Gender difference and genetic variance in lipoprotein receptor-related protein 1 is associated with mortality
2019 (English)In: BIOMEDICAL REPORTS, ISSN 2049-9434, Vol. 11, no 1Article in journal (Refereed) Published
Abstract [en]
Cardiovascular diseases are an important health resource problem and studies have shown a genetic association between single nucleotide polymorphisms (SNPs) and cardiovascular diseases. According to the literature, lipoprotein receptor-related protein 1 (LRP1) is associated with coronary artery disease. The aim of the present study was to evaluate a possible association between different genotypes of LRP1 and all-cause and cardiovascular mortality from a gender perspective. In the present study, 489 elderly community-living people were invited to participate. Clinical examination, echocardiography and blood sampling including SNP analyses of LRP1 (rs1466535) were performed, including the T/T, C/T and C/C genotypes, and the participants were followed for 6.7 years. During the follow-up period, 116 (24%) all-cause and 75 (15%) cardiovascular deaths were registered. In the female population, the LRP1 of the T/T or C/T genotype exhibited a 5.6-fold increased risk of cardiovascular mortality and a 2.8-fold increased risk of all-cause mortality compared with the C/C genotype. No such genotype differences could be seen in the male population. Gender differences could be seen regarding the risk of mortality in the different genotypes. Females with the LRP1 T/T or C/T genotypes exhibited a significantly increased risk of both all-cause and cardiovascular mortality compared with the C/C genotypes. Therefore, more individualized cardiovascular prevention and treatment should be prioritized. However, since this was a small study, the observations should only be regarded as hypothesis-generating.
Place, publisher, year, edition, pages
SPANDIDOS PUBL LTD , 2019. Vol. 11, no 1
Keywords [en]
low-density lipoprotein receptor-related protein 1; genotypes; elderly; genders; mortality
National Category
Geriatrics
Identifiers
URN: urn:nbn:se:liu:diva-159152DOI: 10.3892/br.2019.1217ISI: 000474635900003PubMedID: 31258899OAI: oai:DiVA.org:liu-159152DiVA, id: diva2:1339653
Note
Funding Agencies|County Council of Ostergotland, University of Linkoping, Linkoping, Sweden; Swedish Heart and Lung Foundation
2019-07-302019-07-302019-11-13