PMID- 28301833 OWN - NLM STAT- MEDLINE DCOM- 20180207 LR - 20180514 IS - 1421-9697 (Electronic) IS - 0250-6807 (Linking) VI - 70 IP - 3 DP - 2017 TI - Persistent Environmental Toxicants in Breast Milk and Rapid Infant Growth. PG - 210-216 LID - 10.1159/000463394 [doi] AB - BACKGROUND/AIMS: Many environmental toxicants are passed to infants in utero and through breast milk. Exposure to toxicants during the perinatal period can alter growth patterns, impairing growth or increasing obesity risk. Previous studies have focused on only a few toxicants at a time, which may confound results. We investigated levels of 26 toxicants in breast milk and their associations with rapid infant growth, a risk factor for later obesity. METHODS: We used data from the Norwegian HUMIS study, a multi-center cohort of 2,606 mothers and newborns enrolled between 2002 and 2008. Milk samples collected 1 month after delivery from a subset of 789 women oversampled by overweight were analyzed for toxicants including polychlorinated biphenyls (PCBs), heavy metals, and pesticides. Growth was defined as change in weight-for-age z-score between 0 and 6 months among the HUMIS population, and rapid growth was defined as change in z-score above 0.67. We used a Bayesian variable selection method to determine the exposures that most explained variation in the outcome. Identified toxicants were included in logistic and linear regression models to estimate associations with growth, adjusting for maternal age, smoking, education, pre-pregnancy body mass index (BMI), gestational weight gain, parity, child sex, cumulative breastfeeding, birth weight, gestational age, and preterm status. RESULTS: Of 789 infants, 19.2% displayed rapid growth. The median maternal age was 29.6 years, and the median pre-pregnancy BMI was 24.0 kg/m2, with 45.3% of mothers overweight or obese. Rapid growers were more likely to be firstborn. Hexachlorobenzene, beta-hexachlorocyclohexane (beta-HCH), and PCB-74 were identified in the variable selection method. An interquartile range (IQR) increase in beta-HCH exposure was associated with a lower odds of rapid growth (OR 0.63, 95% CI 0.42-0.94). Newborns exposed to high levels of beta-HCH showed reduced infant growth (beta = -0.03, 95% CI -0.05 to -0.01 for IQR increase in breast milk concentration). No other significant associations were found. CONCLUSIONS: Our results suggest that early life beta-HCH exposure may be linked to slowed growth. Further research is warranted on the potential mechanism behind this association and the longer-term metabolic effects of perinatal beta-HCH exposure. CI - (c) 2017 S. Karger AG, Basel. FAU - Criswell, Rachel AU - Criswell R AD - Department of Environmental Exposure and Epidemiology, Norwegian Institute of Public Health, Oslo, Norway. FAU - Lenters, Virissa AU - Lenters V FAU - Mandal, Siddhartha AU - Mandal S FAU - Stigum, Hein AU - Stigum H FAU - Iszatt, Nina AU - Iszatt N FAU - Eggesbo, Merete AU - Eggesbo M LA - eng PT - Journal Article PT - Multicenter Study PT - Research Support, Non-U.S. Gov't DEP - 20170317 PL - Switzerland TA - Ann Nutr Metab JT - Annals of nutrition & metabolism JID - 8105511 RN - 0 (Metals, Heavy) RN - 0 (Pesticides) RN - DFC2HB4I0K (Polychlorinated Biphenyls) SB - IM MH - Adult MH - Bayes Theorem MH - Birth Weight MH - Body Mass Index MH - Body Weight/*physiology MH - Cohort Studies MH - Female MH - Gestational Age MH - Growth/*physiology MH - Humans MH - Infant MH - Infant, Newborn MH - Logistic Models MH - Male MH - Maternal Age MH - Maternal Exposure/*adverse effects MH - Metals, Heavy/analysis/toxicity MH - Milk, Human/*chemistry MH - Norway MH - Obesity/physiopathology MH - Pesticides/analysis/toxicity MH - Polychlorinated Biphenyls/analysis/toxicity MH - Pregnancy MH - Pregnancy Complications/physiopathology MH - Prenatal Exposure Delayed Effects/chemically induced/*physiopathology OTO - NOTNLM OT - Breast milk OT - Environmental toxicants OT - Infant growth OT - Obesity OT - beta-Hexachlorocyclohexane EDAT- 2017/03/17 06:00 MHDA- 2018/02/08 06:00 CRDT- 2017/03/17 06:00 PHST- 2016/12/02 00:00 [received] PHST- 2017/02/13 00:00 [accepted] PHST- 2017/03/17 06:00 [pubmed] PHST- 2018/02/08 06:00 [medline] PHST- 2017/03/17 06:00 [entrez] AID - 000463394 [pii] AID - 10.1159/000463394 [doi] PST - ppublish SO - Ann Nutr Metab. 2017;70(3):210-216. doi: 10.1159/000463394. Epub 2017 Mar 17.