Holistic vibrational spectromics assessment of human cartilage for osteoarthritis diagnosis.

IF 2.9 2区 医学 Q2 BIOCHEMICAL RESEARCH METHODS Biomedical optics express Pub Date : 2024-06-13 eCollection Date: 2024-07-01 DOI:10.1364/BOE.520171
Hiroki Cook, Anna Crisford, Konstantinos Bourdakos, Douglas Dunlop, Richard O C Oreffo, Sumeet Mahajan
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Abstract

Osteoarthritis (OA) is the most common degenerative joint disease, presented as wearing down of articular cartilage and resulting in pain and limited mobility for 1 in 10 adults in the UK [Osteoarthr. Cartil.28(6), 792 (2020)10.1016/j.joca.2020.03.004]. There is an unmet need for patient friendly paradigms for clinical assessment that do not use ionizing radiation (CT), exogenous contrast enhancing dyes (MRI), and biopsy. Hence, techniques that use non-destructive, near- and shortwave infrared light (NIR, SWIR) may be ideal for providing label-free, deep tissue interrogation. This study demonstrates multimodal "spectromics", low-level abstraction data fusion of non-destructive NIR Raman scattering spectroscopy and NIR-SWIR absorption spectroscopy, providing an enhanced, interpretable "fingerprint" for diagnosis of OA in human cartilage. This is proposed as method level innovation applicable to both arthro- or endoscopic (minimally invasive) or potential exoscopic (non-invasive) optical approaches. Samples were excised from femoral heads post hip arthroplasty from OA patients (n = 13) and age-matched control (osteoporosis) patients (n = 14). Under multivariate statistical analysis and supervised machine learning, tissue was classified to high precision: 100% segregation of tissue classes (using 10 principal components), and a classification accuracy of 95% (control) and 80% (OA), using the combined vibrational data. There was a marked performance improvement (5 to 6-fold for multivariate analysis) using the spectromics fingerprint compared to results obtained from solely Raman or NIR-SWIR data. Furthermore, clinically relevant tissue components were identified through discriminatory spectral features - spectromics biomarkers - allowing interpretable feedback from the enhanced fingerprint. In summary, spectromics provides comprehensive information for early OA detection and disease stratification, imperative for effective intervention in treating the degenerative onset disease for an aging demographic. This novel and elegant approach for data fusion is compatible with various NIR-SWIR optical devices that will allow deep non-destructive penetration.

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用于骨关节炎诊断的人体软骨整体振动光谱评估。
骨关节炎(OA)是最常见的退行性关节疾病,表现为关节软骨磨损,英国每 10 个成年人中就有 1 人因此而感到疼痛和活动受限 [Osteoarthr.Cartil.28(6),792(2020)10.1016/j.joca.2020.03.004]。对于不使用电离辐射(CT)、外源性对比增强染料(MRI)和活组织检查的患者友好型临床评估范例的需求尚未得到满足。因此,使用非破坏性近红外和短波红外光(NIR、SWIR)的技术可能是提供无标记深层组织检查的理想选择。本研究展示了多模态 "光谱学"、非破坏性近红外拉曼散射光谱和近红外-短波红外吸收光谱的低级抽象数据融合,为诊断人体软骨的 OA 提供了增强的、可解释的 "指纹"。这是方法层面的创新,适用于关节镜或内窥镜(微创)或潜在的外窥镜(无创)光学方法。样本取自髋关节置换术后的股骨头,分别来自 OA 患者(13 人)和年龄匹配的对照组(骨质疏松症)患者(14 人)。通过多变量统计分析和监督机器学习,对组织进行了高精度分类:使用综合振动数据,组织类别分离率达 100%(使用 10 个主成分),分类准确率达 95%(对照组)和 80%(OA)。与仅使用拉曼或近红外-西红外数据得出的结果相比,使用光谱指纹的性能有了显著提高(多变量分析提高了 5 到 6 倍)。此外,通过鉴别性光谱特征(光谱生物标记)确定了与临床相关的组织成分,从而可以从增强的指纹中获得可解释的反馈。总之,光谱学为早期 OA 检测和疾病分层提供了全面的信息,对于有效干预老龄人口的退行性疾病治疗至关重要。这种新颖、优雅的数据融合方法与各种近红外-西红外光学设备兼容,可实现非破坏性的深度渗透。
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来源期刊
Biomedical optics express
Biomedical optics express BIOCHEMICAL RESEARCH METHODS-OPTICS
CiteScore
6.80
自引率
11.80%
发文量
633
审稿时长
1 months
期刊介绍: The journal''s scope encompasses fundamental research, technology development, biomedical studies and clinical applications. BOEx focuses on the leading edge topics in the field, including: Tissue optics and spectroscopy Novel microscopies Optical coherence tomography Diffuse and fluorescence tomography Photoacoustic and multimodal imaging Molecular imaging and therapies Nanophotonic biosensing Optical biophysics/photobiology Microfluidic optical devices Vision research.
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