Cellular and extracellular white matter abnormalities in Obsessive-Compulsive Disorder: a diffusion MRI study

While previous studies have implicated white matter (WM) as a core pathology of Obsessive-Compulsive Disorder (OCD), the underlying neurobiological processes remain elusive. This study utilizes free-water imaging derived from diffusion MRI to identify cellular and extracellular WM abnormalities in p...

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Veröffentlicht in:Biological psychiatry : cognitive neuroscience and neuroimaging 2021-04, Vol.6 (10), p.983-991
Hauptverfasser: Maziero, Maria Paula, Seitz-Holland, Johanna, Cho, Kang Ik K, Goldenberg, Joshua E, Tanamatis, Taís W, Diniz, Juliana B, Cappi, Carolina, Alice de Mathis, Maria, Otaduy, Maria C G, da Graça Morais Martin, Maria, de Melo Felipe da Silva, Renata, Shavitt, Roseli G, Batistuzzo, Marcelo C, Lopes, Antonio C, Miguel, Eurípedes C, Pasternak, Ofer, Hoexter, Marcelo Q
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Sprache:eng
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Zusammenfassung:While previous studies have implicated white matter (WM) as a core pathology of Obsessive-Compulsive Disorder (OCD), the underlying neurobiological processes remain elusive. This study utilizes free-water imaging derived from diffusion MRI to identify cellular and extracellular WM abnormalities in patients with OCD compared to controls (Cs). Next, we investigate the association between diffusion measures, and clinical variables in patients. We collected diffusion-weighted MRI and clinical data from eighty-three patients with OCD (56 females/27 males, age=37.7 ± 10.6) and 52 Cs (27 females/25 males, age=32.8 ± 11.5). Fractional anisotropy (FA), fractional anisotropy of cellular tissue (FAT), and extracellular free-water (FW) maps were extracted and compared between patients and Cs using tract-based spatial statistics, and voxel-wise comparison in FSL's Randomise. Next, we correlated these WM measures with clinical variables (age-of-onset and symptom severity) and compared them between patients with and without comorbidities and patients with and without psychiatric medication. Patients with OCD demonstrated lower FA (43.4% of the WM skeleton), FAт (31% of the WM skeleton), and higher FW (22.5% of the WM skeleton) compared to Cs. We did not observe significant correlations between diffusion measures and clinical variables. Comorbidities and medication status did not influence diffusion measures. Our findings of widespread FA, FAт, and FW abnormalities suggest that OCD is associated with both microstructural cellular and extracellular abnormalities beyond the cortico-striato-thalamo-cortical circuits. Future multimodal longitudinal studies are needed to understand better the influence of essential clinical variables across the illness trajectory.
ISSN:2451-9022
2451-9030
DOI:10.1016/j.bpsc.2021.04.001