A multicenter 1 H-MRS study of the medial temporal lobe in AD and MCI
Authors:
- F. JessenFJF. Jessen
- O. GürOGO. Gür
- W. BlockWBW. Block
- G. EndeGEG. Ende
- L. FrölIchLFL. FrölIch
- T. HammenTHT. Hammen
- J. WiltfangJWJ. Wiltfang
- T. KucinskiTKT. Kucinski
- H. JahnHJH. Jahn
- R. HeunRHR. Heun
- W. MaierWMW. Maier
- H. KölSchHKH. KölSch
- 19 May 2009
- journal article
- research article
- Published by Wolters Kluwer Health in Neurology
- Vol. 72 (20) , 1735-1740
Abstract
Objective: The need for biological markers of Alzheimer disease (AD) is constantly increasing. Proton magnetic resonance spectroscopy (1H-MRS) studies have provided consistent evidence for a reduction of the neuronal marker N-acetylaspartate (NAA) in patients with AD. Within the German Competence Network on Dementia, we conducted a 1H-MRS study in patients with mild dementia and mild cognitive impairment (MCI) at four sites to investigate the multicenter feasibility of 1H-MRS. Methods: In total, 130 patients with dementia (98 AD, 32 non-AD), 136 subjects with MCI (70 of AD type, 66 of non-AD type), and 45 unimpaired control subjects were included. Single-volume 1H-MRS of the left medial temporal lobe was performed at long and short echo times. Metabolites were quantified and metabolic ratios were determined. Results: We found a significant reduction of NAA concentration in patients with AD as compared to healthy volunteers and compared to patients with MCI of AD type. NAA/Cr (creatine/phosphocreatine) was also lower in patients with AD compared to control subjects. NAA, choline compounds, and Cr were lower in patients with AD compared to patients with non-AD dementia. Conclusions: We demonstrated the multicenter feasibility of proton magnetic resonance spectroscopy (1H-MRS) of the medial temporal lobe in mild dementia and mild cognitive impairment, which is a prerequisite for the application of 1H-MRS in large-scale clinical trials. Since the concentration measures of the metabolites are adjusted for brain tissue volume, these findings are indicators of biochemical pathology beyond brain atrophy.Keywords
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