Dietary trans fatty acid intake is associated with increased fetal loss

• Published in: Fertility and sterility Vol. 90; no. 2; pp. 385 - 390
• Main Authors: Morrison, John A., Ph.D, Glueck, Charles J., M.D, Wang, Ping, Ph.D
• Format: Journal Article
• Language: English
• Published: New York, NY Elsevier Inc 01.08.2008; Elsevier Science
• Subjects: Adult; Biological and medical sciences; Dietary Fats - adverse effects; Dietary trans fatty acids (TFAs); Diseases of mother, fetus and pregnancy; Energy Intake; Female; Fetal Death - etiology; Gynecology. Andrology. Obstetrics; Humans; Internal Medicine; Logistic Models; Medical sciences; Middle Aged; Obstetrics and Gynecology; Pregnancy; pregnancy loss; Pregnancy. Fetus. Placenta; Retrospective Studies; Trans Fatty Acids - adverse effects; pregnancy loss; Dietary trans fatty acids (TFAs); pregnancy; Pregnancy disorders; Nutrition; Gynecology; Abortion; Obstetrics; Death in utero; Feeding; Pregnancy loss; Pregnancy; Association; Trans fatty acid; Diet; Female
• ISSN: 0015-0282; 1556-5653
• DOI: 10.1016/j.fertnstert.2007.06.037

Objective To examine whether dietary trans fatty acids (TFAs) were associated with fetal loss (no. of pregnancies − no. of live births). The basis of our inquiry derives from the facts that the PPAR-gamma receptor plays a pivotal role in placental function and that TFAs down-regulate PPAR-gamma gene mRNA expression. Design Retrospective study comparing dietary data on TFAs and total calories from Block 98 quantitative food frequency questionnaire on 104 women with insulin data and reporting one or more pregnancies. Setting Twenty-five- to 30-year follow-up as young adults (age 39.5 ± 4.5 years) of schoolgirls in the Princeton School cardiovascular risk study. Patient(s) Former participants in school-based research program at ages 6–18 years (1973–78), screened as part of follow-up study (1998–2003). Main Outcome Measure(s) Fetal loss. Result(s) By stepwise logistic regression, with fetal loss (≥1 vs. 0) as the dependent variable and total calories, percent calories from TFAs (linear and squared terms), diabetes (yes/no), serum insulin, age, race, body mass index, leisure and work physical activity, and education as explanatory variables, percent calories from TFAs was positively, curvilinearly, independently associated with fetal loss. For each 1-unit increase in the squared term of percent calories from TFAs, the odds of having fetal loss versus no fetal loss increased 1.106 times (odds ratio = 1.106; 95% confidence interval 1.026–1.192). Conclusion(s) Since PPAR-gamma plays a pivotal role in placental biology and is down-regulated by TFAs, TFAs may be a reversible risk factor for fetal loss.