MicroRNA signature for early prediction of knee osteoarthritis structural progression using integrated machine and deep learning approaches

被引:0
|
作者
Jamshidi, Afshin [1 ]
Espin-Garcia, Osvaldo [2 ,3 ,4 ,5 ,6 ]
Wilson, Thomas G. [7 ]
Loveless, Ian [7 ]
Pelletier, Jean-Pierre [1 ]
Martel-Pelletier, Johanne [1 ]
Ali, Shabana Amanda [7 ,8 ]
机构
[1] Univ Montreal Hosp Res Ctr CRCHUM, Osteoarthrit Res Unit, 900 St Denis R11 412B, Montreal, PQ H2X 0A9, Canada
[2] Univ Hlth Network, Schroeder Arthrit Inst, Dept Biostat, Toronto, ON, Canada
[3] Univ Hlth Network, Krembil Res Inst, Toronto, ON, Canada
[4] Univ Toronto, Dalla Lana Sch Publ Hlth, Toronto, ON, Canada
[5] Univ Toronto, Dept Stat Sci, Toronto, ON, Canada
[6] Univ Western Ontario, Dept Epidemiol & Biostat, Toronto, ON, Canada
[7] Michigan State Univ Hlth Sci, Henry Ford Hlth, Detroit, MI USA
[8] Wayne State Univ, Ctr Mol Med & Genet, Detroit, MI USA
基金
美国国家卫生研究院;
关键词
Prognostic prediction model; Machine/deep learning; MicroRNA; Biomarkers; Osteoarthritis; Knee structural progression; INTERVAL ESTIMATION; SELECTION; SURVIVAL;
D O I
10.1016/j.joca.2024.11.008
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
Objective: Conventional methodologies are ineffective in predicting the rapid progression of knee osteoarthritis (OA). MicroRNAs (miRNAs) show promise as biomarkers for patient stratification. We aimed to develop a miRNA prognosis model for identifying knee OA structural progressors/non-progressors using integrated machine/deep learning tools. Methods: Baseline serum miRNAs from Osteoarthritis Initiative (OAI) participants were isolated and sequenced. Participants were categorized based on their likelihood of knee structural progression/non-progression using magnetic resonance imaging and X-ray data. For prediction model development, 152 OAI participants (91 progressors, 61 non-progressors) were used. MiRNA features were reduced through VarClusHi clustering. Key miRNAs and OA determinants (age, sex, body mass index, race) were identified using seven machine learning tools. The final prediction model was developed using advanced machine/ deep learning techniques. Model performance was assessed with area under the curve (AUC) (95% confidence intervals) and accuracy. Monte Carlo cross-validation ensured robustness. Model validation used 30 OAI baseline plasma samples from an independent set of participants (14 progressors, 16 non-progressors). Results: Feature clustering selected 107 miRNAs. Elastic Net was chosen for feature selection. An optimized prediction model based on an Artificial Neural Network comprising age and four miRNAs (hsa-miR-556-3p, hsa-miR-3157-5p, hsa-miR-200a-5p, hsa-miR-141-3p) exhibited excellent performance (AUC, 0.94 [0.89, 0.97]; accuracy, 0.84 [0.77, 0.89]). Model validation performance (AUC, 0.81 [0.63, 0.92]; accuracy, 0.83 [0.66, 0.93]) demonstrated the potential for generalization. Conclusion: This study introduces a novel miRNA prognosis model for knee OA patients at risk of structural progression. It requires five baseline features, demonstrates excellent performance, is validated with an independent set, and holds promise for future personalized therapeutic monitoring. (c) 2024 Osteoarthritis Research Society International. Published by Elsevier Ltd. All rights are reserved, including those for text and data mining, AI training, and similar technologies.
引用
收藏
页码:330 / 340
页数:11
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