4.6 Article

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

Journal

ALZHEIMERS RESEARCH & THERAPY
Volume 14, Issue 1, Pages -

Publisher

BMC
DOI: 10.1186/s13195-022-00978-w

Keywords

Cognitive impairment; Alzheimer's disease; fNIRS; Mild cognitive impairment

Funding

  1. Korea Health Industry Development Institute (KHIDI) - Ministry of Health Welfare
  2. Ministry of Health & Brain Research Program - National Research Foundation of Korea [NRF-2016M3C7A1905475]
  3. KBRI basic research program through Korea Brain Research Institute - Ministry of Science and ICT [21-BR-03-05]
  4. Original Technology Research Program for Brain Science of the National Research Foundation [NRF-2014M3C7A1046041]
  5. Institute of Information & communications Technology Planning & Evaluation (IITP) (MSIT) - Korean government, MSIT [2020-0-01969]

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The study suggests that olfactory-stimulated fNIRS could be a potential diagnostic tool for early detection of mild cognitive impairment (MCI) and/or Alzheimer's disease (AD).
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.

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