Waisman Center, University of Wisconsin-Madison, Madison, WI, USA.
Wisconsin Institute for Discovery, University of Wisconsin-Madison, Madison, WI, USA.
Sci Rep. 2017 Jun 1;7(1):2674. doi: 10.1038/s41598-017-02682-4.
Millions of people globally are at high risk for neurodegenerative disorders, infertility or having children with a disability as a result of the Fragile X (FX) premutation, a genetic abnormality in FMR1 that is underdiagnosed. Despite the high prevalence of the FX premutation and its effect on public health and family planning, most FX premutation carriers are unaware of their condition. Since genetic testing for the premutation is resource intensive, it is not practical to screen individuals for FX premutation status using genetic testing. In a novel approach to phenotyping, we have utilized audio recordings and cognitive profiling assessed via self-administered questionnaires on 200 females. Machine-learning methods were developed to discriminate FX premutation carriers from mothers of children with autism spectrum disorders, the comparison group. By using a random forest classifier, FX premutation carriers could be identified in an automated fashion with high precision and recall (0.81 F1 score). Linguistic and cognitive phenotypes that were highly associated with FX premutation carriers were high language dysfluency, poor ability to organize material, and low self-monitoring. Our framework sets the foundation for computational phenotyping strategies to pre-screen large populations for this genetic variant with nominal costs.
全球数百万人面临神经退行性疾病、不孕或生育残疾儿童的风险,这是由于脆性 X (FX)前突变引起的,这是 FMR1 中的一种遗传异常,目前诊断不足。尽管 FX 前突变的患病率很高,且对公共卫生和计划生育有影响,但大多数 FX 前突变携带者并不知道自己的病情。由于前突变的基因检测需要大量资源,因此通过基因检测对 FX 前突变状态进行筛查是不切实际的。在一种新的表型方法中,我们利用音频记录和通过自我管理问卷评估的认知概况,对 200 名女性进行了研究。开发了机器学习方法来区分 FX 前突变携带者和自闭症谱系障碍儿童的母亲,即对照组。通过使用随机森林分类器,可以以自动化的方式高精度和高召回率(0.81 F1 得分)识别 FX 前突变携带者。与 FX 前突变携带者高度相关的语言和认知表型包括语言不流畅、组织材料能力差和自我监控能力低。我们的框架为计算表型策略奠定了基础,这些策略可以用名义成本对大量人群进行这种遗传变异的预筛查。