2015
Association of polymorphisms in the endocannabinoid system genes with myocardial infarction and plasma cholesterol levels
CHMELÍKOVÁ, Monika; Lukáš PÁCAL; Lenka ŠPINAROVÁ and Anna VAŠKŮBasic information
Original name
Association of polymorphisms in the endocannabinoid system genes with myocardial infarction and plasma cholesterol levels
Name in Czech
Asociace polymorfizmů v genech endokanabinoidního systému s infarktem myokardu a plazmatickou hladinou cholesterolu
Authors
CHMELÍKOVÁ, Monika (203 Czech Republic, guarantor, belonging to the institution); Lukáš PÁCAL (203 Czech Republic, belonging to the institution); Lenka ŠPINAROVÁ (203 Czech Republic) and Anna VAŠKŮ (203 Czech Republic, belonging to the institution)
Edition
Biomedical Papers, Olomouc, Palacky University, 2015, 1213-8118
Other information
Language
English
Type of outcome
Article in a journal
Field of Study
30000 3. Medical and Health Sciences
Country of publisher
Czech Republic
Confidentiality degree
is not subject to a state or trade secret
Impact factor
Impact factor: 0.924
RIV identification code
RIV/00216224:14110/15:00082099
Organization unit
Faculty of Medicine
UT WoS
000366566700004
EID Scopus
2-s2.0-84949642993
Keywords (in Czech)
chronické srdeční selhání; endokanabinoidní systém; hydroláza amidů mastných kyselin
Keywords in English
chronic heart failure; endocannabinoid system; fatty acid amide hydrolase; cannabinoid receptor; myocardial infarction cholesterol
Tags
Tags
International impact, Reviewed
Changed: 8/4/2016 09:44, Ing. Mgr. Věra Pospíšilíková
Abstract
In the original language
Aims. The aim of this study was to investigate the relationship between selected symptoms of chronic heart failure (myocardial infarction, plasma cholesterol level) and single nucleotide polymorphisms (SNPs) in the FAAH and CNR1 genes. Methods. A case – control study involving 155 patients with chronic heart failure and 169 age- and sex-matched healthy subjects. We detected SNPs 385 C/A (rs324420) in the FAAH and 1359 G/A (rs1049353) in the CNR1 genes using the polymerase chain reaction and restriction analysis. Genotype and allele frequencies were compared between patients and controls as well as between patients with and without myocardial infarction. Results. No significant differences in genotype or allelic frequencies between patients and controls were found (P > 0.05). Carriers of the FAAH A allele had a 2.37-fold increase in the risk of myocardial infarction (odds ratio 2.37, 95% confidence interval 1.36-6.93, P = 0.01). Homozygous carriers of genotype AA of CNR1 SNP 1359 had significantly higher plasma cholesterol levels than carriers of GG and GA genotypes in patients (P = 0.04). Conclusions. The study results suggest a role for allele A of the FAAH 385 variant as a risk factor for myocardial infarction. Genotype AA of CNR1 1359 variant probably affects plasma cholesterol levels. Pharmacological intervention in this system could modify the therapeutic approach to certain cardiovascular disorders.