Effect of genetic variant (rs11887534) in ABCG8 gene in coronary artery disease and response to atorvastatin therapy.

doi:10.3233/DMA-2010-0710

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Community

Back to search

Article

Effect of genetic variant (rs11887534) in ABCG8 gene in coronary artery disease and response to atorvastatin therapy.

Disease markers - 1 Jan 2010

Srivastava Anshika, Garg Naveen, Srivastava Anvesha, Srivastava Kshitij, Mittal Balraj

Abstract excerpt

BACKGROUND: ATP-binding cassette transporter ABCG8 plays an important role in excretion of cholesterol from liver. Common genetic polymorphisms in ABCG8 gene may genetically predispose an individual to coronary artery disease (CAD) along with response to atorvastatin therapy. Thus, we aimed to examine the role of ABCG8 D19H polymorphism (rs11887534) in susceptibility to CAD and its influence on atorvastatin...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Anticholesteremic Agents

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Atorvastatin

Share to ATP Binding Cassette Transporter, Subfamily G, Member 8

Share to ATP-Binding Cassette Transporters

Share to Coronary Artery Disease

Share to Heptanoic Acids

Share to Lipids

Share to Pyrroles

Source

Open in PubMed Open full text

Identifiers

PMID: 20592455
DOI: 10.3233/DMA-2010-0710
PMCID: PMC3833422

Genes

ABCG8
CAD

Variants

rs11887534

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Effect of genetic variant (rs11887534) in ABCG8 gene in coronary artery disease and response to atorvastatin therapy.PMID 20592455Read ↗

ABCG8 gene polymorphisms, plasma cholesterol concentrations, and risk of cardiovascular disease in familial hypercholesterolemia.Semantic proximity Read ↗

ATP binding cassette transporter G5 and G8 genotypes and plasma lipoprotein levels before and after treatment with atorvastatin.Semantic proximity Read ↗

Contribution of CYP19A1, CYP1A1, and CYP1A2 polymorphisms in coronary heart disease risk among the Chinese Han population.Semantic proximity Read ↗

Genetic variation in ABCA1 predicts ischemic heart disease in the general population.Semantic proximity Read ↗

Genetic determinants of lipid-lowering response to atorvastatin therapy in an Indian population.Semantic proximity Read ↗

Association of ATP-binding cassette transporter A1 gene polymorphisms with plasma lipid variability and coronary heart disease risk.Semantic proximity Read ↗

ABCG5/8 variants are associated with susceptibility to coronary heart disease.Semantic proximity Read ↗

Common variants in the ATP-binding cassette transporter 1 gene with decreased HDL-cholesterol levels and coronary artery disease.Semantic proximity Read ↗

CYP7A1 gene polymorphism located in the 5' upstream region modifies the risk of coronary artery disease.Semantic proximity Read ↗

ApoB gene polymorphism (rs676210) and its pharmacogenetics impact on atorvastatin response among Iraqi population with coronary artery diseaseSemantic proximity Read ↗

A novel haplotype in ABCA1 gene effects plasma HDL-C concentration.Semantic proximity Read ↗

ABCG5/G8 polymorphisms and markers of cholesterol metabolism: systematic review and meta-analysis.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.