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dc.contributor.authorLopera, F.
dc.contributor.authorMarino, C.
dc.contributor.authorChandrahas, A.S.
dc.contributor.authorO’Hare, M.
dc.contributor.authorVillalba-Moreno, N.D.
dc.contributor.authorAguillon, D.
dc.contributor.authorBaena, A.
dc.contributor.authorSanchez, J.S.
dc.contributor.authorVila-Castelar, C.
dc.contributor.authorRamirez, Gomez, L.
dc.contributor.authorChmielewska, N.
dc.contributor.authorOliveira, G.M.
dc.contributor.authorLittau, J.L.
dc.contributor.authorHartmann, K.
dc.contributor.authorPark, K.
dc.contributor.authorKrasemann, S.
dc.contributor.authorGlatzel, M.
dc.contributor.authorSchoemaker, D.
dc.contributor.authorGonzalez-Buendia, L.
dc.contributor.authorDelgado-Tirado, S.
dc.contributor.authorArevalo-Alquichire, S.
dc.contributor.authorSaez-Torres, K.L.
dc.contributor.authorAmarnani, D.
dc.contributor.authorKim, L.A.
dc.contributor.authorMazzarino, R.C.
dc.contributor.authorGordon, H.
dc.contributor.authorBocanegra, Y.
dc.contributor.authorVillegas, A.
dc.contributor.authorGai, X.
dc.contributor.authorBootwalla, M.
dc.contributor.authorJi, J.
dc.contributor.authorShen, L.
dc.contributor.authorKosik, K.S.
dc.contributor.authorSu, Y.
dc.contributor.authorChen, Y.
dc.contributor.authorSchultz, A.
dc.contributor.authorSperling, R.A.
dc.contributor.authorJohnson, K.
dc.contributor.authorReiman, E.M.
dc.contributor.authorSepulveda-Falla, D.
dc.contributor.authorArboleda-Velasquez, J.F.
dc.contributor.authorQuiroz, Y.T.
dc.date.accessioned2024-08-09T00:15:42Z
dc.date.available2024-08-09T00:15:42Z
dc.date.issued2023-05-15
dc.identifier.citationLopera, F., Marino, C., Chandrahas, A.S. et al. Resilience to autosomal dominant Alzheimer’s disease in a Reelin-COLBOS heterozygous man. Nat Med 29, 1243–1252 (2023). https://doi.org/10.1038/s41591-023-02318-3
dc.identifier.issn1078-8956
dc.identifier.pmid37188781
dc.identifier.doi10.1038/s41591-023-02318-3
dc.identifier.urihttp://hdl.handle.net/10150/674030
dc.description.abstractWe characterized the world’s second case with ascertained extreme resilience to autosomal dominant Alzheimer’s disease (ADAD). Side-by-side comparisons of this male case and the previously reported female case with ADAD homozygote for the APOE3 Christchurch (APOECh) variant allowed us to discern common features. The male remained cognitively intact until 67 years of age despite carrying a PSEN1-E280A mutation. Like the APOECh carrier, he had extremely elevated amyloid plaque burden and limited entorhinal Tau tangle burden. He did not carry the APOECh variant but was heterozygous for a rare variant in RELN (H3447R, termed COLBOS after the Colombia–Boston biomarker research study), a ligand that like apolipoprotein E binds to the VLDLr and APOEr2 receptors. RELN-COLBOS is a gain-of-function variant showing stronger ability to activate its canonical protein target Dab1 and reduce human Tau phosphorylation in a knockin mouse. A genetic variant in a case protected from ADAD suggests a role for RELN signaling in resilience to dementia. © 2023, The Author(s).
dc.language.isoen
dc.publisherNature Research
dc.rights© The Author(s) 2023. This article is licensed under a Creative Commons Attribution 4.0 International License.
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/
dc.titleResilience to autosomal dominant Alzheimer’s disease in a Reelin-COLBOS heterozygous man
dc.typeArticle
dc.typetext
dc.contributor.departmentUniversity of Arizona
dc.identifier.journalNature Medicine
dc.description.noteOpen access article
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.
dc.eprint.versionFinal Published Version
dc.source.journaltitleNature Medicine
refterms.dateFOA2024-08-09T00:15:42Z


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© The Author(s) 2023. This article is licensed under a Creative Commons Attribution 4.0 International License.
Except where otherwise noted, this item's license is described as © The Author(s) 2023. This article is licensed under a Creative Commons Attribution 4.0 International License.