Abnormalities in the white matter tracts in patients with Parkinson disease and psychosis

Abhishek Lenka, Madhura Ingalhalikar, Apurva Shah, Jitender Saini, Shyam Sundar Arumugham, Shantala Hegde, Lija George, Ravi Yadav, Pramod Kumar Pal*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

26 Citations (Scopus)

Abstract

Objective: The objective of the current study was to compare the microstructural integrity of the white matter (WM) tracts in patients having Parkinson disease (PD) with and without psychosis (PD-P and PD-NP) through diffusion tensor imaging (DTI). Methods: This cross-sectional study involved 48 PD-NP and 42 PD-P who were matched for age, sex, and education. Tract-based spatial statistics (TBSS) was used to compare several DTI metrics from the diffusion-weighted MRIs obtained through a 3-Tesla scanner. A set of neuropsychological tests was used for the cognitive evaluation of all patients. Results: The severity and stage of PD were not statistically different between the groups. The PD-P group performed poorly in all the neuropsychological domains compared with the PD-NP group. TBSS analysis revealed widespread patterns of abnormality in the fractional anisotropy (FA) in the PD-P group, which also correlated with some of the cognitive scores. These tracts include inferior longitudinal fasciculus, inferior fronto-occipital fasciculus, right parieto-occipital WM, body of the corpus callosum, and corticospinal tract. Conclusion: This study provides novel insights into the putative role of WM tract abnormalities in the pathogenesis of PD-P by demonstrating significant alterations in several WM tracts. Additional longitudinal studies are warranted to confirm the findings of our research.

Original languageEnglish
Pages (from-to)e1876-e1884
Number of pages9
JournalNeurology
Volume94
Issue number18
DOIs
Publication statusPublished - 5 May 2020
Externally publishedYes

Fingerprint

Dive into the research topics of 'Abnormalities in the white matter tracts in patients with Parkinson disease and psychosis'. Together they form a unique fingerprint.

Cite this