Improving Organochlorine Biomarker Models for Cancer Research

Multivariate methods were used to predict levels of dichlorodiphenyldichloroethene (DDE) and polychlorinated biphenyl (PCB) concentrations in plasma from characteristics that included age, diet, race, reproductive history, socioeconomic status, and reported body mass index (BMI) at several decades o...

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Veröffentlicht in:Cancer epidemiology, biomarkers & prevention biomarkers & prevention, 2005-09, Vol.14 (9), p.2224-2236
Hauptverfasser: WOLFF, Mary S, BRITTON, Julie A, TEITELBAUM, Susan L, ENG, Sybil, DEYCH, Elena, IRELAND, Karen, ZHISONG LIU, NEUGUT, Alfred I, SANTELLA, Regina M, GAMMON, Marilie D
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container_end_page 2236
container_issue 9
container_start_page 2224
container_title Cancer epidemiology, biomarkers & prevention
container_volume 14
creator WOLFF, Mary S
BRITTON, Julie A
TEITELBAUM, Susan L
ENG, Sybil
DEYCH, Elena
IRELAND, Karen
ZHISONG LIU
NEUGUT, Alfred I
SANTELLA, Regina M
GAMMON, Marilie D
description Multivariate methods were used to predict levels of dichlorodiphenyldichloroethene (DDE) and polychlorinated biphenyl (PCB) concentrations in plasma from characteristics that included age, diet, race, reproductive history, socioeconomic status, and reported body mass index (BMI) at several decades of life before blood collection. Measurements were available for organochlorine compound (organochlorines), cholesterol, and triglycerides in plasma from 1,008 women participants in a population-based case-control study of breast cancer undertaken in 1996 to 1997 on Long Island, NY. Organochlorine compound levels were associated with age, race, lactation history, body size characteristics, and plasma lipids. PCB predictors also included fish consumption. DDE was correlated with current BMI, BMI at every decade of age from ages 20 to 60 years, and BMI-gain (from ages 20 or 30 years to 1997). In contrast, PCBs were correlated inversely with both BMI (fifth to seventh decades of age) and BMI-gain. After adjusting for covariates, DDE and PCB were both positively associated with BMI and inversely with BMI-gain; they were lowest with low BMI, high BMI-gain, and longer lactation. This pattern is consistent with a pharmacokinetic model that predicts higher body burdens during windows of highest uptake, faster elimination of organochlorine compounds in leaner women, and lowered levels accompanying BMI-gain. As a result, lifetime intake for specific organochlorine compound may lead to different plasma levels dependent on changes in body size, absolute intensity of intake, and whether exposure is ongoing (i.e., PCB) or long discontinued (i.e., DDE).
doi_str_mv 10.1158/1055-9965.EPI-05-0173
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Measurements were available for organochlorine compound (organochlorines), cholesterol, and triglycerides in plasma from 1,008 women participants in a population-based case-control study of breast cancer undertaken in 1996 to 1997 on Long Island, NY. Organochlorine compound levels were associated with age, race, lactation history, body size characteristics, and plasma lipids. PCB predictors also included fish consumption. DDE was correlated with current BMI, BMI at every decade of age from ages 20 to 60 years, and BMI-gain (from ages 20 or 30 years to 1997). In contrast, PCBs were correlated inversely with both BMI (fifth to seventh decades of age) and BMI-gain. After adjusting for covariates, DDE and PCB were both positively associated with BMI and inversely with BMI-gain; they were lowest with low BMI, high BMI-gain, and longer lactation. 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Measurements were available for organochlorine compound (organochlorines), cholesterol, and triglycerides in plasma from 1,008 women participants in a population-based case-control study of breast cancer undertaken in 1996 to 1997 on Long Island, NY. Organochlorine compound levels were associated with age, race, lactation history, body size characteristics, and plasma lipids. PCB predictors also included fish consumption. DDE was correlated with current BMI, BMI at every decade of age from ages 20 to 60 years, and BMI-gain (from ages 20 or 30 years to 1997). In contrast, PCBs were correlated inversely with both BMI (fifth to seventh decades of age) and BMI-gain. After adjusting for covariates, DDE and PCB were both positively associated with BMI and inversely with BMI-gain; they were lowest with low BMI, high BMI-gain, and longer lactation. This pattern is consistent with a pharmacokinetic model that predicts higher body burdens during windows of highest uptake, faster elimination of organochlorine compounds in leaner women, and lowered levels accompanying BMI-gain. As a result, lifetime intake for specific organochlorine compound may lead to different plasma levels dependent on changes in body size, absolute intensity of intake, and whether exposure is ongoing (i.e., PCB) or long discontinued (i.e., DDE).</abstract><cop>Philadelphia, PA</cop><pub>American Association for Cancer Research</pub><pmid>16172236</pmid><doi>10.1158/1055-9965.EPI-05-0173</doi><tpages>13</tpages></addata></record>
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subjects Adult
Aged
Biological and medical sciences
Biomarkers - analysis
BMI
Body Mass Index
Breast Neoplasms - epidemiology
Breast Neoplasms - etiology
Case-Control Studies
DDE
Dichlorodiphenyl Dichloroethylene - blood
Diet
Environmental Exposure
Environmental Pollutants - blood
Epidemiology
Female
Humans
Insecticides - blood
Lactation
Medical sciences
Middle Aged
Models, Theoretical
Multivariate Analysis
Neoplasms - epidemiology
Neoplasms - etiology
organochlorines
PCB
pharmacokinetic
Polychlorinated Biphenyls - blood
Risk Assessment
Tumors
windows of exposure
title Improving Organochlorine Biomarker Models for Cancer Research
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