首页> 外文期刊>Neurotoxicology and teratology >Development of inhibitory control among prenatally cocaine exposed and non-cocaine exposed youths from late childhood to early adolescence: The effects of gender and risk and subsequent aggressive behavior.
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Development of inhibitory control among prenatally cocaine exposed and non-cocaine exposed youths from late childhood to early adolescence: The effects of gender and risk and subsequent aggressive behavior.

机译:从儿童晚期到青春期,在暴露于可卡因的产前和未暴露可卡因的年轻人中,抑制性控制的发展:性别和风险以及随后的攻击行为的影响。

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摘要

The goal of the present investigation was to characterize the development of inhibitory control, an aspect of executive functions, in a sample of prenatally cocaine exposed (CE; n=165) children compared to an at risk, but prenatally cocaine unexposed (NCE; n=119) sample across time (i.e. 7.5 to 11.5 years of age). Gender and cumulative risk, a combination of postnatal medical (i.e. low birth weight and APGAR scores) and demographic risk, indexed by maternal educational attainment, were examined as predictors of change in inhibitory control across time and aggression was modeled as an outcome when children reached 14 years of age. Multiple group latent growth models indicated that CE children made more errors at 7.5 years of age during a standard Stroop interference task, however, over time CE children had greater age-related improvements, narrowing the initial gap, with NCE children in the ability to inhibit errors. Gender effects at 7.5 years within the NCE group were identified with NCE boys making initially more errors than NCE girls; both NCE and CE girls improved faster across development compared to NCE and CE boys, respectively. Greater cumulative risk was associated with more errors at 7.5 years in the CE and NCE groups. No differences were observed between CE and NCE children on time to complete the Stroop task at 7.5 years. However, NCE children had greater age-related improvements in their time to complete the Stroop interference task relative to their CE counterparts. NCE girls improved the fastest over time relative to NCE boys; a similar trend emerged (p<0.10) with CE girls improving faster over time than CE boys. Although all participants improved across development, higher cumulative risk in both groups was associated with slower age-related improvements (i.e. higher slopes) in the time to complete the Stroop task across development. After accounting for gender and cumulative risk, findings in both groups indicated that those who made more errors at 7.5 years of age and/or who had slower age-related changes (i.e. higher slopes) of time to complete the Stroop task across development were more aggressive as rated by caregivers at 14 years of age. Although qualified by gender and cumulative risk, these findings are consistent with reduced cognitive processing efficiency and executive function difficulties in CE children relative to NCE children. Findings suggest that executive function difficulties in CE children may be subtle as development continues to unfold over time. Furthermore, these findings indicate that development of inhibitory control may be an important mechanism linking prenatal cocaine exposure, gender, and cumulative risk to later adverse outcomes.
机译:本研究的目的是在暴露于可卡因的儿童中(CE; n = 165)与处于危险之中但未暴露于可卡因的儿童(NCE; n)相比,表征抑制控制的发展,这是执行功能的一个方面。 = 119)跨时间(即7.5至11.5岁)的样本。性别和累积风险,结合产后医疗(即低出生体重和APGAR得分)和人口统计学风险(通过母体受教育程度进行评估),作为随时间变化的抑制控制变化的预测指标,而侵略性则被建模为儿童达到14岁。多个小组的潜在生长模型表明,在标准Stroop干预任务中,CE儿童在7.5岁时犯了更多的错误,但是,随着时间的流逝,CE儿童具有与年龄有关的更大改善,缩小了最初的差距,而NCE儿童具有抑制的能力。错误。 NCE组中7.5岁时的性别影响被确定为NCE男孩最初比NCE女孩犯更多错误;与NCE和CE男孩相比,NCE和CE女孩在发展过程中的进步更快。 CE和NCE组在7.5年时,更大的累积风险与更多错误相关。 CE和NCE儿童在按时完成7.5岁的Stroop任务时未观察到差异。但是,相对于与CE相对应的孩子,NCE的孩子在完成Stroop干扰任务上的时间与年龄相关的改善更大。与NCE男孩相比,NCE女孩随着时间的推移进步最快。出现了类似的趋势(p <0.10),CE女生比CE女生随着时间的推移进步更快。尽管所有参与者在整个开发过程中均得到改善,但两组中较高的累积风险与完成与开发相关的Stroop任务的时间相关的与年龄相关的改进变慢(即较高的坡度)。在考虑了性别和累积风险之后,两组的研究结果表明,那些在7.5岁时犯更多错误和/或与年龄相关的变化较慢(例如,较高的斜率)以完成跨开发的Stroop任务的人更多。由14岁的照护者评定为具有侵略性。尽管通过性别和累积风险进行了限定,但这些发现与相对于NCE儿童而言,CE儿童的认知加工效率降低和执行功能困难相一致。研究结果表明,随着年龄的增长,CE儿童的执行功能困难可能会很细微。此外,这些发现表明抑制性控制的发展可能是将产前可卡因暴露,性别和累积风险与以后不良后果联系起来的重要机制。

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