Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma.

Abstract:

:Survival following a diagnosis of multiple myeloma (MM) varies between patients and some of these differences may be a consequence of inherited genetic variation. In this study, to identify genetic markers associated with MM overall survival (MM-OS), we conduct a meta-analysis of four patient series of European ancestry, totalling 3,256 patients with 1,200 MM-associated deaths. Each series is genotyped for ∼600,000 single nucleotide polymorphisms across the genome; genotypes for six million common variants are imputed using 1000 Genomes Project and UK10K as the reference. The association between genotype and OS is assessed by Cox proportional hazards model adjusting for age, sex, International staging system and treatment. We identify a locus at 6q25.1 marked by rs12374648 associated with MM-OS (hazard ratio=1.34, 95% confidence interval=1.22-1.48, P=4.69 × 10(-9)). Our findings have potential clinical implications since they demonstrate that inherited genotypes can provide prognostic information in addition to conventional tumor acquired prognostic factors.

journal_name

Nat Commun

journal_title

Nature communications

authors

Johnson DC,Weinhold N,Mitchell JS,Chen B,Kaiser M,Begum DB,Hillengass J,Bertsch U,Gregory WA,Cairns D,Jackson GH,Försti A,Nickel J,Hoffmann P,Nöethen MM,Stephens OW,Barlogie B,Davis FE,Hemminki K,Goldschmidt H,Hou

doi

10.1038/ncomms10290

subject

Has Abstract

pub_date

2016-01-08 00:00:00

pages

10290

issn

2041-1723

pii

ncomms10290

journal_volume

7

pub_type

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