Please use this identifier to cite or link to this item: https://www.um.edu.mt/library/oar/handle/123456789/93694
Full metadata record
DC FieldValueLanguage
dc.contributor.authorMinkelen, Rick van-
dc.contributor.authorBezzina Wettinger, Stephanie-
dc.contributor.authorDe Visser, Marieke C.H.-
dc.contributor.authorVos, Hans L.-
dc.contributor.authorReitsma, Pieter H.-
dc.contributor.authorRosendaal, Frits R.-
dc.contributor.authorBertina, Rogier M.-
dc.contributor.authorDoggen, Carine J. M.-
dc.date.accessioned2022-04-13T09:57:56Z-
dc.date.available2022-04-13T09:57:56Z-
dc.date.issued2009-03-
dc.identifier.citationVan Minkelen, R., Wettinger, S., De Visser, M., Vos, H., Reitsma, P., Rosendaal, F., . . . Doggen, C. (2008). Haplotypes of the interleukin-1 receptor antagonist gene, interleukin-1 receptor antagonist mRNA levels and the risk of myocardial infarction. Atherosclerosis, 203(1), 201-205.en_GB
dc.identifier.urihttps://www.um.edu.mt/library/oar/handle/123456789/93694-
dc.description.abstractBACKGROUND: The overall effect of the major pro-inflammatory cytokine interleukin-1 (IL-1) on coagulation and fibrinolysis is prothrombotic. We recently found that haplotype 5 (H5) of the gene (IL1RN) coding for the interleukin-1 receptor antagonist (IL-1Ra), the natural inhibitor of IL-1, is associated with an increased risk of venous thrombosis. It is unclear whether variations in IL1RN affect the risk of myocardial infarction.en_GB
dc.description.abstractOBJECTIVES: The aim of this study was to investigate the effect of the five most common haplotype groups of IL1RN on the risk of myocardial infarction and on IL1RN mRNA levels.en_GB
dc.description.abstractPATIENTS/METHODS: We genotyped 5 single nucleotide polymorphisms (SNPs) in IL1RN in 560 male patients and 646 male control subjects of a population-based case–control study on myocardial infarction, enabling us to tag the five common haplotype groups of IL1RN. For all haplotype groups the relationship with the risk of myocardial infarction and IL1RN mRNA levels was determined.en_GB
dc.description.abstractRESULTS: An increased risk of myocardial infarction was found for haplotype 3 (H3) carriers (tagged by SNP 13760T/C, odds ratio = 1.3; 95% confidence interval: 1.1–1.7) compared to non-H3 carriers. No effect on myocardial infarction risk was found for the other haplotypes. H3 carriers had decreased IL1RN mRNA levels compared to non-H3 carriers (p < 0.01), whereas mRNA levels were higher in H2 carriers compared to non-H2 carriers (p < 0.01).en_GB
dc.description.abstractCONCLUSIONS: We found that H3 carriership increases the risk of myocardial infarction. This effect could be explained by the reduced IL1RN expression in H3 carriers, which is expected to result in reduced levels of IL-1Ra, the principal antagonist of IL-1.en_GB
dc.language.isoenen_GB
dc.publisherElsevieren_GB
dc.rightsinfo:eu-repo/semantics/restrictedAccessen_GB
dc.subjectMyocardial infarction -- Risk factorsen_GB
dc.subjectHaplotypesen_GB
dc.subjectInterleukin-1en_GB
dc.subjectMessenger RNAen_GB
dc.titleHaplotypes of the interleukin-1 receptor antagonist gene, interleukin-1 receptor antagonist mRNA levels and the risk of myocardial infarctionen_GB
dc.typearticleen_GB
dc.rights.holderThe copyright of this work belongs to the author(s)/publisher. The rights of this work are as defined by the appropriate Copyright Legislation or as modified by any successive legislation. Users may access this work and can make use of the information contained in accordance with the Copyright Legislation provided that the author must be properly acknowledged. Further distribution or reproduction in any format is prohibited without the prior permission of the copyright holder.en_GB
dc.description.reviewedpeer-revieweden_GB
dc.identifier.doi10.1016/j.atherosclerosis.2008.06.029-
dc.publication.titleAtherosclerosisen_GB
Appears in Collections:Scholarly Works - FacHScABS

Files in This Item:
File Description SizeFormat 
Haplotypes of the interleukin-1 receptor antagonist gene.pdf
  Restricted Access
140.76 kBAdobe PDFView/Open Request a copy


Items in OAR@UM are protected by copyright, with all rights reserved, unless otherwise indicated.