The power of sample size through a multi-scanner approach in MR neuroimaging regression analysis: evidence from Alzheimer's disease with and without depression.


Journal

Australasian physical & engineering sciences in medicine
ISSN: 1879-5447
Titre abrégé: Australas Phys Eng Sci Med
Pays: Netherlands
ID NLM: 8208130

Informations de publication

Date de publication:
Jun 2019
Historique:
received: 23 05 2018
accepted: 27 04 2019
pubmed: 6 5 2019
medline: 18 12 2019
entrez: 5 5 2019
Statut: ppublish

Résumé

The inconsistency of volumetric results often seen in MR neuroimaging studies can be partially attributed to small sample sizes and variable data analysis approaches. Increased sample size through multi-scanner studies can tackle the former, but combining data across different scanner platforms and field-strengths may introduce a variability factor capable of masking subtle statistical differences. To investigate the sample size effect on regression analysis between depressive symptoms and grey matter volume (GMV) loss in Alzheimer's disease (AD), a retrospective multi-scanner investigation was conducted. A cohort of 172 AD patients, with or without comorbid depressive symptoms, was studied. Patients were scanned with different imaging protocols in four different MRI scanners operating at either 1.5 T or 3.0 T. Acquired data were uniformly analyzed using the computational anatomy toolbox (CAT12) of the statistical parametric mapping (SPM12) software. Single- and multi-scanner regression analyses were applied to identify the anatomical pattern of correlation between GM loss and depression severity. A common anatomical pattern of correlation between GMV loss and increased depression severity, mostly involving sensorimotor areas, was identified in all patient subgroups imaged in different scanners. Analysis of the pooled multi-scanner data confirmed the above finding employing a more conservative statistical criterion. In the retrospective multi-scanner setting, a significant correlation was also exhibited for temporal and frontal areas. Increasing the sample size by retrospectively pooling multi-scanner data, irrespective of the acquisition platform and parameters employed, can facilitate the identification of anatomical areas with a strong correlation between GMV changes and depression symptoms in AD patients.

Identifiants

pubmed: 31054027
doi: 10.1007/s13246-019-00758-1
pii: 10.1007/s13246-019-00758-1
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

563-571

Auteurs

Efstratios Karavasilis (E)

Second Department of Radiology, University General Hospital 'Attikon', Medical School, National and Kapodistrian University of Athens, 19 Papadiamantopoulou Street, Athens, Greece. stratoskaravasilis@yahoo.gr.
Department of Medical Physics, Medical School, Democritus University of Thrace, Alexandroupolis, Greece. stratoskaravasilis@yahoo.gr.

Theodore P Parthimos (TP)

3rd Age Day Care Center IASIS, Glyfada, Greece.

John D Papatriantafyllou (JD)

3rd Age Day Care Center IASIS, Glyfada, Greece.

Foteini Christidi (F)

First Department of Neurology, Aeginition Hospital, Medical School, National and Kapodistrian University of Athens, Athens, Greece.

Sokratis G Papageorgiou (SG)

Second Department of Neurology, University General Hospital 'Attikon', Medical School, National and Kapodistrian University of Athens, Athens, Greece.

George Kapsas (G)

Department of Radiology, 424 General Military Hospital, Thessaloníki, Greece.

Andrew C Papanicolaou (AC)

Division of Clinical Neurosciences, Department of Pediatrics, University of Tennessee Health Science Center, Memphis, USA.
Department of Anatomy and Neurobiology, University of Tennessee Health Science Center, Memphis, USA.
Neuroscience Institute, Le Bonheur Children's Hospital, Memphis, USA.

Ioannis Seimenis (I)

Department of Medical Physics, Medical School, Democritus University of Thrace, Alexandroupolis, Greece.

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Classifications MeSH