xRead - Olfactory Disorders (September 2023)
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INTERNATIONAL CONSENSUS ON OLFACTION
TABLE VII.12 (Continued)
Study design Study groups
Clinical end point
Topic
Study
Year LOE
Conclusions
Servello et al 635
SS-TDI
ADscores < MCI < HCs Same pattern for subtests No correlations between test scores and OBV 12UPSIT R items identified using machine learning that best differentiated ADfromHCs AD and aMCI had lower UPSIT R scores than HCs ApoE ε 4 allele frequency higher in AD and aMCI, and inversely associated withUPSIT R scores In aMCI, olfactory test scores correlated with neocortical volumes, hippocampal volumes, and amygdala volumes performance was correlated with deep gray matter, cortical, and central atrophy Over 3.5 years of follow-up, 250 incident cases of MCI (17.5%). Decrease in B-SIT scores associated with increased risk of aMCI but not naMCI. Scores also predicted progression from aMCI to AD dementia, with significant dose-response with worsening B-SIT quartiles None of the AD had zero errors. In blinded study, diagnosis of probably AD was 48%, MCI 24%, VD 8%, alcohol-induced impairment 12%, depression 4% and PD andLBD2% Intranasal anticholinergic challenge–induced odor ID decline, which reflects greater cholinergic deficiency, was associated with subsequent better cognitive efficacy from 8-week treatment with a cholinesterase inhibitor In AD, olfactory
2015 4
Case
25mildAD 25 aMCI 28HCs
control
Velayudhan et al 636
2015 4
Case
54mild to
Subset of
control
moderate AD 40 matched HCs
UPSIT R items that best differentiated early AD from HCs
Hagemeier et al 637
UPSIT R Cognitive
2016 4
Case
42AD 19aMCI 19HCs
control
measures
Roberts et al 638
2016 3
Cohort
1430 cognitively normal older patients at baseline
B-SIT (version A)
Christensen et al 639
PST (2-and 3-item versions)
2017 4
Case
20ADand20 HCs (nonblinded study) 24ADand26 HCs (blinded study)
control
Devanand et al 640
2017 3
Cohort
37MCI
UPSIT R Changes in SRT
total immediate recall and ADAS-Cog total score from baseline to 26 and 52 weeks
(Continues)
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