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bioRxiv · 10.1101/2024.11.27.625603

White matter microstructure links with brain, bodily and genetic attributes in adolescence, mid- and late life

Korbmacher, M.·Tranfa, M.·Pontillo, G.·van der Meer, D.·Wang, M.-Y.·Andreassen, O. A.·Westlye, L. T.·Maximov, I. I.
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Abstract

Advanced diffusion magnetic resonance imaging (dMRI) allows one to probe and assess brain white matter (WM) organization and microstructure in vivo. Various dMRI models with different theoretical and practical assumptions have been developed, representing partly overlapping characteristics of the underlying brain biology with potentially complemen-tary value in the cognitive and clinical neurosciences. To which degree the different dMRI metrics relate to clinically relevant geno-and phenotypes is still debated. Hence, we inves-tigate how tract-based and whole WM skeleton parameters from different single- and multi-compartment dMRI approaches associate with clinically relevant and white matter-related phenotypes (sex, age, pulse pressure (PP), body-mass-index (BMI), brain asymmetry) and genetic markers in the UK Biobank (UKB, n=52, 140) and the Adolescent Brain Cognitive Development (ABCD) Study (n=5, 844). Multi-compartment dMRI approaches provided the strongest WM associations with age, and unique insights into brain asymmetry. Kurto-sis was most indicative of PP and BMI. WM-based sex classifications and polygenic score associations for common psychiatric disorders and Alzheimers disease were similar across diffusion approaches. We conclude that WM microstructure is differentially associated with clinically relevant pheno- and genotypes at different points in life. Multi-compartment dMRI approaches, and particularly the examined Bayesian approach, provide additional information to conventional approaches in such examinations.

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Korbmacher, M., Tranfa, M., Pontillo, G., van der Meer, D., Wang, M.-Y., Andreassen, O. A., Westlye, L. T., Maximov, I. I.. 2024-11-27. White matter microstructure links with brain, bodily and genetic attributes in adolescence, mid- and late life. https://doi.org/10.1101/2024.11.27.625603

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