TY - JOUR
T1 - Multimodal investigation of neuropathology and neurometabolites in mild cognitive impairment and late-life depression with 11C-PiB beta-amyloid PET and 7T magnetic resonance spectroscopy
AU - Davies-Jenkins, Christopher W.
AU - Workman, Clifford I.
AU - Hupfeld, Kathleen E.
AU - Zöllner, Helge J.
AU - Leoutsakos, Jeannie Marie
AU - Kraut, Michael A.
AU - Barker, Peter B.
AU - Smith, Gwenn S.
AU - Oeltzschner, Georg
N1 - Publisher Copyright:
© 2024 Elsevier Inc.
PY - 2024/10
Y1 - 2024/10
N2 - Positron emission tomography (PET) and magnetic resonance spectroscopy (1H-MRS) are complementary techniques that can be applied to study how proteinopathy and neurometabolism relate to cognitive deficits in preclinical stages of Alzheimer's disease (AD)—mild cognitive impairment (MCI) and late-life depression (LLD). We acquired beta-amyloid (Aβ) PET and 7 T 1H-MRS measures of GABA, glutamate, glutathione, N-acetylaspartate, N-acetylaspartylglutamate, myo-inositol, choline, and lactate in the anterior and posterior cingulate cortices (ACC, PCC) in 13 MCI and 9 LLD patients, and 13 controls. We used linear regression to examine associations between metabolites, Aβ, and cognitive scores, and whether metabolites and Aβ explained cognitive scores better than Aβ alone. In the ACC, higher Aβ was associated with lower GABA in controls but not MCI or LLD patients, but results depended upon MRS data quality control criteria. Greater variance in California Verbal Learning Test scores was better explained by a model that combined ACC glutamate and Aβ deposition than by models that only included one of these variables. These findings identify preliminary associations between Aβ, neurometabolites, and cognition.
AB - Positron emission tomography (PET) and magnetic resonance spectroscopy (1H-MRS) are complementary techniques that can be applied to study how proteinopathy and neurometabolism relate to cognitive deficits in preclinical stages of Alzheimer's disease (AD)—mild cognitive impairment (MCI) and late-life depression (LLD). We acquired beta-amyloid (Aβ) PET and 7 T 1H-MRS measures of GABA, glutamate, glutathione, N-acetylaspartate, N-acetylaspartylglutamate, myo-inositol, choline, and lactate in the anterior and posterior cingulate cortices (ACC, PCC) in 13 MCI and 9 LLD patients, and 13 controls. We used linear regression to examine associations between metabolites, Aβ, and cognitive scores, and whether metabolites and Aβ explained cognitive scores better than Aβ alone. In the ACC, higher Aβ was associated with lower GABA in controls but not MCI or LLD patients, but results depended upon MRS data quality control criteria. Greater variance in California Verbal Learning Test scores was better explained by a model that combined ACC glutamate and Aβ deposition than by models that only included one of these variables. These findings identify preliminary associations between Aβ, neurometabolites, and cognition.
KW - GABA
KW - beta-amyloid
KW - glutamate
KW - late-life depression
KW - magnetic resonance spectroscopy
KW - mild cognitive impairment
UR - http://www.scopus.com/inward/record.url?scp=85200603806&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85200603806&partnerID=8YFLogxK
U2 - 10.1016/j.neurobiolaging.2024.06.003
DO - 10.1016/j.neurobiolaging.2024.06.003
M3 - Article
C2 - 39111221
AN - SCOPUS:85200603806
SN - 0197-4580
VL - 142
SP - 27
EP - 40
JO - Neurobiology of aging
JF - Neurobiology of aging
ER -