多组学技术用于心血管疾病发病机制与药物靶标研究的Meta分析

邱靖雯, 佘佩谦, 胡翔, 陈安基, 张晶晶

湖南师范大学学报医学版 ›› 2025, Vol. 22 ›› Issue (5) : 142-149.

PDF(2007 KB)
PDF(2007 KB)
湖南师范大学学报医学版 ›› 2025, Vol. 22 ›› Issue (5) : 142-149.
临床医学

多组学技术用于心血管疾病发病机制与药物靶标研究的Meta分析

  • 邱靖雯1,2, 佘佩谦1,3, 胡翔2, 陈安基1, 张晶晶1
作者信息 +

Meta Analysis of Multi Omics Techniques for Investigating the Pathogenesis and Drug Targets of Cardiovascular Diseases

  • QIU Jingwen1,2, SHE Peiqian1,3, HU Xiang2, CHEN Anji1, ZHANG Jingjing1
Author information +
文章历史 +

摘要

目的 通过荟萃分析(Meta分析)系统评价基于多组学技术治疗心血管疾病(cardiovascular disease,CVD)的证据,为CVD患者提供治疗新方向。方法 系统检索中国生物医学文献数据库、中国知网等中文数据库,以及PubMed、Web of Science等外文数据库,2015年4月至2025年4月公开发表的基于多组学技术治疗CVD的相关文献,观测白细胞介素-6(interleukin-6,IL-6)、肿瘤坏死因子-α(tumor necrosis factor-α,TNF-α)、甘油三酯(triglyceride,TG)、总胆固醇(total cholesterol,TC)、低密度脂蛋白胆固醇(low-density lipoprotein cholesterol,LDL-C)、高密度脂蛋白胆固醇(high-density lipoprotein cholesterol,HDL-C)、收缩压(systolic blood pressure,SBP)、舒张压(diastolic blood pressure,DBP)等研究指标以探索多组学技术对CVD的影响,选用Review Manager 5.4软件进行Meta分析,并采用Egger检验对发表偏倚进行分析。结果 最终纳入6篇文献,共纳入588例患者。Meta分析结果显示,基于多组学技术治疗组的CVD患者的TNF-α水平显著低于多组学技术应用之前的TNF-α水平(SMD=-0.78,95%CI:-1.10~-0.46,P<0.05),且漏斗图呈对称状,发表偏倚可能性较小;而基于多组学技术治疗后,CVD患者的其他传统临床指标未出现明显改变,部分指标无统计学意义。结论 在治疗CVD中,多组学技术能够通过调控血管功能相关分子网络并下调促炎因子的表达,同时可能更多针对非传统通路。

Abstract

Objective Meta-analysis was used in order to systematically evaluate the evidence for multi-omics technology in treating cardiovascular disease (CVD) aiming to provide new treatment avenues for CVD patients. Methods A systematic search was conducted across Chinese databases (such as China Biology Medicine disc and China National Knowledge Infrastructure) and international databases (including PubMed and Web of Science) for literature published between April 2015 and April 2025 on multi-omics-based interventions for CVD. Research indicators such as interleukin-6 (IL-6), tumor necrosis factor-α (TNF-α), triglyceride (TG), total cholesterol (TC), low-density lipoprotein cholesterol (LDL-C), high-density lipoprotein cholesterol (HDL-C), systolic blood pressure (SBP), diastolic blood pressure (DBP) were observed to explore the impact of multi-omics technology on cardiovascular diseases, and Review Manager 5.4 software was selected for Meta-analysis, and Egger's test was used to Publication bias was analyzed. Results Six papers with a total of 588 patients were finally included. Meta-analysis results showed that the TNF-α level in the treatment group based on multi-omics technology was significantly lower than the TNF-α level before the application of multi-omics technology (SMD=-0.78, 95% CI: -1.10 to -0.46, P<0.05). Moreover, the funnel plot exhibits symmetry, indicating a low likelihood of publication bias. And after the treatment based on multi-omics technology, the other traditional clinical indexes in patients with cardiovascular diseases did not show significant changes, and some of the indexes were not statistically significant. Conclusion In the treatment of cardiovascular diseases, multi-omics technology can be used to regulate vascular function-related molecular networks and down-regulate the expression of pro-inflammatory factors by modulating the vascular function-related molecular networks, while possibly targeting more non-traditional pathways.

关键词

多组学技术 / 心血管疾病 / Meta分析 / 炎症因子 / 血脂代谢

Key words

multi-omics technology / cardiovascular disease / meta-analysis / inflammatory factors / lipid metabolism

引用本文

导出引用
邱靖雯, 佘佩谦, 胡翔, 陈安基, 张晶晶. 多组学技术用于心血管疾病发病机制与药物靶标研究的Meta分析[J]. 湖南师范大学学报医学版. 2025, 22(5): 142-149
QIU Jingwen, SHE Peiqian, HU Xiang, CHEN Anji, ZHANG Jingjing. Meta Analysis of Multi Omics Techniques for Investigating the Pathogenesis and Drug Targets of Cardiovascular Diseases[J]. Journal of Hunan Normal University(Medical Science). 2025, 22(5): 142-149
中图分类号: R540.4   

参考文献

[1] 刘明波, 何新叶, 杨晓红, 等. 《中国心血管健康与疾病报告2023》要点解读[J]. 中国心血管杂志, 2024, 29(04): 305-324.
[2] 杨乔西, 蔡军. 心血管疾病治疗药物研究进展[J]. 临床药物治疗杂志, 2025, 23(01): 40-48.
[3] ZHANG Y, FONSLOW BR, SHAN B, et al.Protein analysis by shotgun/bottom-up proteomics[J]. Chem Rev, 2013, 113(4): 2343-2394.
[4] 周旭. 基于代谢组学的心血管疾病生物标志物发现与机器学习模型[D]. 贵阳: 贵州医科大学, 2024.
[5] 蒋之林. 基于多组学整合探讨活血化痰中药治疗冠心病痰瘀互结证机制研究[D]. 北京: 中国中医科学院, 2024.
[6] BERNINI LJ, SIMAO ANC, ALFIERI DF, et al.Beneficial effects of Bifidobacterium lactis on lipid profile and cytokines in patients with metabolic syndrome: A randomized trial. Effects of probiotics on metabolic syndrome[J]. Nutrition, 2016, 32(6): 716-719.
[7] SZULINSKA M, LONIEWSKI I, SKRYPNIK K, et al.Multispecies probiotic supplementation favorably affects vascular function and reduces arterial stiffness in obese postmenopausal Women-A 12-Week Placebo-Controlled and randomized clinical study[J]. Nutrients, 2018, 10(11): 1672.
[8] HU X, LI H, ZHAO X, et al.Multi-omics study reveals that statin therapy is associated with restoration of gut microbiota homeostasis and improvement in outcomes in patients with acute coronary syndrome[J]. Theranostics, 2021, 11(12): 5778-5793.
[9] SANCHEZ-CABO F, FUSTER V, SILLA-CASTRO JC, et al.Subclinical atherosclerosis and accelerated epigenetic age mediated by inflammation: A multi-omics study[J]. Eur Heart J, 2023, 44(29): 2698-2709.
[10] MADJD A, TAYLOR MA, MOUSAVI N, et al.Comparison of the effect of daily consumption of probiotic compared with low-fat conventional yogurt on weight loss in healthy obese women following an energy-restricted diet: A randomized controlled trial[J]. Am J Clin Nutr, 2016, 103(2): 323-329.
[11] 刘海宁, 吴昊, 姚灿, 等. Meta分析中连续性数据的深度提取方法[J]. 中国循证医学杂志, 2017, 17(01): 117-121.
[12] NIDORF SM, FIOLET ATL, MOSTERD A, et al.Colchicine in patients with chronic coronary disease[J]. N Engl J Med, 2020, 383(19): 1838-1847.
[13] 李容, 于润, 杜鹏. AP-1家族基因与相关信号通路、肿瘤、发育和衰老进程[J]. 中国科学: 生命科学, 2025, 55(05): 898-911.
[14] YU T, XU X, WEI J, et al.Ginsenoside Rg5 alleviates Ang II-induced cardiac inflammation and remodeling by inhibiting the JNK/AP-1 pathway[J]. Int Immunopharmacol, 2023, 120: 110408.
[15] ZHANG H, DHALLA NS.The role of pro-inflammatory cytokines in the pathogenesis of cardiovascular disease[J]. Int J Mol Sci, 2024, 25(2): 1082.
[16] WEBER BN, GILES JT, LIAO KP.Shared inflammatory pathways of rheumatoid arthritis and atherosclerotic cardiovascular disease[J]. Nat Rev Rheumatol, 2023, 19(7): 417-428.
[17] KANG S, KISHIMOTO T.Interplay between interleukin-6 signaling and the vascular endothelium in cytokine storms[J]. Exp Mol Med, 2021, 53(7): 1116-1123.

PDF(2007 KB)

Accesses

Citation

Detail

段落导航
相关文章

/