• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

载脂蛋白 A1 和 A5 多态性与台湾汉族人群中风亚型的关联。

Association of apolipoprotein A1 and A5 polymorphisms with stroke subtypes in Han Chinese people in Taiwan.

机构信息

Department of Neurology, Taipei Veterans General Hospital, Taipei, Taiwan; National Yang-Ming University school of Medicine, Taipei, Taiwan.

Institutes of Biochemistry, Microbiology, and Immunology, Chung Shan Medical University, Taichung, Taiwan; Clinical Laboratory, Chung Shan Medical University Hospital, Taichung, Taiwan.

出版信息

Gene. 2019 Feb 5;684:76-81. doi: 10.1016/j.gene.2018.10.050. Epub 2018 Oct 24.

DOI:10.1016/j.gene.2018.10.050
PMID:30367981
Abstract

BACKGROUND AND PURPOSES

Stroke is a leading cause of death and serious disability worldwide. Now, evidences indicate that dyslipidemia may play an important role in stroke. APOA1 and APOA5 involve in lipid metabolism. In this study, we investigated the association of APOA1 rs670 and APOA5 rs662799 with different stroke subtypes in the Han Chinese population of Taiwan.

METHODS

A total of 1751 participants, including 459 control subjects, 606 large artery atherosclerosis (LAA), 339 small vessel occlusion (SVO), and 347 hypertensive intracranial hemorrhage (HICH), were enrolled. The presence of rs670 and rs662799 was analyzed through polymerase chain react ion and matrix-assisted laser desorption/ionization-time-of-flight-mass spectrometry.

RESULTS

Notably, the frequency of the rs662799 C allele was significantly lower in the SVO patients than in the controls (24.36% vs. 29.74%, P = 0.024). The frequencies of heterozygote TC [odd ratio (OR) = 0.732, 95% confidence interval (CI) = 0.544-0.984, P = 0.038] and TC + CC (OR = 0.719, 95% CI = 0.542-0.953, P = 0.022) genotypes were significantly lower in the SVO patients than in the controls. In addition, triglyceride levels in individuals carrying the rs662799 TC + CC genotype were significantly higher than in those carrying the TT genotype, especially in older age, female, and body mass index (BMI) ≥ 25 groups. On the contrary, the low-density lipoprotein-cholesterol (LDL-C) was significantly lower in rs662799 TC + CC genotype than TT genotype. The BMI was significantly lower in subjects with rs662799 TC + CC genotype than those with TT genotype, especially in older age and female. High-density lipoprotein-cholesterol (HDL-C) levels were higher in individuals carrying the rs670 GG genotype than in those carrying the AG + AA genotype, especially in BMI < 25 group. Logistic regression analysis showed that the rs662799 C allele (TC + CC) was an independent protective factor for SVO after adjustment for conventional risk factors (OR = 0.709, 95% CI = 0.526-0.956; P = 0.024).

CONCLUSION

GG genotype of rs670 is correlated with high serum HDL-C levels, whereas TC + CC genotype of rs662799 is associated with high serum triglyceride and low LDL and BMI levels. In addition, the rs662799 C allele (TC + CC) is an independent protective factor for SVO in the Han Chinese population in Taiwan.

摘要

背景与目的

卒中是全世界范围内导致死亡和严重残疾的主要原因。目前,有证据表明血脂异常可能在卒中发病中起重要作用。APOA1 和 APOA5 参与脂质代谢。本研究旨在探讨载脂蛋白 A1(APOA1)rs670 和载脂蛋白 A5(APOA5)rs662799 与台湾汉族人群不同卒中亚型的相关性。

方法

共纳入 1751 例受试者,包括 459 例对照、606 例大动脉粥样硬化性卒中(LAA)、339 例小血管闭塞性卒中(SVO)和 347 例高血压性颅内出血(HICH)。采用聚合酶链反应和基质辅助激光解吸/电离-飞行时间质谱法分析 rs670 和 rs662799 的存在情况。

结果

值得注意的是,SVO 患者 rs662799 C 等位基因的频率明显低于对照组(24.36%比 29.74%,P=0.024)。杂合子 TC [比值比(OR)=0.732,95%置信区间(CI)=0.544-0.984,P=0.038]和 TC+CC(OR=0.719,95%CI=0.542-0.953,P=0.022)基因型在 SVO 患者中的频率明显低于对照组。此外,携带 rs662799 TC+CC 基因型的个体的甘油三酯水平明显高于携带 TT 基因型的个体,尤其是在年龄较大、女性和 BMI≥25 组。相反,rs662799 TC+CC 基因型的低密度脂蛋白胆固醇(LDL-C)水平明显低于 TT 基因型。携带 rs662799 TC+CC 基因型的个体的 BMI 明显低于携带 TT 基因型的个体,尤其是在年龄较大和女性中。携带 rs670 GG 基因型的个体高密度脂蛋白胆固醇(HDL-C)水平高于携带 AG+AA 基因型的个体,尤其是在 BMI<25 组。Logistic 回归分析显示,在调整传统危险因素后,rs662799 C 等位基因(TC+CC)是 SVO 的独立保护因素(OR=0.709,95%CI=0.526-0.956;P=0.024)。

结论

rs670 的 GG 基因型与血清 HDL-C 水平升高相关,而 rs662799 的 TC+CC 基因型与血清甘油三酯升高、LDL-C 降低和 BMI 降低相关。此外,rs662799 C 等位基因(TC+CC)是台湾汉族人群 SVO 的独立保护因素。

相似文献

1
Association of apolipoprotein A1 and A5 polymorphisms with stroke subtypes in Han Chinese people in Taiwan.载脂蛋白 A1 和 A5 多态性与台湾汉族人群中风亚型的关联。
Gene. 2019 Feb 5;684:76-81. doi: 10.1016/j.gene.2018.10.050. Epub 2018 Oct 24.
2
The association between apolipoprotein A1-C3-A5 gene cluster promoter polymorphisms and risk of ischemic stroke in the northern Chinese Han population.载脂蛋白A1-C3-A5基因簇启动子多态性与中国北方汉族人群缺血性脑卒中风险的关联
J Int Med Res. 2017 Dec;45(6):2042-2052. doi: 10.1177/0300060517713517. Epub 2017 Jun 21.
3
Interactions of Environmental Factors and APOA1-APOC3-APOA4-APOA5 Gene Cluster Gene Polymorphisms with Metabolic Syndrome.环境因素与APOA1-APOC3-APOA4-APOA5基因簇基因多态性与代谢综合征的相互作用
PLoS One. 2016 Jan 29;11(1):e0147946. doi: 10.1371/journal.pone.0147946. eCollection 2016.
4
Apolipoprotein A5 gene promoter region-1131T/C polymorphism is associated with risk of ischemic stroke and elevated triglyceride levels: a meta-analysis.载脂蛋白 A5 基因启动子区域-1131T/C 多态性与缺血性脑卒中风险及甘油三酯水平升高相关:一项荟萃分析。
Cerebrovasc Dis. 2012;33(6):558-65. doi: 10.1159/000338781. Epub 2012 Jun 8.
5
The association of lipid metabolism relative gene polymorphisms and ischemic stroke in Han and Uighur population of Xinjiang.新疆汉族和维吾尔族人群脂质代谢相关基因多态性与缺血性脑卒中的关联
Lipids Health Dis. 2017 Jun 17;16(1):120. doi: 10.1186/s12944-017-0491-9.
6
Association of apolipoprotein A5 gene promoter region -1131T>C with risk of stroke in Han Chinese.载脂蛋白 A5 基因启动子区-1131T>C 与汉族人群脑卒中风险的关联。
Eur J Intern Med. 2011 Feb;22(1):99-102. doi: 10.1016/j.ejim.2010.07.012. Epub 2010 Aug 14.
7
Interactions between the apolipoprotein a1/c3/a5 haplotypes and alcohol consumption on serum lipid levels.载脂蛋白 a1/c3/a5 单倍型与饮酒对血脂水平的相互影响。
Alcohol Clin Exp Res. 2013 Feb;37(2):234-43. doi: 10.1111/j.1530-0277.2012.01918.x. Epub 2012 Aug 24.
8
Habitual aerobic exercise, gene APOA5 named rs662799 SNP and response of blood lipid and lipoprotein phenotypes among older Chinese adult.习惯性有氧运动、基因 APOA5 命名的 rs662799SNP 与老年中国成年人血脂和脂蛋白表型的反应。
Exp Gerontol. 2018 Sep;110:46-53. doi: 10.1016/j.exger.2018.05.007. Epub 2018 May 26.
9
The Association Between APOA5 Gene Polymorphisms and Plasma Lipids in the Turkish Cypriot Population: A Possible Biomarker for Preventing Cardiovascular Diseases.塞浦路斯土耳其族人群中APOA5基因多态性与血脂的关联:一种预防心血管疾病的潜在生物标志物
Biochem Genet. 2018 Jun;56(3):176-187. doi: 10.1007/s10528-017-9836-3. Epub 2017 Dec 20.
10
Triglyceride-raising APOA5 genetic variants are associated with obesity and non-HDL-C in Chinese children and adolescents.载脂蛋白 A5 升高的甘油三酯基因变异与中国儿童和青少年的肥胖和非高密度脂蛋白胆固醇有关。
Lipids Health Dis. 2014 Jun 5;13:93. doi: 10.1186/1476-511X-13-93.

引用本文的文献

1
Apolipoprotein A (ApoA) in Neurological Disorders: Connections and Insights.载脂蛋白A(ApoA)在神经系统疾病中的关联与见解
Int J Mol Sci. 2025 Aug 16;26(16):7908. doi: 10.3390/ijms26167908.
2
Apolipoprotein A5 gene polymorphism (rs662799) and cardiovascular disease in end-stage kidney disease patients.载脂蛋白 A5 基因多态性(rs662799)与终末期肾病患者的心血管疾病。
BMC Nephrol. 2022 Sep 7;23(1):307. doi: 10.1186/s12882-022-02925-1.
3
Associations between Aquaglyceroporin Gene Polymorphisms and Risk of Stroke among Patients with Hypertension.
水通道蛋白基因多态性与高血压患者卒中风险的关系。
Biomed Res Int. 2020 Mar 25;2020:9358290. doi: 10.1155/2020/9358290. eCollection 2020.