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Advanced Neurology                                          X chromosome-mediated risk in Alzheimer’s disease



              The new directions proposed by the present research      doi: 10.1212/WNL.0b013e31828726f5
            may lead to an improved understanding of the transmission   2.   D’errico P, Meyer-Luehmann M. Mechanisms of pathogenic
            of familial LOAD and the role played by the X chromosome.  Tau and Aβ protein spreading in Alzheimer’s disease. Front
                                                                  Aging Neurosci. 2020;12:265.
            Acknowledgments
                                                                  doi: 10.3389/fnagi.2020.00265
            None.
                                                               3.   Soreq L, Bird H, Mohamed W, Hardy J. Single-cell RNA
            Funding                                               sequencing analysis of human Alzheimer’s disease brain
                                                                  samples reveals neuronal and glial specific cells differential
            This research was funded by the National Institute of Health   expression. PLoS One. 2023;18(2):e0277630.
            National Institute on Aging 1 (RF1 AG054052-01). Partial      doi: 10.1371/journal.pone.0277630
            support for all data sets within the UPDB was provided
            by the Huntsman Cancer Institute, Huntsman Cancer   4.   Bellenguez C, Grenier-Boley B, Lambert JC. Genetics of
            Foundation, the University of Utah, and the Huntsman   Alzheimer’s disease: Where we are, and where we are going.
            Cancer Institute’s Cancer Center Support Grant (P30   Curr Opin Neurobiol. 2020;61:40-48.
            CA42014) from the National Cancer Institute. L.A.C.-A.      doi: 10.1016/j.conb.2019.11.024
            received support from the Huntsman Cancer Foundation   5.   Guerreiro R, Wojtas A, Bras J,  et al. TREM2 variants in
            and George E. Wahlen Department of Veterans Affairs   Alzheimer’s disease. N Engl J Med. 2013;368:117-127.
            Medical Center, Salt Lake City, Utah.
                                                                  doi: 10.1056/NEJMoa1211851
            Conflict of interest                               6.   Cannon-Albright LA, Foster NL, Schliep K, et al. Relative
            The authors declare no conflicts of interest.         risk for Alzheimer disease based on complete family history.
                                                                  Neurology. 2019;92:e1745-e1753.
            Author contributions                                  doi: 10.1212/WNL.0000000000007231
            Conceptualization:  Carmel Armon, Lisa A. Cannon-   7.   Edland SD, Silverman JM, Peskind ER, Tsuang D,
               Albright, Sharon Wolfson                           Wijsman  E, Morris JC. Increased risk of dementia in
            Investigation: Carmel Armon                           mothers of Alzheimer’s disease cases: Evidence for maternal
            Methodology: Carmel Armon, Sharon Wolfson             inheritance. Neurology. 1996;47:254-246.
            Writing–original draft:  Carmel Armon, Lisa A. Cannon-      doi: 10.1212/wnl.47.1.254
               Albright
            Writing–review  &  editing:  Kristina Allen-Brady, Sharon   8.   Honea RA, Swerdlow RH, Vidoni ED, Burns JM. Progressive
                                                                  regional atrophy in normal adults with a maternal history of
               Wolfson                                            Alzheimer disease. Neurology. 2011;76:822-829.
            Ethics approval and consent to participate            doi: 10.1212/WNL.0b013e31820e7b74

            The study was approved by the University of Utah   9.   Honea RA, Vidoni ED, Swerdlow RH, Burns JM, Alzheimer’s
            Institutional Review Board and the Utah Resource      Disease Neuroimaging Initiative. Maternal family history is
            for Genetic Epidemiological Research (approval no.:   associated with Alzheimer’s disease biomarkers. J Alzheimers
                                                                  Dis. 2012;31:659-668.
            IRB_00057751), which collectively oversee the use of
            UPDB data. Individual consent was not required to access      doi: 10.3233/JAD-2012-120676
            the data or to publish.                            10.  Roberts RO, Geda YE, Knopman DS, et al. The incidence
                                                                  of MCI differs by subtype and is higher in men: The mayo
            Consent for publication                               clinic study of aging. Neurology. 2012;78:342-351.
            Not applicable.                                       doi: 10.1212/WNL.0b013e3182452862

            Availability of data                               11.  Mielke MM, Vemuri P, Rocca WA. Clinical epidemiology of
                                                                  Alzheimer’s disease: Assessing sex and gender differences.
            Access to UPDB data are allowed with appropriate      Clin Epidemiol. 2014;6:37-48.
            application and approval.
                                                                  doi: 10.2147/CLEP.S37929
            References                                         12.  Bajic VP, Essack M, Zivkovic L,  et al. The X Files: “The
                                                                  mystery of X chromosome instability in Alzheimer’s
            1.   Herbert LE, Weuve J, Scherr PA, Evans DA. Alzheimer
               disease in the United States (2010-2050) estimated using the   disease”. Front Genet. 2020;10:1368.
               2010 census. Neurology. 2013;80:1778-1783.         doi: 10.3389/fgene.2019.01368


            Volume 3 Issue 2 (2024)                         9                                doi: 10.36922/an.3122
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