Increased cardiovascular mortality in females with the a/a genotype of the SNPs rs1478604 and rs2228262 of thrombospondin-1.

4区 医学 Q4 Medicine
Urban Alehagen, Levar Shamoun, Dick Wågsäter
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引用次数: 2

Abstract

Background: Cardiovascular diseases are still the major cause of death in the Western world, with different outcomes between the two genders. Efforts to identify those at risk are therefore given priority in the handling of health resources. Thrombospondins (TSP) are extracellular matrix proteins associated with cardiovascular diseases. The aim of this study was to investigate variations in single nucleotide polymorphisms (SNPs) of TSP-1 and plasma expression, and associations with mortality from a gender perspective.

Methods: A population of 470 community-living persons were invited to participate. The participants were followed for 7.9 years and underwent a clinical examination and blood sampling. SNP analyses of TSP-1 rs1478604 and rs2228262 using allelic discrimination and plasma measurement of TSP-1 using ELISA were performed, RESULTS: During the follow-up period, 135 (28.7%) all-cause and 83 (17.7%) cardiovascular deaths were registered. In the female population, the A/A genotype of rs2228262 and the T/T genotype of rs1478604 exhibited significantly more cardiovascular deaths compared with the A/G and G/G, or the T/C and C/C genotypes amalgamated (rs2228262: 13.7% vs 2.0%; Χ2:5.29; P = 0.02; rs1478604:17.7% vs 4.7%; Χ2:9.50; P = 0.002). Applied in a risk evaluation, the A/A, or T/T genotypes exhibited an increased risk of cardiovascular mortality (rs2228262: HR: 7.1; 95%CI 1.11-45.8; P = 0.04; rs1478604: HR: 3.18; 95%CI 1.35-7.50; p = 0.008). No differences among the three genotypes could be seen in the male group.

Conclusion: In this study the female group having the A/A genotype of rs2228262, or the T/T genotype of rs1478604 of TSP-1 exhibited higher cardiovascular mortality after a follow-up of almost 8 years. No corresponding genotype differences could be found in the male group. Genotype evaluations should be considered as one of the options to identify individuals at risk. However, this study should be regarded as hypothesis-generating, and more research in the field is needed.

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携带血栓反应蛋白-1 snp rs1478604和rs2228262 a/a基因型的女性心血管死亡率增加
背景:心血管疾病仍然是西方世界死亡的主要原因,两性之间的结果不同。因此,在处理卫生资源时应优先努力查明高危人群。血小板反应蛋白(TSP)是与心血管疾病相关的细胞外基质蛋白。本研究的目的是从性别角度探讨TSP-1单核苷酸多态性(snp)和血浆表达的变化及其与死亡率的关系。方法:对470名社区居民进行问卷调查。参与者被跟踪了7.9年,并接受了临床检查和血液采样。结果:随访期间共发生全因死亡135例(28.7%),心血管死亡83例(17.7%)。在女性人群中,rs2228262的A/A基因型和rs1478604的T/T基因型比A/G和G/G基因型,或T/C和C/C基因型合并(rs2228262: 13.7% vs 2.0%;Χ2:5.29;p = 0.02;Rs1478604:17.7% vs 4.7%;Χ2:9.50;p = 0.002)。应用于风险评估,a / a或T/T基因型显示心血管死亡风险增加(rs2228262: HR: 7.1;95%可信区间1.11 - -45.8;p = 0.04;rs1478604: HR: 3.18;95%可信区间1.35 - -7.50;p = 0.008)。在男性组中,三种基因型之间没有差异。结论:在本研究中,具有rs2228262的A/A基因型或TSP-1的rs1478604的T/T基因型的女性组在近8年的随访后心血管死亡率更高。在男性组中未发现相应的基因型差异。基因型评估应被视为识别高危个体的选择之一。然而,本研究应被视为假设生成,需要在该领域进行更多的研究。
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来源期刊
BMC Medical Genetics
BMC Medical Genetics 医学-遗传学
自引率
0.00%
发文量
0
审稿时长
12 months
期刊介绍: BMC Medical Genetics is an open access journal publishing original peer-reviewed research articles in the effects of genetic variation in individuals, families and among populations in relation to human health and disease. Note: BMC Medical Genetics is now closed. This journal has merged with BMC Medical Genomics, a broad-scope, open access community journal for all medical genetics and genomics research.
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