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鱼油减少孕期女性吸烟(FORTUNE)可行性试验

The Fish Oil to Reduce Tobacco Use iN Expectant mothers (FORTUNE) feasibility trial.

作者信息

Murff Harvey J, Greevy Robert A, Sternlieb Sarah, Gilliam Karen, King Stephen, Sanghani Reesha, Tindle Hilary A

机构信息

Division of General Internal Medicine and Public Health, Vanderbilt University Medical Center, Nashville, TN (Drs Murff and Sternlieb, Ms Gilliam, Mr King, and Dr Tindle); Geriatric Research, Education, and Clinical Centers, United States Department of Veterans Affairs, VA Tennessee Valley Healthcare System, Nashville, TN (Drs Murff and Tindle); Vanderbilt-Ingram Cancer Center, Vanderbilt University Medical Center, Nashville, TN (Drs Murff and Tindle).

Departments of Biostatistics (Dr Greevy), Vanderbilt University Medical Center, Nashville, TN.

出版信息

Am J Obstet Gynecol MFM. 2022 Nov;4(6):100707. doi: 10.1016/j.ajogmf.2022.100707. Epub 2022 Aug 7.

Abstract

BACKGROUND

Three small clinical trials have suggested that supplementation with n-3 long-chain polyunsaturated fatty acids (eicosapentaenoic acid and docosahexaenoic acid) found in fish oils may reduce nicotine cravings and at higher doses reduce cigarette consumption. Pregnant women who smoke have fewer pharmacologic options to aid them with smoking cessation. Although n-3 long-chain polyunsaturated fatty acid supplementation has been studied in pregnancy, few studies have evaluated doses of ≥4 g per day, and no previous studies have selectively enrolled pregnant women who smoke. High-dose n-3 long-chain polyunsaturated fatty acids may aid cessation but could be poorly tolerated in pregnant women who smoke because of gastrointestinal side effects.

OBJECTIVE

We conducted a feasibility trial to determine the tolerability of high-dose n-3 long-chain polyunsaturated fatty acid supplementation in pregnant women who smoked. We hypothesized that n-3 long-chain polyunsaturated fatty acid doses of 4.2 g a day would be well-tolerated relative to an olive oil placebo. We assessed red blood cell phospholipid membrane concentrations at baseline and end of therapy (4 weeks) and piloted outcomes for a future efficacy trial of n-3 long-chain polyunsaturated fatty acid supplementation for smoking cessation in pregnancy.

STUDY DESIGN

We recruited 28 pregnant women between the gestational ages of 6 and 36 weeks who reported daily cigarette smoking and were motivated to quit to participate in a double-blind placebo-controlled randomized feasibility trial of 4.2 g per day of n-3 long-chain polyunsaturated fatty acid supplementation. Participants reported cigarettes per day, completed the Fagerström Test for Cigarette Dependence, and provided blood, urine, and exhaled CO samples. We used repeated-measures analysis of variance to pilot analyses of changes in cigarettes per day and Fagerström Test for Cigarette Dependence scores.

RESULTS

At baseline, red blood cell membrane eicosapentaenoic acid concentrations were negatively correlated with cigarettes per day (r=-0.44; P=.04). By 4 weeks, circulating n-3 long-chain polyunsaturated fatty acid levels increased by 18% in the n-3 long-chain polyunsaturated fatty acid supplementation arm vs a decrease of 3% in the placebo arm. Occurrence of gastrointestinal side effects such as burping, heartburn, diarrhea, abdominal pain, or nausea did not differ statistically between study arms. At 4 weeks, participants allocated to the n-3 long-chain polyunsaturated fatty acids arm reported a median of 3 cigarettes per day (interquartile range, 1-8) vs 7 cigarettes per day (interquartile range, 1-14) in the placebo arm, which was not statistically significant (P=.99). Participants allocated to the n-3 long-chain polyunsaturated fatty acids arm had a decrease of 1 (interquartile range, 0-1) on the Fagerström Test for Cigarette Dependence score vs 0 (interquartile range, 0-0) for placebo (P=.46).

CONCLUSION

High-dose n-3 long-chain polyunsaturated fatty acids may be tolerated in pregnant women who smoke; however, there was a high level of participant dropout, with more participants allocated to the fish oil arm becoming lost to follow-up. These results will inform the design of a future large-scale randomized controlled trial to test the impact of fish oil supplements on smoking cessation in pregnancy.

摘要

背景

三项小型临床试验表明,补充鱼油中含有的n-3长链多不饱和脂肪酸(二十碳五烯酸和二十二碳六烯酸)可能会减少对尼古丁的渴望,且更高剂量时可减少香烟消费量。吸烟的孕妇在戒烟方面的药物选择较少。虽然已对孕期补充n-3长链多不饱和脂肪酸进行了研究,但很少有研究评估每日剂量≥4克的情况,且之前没有研究专门纳入吸烟的孕妇。高剂量的n-3长链多不饱和脂肪酸可能有助于戒烟,但由于胃肠道副作用,吸烟的孕妇可能耐受性较差。

目的

我们进行了一项可行性试验,以确定高剂量n-3长链多不饱和脂肪酸补充剂在吸烟孕妇中的耐受性。我们假设相对于橄榄油安慰剂,每天4.2克的n-3长链多不饱和脂肪酸剂量耐受性良好。我们在基线和治疗结束时(4周)评估了红细胞磷脂膜浓度,并为未来关于孕期补充n-3长链多不饱和脂肪酸戒烟的疗效试验初步确定了结果。

研究设计

我们招募了28名孕周在6至36周之间、报告每日吸烟且有戒烟意愿的孕妇,参与一项每日补充4.2克n-3长链多不饱和脂肪酸的双盲安慰剂对照随机可行性试验。参与者报告每日吸烟量,完成香烟依赖的Fagerström测试,并提供血液、尿液和呼出的一氧化碳样本。我们使用重复测量方差分析对每日吸烟量和香烟依赖Fagerström测试分数的变化进行初步分析。

结果

在基线时,红细胞膜二十碳五烯酸浓度与每日吸烟量呈负相关(r = -0.44;P = 0.04)。到4周时,n-3长链多不饱和脂肪酸补充组中循环n-3长链多不饱和脂肪酸水平增加了18%,而安慰剂组下降了3%。研究组之间打嗝、烧心、腹泻、腹痛或恶心等胃肠道副作用的发生率在统计学上没有差异。在4周时,分配到n-3长链多不饱和脂肪酸组的参与者报告每日吸烟中位数为3支(四分位间距,1 - 8支),而安慰剂组为7支(四分位间距,1 - 14支),差异无统计学意义(P = 0.99)。分配到n-3长链多不饱和脂肪酸组的参与者在香烟依赖Fagerström测试分数上下降了1分(四分位间距,0 - 1分),而安慰剂组下降了0分(四分位间距,0 - 0分)(P = 0.46)。

结论

高剂量n-3长链多不饱和脂肪酸在吸烟孕妇中可能是可耐受的;然而,参与者脱落率较高,分配到鱼油组的更多参与者失访。这些结果将为未来大规模随机对照试验的设计提供信息,以测试鱼油补充剂对孕期戒烟的影响。

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