超越 BMI:通过智能手机图像评估心脏代谢风险
Seeing beyond BMI: Estimating cardiometabolic risk with smartphone imagery

原始链接: https://research.google/blog/seeing-beyond-bmi-estimating-cardiometabolic-risk-with-smartphone-imagery/

本研究评估了在 MetabolicMosaic 队列中使用梯度提升分类器预测胰岛素抵抗(IR)时,不同数据源的有效性。为确保结果公正,研究人员采用了严格的平衡测试框架,对比了五组特征:基础人口统计学数据、皮尺测量、智能手表 BIA、基于智能手机的 PhotoScan 以及临床 DXA 扫描。 性能评估采用受试者工作特征曲线下面积(AUROC)和净重新分类指数(NRI)。基础人口统计学模型的 AUROC 为 0.692。整合 PhotoScan 指标后,准确率显著提升至 AUROC 0.760 和 NRI 0.593,表现与金标准 DXA(AUROC 0.773;NRI 0.748)几乎相当。相反,整合智能手表 BIA 并未改善预测效果,因为它缺乏 PhotoScan 所能捕捉到的细致身体成分数据,如 A/G 比值和 V/S 比值。 研究结果表明,基于智能手机的光学表型分析具有极高的临床应用价值,是识别胰岛素抵抗的一种可行且便捷的替代方案。

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原文

Insulin resistance classification

Next, we compared how well different combinations of data predicted insulin resistance, stacking our baseline demographics against combining it with standard tape measurements, smartwatch BIA sensors, PhotoScan, and gold-standard DXA scans.

We tested our models on the MetabolicMosaic cohort using a gradient boosting classifier to identify subjects with insulin resistance. To ensure our results were completely unbiased and leak-free, we implemented a rigorous testing process that repeatedly evaluated the model on unseen data. We also made sure each test group was evenly balanced by both BMI and insulin resistance status, ensuring a fair and realistic performance test. With this robust framework in place, we systematically fed the classifier five distinct feature sets to compare their predictive power, baseline demographics like age, sex, and body mass index, standard tape measure anthropometrics, smartwatch bioelectrical impedance, our smartphone PhotoScan metrics, and the clinical gold-standard DXA scans. By comparing how the model performed with each of these isolated inputs, we established the clinical value of our smartphone optical phenotyping.

To evaluate our models, we focused on two key metrics: the Area Under the Receiver Operating Characteristic curve (AUROC) and the Net Reclassification Index (NRI). Simply put, AUROC measures how accurately a model can distinguish between someone who has insulin resistance and someone who does not (higher is better). NRI, on the other hand, quantifies exactly how much our new digital metrics improve our ability to correctly categorize people compared to our old baseline model. As the figure below indicates, our baseline demographic model achieved an AUROC of 0.692. When we added the photoscan-based body composition features (demo + photoscan), the classification accuracy improved to an AUROC to 0.760 and NRI improved to 0.593, nearly as effective as using clinical DXA data itself, which topped out at an AUROC of 0.773 and an NRI of 0.748. In contrast, adding BIA with demographics (demo + bia below) yielded no improvement in AUROC or NRI for insulin resistance classification for IR classification, as BIA only provides BF% estimation, whose feature importance is significantly lower than A/G ratio and V/S ratio in the demo + photoscan model.

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