TY - JOUR
T1 - Odorant Item Specific Olfactory Identification Deficit May Differentiate Alzheimer Disease From Aging
AU - Texas Alzheimer's Research, Care Consortium
AU - Woodward, Matthew R.
AU - Hafeez, Muhammad Ubaid
AU - Qi, Qianya
AU - Riaz, Ahmed
AU - Benedict, Ralph H.B.
AU - Yan, Li
AU - Szigeti, Kinga
AU - Pavlik, Valory
AU - Massman, Paul
AU - Darby, Eveleen
AU - Rodriguear, Monica
AU - Khaleeq Ansari, Aisha
AU - DeToledo, John C.
AU - Reddy, Hemachandra
AU - Wilms, Henrick
AU - Johnson, Kim
AU - Perez, Victoria
AU - Fairchild, Thomas
AU - Knebl, Janice
AU - O'Bryant, Sid E.
AU - Hall, James R.
AU - Johnson, Leigh
AU - Barber, Robert C.
AU - Mains, Douglas
AU - Alvarez, Lisa
AU - Cullum, Munro
AU - Rosenberg, Roger
AU - Williams, Benjamin
AU - Quiceno, Mary
AU - Reisch, Joan
AU - Hynan, Linda S.
AU - Huebinger, Ryan
AU - Smith, Janet
AU - Nguyen, Trung
AU - Royall, Donald
AU - Palmer, Raymond
AU - Polk, Marsha
AU - Stevens, Alan
AU - Ory, Marcia
AU - Paydarfar, David
AU - Bertelson, John
AU - Woon, Martin
AU - Ayres, Gayle
AU - Aguirre, Alyssa
AU - Wilhelmsen, Kirk C.
AU - Tilson, Jeffrey L.
N1 - Publisher Copyright:
© 2018 American Association for Geriatric Psychiatry
PY - 2018/8
Y1 - 2018/8
N2 - Objectives: To explore whether the ability to recognize specific odorant items is differentially affected in aging versus Alzheimer disease (AD); to refine olfactory identification deficit (OID) as a biomarker of prodromal and early AD. Design: Prospective multicenter cross-sectional study with a longitudinal arm. Setting: Outpatient memory diagnostic clinics in New York and Texas. Participants: Adults aged 65 and older with amnestic mild cognitive impairment (aMCI) and AD and healthy aging (HA) subjects in the comparison group. Measurements: Participants completed the University of Pennsylvania Smell Identification Test (UPSIT) and neuropsychological testing. AD-associated odorants (AD-10) were selected based on a model of ordinal logistic regression. Age-associated odorants (Age-10) were identified using a linear model. Results: For the 841 participants (234 HA, 192 aMCI, 415 AD), AD-10 was superior to Age-10 in separating HA and AD. AD-10 was associated with a more widespread cognitive deficit across multiple domains, in contrast to Age-10. The disease- and age-associated odorants clustered separately in age and AD. AD-10 predicted conversion from aMCI to AD. Conclusions: Nonoverlapping UPSIT items were identified that were individually associated with age and disease. Despite a modest predictive value of the AD-specific items for conversion to AD, the AD-specific items may be useful in enriching samples to better identify those at risk for AD. Further studies are needed with monomolecular and unilateral stimulation and orthogonal biomarker validation to further refine disease- and age-associated signals.
AB - Objectives: To explore whether the ability to recognize specific odorant items is differentially affected in aging versus Alzheimer disease (AD); to refine olfactory identification deficit (OID) as a biomarker of prodromal and early AD. Design: Prospective multicenter cross-sectional study with a longitudinal arm. Setting: Outpatient memory diagnostic clinics in New York and Texas. Participants: Adults aged 65 and older with amnestic mild cognitive impairment (aMCI) and AD and healthy aging (HA) subjects in the comparison group. Measurements: Participants completed the University of Pennsylvania Smell Identification Test (UPSIT) and neuropsychological testing. AD-associated odorants (AD-10) were selected based on a model of ordinal logistic regression. Age-associated odorants (Age-10) were identified using a linear model. Results: For the 841 participants (234 HA, 192 aMCI, 415 AD), AD-10 was superior to Age-10 in separating HA and AD. AD-10 was associated with a more widespread cognitive deficit across multiple domains, in contrast to Age-10. The disease- and age-associated odorants clustered separately in age and AD. AD-10 predicted conversion from aMCI to AD. Conclusions: Nonoverlapping UPSIT items were identified that were individually associated with age and disease. Despite a modest predictive value of the AD-specific items for conversion to AD, the AD-specific items may be useful in enriching samples to better identify those at risk for AD. Further studies are needed with monomolecular and unilateral stimulation and orthogonal biomarker validation to further refine disease- and age-associated signals.
KW - Alzheimer disease
KW - cognitive aging
KW - mild cognitive impairment
KW - olfactory identification
KW - smell
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U2 - 10.1016/j.jagp.2018.02.008
DO - 10.1016/j.jagp.2018.02.008
M3 - Article
C2 - 29858162
AN - SCOPUS:85047551355
SN - 1064-7481
VL - 26
SP - 835
EP - 846
JO - American Journal of Geriatric Psychiatry
JF - American Journal of Geriatric Psychiatry
IS - 8
ER -