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E280A PS‐1 mutation causes Alzheimer's disease but age of onset is not modified by ApoE alleles
Author(s) -
Lendon Corinne L.,
Martinez Alonso,
Behrens Isabel Maria,
Kosik Kenneth S.,
Madrigal Lucia,
Norton Joanne,
Neuman Rosalind,
Myers Amanda,
Busfield Frances,
Wragg Michelle,
Arcos Mauricio,
Viana Juan Carlos Arango,
Ossa Jorge,
Ruiz Andres,
Goate Alison M.,
Lopera Francisco
Publication year - 1997
Publication title -
human mutation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.981
H-Index - 162
eISSN - 1098-1004
pISSN - 1059-7794
DOI - 10.1002/(sici)1098-1004(1997)10:3<186::aid-humu2>3.0.co;2-h
Subject(s) - biology , genetics , apolipoprotein e , allele , genotype , haplotype , age of onset , founder effect , mutation , point mutation , disease , gene , medicine
A single base substitution of a glutamic acid to an alanine codon 280 was found in the presenilin‐1 ( PS‐1 ) gene on chromosome 14 in affected individuals in each of seven Colombian early‐onset Alzheimer's disease (AD) kindreds. The mutation segregated with disease in kindreds tested. In the largest kindred (C2), the maximum two‐point lod score between the mutation and AD was Z = 8.14 at θ = 0. The presence of a single mutation and the common geographic origin, with all families from the state of Antioquia, suggest a founder effect in this population. This finding is supported by the observation of a rare haplotype inherited with AD in all kindreds. These kindreds form the largest collection of AD cases with the same PS‐1 mutation and the same educational, environmental, and ethnic background in which to study the phenotypic effect of putative risk factors, such as the ϵ4 allele of apolipoprotein E (ApoE) or head trauma. Of the few AD cases having a history of head trauma, the age of onset was not lowered. No effect of ApoE genotype on the age of onset was detected. Previous investigations of the effect of ApoE genotype on the age of onset were confounded by small patient numbers, familial clustering of ApoE genotypes, and combining data from unrelated families with different mutations. Hum Mutat 10:186–195, 1997. © 1997 Wiley‐Liss, Inc.