Genetic associations with age at dementia onset in the PSEN1 E280A Colombian kindred

Author:

Cochran Jesse Nicholas1ORCID,Acosta‐Uribe Juliana23,Esposito Bianca T.4,Madrigal Lucia3,Aguillón David3,Giraldo Margarita M.3,Taylor Jared W.1,Bradley Joseph5,Fulton‐Howard Brian4,Andrews Shea J.4,Acosta‐Baena Natalia3,Alzate Diana3,Garcia Gloria P.3,Piedrahita Francisco3,Lopez Hugo E.3,Anderson Ashlyn G.1,Rodriguez‐Nunez Ivan1,Roberts Kevin1,Dominantly Inherited Alzheimer Network 5,Absher Devin1,Myers Richard M.1,Beecham Gary W.6,Reitz Christiane7,Rizzardi Lindsay F.1,Fernandez Maria Victoria5,Goate Alison M.4,Cruchaga Carlos5,Renton Alan E.4,Lopera Francisco3,Kosik Kenneth S.2

Affiliation:

1. HudsonAlpha Institute for Biotechnology Huntsville Alabama USA

2. Neuroscience Research Institute University of California, Santa Barbara, California, and Department of Molecular Cellular and Developmental Biology University of California Santa Barbara California USA

3. Grupo de Neurociencias de Antioquia. School of Medicine. Universidad de Antioquia Medellín Antioquia Colombia

4. Department of Genetics & Genomic Sciences Icahn School of Medicine at Mount Sinai New York New York USA

5. Washington University School of Medicine St. Louis Missouri USA

6. The John P. Hussman Institute for Human Genomics University of Miami Miami Florida USA

7. Department of Epidemiology, Sergievsky Center, Taub Institute for Research on the Aging Brain Columbia University New York New York USA

Abstract

AbstractINTRODUCTIONGenetic associations with Alzheimer's disease (AD) age at onset (AAO) could reveal genetic variants with therapeutic applications. We present a large Colombian kindred with autosomal dominant AD (ADAD) as a unique opportunity to discover AAO genetic associations.METHODSA genetic association study was conducted to examine ADAD AAO in 340 individuals with the PSEN1 E280A mutation via TOPMed array imputation. Replication was assessed in two ADAD cohorts, one sporadic early‐onset AD study and four late‐onset AD studies.RESULTS13 variants had p<1×10−7 or p<1×10−5 with replication including three independent loci with candidate associations with clusterin including near CLU. Other suggestive associations were identified in or near HS3ST1, HSPG2, ACE, LRP1B, TSPAN10, and TSPAN14.DISCUSSIONVariants with suggestive associations with AAO were associated with biological processes including clusterin, heparin sulfate, and amyloid processing. The detection of these effects in the presence of a strong mutation for ADAD reinforces their potentially impactful role.

Funder

Larry L. Hillblom Foundation

National Institute on Aging

Michael J. Fox Foundation for Parkinson's Research

Publisher

Wiley

Subject

Psychiatry and Mental health,Cellular and Molecular Neuroscience,Geriatrics and Gerontology,Neurology (clinical),Developmental Neuroscience,Health Policy,Epidemiology

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