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

被引:1
|
作者
Davies-Jenkins, Christopher W. [1 ,2 ]
Workman, Clifford I. [3 ,5 ]
Hupfeld, Kathleen E. [1 ,2 ]
Zollner, Helge J. [1 ,2 ]
Leoutsakos, Jeannie-Marie [3 ,4 ]
Kraut, Michael A. [1 ]
Barker, Peter B. [1 ,2 ]
Smith, Gwenn S. [3 ,5 ]
Oeltzschner, Georg [1 ,2 ]
机构
[1] Johns Hopkins Univ, Russell H Morgan Dept Radiol & Radiol Sci, Sch Med, Baltimore, MD USA
[2] Kennedy Krieger Inst, FM Kirby Res Ctr Funct Brain Imaging, Baltimore, MD USA
[3] Johns Hopkins Univ, Sch Med, Dept Psychiat & Behav Sci, Div Geriatr Psychiat & Neuropsychiat, Baltimore, MD USA
[4] Johns Hopkins Bloomberg Sch Publ Hlth, Baltimore, MD USA
[5] Johns Hopkins Univ, Sch Med, Russell H Morgan Dept Radiol & Radiol Sci, Div Nucl Med & Mol Imaging, Baltimore, MD 21205 USA
关键词
mild cognitive impairment; late-life depression; magnetic resonance spectroscopy; beta-amyloid; GABA; glutamate; ALZHEIMERS-DISEASE BRAIN; GAMMA-AMINOBUTYRIC-ACID; PROTON MR SPECTROSCOPY; OXIDATIVE STRESS; N-ACETYLASPARTATE; MITOCHONDRIAL DYSFUNCTION; METABOLITE CONCENTRATIONS; MAJOR DEPRESSION; CINGULATE CORTEX; RAT-BRAIN;
D O I
10.1016/j.neurobiolaging.2024.06.003
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
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 (A(3) 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, A(3, and cognitive scores, and whether metabolites and A(3 explained cognitive scores better than A(3 alone. In the ACC, higher A(3 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 A(3 deposition than by models that only included one of these variables. These findings identify preliminary associations between A(3, neurometabolites, and cognition.
引用
收藏
页码:27 / 40
页数:14
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