Division of Pulmonary and Critical Care Medicine, Department of Medicine, Brigham and Women's Hospital, Boston, MA, USA.
Applied Chest Imaging Laboratory, Brigham and Women's Hospital, Boston, MA, USA.
Sci Rep. 2024 Aug 3;14(1):17981. doi: 10.1038/s41598-024-68447-y.
Low muscle mass is associated with numerous adverse outcomes independent of other associated comorbid diseases. We aimed to predict and understand an individual's risk for developing low muscle mass using proteomics and machine learning. We identified eight biomarkers associated with low pectoralis muscle area (PMA). We built three random forest classification models that used either clinical measures, feature selected biomarkers, or both to predict development of low PMA. The area under the receiver operating characteristic curve for each model was: clinical-only = 0.646, biomarker-only = 0.740, and combined = 0.744. We displayed the heterogenetic nature of an individual's risk for developing low PMA and identified two distinct subtypes of participants who developed low PMA. While additional validation is required, our methods for identifying and understanding individual and group risk for low muscle mass could be used to enable developments in the personalized prevention of low muscle mass.
肌肉量低与许多不良预后相关,独立于其他相关合并症。我们旨在使用蛋白质组学和机器学习来预测和了解个体发生肌肉量低的风险。我们确定了 8 个与胸肌面积(PMA)低相关的生物标志物。我们构建了三个随机森林分类模型,这些模型分别使用临床指标、特征选择的生物标志物或两者来预测低 PMA 的发展。每个模型的接收者操作特征曲线下的面积分别为:仅临床指标=0.646、仅生物标志物=0.740、组合=0.744。我们展示了个体发生低 PMA 风险的异质性,并确定了两种不同的低 PMA 发展参与者亚型。虽然还需要进一步验证,但我们用于识别和理解个体和群体低肌肉量风险的方法可用于促进低肌肉量的个性化预防。