| Literature DB >> 30242727 |
Sebastian Ocklenburg1, Catrona Anderson2,3, Wanda M Gerding4, Christoph Fraenz2, Caroline Schlüter2, Patrick Friedrich2, Maximilian Raane5, Burkhard Mädler6, Lara Schlaffke7, Larissa Arning4, Jörg T Epplen4,5, Onur Güntürkün2, Christian Beste8, Erhan Genç2.
Abstract
Myelination of axons in the central nervous system is critical for human cognition and behavior. The predominant protein in myelin is proteolipid protein-making PLP1, the gene that encodes for proteolipid protein, one of the primary candidate genes for white matter structure in the human brain. Here, we investigated the relation of genetic variation within PLP1 and white matter microstructure as assessed with myelin water fraction imaging, a neuroimaging technique that has the advantage over conventional diffusion tensor imaging in that it allows for a more direct assessment of myelin content. We observed significant asymmetries in myelin water fraction that were strongest and rightward in the parietal lobe. Importantly, these parietal myelin water fraction asymmetries were associated with genetic variation in PLP1. These findings support the assumption that genetic variation in PLP1 affects white matter myelination in the healthy human brain.Entities:
Keywords: 3D multi-echo gradient spin echo (3D ME-GRASE); Brain; Hemispheric asymmetries; Laterality; Multi-exponential T2 relaxation; Myelin; Myelin water fraction; PLP1; Proteolipid protein; White matter
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Year: 2018 PMID: 30242727 DOI: 10.1007/s12035-018-1351-y
Source DB: PubMed Journal: Mol Neurobiol ISSN: 0893-7648 Impact factor: 5.590