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Article

Association of C34T AMPD1 gene polymorphism with features of metabolic syndrome in patients with coronary artery disease or heart failure.

Scandinavian journal of clinical and laboratory investigation - 1 Jan 2009

Safranow Krzysztof, Czyzycka Edyta, Binczak-Kuleta Agnieszka, Rzeuski Ryszard, Skowronek Janusz, Wojtarowicz Andrzej, Jakubowska Katarzyna, Olszewska Maria, Loniewska Beata, Kaliszczak Robert, Kornacewicz-Jach Zdzislawa, Ciechanowicz Andrzej, Chlubek Dariusz

Abstract excerpt

OBJECTIVE: The common C34T polymorphism in the AMP deaminase-1 (AMPD1) gene results in an inactive enzyme in homozygotes for the mutated T allele. Some studies have shown an association of T allele with longer survival in heart failure (HF) and/or coronary artery disease (CAD). The aim of this study was to assess genotype-phenotype correlations in such patients, with emphasis on components of the metabolic...

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Source

Identifiers

PMID: 18855224
DOI: 10.1080/00365510802430964

Genes

CAD
AMPD1

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.

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Association of C34T AMPD1 gene polymorphism with features of metabolic syndrome in patients with coronary artery disease or heart failure.PMID 18855224Read ↗

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AMP deaminase 1 gene polymorphism and heart disease-a genetic association that highlights new treatment.Semantic proximity Read ↗

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