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Review
. 2018 Feb 20;10(1):21.
doi: 10.1186/s13195-018-0347-1.

Effects of pharmacological and nonpharmacological treatments on brain functional magnetic resonance imaging in Alzheimer's disease and mild cognitive impairment: a critical review

Affiliations
Review

Effects of pharmacological and nonpharmacological treatments on brain functional magnetic resonance imaging in Alzheimer's disease and mild cognitive impairment: a critical review

Elisa Canu et al. Alzheimers Res Ther. .

Abstract

Background: A growing number of pharmacological and nonpharmacological trials have been performed to test the efficacy of approved or experimental treatments in Alzheimer disease (AD) and mild cognitive impairment (MCI). In this context, functional magnetic resonance imaging (fMRI) may be a good candidate to detect brain changes after a short period of treatment.

Main body: This critical review aimed to identify and discuss the available studies that have tested the efficacy of pharmacological and nonpharmacological treatments in AD and MCI cases using task-based or resting-state fMRI measures as primary outcomes. A PubMed-based literature search was performed with the use of the three macro-areas: 'disease', 'type of MRI', and 'type of treatment'. Each contribution was individually reviewed according to the Cochrane Collaboration's tool for assessing risk of bias. Study limitations were systematically detected and critically discussed. We selected 34 pharmacological and 13 nonpharmacological articles. According to the Cochrane Collaboration's tool for assessing risk of bias, 40% of these studies were randomized but only a few described clearly the randomization procedure, 36% declared the blindness of participants and personnel, and only 21% reported the blindness of outcome assessment. In addition, 28% of the studies presented more than 20% drop-outs at short- and/or long-term assessments. Additional common shortcomings of the reviewed works were related to study design, patient selection, sample size, choice of outcome measures, management of drop-out cases, and fMRI methods.

Conclusion: There is an urgent need to obtain efficient treatments for AD and MCI. fMRI is powerful enough to detect even subtle changes over a short period of treatment; however, the soundness of methods should be improved to enable meaningful data interpretation.

Keywords: Alzheimer’s disease (AD); Cognition; Functional magnetic resonance imaging (MRI); Mild cognitive impairment (MCI); Nonpharmacological treatments; Pharmacological treatments; Training.

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Conflict of interest statement

Authors’ information

EC: MSc, PhD with background in neuropsychology and neuroimaging.

ES: PT with background in clinical physiotherapy and neuroimaging.

MF: MD, FEAN with background in clinical neurology and neuroimaging.

FA: MD, PhD with background in clinical neurology and neuroimaging.

All authors have specific training and expertise in MRI and neurodegenerative diseases.

Ethics approval and consent to participate

Not applicable.

Consent for publication

Not applicable.

Competing interests

EC has received research support from the Italian Ministry of Health; MF is Editor-in-Chief of Journal of Neurology; serves on a scientific advisory board for Teva Pharmaceutical Industries; has received compensation for consulting services and/or speaking activities from Bayer Schering Pharma, Biogen Idec, EXCEMED, Merck Serono, and Teva Pharmaceutical Industries; and receives research support from Bayer Schering Pharma, Biogen Idec, Merck Serono, Teva Pharmaceutical Industries, Italian Ministry of Health, Fondazione Italiana Sclerosi Multipla, Cure PSP, Alzheimer’s and Drug Discovery Foundation, and the Jacques and Gloria Gossweiler Foundation (Switzerland); FA is a Section Editor for NeuroImage: Clinical; has received speaker honoraria from EXCEMED—Excellence in Medical Education and Biogen Idec; and receives research supports from the Italian Ministry of Health, AriSLA (Fondazione Italiana di Ricerca per la SLA), and the European Research Council. ES declares that she has no competing interests.

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Figures

Fig. 1
Fig. 1
Flowchart of literature review process (pharmacological functional magnetic resonance imaging studies)
Fig. 2
Fig. 2
Judgments of articles according to the seven categories of the Cochrane Collaboration’s tool for assessing risk of bias. Positive marks denote low risk or no bias; negative marks denote high-risk bias; question marks denote unclear information. NA not applicable
Fig. 3
Fig. 3
Flowchart of literature review process (nonpharmacological functional magnetic resonance imaging studies)

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