基于机器学习的聚类分析确定了退行性颈椎病患者的四种独特表型,这些表型具有不同的临床特征以及长期功能和神经功能预后。

IF 9.7 1区 医学 Q1 MEDICINE, RESEARCH & EXPERIMENTAL EBioMedicine Pub Date : 2024-08-01 Epub Date: 2024-07-04 DOI:10.1016/j.ebiom.2024.105226
Karlo M Pedro, Mohammed Ali Alvi, Nader Hejrati, Ayesha I Quddusi, Anoushka Singh, Michael G Fehlings
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引用次数: 0

摘要

背景:退行性颈椎脊髓病(DCM)是导致成人脊髓功能障碍的主要原因,它表现出多种相互关联的症状,临床表现具有显著的异质性。本研究试图利用基于机器学习的聚类算法来识别不同患者的临床特征和手术干预后的功能轨迹:在这项研究中,我们利用来自三项主要 DCM 试验的汇总数据,采用 k-means 和潜在特征分析(LPA)来识别患者表型。Nurick评分、NDI(颈部残疾指数)、颈部疼痛以及运动和感觉评分的组合有助于聚类。拟合优度指数用于确定最佳聚类数。方差分析和事后Tukey's检验评估了结果差异,而多项式逻辑回归则确定了组别成员的重要预测因素:共有 1047 名 DCM 患者(平均 [SD] 年龄:56.80 [11.39] 岁,女性 411 [39%])完成了术后一年的结果评估。潜在特征分析确定了四种 DCM 表型:"严重多模态损伤 "组(286 人)、"轻微损伤 "组(116 人)、"运动主导 "组(88 人)和 "疼痛主导 "组(557 人)。每种表型都表现出独特的症状特征和不同的功能恢复轨迹。由年老体弱的患者组成的 "严重多模态损伤组 "在一年后的总体预后最差(SF-36 PCS 平均值 [SD]: 40.01 [9.75];SF-36 MCS 平均值 [SD], 46.08 [11.50]),但手术后神经功能得到了很大恢复(ΔmJOA 平均值 [SD]: 3.83 [2.98])。应用 k-means 算法得出了类似的四类解决方案。较高的虚弱评分和阳性吸烟状态预示着患者属于 "严重多模态损伤 "组(OR 分别为 1.47 [95% CI 1.07-2.02] 和 1.58 [95% CI 1.25-1.99]),而接受前路手术和症状持续时间较长则与 "疼痛为主 "组相关(OR 分别为 2.0 [95% CI 1.06-3.80] 和 3.1 [95% CI 1.38-6.89]):对多种临床指标的无监督学习可预测不同的患者表型。症状聚类为识别DCM亚群提供了一个有价值的框架,超越了像mJOA这样的单一患者报告结果测量:本研究未获得任何资助。原始研究由 AO Spine North America 资助。
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Machine learning-based cluster analysis identifies four unique phenotypes of patients with degenerative cervical myelopathy with distinct clinical profiles and long-term functional and neurological outcomes.

Background: Degenerative cervical myelopathy (DCM), the predominant cause of spinal cord dysfunction among adults, exhibits diverse interrelated symptoms and significant heterogeneity in clinical presentation. This study sought to use machine learning-based clustering algorithms to identify distinct patient clinical profiles and functional trajectories following surgical intervention.

Methods: In this study, we applied k-means and latent profile analysis (LPA) to identify patient phenotypes, using aggregated data from three major DCM trials. The combination of Nurick score, NDI (neck disability index), neck pain, as well as motor and sensory scores facilitated clustering. Goodness-of-fit indices were used to determine the optimal cluster number. ANOVA and post hoc Tukey's test assessed outcome differences, while multinomial logistic regression identified significant predictors of group membership.

Findings: A total of 1047 patients with DCM (mean [SD] age: 56.80 [11.39] years, 411 [39%] females) had complete one year outcome assessment post-surgery. Latent profile analysis identified four DCM phenotypes: "severe multimodal impairment" (n = 286), "minimal impairment" (n = 116), "motor-dominant" (n = 88) and "pain-dominant" (n = 557) groups. Each phenotype exhibited a unique symptom profile and distinct functional recovery trajectories. The "severe multimodal impairment group", comprising frail elderly patients, demonstrated the worst overall outcomes at one year (SF-36 PCS mean [SD]: 40.01 [9.75]; SF-36 MCS mean [SD], 46.08 [11.50]) but experienced substantial neurological recovery post-surgery (ΔmJOA mean [SD]: 3.83 [2.98]). Applying the k-means algorithm yielded a similar four-class solution. A higher frailty score and positive smoking status predicted membership in the "severe multimodal impairment" group (OR 1.47 [95% CI 1.07-2.02] and 1.58 [95% CI 1.25-1.99, respectively]), while undergoing anterior surgery and a longer symptom duration were associated with the "pain-dominant" group (OR 2.0 [95% CI 1.06-3.80] and 3.1 [95% CI 1.38-6.89], respectively).

Interpretation: Unsupervised learning on multiple clinical metrics predicted distinct patient phenotypes. Symptom clustering offers a valuable framework to identify DCM subpopulations, surpassing single patient reported outcome measures like the mJOA.

Funding: No funding was received for the present work. The original studies were funded by AO Spine North America.

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来源期刊
EBioMedicine
EBioMedicine Biochemistry, Genetics and Molecular Biology-General Biochemistry,Genetics and Molecular Biology
CiteScore
17.70
自引率
0.90%
发文量
579
审稿时长
5 weeks
期刊介绍: eBioMedicine is a comprehensive biomedical research journal that covers a wide range of studies that are relevant to human health. Our focus is on original research that explores the fundamental factors influencing human health and disease, including the discovery of new therapeutic targets and treatments, the identification of biomarkers and diagnostic tools, and the investigation and modification of disease pathways and mechanisms. We welcome studies from any biomedical discipline that contribute to our understanding of disease and aim to improve human health.
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