xRead - Olfactory Disorders (September 2023)
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PATEL et al.
TABLE VII.12 (Continued)
Study design Study groups
Clinical end point
Topic
Study
Year LOE
Conclusions
UPSIT R Cognitive
Reduced smell test scores associated with lower cognitive scores and older age, as well as increased ratios of CSF T-tau and P-tau toA β 1-42 Suggests OI reflects degree of preclinical AD pathology AD scores lower than NPH scores NPH scores below HC testing may be useful in differentiating AD from NPH Better SS-ID scores in HCs MCI outperformed AD Combining olfactory and cognitive measures improved diagnosis of AD andMCI At baseline, lower B-SIT scores correlated with increased CSF t-tau and were lower than HCs in all diagnostic groups Lower scores predicted MMSE decline in total recall in ApoE ε 4carriers and those with abnormal A β 42 Concluded OD may reflect neuronal injury rather than amyloid pathology Lower UPSIT R scores associated with increased temporal and parietal tau, but not amyloid, burden Quantitative meta-analysis indicates robust olfactory deficits in patients with MCI Olfactory ID test may be useful in early screening for cognitive impairment and dementia group, and word list learning and delayed scores, although still within normal limits Suggests that olfactory
Lafaille-Magnan et al 641
2017 3
Cross
274 healthy
sectional
older persons with parental or multiple sibling history ofAD
measures CSF levels of
T-tau, P-tau, and ratios with A β 1-42
Passler et al 642
2017 4
Case
7AD 22NPH 14HCs
UPSIT R
control
Quarmley et al 643
SS-ID (16 odors) MoCA
2017 4
Case
262AD 150aMCI 24naMCI 292HCs
control
Reijs 644
2017 3
Case
42AD 45MCI 26non-AD dementia 40HCs
B-SIT Cognitive
control and cohort
measures
CSFA β 42 CSF t-tau ApoE genotype
Risacher et al 645
Association of
2017 4
Case
10SCD 5MCI 19HCs
UPSIT R scores withPET measures of tau and amyloid burden
control
Roalf et al 646
2017 1
Meta
1993MCI 2861HCs
Psychophysical examinations (eg,UPSIT R and SS-TDI)
analysis of case control and cohort studies
(Continues)
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