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1.
PLoS One ; 9(10): e106446, 2014.
Article in English | MEDLINE | ID: mdl-25337852

ABSTRACT

OBJECTIVE: To investigate the association between cigarette use during pregnancy and pregnancy-induced hypertension/preeclampsia/eclampsia (PIH) by maternal race/ethnicity and age. METHODS: This retrospective cohort study was based on the U.S. 2010 natality data. Our study sample included U.S. women who delivered singleton pregnancies between 20 and 44 weeks of gestation without major fetal anomalies in 2010 (n = 3,113,164). Multivariate logistic regression models were fit to estimate crude and adjusted odds ratios and the corresponding 95% confidence intervals. RESULTS: We observed that the association between maternal smoking and PIH varied by maternal race/ethnicity and age. Compared with non-smokers, reduced odds of PIH among pregnant smokers was only evident for non-Hispanic white and non-Hispanic American Indian women aged less than 35 years. Non-Hispanic Asian/Pacific Islander women who smoked during pregnancy had increased odds of PIH regardless of maternal age. Non-Hispanic white and non-Hispanic black women 35 years or older who smoked during pregnancy also had increased odds of PIH. CONCLUSION: Our study findings suggest important differences by maternal race/ethnicity and age in the association between cigarette use during pregnancy and PIH. More research is needed to establish the biologic and social mechanisms that might explain the variations with maternal age and race/ethnicity that were observed in our study.


Subject(s)
Eclampsia/genetics , Pre-Eclampsia/genetics , Pregnancy Complications/genetics , Smoking/genetics , Adult , Cohort Studies , Ethnicity , Female , Genetic Association Studies , Humans , Maternal Age , Pre-Eclampsia/pathology , Pregnancy , Risk Factors , Smoking/adverse effects , United States , Young Adult
2.
Breast Cancer Res ; 9(3): R29, 2007.
Article in English | MEDLINE | ID: mdl-17501995

ABSTRACT

INTRODUCTION: Prenatal levels of mitogens may influence the lifetime breast cancer risk by driving stem cell proliferation and increasing the number of target cells, and thereby increasing the chance of mutation events that initiate oncogenesis. We examined in umbilical cord blood the correlation of potential breast epithelial mitogens, including hormones and growth factors, with hematopoietic stem cell concentrations serving as surrogates of overall stem cell potential. METHODS: We analyzed cord blood samples from 289 deliveries. Levels of hormones and growth factors were correlated with concentrations of stem cell and progenitor populations (CD34+ cells, CD34+CD38- cells, CD34+c-kit+ cells, and granulocyte-macrophage colony-forming units). Changes in stem cell concentration associated with each standard deviation change in mitogens and the associated 95% confidence intervals were calculated from multiple regression analysis. RESULTS: Cord blood plasma levels of insulin-like growth factor-1 (IGF-1) were strongly correlated with all the hematopoietic stem and progenitor concentrations examined (one standard-deviation increase in IGF-1 being associated with a 15-19% increase in stem/progenitor concentrations, all P < 0.02). Estriol and insulin-like growth factor binding protein-3 levels were positively and significantly correlated with some of these cell populations. Sex hormone-binding globulin levels were negatively correlated with these stem/progenitor pools. These relationships were stronger in Caucasians and Hispanics and were weaker or not present in Asian-Americans and African-Americans. CONCLUSION: Our data support the concept that in utero mitogens may drive the expansion of stem cell populations. The correlations with IGF-1 and estrogen are noteworthy, as both are crucial for mammary gland development.


Subject(s)
Breast Neoplasms/embryology , Fetal Blood/chemistry , Growth Substances/blood , Hematopoietic Stem Cells/cytology , Hormones/blood , Antigens, CD/analysis , Breast Neoplasms/epidemiology , Cell Division , Erythroid Precursor Cells/cytology , Erythroid Precursor Cells/physiology , Female , Fetal Blood/cytology , Hematopoietic Stem Cells/immunology , Humans , Infant, Newborn , Insulin-Like Growth Factor I/analysis , Pregnancy
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