Lana Vasung, Junshen Xu, Esra Abaci-Turk, Cindy Zhou, Elizabeth Holland, William H Barth, Carol Barnewolt, Susan Connolly, Judy Estroff, Polina Golland, Henry A Feldman, Elfar Adalsteinsson, P Ellen Grant
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Pregnant women were scanned for 5-10 min while breathing room air (21% O2) and for 5-10 min while breathing 100% FiO2 in supine and/or lateral position. BOLD acquisition time was 20 min in total with effective temporal resolution approximately 3 s. To quantify upper and lower limb kinematics, we used a 3D convolutional neural network previously trained to track fetal key points (wrists, elbows, shoulders, ankles, knees, hips) on similar BOLD time series. Tracking was visually assessed, errors were manually corrected, and the absolute movement time (AMT) for each joint was calculated. To identify variables that had a significant association with AMT, we constructed a mixed-model ANOVA with interaction terms. Fetuses showed significantly longer duration of limb movements during maternal hyperoxia. We also found a significant centrifugal increase of AMT across limbs and significantly longer AMT of upper extremities <31 GW and longer AMT of lower extremities >35 GW. In conclusion, using ML we successfully quantified complex 3D fetal limb motion in utero and across gestation, showing maternal factors (hyperoxia) and fetal factors (gestational age, joint) that impact movement. 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引用次数: 0
摘要
胎动的早期变化是中枢神经系统健康发育的标志。然而,目前还没有自动方法来量化宫内发育中胎儿复杂的三维运动。这项前瞻性研究的目的是在宫内核磁共振成像上使用机器学习(ML)对胎儿肢体运动进行定量运动学分析,评估母体、胎盘和胎儿因素的影响。在这项横断面观察性研究中,我们使用了 52 名典型孕妇(18-45 岁)的 76 组胎儿(24-40 孕周 [GW])血氧饱和度依赖性(BOLD)磁共振成像扫描。孕妇在仰卧和/或侧卧位时,呼吸室内空气(21% O2)5-10 分钟,呼吸 100% FiO2 5-10 分钟。为了量化上肢和下肢的运动学特征,我们使用了之前训练过的三维卷积神经网络,在类似的 BOLD 时间序列上追踪胎儿的关键点(手腕、肘部、肩部、脚踝、膝盖、臀部)。对跟踪进行目测评估,对误差进行人工校正,并计算每个关节的绝对运动时间(AMT)。为了确定与绝对运动时间有显著关联的变量,我们构建了一个带有交互项的混合模式方差分析。在母体高氧状态下,胎儿的肢体运动时间明显更长。我们还发现肢体间的 AMT 有明显的离心增加,上肢的 AMT 明显更长 35 GW。总之,我们利用 ML 成功地量化了胎儿在宫内和整个孕期的复杂三维肢体运动,显示了影响运动的母体因素(高氧)和胎儿因素(胎龄、关节)。核磁共振成像上的胎儿运动量化是胎儿健康和神经肌肉发育的潜在新生物标志物。
Cross-Sectional Observational Study of Typical in utero Fetal Movements Using Machine Learning.
Early variations of fetal movements are the hallmark of a healthy developing central nervous system. However, there are no automatic methods to quantify the complex 3D motion of the developing fetus in utero. The aim of this prospective study was to use machine learning (ML) on in utero MRI to perform quantitative kinematic analysis of fetal limb movement, assessing the impact of maternal, placental, and fetal factors. In this cross-sectional, observational study, we used 76 sets of fetal (24-40 gestational weeks [GW]) blood oxygenation level-dependent (BOLD) MRI scans of 52 women (18-45 years old) during typical pregnancies. Pregnant women were scanned for 5-10 min while breathing room air (21% O2) and for 5-10 min while breathing 100% FiO2 in supine and/or lateral position. BOLD acquisition time was 20 min in total with effective temporal resolution approximately 3 s. To quantify upper and lower limb kinematics, we used a 3D convolutional neural network previously trained to track fetal key points (wrists, elbows, shoulders, ankles, knees, hips) on similar BOLD time series. Tracking was visually assessed, errors were manually corrected, and the absolute movement time (AMT) for each joint was calculated. To identify variables that had a significant association with AMT, we constructed a mixed-model ANOVA with interaction terms. Fetuses showed significantly longer duration of limb movements during maternal hyperoxia. We also found a significant centrifugal increase of AMT across limbs and significantly longer AMT of upper extremities <31 GW and longer AMT of lower extremities >35 GW. In conclusion, using ML we successfully quantified complex 3D fetal limb motion in utero and across gestation, showing maternal factors (hyperoxia) and fetal factors (gestational age, joint) that impact movement. Quantification of fetal motion on MRI is a potential new biomarker of fetal health and neuromuscular development.
期刊介绍:
''Developmental Neuroscience'' is a multidisciplinary journal publishing papers covering all stages of invertebrate, vertebrate and human brain development. Emphasis is placed on publishing fundamental as well as translational studies that contribute to our understanding of mechanisms of normal development as well as genetic and environmental causes of abnormal brain development. The journal thus provides valuable information for both physicians and biologists. To meet the rapidly expanding information needs of its readers, the journal combines original papers that report on progress and advances in developmental neuroscience with concise mini-reviews that provide a timely overview of key topics, new insights and ongoing controversies. The editorial standards of ''Developmental Neuroscience'' are high. We are committed to publishing only high quality, complete papers that make significant contributions to the field.