Keenan Kate, Hipwell Alison, McAloon Rose, Hoffmann Amy, Mohanty Arpita, Magee Kelsey
University of Chicago, Department of Psychiatry and Behavioral Neuroscience, University of Chicago, 5841 South Maryland Avenue, Chicago IL, 60637, USA.
University of Pittsburgh, Western Psychiatric Institute and Clinic, 3811 O'Hara Street, Pittsburgh, PA, 15213, USA.
Psychoneuroendocrinology. 2016 Sep;71:170-5. doi: 10.1016/j.psyneuen.2016.05.023. Epub 2016 May 25.
African American women living in urban, low-income environments are at high risk for poor nutrition during pregnancy and birth complications.
To test the effectiveness of prenatal docosahexaenoic acid (DHA) supplementation on birth outcomes and infant development in a sample of African American women with Medicaid insurance and living in the city of Pittsburgh.
The Nutrition and Pregnancy Study (NAPS) is a double-blind, randomized controlled trial of prenatal DHA supplementation conducted between 2012 and 2014.
Participants were recruited from obstetric clinics at the University of Pittsburgh Medical Center.
Sixty-four pregnant, African American women were enrolled at 16-21 weeks of gestation and randomized to either 450mg/day of DHA (22:6n-3)(n=43) or a soybean placebo (n=21). Four women (6.3%) withdrew from the study: two participants from each study arm; complete data were obtained for 49 infants (76.5%) at the 3-month assessment.
Supplementation with DHA or placebo continued from the beginning of enrollment through delivery.
Data on birth outcomes were collected from medical records. At approximately 3 months post-partum, mothers brought their infants to the laboratory where the Bayley Scales of Infant Development (BSID-III) were administered and cortisol response to the Face-to-Face Still-Face (FFSF) paradigm was assessed.
Infants of mothers who received DHA supplementation had higher birth weight (3.174g versus 2.890g) than infants of mothers receiving placebo (F [2.40]=6.09, p=0.018, eta=0.36), and were more likely to have a 1-min Apgar score greater than 8 (OR=5.99 [95% CI=1.25-28.75], p=0.025). Infants of mothers who received DHA compared with infants of mothers receiving placebo had lower levels of cortisol in response to the FFSF paradigm (F [1.32]=5.36, p=0.018, eta=0.36). None of the scores on the BSID-III differed as a function of active supplement versus placebo.
Infants of women living in urban, low-income environments who received DHA supplementation had more optimal birth outcomes and more modulated cortisol response to a stressor. DHA supplementation may be effective in attenuating the negative effects of prenatal stress on offspring development.
生活在城市低收入环境中的非裔美国女性在孕期面临营养不良及分娩并发症的高风险。
在有医疗补助保险且居住在匹兹堡市的非裔美国女性样本中,测试产前补充二十二碳六烯酸(DHA)对分娩结局及婴儿发育的有效性。
营养与妊娠研究(NAPS)是一项在2012年至2014年期间进行的关于产前补充DHA的双盲随机对照试验。
参与者从匹兹堡大学医学中心的产科诊所招募。
64名怀孕的非裔美国女性在妊娠16 - 21周时入组,并随机分为两组,一组每天补充450毫克DHA(22:6n - 3)(n = 43),另一组服用大豆安慰剂(n = 21)。4名女性(6.3%)退出研究:每组各两名参与者;在3个月评估时,为49名婴儿(76.5%)获取了完整数据。
从入组开始至分娩持续补充DHA或安慰剂。
从医疗记录中收集分娩结局数据。产后约3个月,母亲们带婴儿到实验室,进行贝利婴儿发育量表(BSID - III)测试,并评估婴儿对面对面静止脸(FFSF)范式的皮质醇反应。
接受DHA补充剂的母亲所生婴儿的出生体重高于接受安慰剂的母亲所生婴儿(3174克对2890克)(F[2.40]=6.09,p = 0.018,eta = 0.36),且1分钟阿氏评分大于8分的可能性更大(OR = 5.99[95%CI = 1.25 - 28.75],p = 0.025)。与接受安慰剂的母亲所生婴儿相比,接受DHA补充剂的母亲所生婴儿在FFSF范式下的皮质醇水平更低(F[1.32]=5.36,p = 0.018,eta = 0.36)。BSID - III的各项评分在活性补充剂组与安慰剂组之间没有差异。
生活在城市低收入环境中的女性,其婴儿在接受DHA补充剂后,分娩结局更佳,对应激源的皮质醇反应调节更好。补充DHA可能有效减轻产前应激对后代发育的负面影响。