利用生物传感器和患者报告的数据纵向跟踪系统性红斑狼疮(SLE):利用数字信号测量和预测狼疮疾病活动的完全分散移动研究报告- OASIS研究

IF 2.7 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY BioTech Pub Date : 2023-11-09 DOI:10.3390/biotech12040062
Eldon R. Jupe, Gerald H. Lushington, Mohan Purushothaman, Fabricio Pautasso, Georg Armstrong, Arif Sorathia, Jessica Crawley, Vijay R. Nadipelli, Bernard Rubin, Ryan Newhardt, Melissa E. Munroe, Brett Adelman
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引用次数: 0

摘要

(1)目的:系统性红斑狼疮(SLE)是一种复杂的疾病,涉及免疫失调、发作性发作和生活质量差。对于SLE患者的分散数字研究,使用机器学习来评估患者报告的结果(PROs)、生活质量(QOL)和生物特征数据,以预测可能的疾病爆发。(2)方法:参与者从LupusCorner网络社区中招募。自我报告SLE诊断的成年人同意并给予移动应用程序来记录患者概况(PP), PRO和QOL指标,并且入选的参与者接受智能手表进行数字生物识别监测。使用特征选择和分类算法对所得数据进行分析。(3)结果:550名参与者完成了数字调查,144人(26%)同意佩戴智能手表,68人获得了医疗记录(MRs)。对PP、PRO、QOL和生物特征数据的挖掘产生了一个26个特征的模型,用于根据mr识别的疾病爆发风险对参与者进行分类。ROC曲线显著区分真阳性和假阳性(十倍交叉验证:p <0.00023;五重:p <0.00022)。一个25个特征的贝叶斯模型能够对参与者报告的可能的耀斑进行时变预测(P(true) >0.85, p <0.001;P (nonflare)比;0.83, p <0.0001)。(4)结论:定期分析患者的健康状况和生物特征活动可能有助于主动筛查需要临床评估的情况。
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Tracking of Systemic Lupus Erythematosus (SLE) Longitudinally Using Biosensor and Patient-Reported Data: A Report on the Fully Decentralized Mobile Study to Measure and Predict Lupus Disease Activity Using Digital Signals—The OASIS Study
(1) Objective: Systemic lupus erythematosus (SLE) is a complex disease involving immune dysregulation, episodic flares, and poor quality of life (QOL). For a decentralized digital study of SLE patients, machine learning was used to assess patient-reported outcomes (PROs), QOL, and biometric data for predicting possible disease flares. (2) Methods: Participants were recruited from the LupusCorner online community. Adults self-reporting an SLE diagnosis were consented and given a mobile application to record patient profile (PP), PRO, and QOL metrics, and enlisted participants received smartwatches for digital biometric monitoring. The resulting data were profiled using feature selection and classification algorithms. (3) Results: 550 participants completed digital surveys, 144 (26%) agreed to wear smartwatches, and medical records (MRs) were obtained for 68. Mining of PP, PRO, QOL, and biometric data yielded a 26-feature model for classifying participants according to MR-identified disease flare risk. ROC curves significantly distinguished true from false positives (ten-fold cross-validation: p < 0.00023; five-fold: p < 0.00022). A 25-feature Bayesian model enabled time-variant prediction of participant-reported possible flares (P(true) > 0.85, p < 0.001; P(nonflare) > 0.83, p < 0.0001). (4) Conclusions: Regular profiling of patient well-being and biometric activity may support proactive screening for circumstances warranting clinical assessment.
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来源期刊
BioTech
BioTech Immunology and Microbiology-Applied Microbiology and Biotechnology
CiteScore
3.70
自引率
0.00%
发文量
51
审稿时长
11 weeks
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