与美国胎儿酒精谱系障碍连续诊断相关的母亲和父亲风险因素:近端和远端影响。

IF 3 Q2 SUBSTANCE ABUSE
Philip A. May, Julie M. Hasken, Julie M. Stegall, Heather A. Mastro, Amy Baete, Jaymi Russo, Rosemary Bozeman, Mary Kay Burns, Jo-Viviane Jones, Wendy O. Kalberg, David Buckley, Omar Abdul-Rahman, Margaret P. Adam, Tamison Jewett, Luther K. Robinson, Melanie A. Manning, H. Eugene Hoyme
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引用次数: 0

摘要

背景:我们试图确定美国胎儿酒精谱系障碍(FASD)的危险因素。方法:对三个地区参与FASD流行病学合作(CoFASP)的一年级儿童的母亲进行访谈。母亲和父亲的数据由诊断为FASD的儿童的母亲和对照组报告。结果:对患有FASD儿童的母亲(n = 114)和对照组(n = 753)进行了访谈。57%的对照组母亲在怀孕前通常每个饮酒日喝2.7杯(DDD),每月一次,79%患有FASD的孩子的母亲报告每周喝4.2杯1-2次。据报道,患有酒精相关神经发育障碍儿童的母亲总体上饮酒最多:酗酒、饮酒频率、每个孕期饮酒和其他药物使用。患有胎儿酒精综合征(FAS)和部分FAS (PFAS)儿童的母亲少报了消费量。远端产妇的危险因素为肝脏问题、抑郁、妊娠认知和首次产前检查、较低的结婚频率和较低的灵性。产后危险指标为低出生体重和胎龄。回归分析显示,孕前三次DDD报告与FASD连续诊断相关(p 2 = 61.09),妊娠后期识别(p = 0.032, χ2 = 4.58),产前随访(p = 0.036, χ2 = 4.38),终生抑郁(p = 0.002, χ2 = 9.47)是FASD的显著预测因子。最后的10步模型解释了27.4%的FASD风险方差。结论:虽然确定了多个显著的母亲FASD危险因素,但父亲饮酒不是具有统计学意义的独立危险因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Maternal and paternal risk factors associated with diagnoses within the continuum of fetal alcohol spectrum disorders in the USA: Proximal and distal influences

Maternal and paternal risk factors associated with diagnoses within the continuum of fetal alcohol spectrum disorders in the USA: Proximal and distal influences

Background

We sought to determine risk factors for fetal alcohol spectrum disorders (FASD) in the United States.

Method

Mothers of first-grade children participating in the Collaboration on FASD Prevalence (CoFASP) in three regional sites were interviewed. Maternal and paternal data were reported by mothers of children with an FASD diagnosis and controls.

Results

Interviews were conducted with mothers of children with an FASD (n = 114) and controls (n = 753). Fifty-seven percent of control mothers usually drank 2.7 drinks per drinking day (DDD) once per month prior to pregnancy, and 79% of mothers of children with FASD reported drinking 4.2 drinks 1–2 times per week. Mothers of children with alcohol-related neurodevelopmental disorder reported the most alcohol consumption overall: bingeing, drinking frequency, drinking in each trimester, and other drug use. Mothers of children with fetal alcohol syndrome (FAS) and partial FAS (PFAS) underreported consumption. Distal maternal risk factors were liver problems, depression, later pregnancy recognition and first prenatal visit, lower frequency of marriage, and lower spirituality. Postnatal risk indicators were low birthweight and gestational age. Regression analysis indicated that maternal reports of three DDD before pregnancy were associated with a diagnosis within the FASD continuum (p < 0.001, OR = 9.92). First-trimester exposure (p < 0.001, OR = 7.64) and all three trimesters (p < 0.001, OR = 7.77) were associated with a child's FASD diagnosis. An independent association was found between paternal DDD during pregnancy and FASD diagnoses (p = 0.002, OR = 1.08); but, once maternal drinking was a covariate, paternal influence was not significant. Stepwise models indicated that combined maternal alcohol use measures (p < 0.001, χ2 = 61.09), later pregnancy recognition (p = 0.032, χ2 = 4.58), later prenatal visits (p = 0.036, χ2 = 4.38), and depression in lifetime (p = 0.002, χ2 = 9.47) were significant FASD predictors. The final 10-step model explained 27.4% of the variance in FASD risk.

Conclusion

While multiple, significant maternal risk factors for FASD were identified, paternal drinking was not a statistically significant, independent risk factor.

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