Investigating N-3 Fatty Acids to Prevent Neonatal Tobacco-related outcomeS

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Tobacco use is the most important modifiable risk factor associated with adverse pregnancy outcomes and increases the risk of preterm birth, intrauterine growth restriction and sudden infant death syndrome. Over 11% of women report smoking during pregnancy, with higher rates seen in the Southeastern...

Tobacco use is the most important modifiable risk factor associated with adverse pregnancy outcomes and increases the risk of preterm birth, intrauterine growth restriction and sudden infant death syndrome. Over 11% of women report smoking during pregnancy, with higher rates seen in the Southeastern United States. Fewer than half of pregnant smokers are able to quit on their own during pregnancy. Currently, FDA-approved pharmacological strategies for smoking cessation are generally not used in pregnancy: varenicline and bupropion are unsafe and nicotine replacement therapy has limited data to support its efficacy in pregnant smokers. Identifying safe and effective therapies to prevent tobacco-related pregnancy outcomes and/or increase smoking cessation in pregnant women would have a substantial public health impact. Our group and others have reported that cigarette smoking is associated with a relative deficiency in circulating n-3 long-chain polyunsaturated fatty acid (n-3 LCPUFA) levels. Our overarching hypothesis is that smoking-induced n-3 LCPUFA deficiencies contribute to tobacco-related adverse pregnancy outcomes and that supplementation of n-3 LCPUFAs in pregnant smokers may prevent these complications. Support for this hypothesis comes from a recent secondary analysis of the Omega-3 Fatty Acids Supplementation to Prevent Preterm Birth trial which found that only smokers taking n-3 LCPUFAs had a reduction in preterm labor risk as compared to non-smokers. While compelling, this study was a post hoc analysis that included only a small sample of smokers and did not collect data on smoking behaviors during follow up. Yet the ascertainment of longitudinal smoking behavior is critical, as some clinical studies have found that supplemental n-3 LCPUFAs might also reduce nicotine cravings and lower daily cigarette use. Thus, smokers may doubly benefit from replenishing n-3 LCPUFAs via lower risk of preterm labor and/or increased smoking cessation. We conducted a placebo-controlled pilot RCT of n-3 LCPUFAs in 28 pregnant smokers and found the intervention to be feasible and well-tolerated. Compared to placebo, n-3 LCPUFAs lowered both nicotine dependence at 4 weeks (change from baseline in Fagerström Test for Nicotine Dependence -2.5 vs. 0, p = 0.01) and resulted in a non-statistically significant reduction in cigarettes per day and urine cotinine. To address important remaining knowledge gaps we propose the Investigating N-3 Fatty Acids to prevent Neonatal Tobacco related outcomeS (INFANTS). Our proposal has three Specific Aims. Specific Aim 1: To determine the effect of supplemental n-3 LCPUFAs compared to placebo on gestational age at delivery and preterm labor in pregnant smokers. Specific Aim 2: To determine the effect of supplemental n-3 LCPUFAs compared to placebo on tobacco use in pregnant smokers. Specific Aim 3: To determine if the effect of supplemental n-3 LCPUFAs on preterm labor is mediated by changes in smoking behavior and/or increases in circulating n-3 LCPUFAs. The INFANTS study is a multicenter, randomized, double-blind, placebo controlled study that will randomize 400 pregnant smokers to either supplemental n-3 LCPUFAs or placebo. Participants will be enrolled between 12 and 24 weeks gestation and followed until delivery. We will recruit participants from eight clinical centers in the Middle-Tennessee area. We will assess smoking behavior after 12-weeks of supplementation using self-report and validated biomarkers of tobacco exposure (urine cotinine). We will measure response to supplementation using biological markers of n-3 LCPUFA status (red blood cell phospholipid membrane fatty acid percentages). Our primary endpoint will be preterm labor as reflected by gestational age at delivery, which will be extracted from the medical record. Our secondary endpoint will be change from baseline in cigarettes per day at 12 weeks biochemically confirmed through reduction in urine cotinine. We will conduct mediation analysis to better understand the mechanisms contributing to the effects of supplemental n-3 LCPUFAs on birth outcomes in pregnant smokers. Our study is innovative in that it will be the first clinical trial of n-3 LCPUFAs exclusively recruiting pregnant smokers. This will be the first study to evaluate the impact on n-3 LCPUFAs on tobacco use in smokers who wish to quit, thus identifying a novel strategy to reduce tobacco use that could be relevant for all smokers. n-3 LCPUFAs supplements are well tolerated in pregnancy but currently are not recommended as part of routine prenatal care in smokers. Thus if our study demonstrated that supplemental n-3 LCPUFAs are effective at reducing the risk of tobacco-related adverse neonatal outcomes and/or reducing tobacco use during pregnancy, our results could have an immediate and major clinical impact on pregnancy care and neonatal outcomes in the United States.

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