Unsupervised machine-learning algorithms for the identification of clinical phenotypes in the osteoarthritis initiative database

被引:17
作者
Demanse, David [1 ]
Saxer, Franziska [2 ,7 ]
Lustenberger, Patrick [3 ]
Nikolaus, Philipp [3 ]
Rasin, Ilja [3 ]
Brennan, Damian F. [3 ]
Roubenoff, Ronenn [2 ]
Premji, Sumehra [1 ,3 ,4 ]
Conaghan, Philip G. [5 ,6 ]
Schieker, Matthias [2 ]
机构
[1] Novartis Pharm AG, CH-4002 Basel, Switzerland
[2] Novartis Inst Biomed Res, Novartis Campus, CH-4002 Basel, Switzerland
[3] IBM Switzerland AG, Vulkanstr 106, CH-8048 Zurich, Switzerland
[4] Bayer Pharmaceut, CH-4002 Basel, Switzerland
[5] Univ Leeds, Leeds Inst Rheumat & Musculoskeletal Med, Leeds, England
[6] NIHR Leeds Biomed Res Ctr, Leeds, England
[7] Univ Basel, Med Fac, CH-4002 Basel, Switzerland
关键词
Knee osteoarthritis; Machine learning; Cluster analysis; Clinical phenotypes; Patient segments; Precision medicine; KNEE OSTEOARTHRITIS; PHYSICAL-ACTIVITY; PAIN; CARTILAGE; MARKERS; ASSOCIATION; TRIALS; TRAJECTORIES; PROGRESSION; BIOMARKERS;
D O I
10.1016/j.semarthrit.2022.152140
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objectives: Osteoarthritis (OA) is a complex disease comprising diverse underlying patho-mechanisms. To enable the development of effective therapies, segmentation of the heterogenous patient population is critical. This study aimed at identifying such patient clusters using two different machine learning algorithms. Methods: Using the progression and incident cohorts of the Osteoarthritis Initiative (OAI) dataset, deep embedded clustering (DEC) and multiple factor analysis with clustering (MFAC) approaches, including 157 input-variables at baseline, were employed to differentiate specific patient profiles. Results: DEC resulted in 5 and MFAC in 3 distinct patient phenotypes. Both identified a "comorbid" cluster with higher body mass index (BMI), relevant burden of comorbidity and low levels of physical activity. Both methods also identified a younger and physically more active cluster and an elderly cluster with functional limitations, but low disease impact. The additional two clusters identified with DEC were subgroups of the young/physically active and the elderly/physically inactive clusters. Overall pain trajectories over 9 years were stable, only the numeric rating scale (NRS) for pain showed distinct increase, while physical activity decreased in all clusters. Clusters showed different (though non-significant) trajectories of joint space changes over the follow-up period of 8 years. Conclusion: Two different clustering approaches yielded similar patient allocations primarily separating complex "comorbid" patients from healthier subjects, the latter divided in young/physically active vs elderly/physically inactive subjects. The observed association to clinical (pain/physical activity) and structural progression could be helpful for early trial design as strategy to enrich for patients who may specifically benefit from diseasemodifying treatments.
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页数:14
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