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餐后极低密度脂蛋白在代谢综合征心房重构中的作用。

The role of postprandial very-low-density lipoprotein in the development of atrial remodeling in metabolic syndrome.

机构信息

Center for Lipid Biosciences, Kaohsiung Medical University Hospital, Kaohsiung, Taiwan.

Lipid Science and Aging Research Center, College of Medicine, Kaohsiung Medical University, Kaohsiung, Taiwan.

出版信息

Lipids Health Dis. 2020 Sep 22;19(1):210. doi: 10.1186/s12944-020-01386-5.

DOI:10.1186/s12944-020-01386-5
PMID:32962696
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7507670/
Abstract

BACKGROUND

Negatively charged very-low-density lipoprotein (VLDL-χ) in metabolic syndrome (MetS) patients exerts cytotoxic effects on endothelial cells and atrial myocytes. Atrial cardiomyopathy, manifested by atrial remodeling with a dilated diameter, contributes to atrial fibrillation pathogenesis and predicts atrial fibrillation development. The correlation of VLDL-χ with atrial remodeling is unknown. This study investigated the association between VLDL-χ and remodeling of left atrium.

METHODS

Consecutively, 87 MetS and 80 non-MetS individuals between 23 and 74 years old (50.6% men) without overt cardiovascular diseases were included in the prospective cohort study. Blood samples were collected while fasting and postprandially (at 0.5, 1, 2, and 4 h after a unified meal). VLDL was isolated by ultracentrifugation; the percentile concentration of VLDL-χ (%) was determined by ultra-performance liquid chromatography. The correlations of left atrium diameter (LAD) with variables including VLDL-χ, LDL-C, HDL-C, triglycerides, glucose, and blood pressure, were analyzed by multiple linear regression models. A hierarchical linear model was conducted to test the independencies of each variable's correlation with LAD.

RESULTS

The mean LAD was 3.4 ± 0.5 cm in non-MetS subjects and 3.9 ± 0.5 cm in MetS patients (P < 0.01). None of the fasting lipid profiles were associated with LAD. VLDL-χ, BMI, waist circumference, hip circumference, and blood pressure were positively correlated with LAD (all P < 0.05) after adjustment for age and sex. Significant interactions between VLDL-χ and blood pressure, waist circumference, and hip circumference were observed. When adjusted for obesity- and blood pressure-related variables, 2-h postprandial VLDL-χ (mean 1.30 ± 0.61%) showed a positive correlation with LAD in MetS patients. Each 1% VLDL-χ increase was estimated to increase LAD by 0.23 cm.

CONCLUSIONS

Postprandial VLDL-χ is associated with atrial remodeling particularly in the MetS group. VLDL-χ is a novel biomarker and may be a therapeutic target for atrial cardiomyopathy in MetS patients.

TRIAL REGISTRATION

ISRCTN 69295295 . Retrospectively registered 9 June 2020.

摘要

背景

代谢综合征(MetS)患者中带负电荷的极低密度脂蛋白(VLDL-χ)对内皮细胞和心房肌细胞具有细胞毒性作用。心房心肌病以扩张的直径表现为心房重构,导致心房颤动的发病机制,并预测心房颤动的发展。VLDL-χ 与心房重构的相关性尚不清楚。本研究探讨了 VLDL-χ 与左心房重构之间的关系。

方法

连续纳入 87 名 MetS 和 80 名非 MetS 患者(年龄 23-74 岁,50.6%为男性),均无明显心血管疾病。空腹和餐后(统一餐后 0.5、1、2 和 4 小时)采集血样。采用超速离心法分离 VLDL;通过超高效液相色谱法测定 VLDL-χ(%)的百分位数浓度。采用多元线性回归模型分析左心房直径(LAD)与包括 VLDL-χ、LDL-C、HDL-C、甘油三酯、血糖和血压在内的变量之间的相关性。采用分层线性模型检验每个变量与 LAD 的相关性的独立性。

结果

非 MetS 组的平均 LAD 为 3.4±0.5cm,MetS 组为 3.9±0.5cm(P<0.01)。空腹血脂谱均与 LAD 无关。VLDL-χ、BMI、腰围、臀围和血压与 LAD 呈正相关(均 P<0.05),校正年龄和性别后。观察到 VLDL-χ 与血压、腰围和臀围之间存在显著的交互作用。在校正肥胖和血压相关变量后,MetS 患者餐后 2 小时 VLDL-χ(平均 1.30±0.61%)与 LAD 呈正相关。VLDL-χ 每增加 1%,估计 LAD 增加 0.23cm。

结论

餐后 VLDL-χ 与心房重构相关,尤其是在 MetS 组。VLDL-χ 是一种新型生物标志物,可能是 MetS 患者心房心肌病的治疗靶点。

试验注册

ISRCTN69295295。2020 年 6 月 9 日回顾性注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acf3/7507670/dda611b9275d/12944_2020_1386_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acf3/7507670/6c24a0d64cc4/12944_2020_1386_Fig1_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acf3/7507670/a16af4f2559d/12944_2020_1386_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acf3/7507670/dda611b9275d/12944_2020_1386_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acf3/7507670/6c24a0d64cc4/12944_2020_1386_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acf3/7507670/12d91fc03832/12944_2020_1386_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acf3/7507670/0135a9effbe1/12944_2020_1386_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acf3/7507670/0b4f6d7f93d0/12944_2020_1386_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acf3/7507670/a16af4f2559d/12944_2020_1386_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/acf3/7507670/dda611b9275d/12944_2020_1386_Fig6_HTML.jpg

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