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SCIENTIFIC LITERATURE · MED

Parkinson hastalığında kortikal kalınlık: Koordinat tabanlı bir meta-analiz.

Cortical thickness in Parkinson disease: A coordinate-based meta-analysis.

Makine çevirisi · Editoryal inceleme bekliyor

Medicine (Baltimore) · 2020-07-01

DOI: 10.1097/md.0000000000021403PMID: 32756136

Open accessMeta-Analysis; review-article; Journal ArticleKaynağa git ↗

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Aşağıdaki metin kaynak makalenin lisansı doğrulanmış orijinal özetidir. cc by

BackgroundA growing number of studies have used surface-based morphometry (SBM) analyses to investigate gray matter cortical thickness (CTh) abnormalities in Parkinson disease (PD). However, the results across studies are inconsistent and have not been systematically reviewed. A clear picture of CTh alterations in PD remains lacked. Coordinate-based meta-analysis (CBMA) is a powerful tool to quantitatively integrate the results of individual voxel-based neuroimaging studies to identify the functional or structural neural substrates of particular neuropsychiatric disorders. Recently, CBMA has been updated for integrating SBM studies.MethodsThe online databases PubMed, Embase, Web of Science, China National Knowledge Infrastructure (CNKI), WanFang, and SinoMed were comprehensively searched without language limitations from the database inception to February 2, 2020. We will include all SBM studies that compared regional CTh between patients with idiopathic PD and healthy control subjects at the whole-cortex level using Seed-based d Mapping with Permutation of Subject Images (SDM-PSI). In addition to the main CBMA, we will conduct several supplementary analyses to test the robustness of the results, such as jackknife analyses, subgroup analyses, heterogeneity analyses, publication bias analyses, and meta-regression analyses.ResultsThis CBMA will offer the latest evidence of CTh alterations in PD.ConclusionsConsistent and robust evidence of CTh alterations will feature brain morphometry of PD and may facilitate biomarker development.Prospero registration numberCRD42020148775.

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