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APOE and other loci affect age‐at‐onset in Alzheimer's disease families with PS2 mutation
Author(s) -
Wijsman Ellen M.,
Daw E. Warwick,
Yu Xuesong,
Steinbart Ellen J.,
Nochlin David,
Bird Thomas D.,
Schellenberg Gerard D.
Publication year - 2004
Publication title -
american journal of medical genetics part b: neuropsychiatric genetics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.393
H-Index - 126
eISSN - 1552-485X
pISSN - 1552-4841
DOI - 10.1002/ajmg.b.30087
Subject(s) - apolipoprotein e , age of onset , allele , locus (genetics) , biology , genetics , genotype , alzheimer's disease , allelic heterogeneity , dementia , disease , medicine , gene
Several kindreds of Volga German (VG) ancestry have a single PS2 mutation that causes an autosomal dominant form of Alzheimer's disease (AD). These families show a wide range in age‐at‐onset, which suggests the existence of modifying factors other than the PS2 mutation. To examine evidence for a genetic basis of variation in onset age, we performed a Bayesian oligogenic segregation and linkage analysis on nine VG families confirmed to have at least one affected PS2 carrier. This analysis simultaneously estimated the effects of APOE and PS2 and the number and effects of additional loci affecting AD age‐at‐onset. In addition, a family effect accounted for shared environmental effects. This analysis approach has the advantage of full use of the complete pedigree structure, as well as use of information on unsampled individuals with phenotypic data. These analyses provide evidence that APOE plays a small, but significant, role in modifying the age‐at‐onset in these VG families. The effects estimated for the APOE ε3 and ε4 genotypes were consistent with those estimated in previous analysis of late‐onset AD families, with evidence for a dose‐dependent relationship between number of ε4 alleles and age‐at‐onset. We estimated an ∼83% posterior probability of at least one modifier locus in addition to APOE, and that the fraction of the variance in age‐at‐onset attributable to PS2, APOE, other loci, and family effects is ∼70, ∼2, ∼6.5, and ∼8.5%, respectively. These results provide evidence that APOE and other loci modify onset in AD caused by PS2 mutation. © 2004 Wiley‐Liss, Inc.