Evidence map›Paper›PMID 31216985›Full record

ArticleBMC bioinformatics2019

Cross-population analysis for functional characterization of type II diabetes variants.

Dalia Elmansy, Mehmet Koyutürk

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Article in BMC bioinformatics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
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2citing papers in PubMed
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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Dalia ElmansyDepartment of Electrical Engineering and Computer Science, Case Western Reserve University, 10900 Euclid Ave, Cleveland, OH, 44106, USA. dfe4@case.edu.
Mehmet KoyutürkDepartment of Electrical Engineering and Computer Science, Center for Proteomics and Bioinformatics, Case Western Reserve University, 10900 Euclid Ave, Cleveland, OH, 44106, USA.

Funding

Theoretical Foundations and Software Infrastructure for Biological Network DatabasesU01CA198941 · NCI · CASE WESTERN RESERVE UNIVERSITY · PI KOYUTURK, MEHMET · 2015 to 2017
$1.4M
Enhancing Genome-Wide Association Studies via Integrative Network AnalysisR01LM011247 · NLM · CASE WESTERN RESERVE UNIVERSITY · PI KOYUTURK, MEHMET · 2012 to 2015
$1.3M
NCI NIH HHS U01 CA198941NLM NIH HHS R01 LM011247
6 · The paper itself

Abstract

backgroundAs Genome-Wide Association Studies (GWAS) have been increasingly used with data from various populations, it has been observed that data from different populations reveal different sets of Single Nucleotide Polymorphisms (SNPs) that are associated with the same disease. Using Type II Diabetes (T2D) as a test case, we develop measures and methods to characterize the functional overlap of SNPs associated with the same disease across populations.

resultsWe introduce the notion of an Overlap Matrix as a general means of characterizing the functional overlap between different SNP sets at different genomic and functional granularities. Using SNP-to-gene mapping, functional annotation databases, and functional association networks, we assess the degree of functional overlap across nine populations from Asian and European ethnic origins. We further assess the generalizability of the method by applying it to a dataset for another complex disease - Prostate Cancer. Our results show that more overlap is captured as more functional data is incorporated as we go through the pipeline, starting from SNPs and ending at network overlap analyses. We hypothesize that these observed differences in the functional mechanisms of T2D across populations can also explain the common use of different prescription drugs in different populations. We show that this hypothesis is concordant with the literature on the functional mechanisms of prescription drugs.

conclusionOur results show that although the etiology of a complex disease can be associated with distinct processes that are affected in different populations, network-based annotations can capture more functional overlap across populations. These results support the notion that it can be useful to take ethnicity into account in making personalized treatment decisions for complex diseases.

Indexed as

Genetic Predisposition to DiseaseGenome-Wide Association StudyAsian PeopleDiabetes Mellitus, Type 2EthnicityGenome, HumanHumansMalePolymorphism, Single NucleotideProstatic NeoplasmsProtein Interaction MapsCross-population analysisFunctional annotationNetwork analysisOverlap analysisT2D single nucleotide polymorphismType II diabetes

Identifiers

PMID31216985
PMCPMC6584529

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.