A digital biomarker of diabetes from smartphone-based vascular signals.
A digital biomarker of diabetes from smartphone-based vascular signals.
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基于智能手机血管信号的糖尿病数字生物标志物。
DOI:
10.1038/s41591-020-1010-5
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发表时间:
2020-10
期刊:
影响因子:
82.9
通讯作者:
Tison GH
中科院分区:
文献类型:
--
作者:
Avram R;Olgin JE;Kuhar P;Hughes JW;Marcus GM;Pletcher MJ;Aschbacher K;Tison GH
The global burden of diabetes is rapidly increasing, from 451 million people in 2019 to 693 million by 2045. The insidious onset of type 2 diabetes delays diagnosis and increases morbidity. Given the multifactorial vascular effects of diabetes, we hypothesized that smartphone-based photoplethysmography (PPG) could provide a widely-accessible digital biomarker for diabetes. Here, we developed a deep neural network (DNN) to detect prevalent diabetes using smartphone-based PPG from an initial cohort of 53,870 individuals (the “Primary Cohort”), which was then validated in a separate cohort of 7,806 individuals (the “Contemporary Cohort”), and a cohort of 181 prospectively-enrolled individuals from three clinics (the “Clinic Cohort”). The DNN achieved an area under the curve (AUC) for prevalent diabetes of 0.766 in the Primary Cohort (95% confidence interval (CI): 0.750–0.782; sensitivity 75%, specificity 65%) and 0.740 in the Contemporary Cohort (95% CI: 0.723–0.758; sensitivity 81%, specificity 54%). When the output of the DNN, called the DNN Score, was included in a regression analysis alongside age, gender, race/ethnicity, and body mass index, the AUC was 0.830 and the DNN Score remained independently predictive of diabetes. The performance of the DNN in the Clinic Cohort was similar to that in other validation datasets. There was a significant and positive association between the continuous DNN Score and hemoglobin A1c (HbA1c) (p≤0.001) among those with HbA1c. These findings demonstrate that smartphone-based PPG provides a readily attainable, noninvasive digital biomarker of prevalent diabetes.
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影响因子:
5.5
作者:
Dixit S;Pletcher MJ;Vittinghoff E;Imburgia K;Maguire C;Whitman IR;Glantz SA;Olgin JE;Marcus GM
通讯作者:
Marcus GM
影响因子:
16.2
作者:
Bertoni, AG;Anderson, GF;Brancati, FL
通讯作者:
Brancati, FL
影响因子:
5.1
作者:
Cho, N. H.;Shaw, J. E.;Malanda, B.
通讯作者:
Malanda, B.
影响因子:
1.9
作者:
Elgendi M
通讯作者:
Elgendi M
影响因子:
15.2
作者:
Avram, Robert;Tison, Geoffrey H.;Olgin, Jeffrey
通讯作者:
Olgin, Jeffrey