Alteration patterns of brain glucose metabolism: comparisons of healthy controls, subjective memory impairment and mild cognitive impairment

被引:14
作者
Song, In-Uk [1 ]
Choi, Eun Kyoung [2 ]
Oh, Jin Kyoung [2 ]
Chung, Yong-An [2 ]
Chung, Sung-Woo [1 ]
机构
[1] Catholic Univ Korea, Dept Neurol, Coll Med, Seoul, South Korea
[2] Catholic Univ Korea, Dept Radiol, Coll Med, Seoul, South Korea
基金
新加坡国家研究基金会;
关键词
Dementia; cognition; FDG; PET; ALZHEIMERS-DISEASE; PERIVASCULAR DRAINAGE; DECLINE; HYPOMETABOLISM; PET; PREVALENCE; PREDICTION; COMPLAINTS; PATHOLOGY; DEMENTIA;
D O I
10.1177/0284185114566088
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Background: Some groups have focused on the detection and management of subjective memory impairment (SMI) as the stage that precedes mild cognitive impairment (MCI). However, there have been few clinical studies that have examined biomarkers of SMI to date. Purpose: To investigate the differences in glucose metabolism as a prodromal marker of dementia in patients with SMI, MCI, and healthy controls using brain F-18 fluoro-2-deoxyglucose positron emission tomography (FDG-PET). Material and Methods: Sixty-eight consecutive patients with SMI, 47 patients with MCI, and 42 age-matched healthy subjects were recruited. All subjects underwent FDG-PET and detailed neuropsychological testing. FDG-PET images were analyzed using the statistical parametric mapping (SPM) program. Results: FDG-PET analysis showed glucose hypometabolism in the periventricular regions of patients with SMI and in the parietal, precentral frontal, and periventricular regions of patients with MCI compared with healthy controls. Interestingly, hypometabolism on FDG-PET was noted in the parietal and precentral frontal regions in MCI patients compared to SMI patients. Conclusion: The results suggest that hypometabolism in the periventricular regions as seen on FDG-PET may play a role as a predictive biomarker of pre-dementia, and the extension of reduced glucose metabolism into parietal regions likely reflects progression of cognitive deterioration.
引用
收藏
页码:90 / 97
页数:8
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