{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,11,5]],"date-time":"2026-11-05T07:11:37Z","timestamp":1793862697354,"version":"4.6.1"},"reference-count":101,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"6","license":[{"start":{"date-parts":[[2025,4,29]],"date-time":"2025-04-29T00:00:00Z","timestamp":1745884800000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by\/4.0 http:\/\/creativecommons.org\/licenses\/by\/4.0"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2026,6]]},"abstract":"<jats:p>JOURNAL\/nrgr\/04.03\/01300535-202606000-00068\/figure1\/v\/2026-04-16T195327Z\/r\/image-tiff<\/jats:p>\n                  <jats:p>\n                    Alzheimer\u2019s disease is initially thought to be caused by age-associated accumulation of plaques, in recent years, research has increasingly associated Alzheimer\u2019s disease with lysosomal storage and metabolic disorders, and the explanation of its pathogenesis has shifted from amyloid and tau accumulation to oxidative stress and impaired lipid and glucose metabolism aggravated by hypoxic conditions. However, the underlying mechanisms linking those cellular processes and conditions to disease progression have yet to be defined. Here, we applied a disease similarity approach to identify unknown molecular targets of Alzheimer\u2019s disease by using transcriptomic data from congenital diseases known to increase Alzheimer\u2019s disease risk, namely Down syndrome, Niemann-Pick type C disease, and mucopolysaccharidoses I. We uncovered common pathways, hub genes, and miRNAs across\n                    <jats:italic toggle=\"yes\">in vitro<\/jats:italic>\n                    and\n                    <jats:italic toggle=\"yes\">in vivo<\/jats:italic>\n                    models of these diseases as potential molecular targets for neuroprotection and amelioration of Alzheimer\u2019s disease pathology, many of which have never been associated with Alzheimer\u2019s disease. We then investigated common molecular alterations in brain samples from a Niemann-Pick type C disease mouse model by juxtaposing them with brain samples of both human and mouse models of Alzheimer\u2019s disease. Detailed phenotypic, molecular, chronological, and biological aging analyses revealed that the\n                    <jats:italic toggle=\"yes\">Npc1<\/jats:italic>\n                    <jats:sup>tm(I1061T)Dso<\/jats:sup>\n                    mouse model can serve as a potential short-lived\n                    <jats:italic toggle=\"yes\">in vivo<\/jats:italic>\n                    model for brain aging and Alzheimer\u2019s disease research. This research represents the first comprehensive approach to congenital disease association with neurodegeneration and a new perspective on Alzheimer\u2019s disease research while highlighting shortcomings and lack of correlation in diverse\n                    <jats:italic toggle=\"yes\">in vitro<\/jats:italic>\n                    models. Considering the lack of an Alzheimer\u2019s disease mouse model that recapitulates the physiological hallmarks of brain aging, the short-lived\n                    <jats:italic toggle=\"yes\">Npc1<\/jats:italic>\n                    <jats:sup>tm(I1061T)Dso<\/jats:sup>\n                    mouse model can further accelerate the research in these fields and offer a unique model for understanding the molecular mechanisms of Alzheimer\u2019s disease from a perspective of accelerated brain aging.\n                  <\/jats:p>","DOI":"10.4103\/nrr.nrr-d-24-01190","type":"journal-article","created":{"date-parts":[[2025,5,2]],"date-time":"2025-05-02T07:37:25Z","timestamp":1746171445000},"page":"2531-2542","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":5,"title":["Short-lived Niemann-Pick type C mice with accelerated brain aging as a novel model for Alzheimer\u2019s disease research"],"prefix":"10.4103","volume":"21","author":[{"given":"Vikas Anil","family":"Gujjala","sequence":"first","affiliation":[{"name":"Department of Biology, Virginia Commonwealth University, Richmond, VA, USA"},{"name":"Center for Integrative Life Sciences, Virginia Commonwealth University, Richmond, VA, USA"},{"name":"Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Morteza","family":"Abyadeh","sequence":"additional","affiliation":[{"name":"Department of Biology, Virginia Commonwealth University, Richmond, VA, USA"},{"name":"Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Isaiah","family":"Klimek","sequence":"additional","affiliation":[{"name":"Department of Biology, Virginia Commonwealth University, Richmond, VA, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alexander","family":"Tyshkovskiy","sequence":"additional","affiliation":[{"name":"Division of Genetics, Department of Medicine, Brigham and Women\u2019s Hospital, Harvard Medical School, Boston, MA, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Naci","family":"Oz","sequence":"additional","affiliation":[{"name":"Department of Biology, Virginia Commonwealth University, Richmond, VA, USA"},{"name":"Center for Integrative Life Sciences, Virginia Commonwealth University, Richmond, VA, USA"},{"name":"Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jos\u00e9 Pedro","family":"Castro","sequence":"additional","affiliation":[{"name":"i3S, Instituto de Investiga\u00e7\u00e3o e Inova\u00e7\u00e3o em Sa\u00fade, Universidade do Porto, Porto, Portugal"},{"name":"Aging and Aneuploidy Laboratory, IBMC, Instituto de Biologia Molecular e Celular, Universidade do Porto, Porto, Portugal"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Vadim N.","family":"Gladyshev","sequence":"additional","affiliation":[{"name":"Division of Genetics, Department of Medicine, Brigham and Women\u2019s Hospital, Harvard Medical School, Boston, MA, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-2952-2008","authenticated-orcid":false,"given":"Jason","family":"Newton","sequence":"additional","affiliation":[{"name":"Department of Biology, Virginia Commonwealth University, Richmond, VA, USA"},{"name":"Center for Integrative Life Sciences, Virginia Commonwealth University, Richmond, VA, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-6132-5197","authenticated-orcid":false,"given":"Alaattin","family":"Kaya","sequence":"additional","affiliation":[{"name":"Department of Biology, Virginia Commonwealth University, Richmond, VA, USA"},{"name":"Center for Integrative Life Sciences, Virginia Commonwealth University, Richmond, VA, USA"},{"name":"Department of Biochemistry and Molecular Genetics, University of Virginia School of Medicine, Charlottesville, VA, USA"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2025,4,29]]},"reference":[{"key":"R1-20260416","doi-asserted-by":"crossref","first-page":"97","DOI":"10.1186\/s13195-017-0320-4","article-title":"Rho GTPases as therapeutic targets in Alzheimer\u2019s disease","volume":"9","author":"Aguilar","year":"2017","journal-title":"Alzheimers Res Ther"},{"key":"R2-20260416","article-title":"FastQC: a quality control tool for high throughput sequence data [Online]","author":"Andrews","year":"2010"},{"key":"R3-20260416","doi-asserted-by":"crossref","first-page":"1305","DOI":"10.1093\/hmg\/ddu541","article-title":"Expression of progerin in aging mouse brains 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