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Novel diagnostic tools for identifying cognitive impairment using olfactory- stimulated functional near-infrared spectroscopy: patient-level, single-group, diagnostic trial

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dc.contributor.authorKim, Jaewon-
dc.contributor.authorYon, Dong Keon-
dc.contributor.authorChoi, Kyu Yeong-
dc.contributor.authorLee, Jang Jae-
dc.contributor.authorKim, Namwoo-
dc.contributor.authorLee, Kun Ho-
dc.contributor.authorKim, Jae Gwan-
dc.date.accessioned2023-08-17T02:03:48Z-
dc.date.available2023-08-17T02:03:48Z-
dc.date.created2022-04-06-
dc.date.issued2022-03-
dc.identifier.issn1758-9193-
dc.identifier.urihttp://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/928-
dc.description.abstractIntroduction: Basic studies suggest that olfactory dysfunction and functional near-infrared spectroscopy (fNIRS) can be used as tools for the diagnosis of mild cognitive impairment (MCI); however, real-world evidence is lacking. We investigated the potential diagnostic efficacy of olfactory-stimulated fNIRS for early detection of MCI and/or Alzheimer disease (AD). Methods: We conducted a patient-level, single-group, diagnostic interventional trial involving elderly volunteers (age >60 years) suspected of declining cognitive function. Patients received open-label olfactory-stimulated fNIRS for measurement of oxygenation difference in the orbitofrontal cortex. All participants underwent amyloid PET, MRI, Mini-Mental State Examination (MMSE), and Seoul Neuropsychological Screening Battery (SNSB). Results: Of 97 subjects, 28 (28.9%) were cognitively normal, 32 (33.0%) had preclinical AD, 21 (21.6%) had MCI, and 16 (16.5%) had AD. Olfactory-stimulated oxygenation differences in the orbitofrontal cortex were associated with cognitive impairment; the association was more pronounced with cognitive severity. Olfactory-stimulated oxygenation difference was associated with MMSE (adjusted beta [a beta] 1.001; 95% Cl 0.540-1.463), SNSB language and related function (a beta, 1.218; 95% Cl, 0.020-2.417), SNSB memory (a beta, 1.963; 95% Cl, 0.841-3.084), SNSB frontal/executive function (a beta, 1.715; 95% Cl, 0.401-3.029) scores, standard uptake value ratio from amyloid PET (a beta, -10.083; 95% Cl, -19.063 to -1.103), and hippocampal volume from MRI (a beta, 0.002; 95% Cl, 0.001-0.004). Olfactory-stimulated oxygenation difference in the orbitofrontal cortex was superior in diagnosing MCI and AD (AUC, 0.909; 95% Cl, 0.848-0.971), compared to amyloid PET (AUC, 0.793; 95% Cl, 0.694-0.893) or MRI (AUC, 0.758; 95% Cl, 0.644-0.871). Discussion: Our trial showed that olfactory-stimulated oxygenation differences in the orbitofrontal cortex detected by fNIRS were associated with cognitive impairment and cognitive-related objectives.This novel approach may be a potential diagnostic tool for patients with MCI and/or AD.-
dc.language영어-
dc.language.isoen-
dc.publisherBioMed Central-
dc.titleNovel diagnostic tools for identifying cognitive impairment using olfactory- stimulated functional near-infrared spectroscopy: patient-level, single-group, diagnostic trial-
dc.typeArticle-
dc.contributor.affiliatedAuthorLee, Kun Ho-
dc.identifier.doi10.1186/s13195-022-00978-w-
dc.identifier.wosid000766167900002-
dc.identifier.bibliographicCitationAlzheimer's Research and Therapy, v.14, no.1-
dc.relation.isPartOfAlzheimer's Research and Therapy-
dc.citation.titleAlzheimer's Research and Therapy-
dc.citation.volume14-
dc.citation.number1-
dc.type.rimsART-
dc.type.docTypeArticle-
dc.description.journalClass1-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryClinical Neurology-
dc.relation.journalWebOfScienceCategoryNeurosciences-
dc.subject.keywordPlusALZHEIMERS-DISEASE-
dc.subject.keywordPlusBRAIN ACTIVATION-
dc.subject.keywordPlusINVOLVEMENT-
dc.subject.keywordPlusPATHOLOGY-
dc.subject.keywordPlusDEMENTIA-
dc.subject.keywordPlusTASK-
dc.subject.keywordPlusPET-
dc.subject.keywordAuthorCognitive impairment-
dc.subject.keywordAuthorAlzheimer&apos-
dc.subject.keywordAuthors disease-
dc.subject.keywordAuthorfNIRS-
dc.subject.keywordAuthorMild cognitive impairment-
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