Braithwaite E C, Hill J, Pickles A, Glover V, O'Donnell K, Sharp H
1School of Life Sciences and Education,Staffordshire University,Stoke-on-Trent,UK.
2School of Psychology and Clinical Language Sciences,University of Reading,Reading,UK.
J Dev Orig Health Dis. 2018 Aug;9(4):425-431. doi: 10.1017/S2040174418000181. Epub 2018 Apr 10.
Recent findings highlight that there are prenatal risks for affective disorders that are mediated by glucocorticoid mechanisms, and may be specific to females. There is also evidence of sex differences in prenatal programming mechanisms and developmental psychopathology, whereby effects are in opposite directions in males and females. As birth weight is a risk for affective disorders, we sought to investigate whether maternal prenatal cortisol may have sex-specific effects on fetal growth. Participants were 241 mothers selected from the Wirral Child Health and Development Study (WCHADS) cohort (n=1233) using a psychosocial risk stratifier, so that responses could be weighted back to the general population. Mothers provided saliva samples, which were assayed for cortisol, at home over 2 days at 32 weeks gestation (on waking, 30-min post-waking and during the evening). Measures of infant birth weight (corrected for gestational age) were taken from hospital records. General population estimates of associations between variables were obtained using inverse probability weights. Maternal log of the area under the curve cortisol predicted infant birth weight in a sex-dependent manner (interaction term P=0.029). There was a positive and statistically significant association between prenatal cortisol in males, and a negative association in females that was not statistically significant. A sex interaction in the same direction was evident when using the waking (P=0.015), and 30-min post-waking (P=0.013) cortisol, but not the evening measure. There was no interaction between prenatal cortisol and sex to predict gestational age. Our findings add to an emerging literature that suggests that there may be sex-specific mechanisms that underpin fetal programming.
近期研究结果表明,情感障碍存在由糖皮质激素机制介导的产前风险,且可能具有女性特异性。也有证据显示产前编程机制和发育精神病理学存在性别差异,即男性和女性的影响方向相反。由于出生体重是情感障碍的一个风险因素,我们试图研究母亲产前皮质醇是否对胎儿生长具有性别特异性影响。参与者是从威尔拉尔儿童健康与发展研究(WCHADS)队列(n = 1233)中通过心理社会风险分层选取的241名母亲,以便将结果加权回一般人群。母亲们在妊娠32周时在家中连续2天提供唾液样本,用于检测皮质醇(醒来时、醒来后30分钟和晚上)。婴儿出生体重(根据孕周校正)的测量数据来自医院记录。使用逆概率权重获得变量之间关联的一般人群估计值。母亲皮质醇曲线下面积的对数以性别依赖的方式预测婴儿出生体重(交互项P = 0.029)。男性产前皮质醇与婴儿出生体重呈正相关且具有统计学意义,而女性则呈负相关但无统计学意义。使用醒来时(P = 0.015)和醒来后30分钟(P = 0.013)的皮质醇测量值时,在相同方向上存在性别交互作用,但晚上的测量值不存在。产前皮质醇与性别之间不存在预测孕周的交互作用。我们的研究结果进一步补充了新出现的文献,表明可能存在支撑胎儿编程的性别特异性机制。