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dc.contributor.authorCook, Hiroki
dc.contributor.authorCrisford, Anna
dc.contributor.authorBourdakos, Konstantinos
dc.contributor.authorDunlop, Douglas
dc.contributor.authorOreffo, Richard O.C.
dc.contributor.authorMahajan, Sumeet
dc.date.accessioned2025-02-24T09:01:14Z
dc.date.available2025-02-24T09:01:14Z
dc.date.created2024-08-01T11:39:45Z
dc.date.issued2024
dc.identifier.citationBiomedical Optics Express. 2024, 15 (7), 4264-4280.en_US
dc.identifier.issn2156-7085
dc.identifier.urihttps://hdl.handle.net/11250/3180009
dc.description.abstractOsteoarthritis (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) [CrossRef] ]. 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.en_US
dc.language.isoengen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.subjectosteoarthritisen_US
dc.subjectNIR Raman scattering spectroscopyen_US
dc.subjectNIR-SWIR absorption spectroscopyen_US
dc.titleHolistic vibrational spectromics assessment of human cartilage for osteoarthritis diagnosisen_US
dc.title.alternativeHolistic vibrational spectromics assessment of human cartilage for osteoarthritis diagnosisen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holderJournal © 2024en_US
dc.subject.nsiVDP::Teknologi: 500::Bioteknologi: 590en_US
dc.source.pagenumber4264-4280en_US
dc.source.volume15en_US
dc.source.journalBiomedical Optics Expressen_US
dc.source.issue7en_US
dc.identifier.doi10.1364/BOE.520171
dc.identifier.cristin2283980
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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Navngivelse 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Navngivelse 4.0 Internasjonal