Novel diagnostic tools for identifying cognitive impairment using olfactory- stimulated functional near-infrared spectroscopy: patient-level, single-group, diagnostic trial
DC Field | Value | Language |
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dc.contributor.author | Kim, Jaewon | - |
dc.contributor.author | Yon, Dong Keon | - |
dc.contributor.author | Choi, Kyu Yeong | - |
dc.contributor.author | Lee, Jang Jae | - |
dc.contributor.author | Kim, Namwoo | - |
dc.contributor.author | Lee, Kun Ho | - |
dc.contributor.author | Kim, Jae Gwan | - |
dc.date.accessioned | 2023-08-17T02:03:48Z | - |
dc.date.available | 2023-08-17T02:03:48Z | - |
dc.date.created | 2022-04-06 | - |
dc.date.issued | 2022-03 | - |
dc.identifier.issn | 1758-9193 | - |
dc.identifier.uri | http://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/928 | - |
dc.description.abstract | Introduction: 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.language | 영어 | - |
dc.language.iso | en | - |
dc.publisher | BioMed Central | - |
dc.title | Novel diagnostic tools for identifying cognitive impairment using olfactory- stimulated functional near-infrared spectroscopy: patient-level, single-group, diagnostic trial | - |
dc.type | Article | - |
dc.contributor.affiliatedAuthor | Lee, Kun Ho | - |
dc.identifier.doi | 10.1186/s13195-022-00978-w | - |
dc.identifier.wosid | 000766167900002 | - |
dc.identifier.bibliographicCitation | Alzheimer's Research and Therapy, v.14, no.1 | - |
dc.relation.isPartOf | Alzheimer's Research and Therapy | - |
dc.citation.title | Alzheimer's Research and Therapy | - |
dc.citation.volume | 14 | - |
dc.citation.number | 1 | - |
dc.type.rims | ART | - |
dc.type.docType | Article | - |
dc.description.journalClass | 1 | - |
dc.description.isOpenAccess | Y | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Neurosciences & Neurology | - |
dc.relation.journalWebOfScienceCategory | Clinical Neurology | - |
dc.relation.journalWebOfScienceCategory | Neurosciences | - |
dc.subject.keywordPlus | ALZHEIMERS-DISEASE | - |
dc.subject.keywordPlus | BRAIN ACTIVATION | - |
dc.subject.keywordPlus | INVOLVEMENT | - |
dc.subject.keywordPlus | PATHOLOGY | - |
dc.subject.keywordPlus | DEMENTIA | - |
dc.subject.keywordPlus | TASK | - |
dc.subject.keywordPlus | PET | - |
dc.subject.keywordAuthor | Cognitive impairment | - |
dc.subject.keywordAuthor | Alzheimer&apos | - |
dc.subject.keywordAuthor | s disease | - |
dc.subject.keywordAuthor | fNIRS | - |
dc.subject.keywordAuthor | Mild cognitive impairment | - |
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