Sex, racial, and APOE-ϵ4 allele differences in longitudinal white matter microstructure in multiple cohorts of aging and Alzheimer's disease

Peterson, A.; Sathe, A.; Zaras, D.; Yang, Y.; Durant, A.; Deters, K. D.; Shashikumar, N.; Pechman, K. R.; Kim, M. E.; Gao, C.; Mohd Khairi, N.; Li, Z.; Yao, T.; Huo, Y.; Dumitrescu, L.; Gifford, K.; Wilson, J. E.; Cambronero, F.; Risacher, S. L.; Beason-Held, L. L.; An, Y.; Arfanakis, K.; Erus, G.; Davatzikos, C.; Tosun, D.; Toga, A. W.; Thompson, P. M.; Mormino, E. C.; Zhang, P.; Schilling, K.; Alzheimer's Disease Neuroimaging Initiative,; The BIOCARD Study Team,; The Alzheimer's Disease Sequencing Project,; Albert, M.; Kukull, W.; Biber, S. A.; Landman, B. A.; Johnson, S. C.; Schneider

doi:10.1101/2024.06.10.598357

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bioRxiv · 10.1101/2024.06.10.598357

Sex, racial, and APOE-ϵ4 allele differences in longitudinal white matter microstructure in multiple cohorts of aging and Alzheimer's disease

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Abstract

Structured AbstractO_ST_ABSINTRODUCTIONC_ST_ABSThe effects of sex, race, and Apolipoprotein E (APOE) - Alzheimers disease (AD) risk factors - on white matter integrity are not well characterized. METHODSDiffusion MRI data from nine well-established longitudinal cohorts of aging were free-water (FW)-corrected and harmonized. This dataset included 4,702 participants (age=73.06 {+/-} 9.75) with 9,671 imaging sessions over time. FW and FW-corrected fractional anisotropy (FAFWcorr) were used to assess differences in white matter microstructure by sex, race, and APOE-{varepsilon}4 carrier status. RESULTSSex differences in FAFWcorr in association and projection tracts, racial differences in FAFWcorr in projection tracts, and APOE-{varepsilon}4 differences in FW limbic and occipital transcallosal tracts were most pronounced. DISCUSSIONThere are prominent differences in white matter microstructure by sex, race, and APOE- {varepsilon}4 carrier status. This work adds to our understanding of disparities in AD. Additional work to understand the etiology of these differences is warranted. HighlightsO_LISex, race, and APOE-{varepsilon}4 carrier status relate to white matter microstructural integrity C_LIO_LIFemales generally have lower FAFWcorr compared to males C_LIO_LINon-Hispanic Black adults generally have lower FAFWcorr than non-Hispanic White adults C_LIO_LIAPOE-{varepsilon}4 carriers tended to have higher FW than non-carriers C_LI Research in Context Systematic ReviewThe authors used PubMed and Google Scholar to review literature that used conventional and free-water (FW)-corrected microstructural metrics to evaluate sex, race, and APOE-{varepsilon}4 differences in white matter microstructure. While studies have previously explored differences by sex and APOE-{varepsilon}4 status, less is known about racial differences and no large-scale FW-corrected analysis has been performed. InterpretationSex and race were more associated with FAFWcorr while APOE-{varepsilon}4 status was associated with FW metrics. Association, projection, limbic, and occipital transcallosal tracts showed the greatest differences. Future DirectionFuture studies to determine the biological and social pathways that lead to sex, racial, and APOE-{varepsilon}4 differences are warranted. Consent StatementAll participants provided informed consent in their respective cohort studies.

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Peterson, A., Sathe, A., Zaras, D., Yang, Y., Durant, A., Deters, K. D., Shashikumar, N., Pechman, K. R., Kim, M. E., Gao, C., Mohd Khairi, N., Li, Z., Yao, T., Huo, Y., Dumitrescu, L., Gifford, K., Wilson, J. E., Cambronero, F., Risacher, S. L., Beason-Held, L. L., An, Y., Arfanakis, K., Erus, G., Davatzikos, C., Tosun, D., Toga, A. W., Thompson, P. M., Mormino, E. C., Zhang, P., Schilling, K., Alzheimer's Disease Neuroimaging Initiative,, The BIOCARD Study Team,, The Alzheimer's Disease Sequencing Project,, Albert, M., Kukull, W., Biber, S. A., Landman, B. A., Johnson, S. C., Schneider. 2024-06-12. Sex, racial, and APOE-ϵ4 allele differences in longitudinal white matter microstructure in multiple cohorts of aging and Alzheimer's disease. https://doi.org/10.1101/2024.06.10.598357

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