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  3. Multicenter stability of resting state fMRI in the detection of Alzheimer's disease and amnestic MCI.
 

Multicenter stability of resting state fMRI in the detection of Alzheimer's disease and amnestic MCI.

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BORIS DOI
10.7892/boris.101474
Date of Publication
2017
Publication Type
Article
Division/Institute

Universitätsklinik fü...

Contributor
Teipel, Stefan J
Wohlert, Alexandra
Metzger, Coraline
Grimmer, Timo
Sorg, Christian
Ewers, Michael
Meisenzahl, Eva
Klöppel, Stefan
Universitätsklinik für Alterspsychiatrie und Psychotherapie (APP)
Borchardt, Viola
Grothe, Michel J
Walter, Martin
Dyrba, Martin
Subject(s)

600 - Technology::610...

Series
NeuroImage: Clinical
ISSN or ISBN (if monograph)
2213-1582
Publisher
Elsevier
Language
English
Publisher DOI
10.1016/j.nicl.2017.01.018
PubMed ID
28180077
Description
BACKGROUND

In monocentric studies, patients with mild cognitive impairment (MCI) and Alzheimer's disease (AD) dementia exhibited alterations of functional cortical connectivity in resting-state functional MRI (rs-fMRI) analyses. Multicenter studies provide access to large sample sizes, but rs-fMRI may be particularly sensitive to multiscanner effects.

METHODS

We used data from five centers of the "German resting-state initiative for diagnostic biomarkers" (psymri.org), comprising 367 cases, including AD patients, MCI patients and healthy older controls, to assess the influence of the distributed acquisition on the group effects. We calculated accuracy of group discrimination based on whole brain functional connectivity of the posterior cingulate cortex (PCC) using pooled samples as well as second-level analyses across site-specific group contrast maps.

RESULTS

We found decreased functional connectivity in AD patients vs. controls, including clusters in the precuneus, inferior parietal cortex, lateral temporal cortex and medial prefrontal cortex. MCI subjects showed spatially similar, but less pronounced, differences in PCC connectivity when compared to controls. Group discrimination accuracy for AD vs. controls (MCI vs. controls) in the test data was below 76% (72%) based on the pooled analysis, and even lower based on the second level analysis stratified according to scanner. Only a subset of quality measures was useful to detect relevant scanner effects.

CONCLUSIONS

Multicenter rs-fMRI analysis needs to employ strict quality measures, including visual inspection of all the data, to avoid seriously confounded group effects. While pending further confirmation in biomarker stratified samples, these findings suggest that multicenter acquisition limits the use of rs-fMRI in AD and MCI diagnosis.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/153388
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