SYNE1 gene novel variant is associated with myocardial infarction in young people with a family history of premature atherosclerosis.

Michal Ambroziak, Jakub Franke, Anna Wojcicka, Monika Kolanowska, Andrzej Budaj
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Abstract

Aim. The aim of the study was to investigate the role of genetic variants in young patients (aged <50 years) with myocardial infarction (MI) and a family history of premature atherosclerosis. Methods and Results. The studied group consisted of 70 patients aged 26-49 (mean 43.1, SD ±4.3), 17 women and 53 men, with MI and with a family history of premature atherosclerosis, defined as MI or ischaemic stroke in first-degree relatives at age <65 years in women or <55 years in men. The total DNA was extracted from the peripheral blood samples. The targeted enrichment library was prepared and analyzed using the Next-Generation Sequencing method. Statistical analyses were performed using the R software package (http://www.r-project.org/). The results of sequencing were compared to data from the reference control population consisting of 597 people with no history of MI (418 women, 179 men) aged 18-83 (mean 40.5, SD ± 12.4) as a whole and after matching with a studied group by age and gender in a proportion 1:3 (210 people, 51 women, 159 men, aged 18-77, mean 42.1, SD ±10.6) using Propensity Score Matching. Risks associated with detected variants were evaluated using Fisher?s exact test based on the allelic frequencies of variants in both groups. SYNE1 gene variant rs36215567 (NM_182961.4: c.20396+22A>G) occurs with a significantly higher incidence in the studied group when compared to the control population with OR 4.80 95%CI 1.43-14.45 (p=0.005) as well as when compared to the control population matched by age and gender OR 9.31 95%CI 1.64-95.41 (p=0.004). There were no statistically significant differences in the incidence of variants related to familial hypercholesterolemia such as LDLR c.667G>A, PCSK9 c.658-36G>A, and APOB c.12382G>A between both cohorts. Conclusion. A novel variant of the SYNE1 gene is associated with myocardial infarction in young patients with a family history of premature atherosclerosis.
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SYNE1基因新型变异与有过早动脉粥样硬化家族史的年轻人心肌梗死有关。
研究目的该研究旨在调查遗传变异在年轻心肌梗死(MI)和早发动脉粥样硬化家族史患者(50 岁)中的作用。研究对象包括 70 名年龄在 26-49 岁(平均 43.1 岁,SD ±4.3)的心肌梗死患者,其中女性 17 人,男性 53 人,他们都有早发性动脉粥样硬化家族史,即一级亲属在女性 65 岁或男性 55 岁时发生心肌梗死或缺血性中风。从外周血样本中提取总 DNA。采用下一代测序方法制备并分析靶向富集文库。统计分析使用 R 软件包 (http://www.r-project.org/) 进行。测序结果与参考对照人群的数据进行了比较,参考对照人群包括 597 名无心肌梗死病史者(女性 418 人,男性 179 人),年龄在 18-83 岁之间(平均 40.5 岁,SD ± 12.4),以及使用倾向得分匹配法按年龄和性别以 1:3 的比例与研究人群(210 人,女性 51 人,男性 159 人,年龄在 18-77 岁之间,平均 42.1 岁,SD ± 10.6)进行匹配后的人群。根据两组变异的等位基因频率,使用费雪精确检验评估了与检测到的变异相关的风险。SYNE1 基因变异 rs36215567 (NM_182961.4: c.20396SYNE1基因变异rs36215567(NM_182961.4:c.20396 +22A>G)在研究组中的发生率明显高于对照组,OR为4.80 95%CI为1.43-14.45(P=0.005),与年龄和性别匹配的对照组相比,OR为9.31 95%CI为1.64-95.41(P=0.004)。与家族性高胆固醇血症相关的变体,如 LDLR c.667G>A、PCSK9 c.658-36G>A、APOB c.12382G>A 的发生率在两个队列之间没有统计学差异。结论:SYNE1 基因的新型变异与有过早动脉粥样硬化家族史的年轻患者的心肌梗死有关。
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