Please use this identifier to cite or link to this item: https://doi.org/10.1038/s41598-017-06287-9
Title: Common shared genetic variation behind decreased risk of breast cancer in celiac disease
Authors: Ugalde-Morales, E
Li, J 
Humphreys, K
Ludvigsson, J.F
Yang, H
Hall, P
Czene, K
Keywords: breast tumor
celiac disease
chromosomal mapping
complication
female
gene linkage disequilibrium
genetic predisposition
genetic variation
genetics
human
risk factor
single nucleotide polymorphism
Breast Neoplasms
Celiac Disease
Chromosome Mapping
Female
Genetic Predisposition to Disease
Genetic Variation
Humans
Linkage Disequilibrium
Polymorphism, Single Nucleotide
Risk Factors
Issue Date: 2017
Citation: Ugalde-Morales, E, Li, J, Humphreys, K, Ludvigsson, J.F, Yang, H, Hall, P, Czene, K (2017). Common shared genetic variation behind decreased risk of breast cancer in celiac disease. Scientific Reports 7 (1) : 5942. ScholarBank@NUS Repository. https://doi.org/10.1038/s41598-017-06287-9
Rights: Attribution 4.0 International
Abstract: There is epidemiologic evidence showing that women with celiac disease have reduced risk of later developing breast cancer, however, the etiology of this association is unclear. Here, we assess the extent of genetic overlap between the two diseases. Through analyses of summary statistics on densely genotyped immunogenic regions, we show a significant genetic correlation (r = -0.17, s.e. 0.05, P < 0.001) and overlap (Ppermuted < 0.001) between celiac disease and breast cancer. Using individual-level genotype data from a Swedish cohort, we find higher genetic susceptibility to celiac disease summarized by polygenic risk scores to be associated with lower breast cancer risk (ORper-SD, 0.94, 95% CI 0.91 to 0.98). Common single nucleotide polymorphisms between the two diseases, with low P-values (PCD < 1.00E-05, PBC ? 0.05), mapped onto genes enriched for immunoregulatory and apoptotic processes. Our results suggest that the link between breast cancer and celiac disease is due to a shared polygenic variation of immune related regions, uncovering pathways which might be important for their development. © 2017 The Author(s).
Source Title: Scientific Reports
URI: https://scholarbank.nus.edu.sg/handle/10635/178314
ISSN: 20452322
DOI: 10.1038/s41598-017-06287-9
Rights: Attribution 4.0 International
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