontrib><creatorcontrib>FEIN, Rebecca</creatorcontrib><creatorcontrib>COHEN, Sheldon</creatorcontrib><creatorcontrib>COULL, Brent A</creatorcontrib><title>Disrupted Prenatal Maternal Cortisol, Maternal Obesity, and Childhood Wheeze: Insights into Prenatal Programming</title><title>American journal of respiratory and critical care medicine</title><addtitle>Am J Respir Crit Care Med</addtitle><description>Exploring prenatal factors influencing childhood wheeze may inform programming mechanisms.
We examined associations among prenatal maternal cortisol profiles, maternal obesity, and repeated wheeze up to age 2 years (n = 261).
Salivary cortisol was collected five times per day over 3 days at 29.0 ± 4.9 weeks gestation. Mothers were categorized as obese (body mass index ≥ 30 kg/m(2)) versus nonobese (body mass index < 30 kg/m(2)). Using logistic regression, we examined the influence of log-transformed cortisol metrics (level at each time point, morning rise, diurnal and afternoon slopes) and obesity on wheeze adjusting for covariates. Linear mixed models were implemented to examine associations between cortisol trajectories and wheezing. Interactions between maternal cortisol and obesity were considered.
Mothers were primarily minority (56.5% Hispanic, 24.1% African American), 61% had less than or equal to 12 years of education, 34% were obese, and 8.4% of children had repeated wheeze. An interquartile range increase in mean log cortisol at bedtime (odds ratio, 2.2; 95% confidence interval, 1.09-4.09) and maternal obesity (odds ratio, 3.43; 95% confidence interval, 1.26-9.35) were independently associated with wheeze. Linear mixed models revealed an association between a flatter afternoon slope (slower decline in log cortisol per hour) and repeated wheeze in children of obese mothers (children with [-0.017 change] and without [-0.061 change] wheeze [P = 0.009 for time × wheeze interaction]), but not in children of nonobese mothers (with [-0.050 change] and without [-0.061 change] wheeze [P = 0.51]).
Maternal prenatal cortisol disruption and obesity were independently associated with children's wheeze. Obese women with adverse cortisol profiles were most likely to have children with repeated wheeze.</description><subject>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</subject><subject>Asthma</subject><subject>Biological and medical sciences</subject><subject>Body Mass Index</subject><subject>Children & youth</subject><subject>Childrens health</subject><subject>Chronic obstructive pulmonary disease, asthma</subject><subject>Confidence intervals</subject><subject>Female</subject><subject>Hormones</subject><subject>Humans</subject><subject>Hydrocortisone - biosynthesis</subject><subject>Incidence</subject><subject>Influence</subject><subject>Intensive care medicine</subject><subject>Maternal Exposure - adverse effects</subject><subject>Medical sciences</subject><subject>Metabolic diseases</subject><subject>Obesity</subject><subject>Obesity - complications</subject><subject>Obesity - epidemiology</subject><subject>Obesity - metabolism</subject><subject>Pneumology</subject><subject>Pregnancy</subject><subject>Prenatal Care - methods</subject><subject>Prenatal Exposure Delayed Effects - epidemiology</subject><subject>Prenatal Exposure Delayed Effects - etiology</subject><subject>Prenatal Exposure Delayed Effects - metabolism</subject><subject>Prospective Studies</subject><subject>Respiratory Sounds - etiology</subject><subject>Risk Factors</subject><subject>Saliva - chemistry</subject><subject>United States - epidemiology</subject><subject>Womens health</subject><issn>1073-449X</issn><issn>1535-4970</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>BENPR</sourceid><recordid>eNpVkUtv1DAUhS0Eog_4AyxQJMSuaf1KYrNAQoGWSkXTBQh21o3jTFwl9mB7kNpfj6MZOnTl4-vvnmv7IPSG4HNCan4RtJ7PKSYUi5JUDK_aZ-g4i6rkssHPs8YNKzmXv47QSYx3OKOC4JfoiLJKYlrjY7T5bGPYbpLpi9tgHCSYim-QTHBZtD4kG_10diitOhNtuj8rwPVFO9qpH73vi5-jMQ_mQ3Htol2PKRbWJX9wvA1-HWCerVu_Qi8GmKJ5vV9P0Y_LL9_br-XN6uq6_XRTal7jVNa8lv0AggstMGWy76TQphsaDZWsQMpekKHDMEDHKO_ya6plC7gTkvKGsVP0cee72Xaz6bVxKcCkNsHOEO6VB6uenjg7qrX_ozgneZ7MBu_2BsH_3pqY1J3fLn8QFeFMCtrUZKHojtLBxxjM8DiBYLWkpJaU1C4ltUspN739_26PLf9iycD7PQBRwzQEcNrGA9fwpq4FZn8BSO2eEw</recordid><startdate>20130601</startdate><enddate>20130601</enddate><creator>WRIGHT, Rosalind J</creator><creator>FISHER, Kate</creator><creator>CHIU, Yueh-Hsiu Mathilda</creator><creator>WRIGHT, Robert O</creator><creator>FEIN, Rebecca</creator><creator>COHEN, Sheldon</creator><creator>COULL, Brent A</creator><general>American Thoracic Society</general><scope>IQODW</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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AN0</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>5PM</scope></search><sort><creationdate>20130601</creationdate><title>Disrupted Prenatal Maternal Cortisol, Maternal Obesity, and Childhood Wheeze: Insights into Prenatal Programming</title><author>WRIGHT, Rosalind J ; FISHER, Kate ; CHIU, Yueh-Hsiu Mathilda ; WRIGHT, Robert O ; FEIN, Rebecca ; COHEN, Sheldon ; COULL, Brent A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c460t-6469dfa848c80239db98cebf7ca595a99d81fb0afab324b9025fb0aa0b8924733</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy</topic><topic>Asthma</topic><topic>Biological and medical sciences</topic><topic>Body Mass Index</topic><topic>Children & youth</topic><topic>Childrens health</topic><topic>Chronic obstructive pulmonary disease, asthma</topic><topic>Confidence intervals</topic><topic>Female</topic><topic>Hormones</topic><topic>Humans</topic><topic>Hydrocortisone - biosynthesis</topic><topic>Incidence</topic><topic>Influence</topic><topic>Intensive care medicine</topic><topic>Maternal Exposure - adverse effects</topic><topic>Medical sciences</topic><topic>Metabolic diseases</topic><topic>Obesity</topic><topic>Obesity - complications</topic><topic>Obesity - epidemiology</topic><topic>Obesity - metabolism</topic><topic>Pneumology</topic><topic>Pregnancy</topic><topic>Prenatal Care - methods</topic><topic>Prenatal Exposure Delayed Effects - epidemiology</topic><topic>Prenatal Exposure Delayed Effects - etiology</topic><topic>Prenatal Exposure Delayed Effects - metabolism</topic><topic>Prospective Studies</topic><topic>Respiratory Sounds - etiology</topic><topic>Risk Factors</topic><topic>Saliva - chemistry</topic><topic>United States - epidemiology</topic><topic>Womens health</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>WRIGHT, Rosalind J</creatorcontrib><creatorcontrib>FISHER, Kate</creatorcontrib><creatorcontrib>CHIU, Yueh-Hsiu Mathilda</creatorcontrib><creatorcontrib>WRIGHT, Robert O</creatorcontrib><creatorcontrib>FEIN, Rebecca</creatorcontrib><creatorcontrib>COHEN, Sheldon</creatorcontrib><creatorcontrib>COULL, Brent A</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>British Nursing Database</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of respiratory and critical care medicine</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>WRIGHT, Rosalind J</au><au>FISHER, Kate</au><au>CHIU, Yueh-Hsiu Mathilda</au><au>WRIGHT, Robert O</au><au>FEIN, Rebecca</au><au>COHEN, Sheldon</au><au>COULL, Brent A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Disrupted Prenatal Maternal Cortisol, Maternal Obesity, and Childhood Wheeze: Insights into Prenatal Programming</atitle><jtitle>American journal of respiratory and critical care medicine</jtitle><addtitle>Am J Respir Crit Care Med</addtitle><date>2013-06-01</date><risdate>2013</risdate><volume>187</volume><issue>11</issue><spage>1186</spage><epage>1193</epage><pages>1186-1193</pages><issn>1073-449X</issn><eissn>1535-4970</eissn><abstract>Exploring prenatal factors influencing childhood wheeze may inform programming mechanisms.
We examined associations among prenatal maternal cortisol profiles, maternal obesity, and repeated wheeze up to age 2 years (n = 261).
Salivary cortisol was collected five times per day over 3 days at 29.0 ± 4.9 weeks gestation. Mothers were categorized as obese (body mass index ≥ 30 kg/m(2)) versus nonobese (body mass index < 30 kg/m(2)). Using logistic regression, we examined the influence of log-transformed cortisol metrics (level at each time point, morning rise, diurnal and afternoon slopes) and obesity on wheeze adjusting for covariates. Linear mixed models were implemented to examine associations between cortisol trajectories and wheezing. Interactions between maternal cortisol and obesity were considered.
Mothers were primarily minority (56.5% Hispanic, 24.1% African American), 61% had less than or equal to 12 years of education, 34% were obese, and 8.4% of children had repeated wheeze. An interquartile range increase in mean log cortisol at bedtime (odds ratio, 2.2; 95% confidence interval, 1.09-4.09) and maternal obesity (odds ratio, 3.43; 95% confidence interval, 1.26-9.35) were independently associated with wheeze. Linear mixed models revealed an association between a flatter afternoon slope (slower decline in log cortisol per hour) and repeated wheeze in children of obese mothers (children with [-0.017 change] and without [-0.061 change] wheeze [P = 0.009 for time × wheeze interaction]), but not in children of nonobese mothers (with [-0.050 change] and without [-0.061 change] wheeze [P = 0.51]).
Maternal prenatal cortisol disruption and obesity were independently associated with children's wheeze. Obese women with adverse cortisol profiles were most likely to have children with repeated wheeze.</abstract><cop>New York, NY</cop><pub>American Thoracic Society</pub><pmid>23590260</pmid><doi>10.1164/rccm.201208-1530OC</doi><tpages>8</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Anesthesia. Intensive care medicine. Transfusions. Cell therapy and gene therapy Asthma Biological and medical sciences Body Mass Index Children & youth Childrens health Chronic obstructive pulmonary disease, asthma Confidence intervals Female Hormones Humans Hydrocortisone - biosynthesis Incidence Influence Intensive care medicine Maternal Exposure - adverse effects Medical sciences Metabolic diseases Obesity Obesity - complications Obesity - epidemiology Obesity - metabolism Pneumology Pregnancy Prenatal Care - methods Prenatal Exposure Delayed Effects - epidemiology Prenatal Exposure Delayed Effects - etiology Prenatal Exposure Delayed Effects - metabolism Prospective Studies Respiratory Sounds - etiology Risk Factors Saliva - chemistry United States - epidemiology Womens health |
title | Disrupted Prenatal Maternal Cortisol, Maternal Obesity, and Childhood Wheeze: Insights into Prenatal Programming |
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