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Resilience to autosomal dominant Alzheimer’s disease in a Reelin-COLBOS heterozygous man

Authors :
Francisco Lopera
Claudia Marino
Anita S. Chandrahas
Michael O’Hare
Nelson David Villalba-Moreno
David Aguillon
Ana Baena
Justin S. Sanchez
Clara Vila-Castelar
Liliana Ramirez Gomez
Natalia Chmielewska
Gabriel M. Oliveira
Jessica Lisa Littau
Kristin Hartmann
Kyungeun Park
Susanne Krasemann
Markus Glatzel
Dorothee Schoemaker
Lucia Gonzalez-Buendia
Santiago Delgado-Tirado
Said Arevalo-Alquichire
Kahira L. Saez-Torres
Dhanesh Amarnani
Leo A. Kim
Randall C. Mazzarino
Harper Gordon
Yamile Bocanegra
Andres Villegas
Xiaowu Gai
Moiz Bootwalla
Jianling Ji
Lishuang Shen
Kenneth S. Kosik
Yi Su
Yinghua Chen
Aaron Schultz
Reisa A. Sperling
Keith Johnson
Eric M. Reiman
Diego Sepulveda-Falla
Joseph F. Arboleda-Velasquez
Yakeel T. Quiroz
Source :
Nature Medicine. 29:1243-1252
Publication Year :
2023
Publisher :
Springer Science and Business Media LLC, 2023.

Abstract

We 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.

Details

ISSN :
1546170X and 10788956
Volume :
29
Database :
OpenAIRE
Journal :
Nature Medicine
Accession number :
edsair.doi...........cbe347616c0af69e09ef1427cfb6ea9e
Full Text :
https://doi.org/10.1038/s41591-023-02318-3