Department of Psychiatry, University of Colorado School of Medicine, Aurora, CO.
Department of Obstetrics and Gynecology, Division of Maternal and Fetal Medicine, University of Colorado School of Medicine, Aurora, CO.
Schizophr Bull. 2021 Jul 8;47(4):896-905. doi: 10.1093/schbul/sbaa171.
Black Americans have increased risk for schizophrenia and other mental illnesses with prenatal origins. Prenatal choline promotes infant brain development and behavioral outcomes, but choline has not been specifically assessed in Black Americans. Pregnant women (N = 183, N = 25 Black Americans) enrolled in a study of prenatal stressors and interactions with prenatal choline. Black American women had lower 16-week gestation plasma choline than Whites. Lower choline was not related to obesity, income, or metabolic genotypes. Pregnant women in rural Uganda have higher choline levels than Black American women. Black Americans' lower choline was associated with higher hair cortisol, indicative of higher stress. Lower maternal choline was associated with offsprings' lower gestational age at birth and with decreased auditory P50 inhibition, a marker of inhibitory neuron development. Behavioral development was assessed on the Infant Behavior Questionnaire-R-SF (IBQ-R) at 3 months. Lower Black American maternal gestational choline was associated with lower infant IBQ-R Orienting/Regulation, indicating decreased attention and relation to caregivers. Additional evidence for developmental effects of choline in Black Americans comes from a randomized clinical trial of gestational phosphatidylcholine supplementation versus placebo that included 15 Black Americans. Phosphatidylcholine increased gestational age at birth and newborn P50 inhibition and decreased Social Withdrawn and Attention problems at 40 months of age in Black Americans' offspring compared to placebo. Inhibitory and behavioral deficits associated with lower prenatal choline in offspring of Black American women indicate potential developmental predispositions to later mental illnesses that might be ameliorated by prenatal choline or phosphatidylcholine supplementation.
美国黑人在胎儿期就有更高的患精神分裂症和其他精神疾病的风险。胎儿期胆碱能促进婴儿的大脑发育和行为结果,但尚未对美国黑人进行胆碱的具体评估。这项研究纳入了 183 名孕妇(25 名美国黑人),以评估胎儿期应激源及其与胎儿期胆碱的相互作用。与白人相比,美国黑人孕妇在 16 周妊娠时的血浆胆碱水平较低。胆碱水平较低与肥胖、收入或代谢基因型无关。乌干达农村地区的孕妇的胆碱水平高于美国黑人孕妇。美国黑人的胆碱水平较低与较高的头发皮质醇水平相关,这表明压力较高。较低的母体胆碱与后代出生时较低的胎龄以及听觉 P50 抑制减少有关,这是抑制性神经元发育的标志。在 3 个月时使用婴儿行为问卷-R-SF(IBQ-R)评估行为发育。美国黑人产妇妊娠胆碱水平较低与婴儿 IBQ-R 定向/调节能力较低相关,表明注意力和与照顾者的关系下降。胆碱对美国黑人发育影响的进一步证据来自一项妊娠期磷脂酰胆碱补充与安慰剂的随机临床试验,该试验包括 15 名美国黑人。与安慰剂相比,磷脂酰胆碱增加了美国黑人后代的胎龄、新生儿 P50 抑制,并减少了 40 个月时的社会退缩和注意力问题。与美国黑人女性后代的胎儿期胆碱较低相关的抑制和行为缺陷表明,他们存在日后患精神疾病的潜在发育倾向,这种倾向可能通过胎儿期胆碱或磷脂酰胆碱的补充得到改善。