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      动脉阻塞性疾病患者血浆骨形态发生蛋白-4的表达变化及其与炎症和血管损伤的相关性 Translated title: Expression pattern of the bone morphogenetic protein-4 and its relationship with inflammation, vascular injury in patients suffered the arterial occlusive diseases

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          Abstract

          目的

          骨形态发生蛋白-4(bone morphogenentic protein-4,BMP4)在动脉粥样硬化(atherosclerosis,AS)的病理过程中具有重要调节作用,但相关的临床研究较少。本研究拟观察以AS为主要病理特点的动脉阻塞性疾病(arterial occlusive disease,ACD)患者血浆BMP4的表达情况,并分析血浆中BMP4与炎症因子和血管损伤标志物之间的相关性。

          方法

          共招募38名诊断为ACD的患者(ACD组)和38名体检志愿者(对照组),抽取ACD组患者术前和对照组体检时的静脉血,比较2组血常规指标的差异。采用酶联免疫吸附试验(enzyme linked immunosorbent assay,ELISA)检测血浆中BMP4、肿瘤坏死因子α(tumor necrosis factor-α,TNF-α)、白细胞介素(interleukin,IL)-1β、IL-10及血管内皮钙黏蛋白(vascular endothelial cadherin,VE-cadherin)的表达变化,并进一步分析BMP4与以上各指标之间的相关性。

          结果

          与对照组相比,ACD组患者血常规结果表现为中性粒细胞-淋巴细胞比值[neutrophil to lymphocyte ratio,NLR;1.63 (1.26,1.91) vs 3.43(2.16,6.61)]和血小板-淋巴细胞比值[platelet to lymphocyte ratio,PLR;6.37(5.26,7.74) vs 15.79(7.97,20.53)]升高、淋巴细胞-单核细胞比值[lymphocyte to monocyte ratio,LMR;5.67(4.41,7.14) vs 3.43(2.07,3.74)]下降(均 P<0.05);ACD组患者血浆BMP4[581.26(389.85,735.64) pg/mL vs 653.97(510.95,890.43) pg/mL]、TNF-α[254.16(182.96,340.70) pg/mL vs 293.29(238.90,383.44) pg/mL]及内皮标志物VE-cadherin[1.54 (1.08,2.13) ng/mL vs 1.85 (1.30,2.54) ng/mL]的水平均显著升高,而抗炎因子IL-10的水平显著下降[175.89 (118.39,219.25) pg/mL vs 135.92(95.80,178.04) pg/mL](均 P<0.05)。2组间促炎因子IL-1β的差异无统计学意义[300.39(205.39,403.56) pg/mL vs 378.46 (243.20,448.69) pg/mL; P=0.09]。相关分析结果表明:血浆BMP4水平与促炎因子IL-1β( r=0.35)、TNF-α( r=0.31)以及内皮标志物VE-cadherin( r=0.47)呈正相关,与抗炎因子IL-10呈负相关( r=-0.37;均 P<0.01)。

          结论

          ACD患者血浆BMP4的水平升高,且与患者的炎症水平和血管损伤程度具有相关性。

          Translated abstract

          Objective

          Bone morphogenetic protein-4 (BMP4) has been proved to be an important regulatory factor for the pathological process of atherosclerosis (AS). However, there are few related clinical studies. This study aims to investigate the levels of plasma BMP4 in patients suffering from the arterial occlusive diseases (ACD) characterized by AS, and further to test the relationship between BMP4 and inflammation and vascular injury.

          Methods

          A total of 38 ACD patients (the ACD group) and 38 healthy people for the physical examination (the control group) were enrolled. The plasma in each subject from both groups was obtained to test the levels of BMP4, tumor necrosis factor-α (TNF-α), interleukin-1β (IL-1β), IL-10, and vascular endothelial cadherin (VE-cadherin), and the relationship between BMP4 and the detected indicators above were further analyzed.

          Results

          Compared with the control group, the patients in the ACD group displayed significant elevations in the neutrophil to lymphocyte ratio [NLR, 1.63 (1.26, 1.91) vs 3.43 (2.16, 6.61)] and platelet to lymphocyte ratio [PLR, 6.37 (5.26, 7.74) vs 15.79 (7.97, 20.53)], while decrease in the lymphocyte to monocyte ratio [LMR, 5.67 (4.41, 7.14) vs 3.43 (2.07, 3.74)] (all P<0.05). Besides, the ACD patients displayed significant elevations in plasma BMP4 [581.26 (389.85, 735.64) pg/mL vs 653.97(510.95, 890.43) pg/mL], TNF-α [254.16 (182.96, 340.70) pg/mL vs 293.29(238.90, 383.44) pg/mL], and VE-cadherin [1.54 (1.08, 2.13) ng/mL vs 1.85 (1.30, 2.54) ng/mL], and decrease in IL-10 [175.89 (118.39, 219.25) pg/mL vs 135.92 (95.80, 178.04) pg/mL] (all P<0.05). While the levels of IL-1β remained statistically comparable between the 2 groups ( P=0.09). Furthermore, the plasma BMP4 levels were further revealed to be positively correlated with the levels of IL-1β ( r=0.35), TNF-α ( r=0.31) and VE-cadherin ( r=0.47), while they were negatively correlated with the levels of IL-10 ( r=-0.37; all P<0.01).

          Conclusion

          After ACD occurrence, the patients’ plasma concentrations of BMP4 would be upregulated, which may serve as a candidate to indicate the levels of inflammation and vascular injury.

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          Most cited references26

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          Research Progress on the Relationship between Atherosclerosis and Inflammation

          Atherosclerosis is a chronic inflammatory disease; unstable atherosclerotic plaque rupture, vascular stenosis, or occlusion caused by platelet aggregation and thrombosis lead to acute cardiovascular disease. Atherosclerosis-related inflammation is mediated by proinflammatory cytokines, inflammatory signaling pathways, bioactive lipids, and adhesion molecules. This review discusses the effects of inflammation and the systemic inflammatory signaling pathway on atherosclerosis, the role of related signaling pathways in inflammation, the formation of atherosclerosis plaques, and the prospects of treating atherosclerosis by inhibiting inflammation.
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            Endothelial responses to shear stress in atherosclerosis: a novel role for developmental genes

            Flowing blood generates a frictional force called shear stress that has major effects on vascular function. Branches and bends of arteries are exposed to complex blood flow patterns that exert low or low oscillatory shear stress, a mechanical environment that promotes vascular dysfunction and atherosclerosis. Conversely, physiologically high shear stress is protective. Endothelial cells are critical sensors of shear stress but the mechanisms by which they decode complex shear stress environments to regulate physiological and pathophysiological responses remain incompletely understood. Several laboratories have advanced this field by integrating specialized shear-stress models with systems biology approaches, including transcriptome, methylome and proteome profiling and functional screening platforms, for unbiased identification of novel mechanosensitive signalling pathways in arteries. In this Review, we describe these studies, which reveal that shear stress regulates diverse processes and demonstrate that multiple pathways classically known to be involved in embryonic development, such as BMP-TGFβ, WNT, Notch, HIF1α, TWIST1 and HOX family genes, are regulated by shear stress in arteries in adults. We propose that mechanical activation of these pathways evolved to orchestrate vascular development but also drives atherosclerosis in low shear stress regions of adult arteries.
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              Inflammation and atherosclerosis: signaling pathways and therapeutic intervention

              Atherosclerosis is a chronic inflammatory vascular disease driven by traditional and nontraditional risk factors. Genome-wide association combined with clonal lineage tracing and clinical trials have demonstrated that innate and adaptive immune responses can promote or quell atherosclerosis. Several signaling pathways, that are associated with the inflammatory response, have been implicated within atherosclerosis such as NLRP3 inflammasome, toll-like receptors, proprotein convertase subtilisin/kexin type 9, Notch and Wnt signaling pathways, which are of importance for atherosclerosis development and regression. Targeting inflammatory pathways, especially the NLRP3 inflammasome pathway and its regulated inflammatory cytokine interleukin-1β, could represent an attractive new route for the treatment of atherosclerotic diseases. Herein, we summarize the knowledge on cellular participants and key inflammatory signaling pathways in atherosclerosis, and discuss the preclinical studies targeting these key pathways for atherosclerosis, the clinical trials that are going to target some of these processes, and the effects of quelling inflammation and atherosclerosis in the clinic.
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                Author and article information

                Journal
                Zhong Nan Da Xue Xue Bao Yi Xue Ban
                Zhong Nan Da Xue Xue Bao Yi Xue Ban
                zndx
                Journal of Central South University Medical Sciences
                中南大学出版社 (湖南省长沙市湘雅路110号湘雅医学院 )
                1672-7347
                28 February 2024
                : 49
                : 2
                : 279-285
                Affiliations
                [1] [1 ] 中南大学湘雅二医院检验医学科 长沙 410011 [1 ] Department of Laboratory, Second Xiangya Hospital, Central South University Changsha 410011
                [2] [2 ] 中南大学湘雅二医院麻醉科 长沙 410011 [2 ] Department of Anesthesiology, Second Xiangya Hospital, Central South University Changsha 410011
                [3] [3 ] 中南大学湘雅二医院党委办公室 长沙 410011 [3 ] Office of the CPC Committee, Second Xiangya Hospital, Central South University Changsha 410011 China
                Author notes

                张文娟,Email: akkc-wj@ 123456163.com , ORCID: 0000-0003-3883-9293

                陈若虹,Email: chenruohong@ 123456csu.edu.cn , ORCID: 0000-0002-9488-0226
                刘朝阳,Email: liuzhaoyang4008@ 123456csu.edu.cn , ORCID: 0009-0009-2324-2516
                Article
                1672-7347(2024)02-0279-07 230264
                10.11817/j.issn.1672-7347.2024.230264
                11103063
                38755724
                96196fa7-73b7-4709-9d59-87e6200427f5
                ©Journal of Central South University (Medical Science). All rights reserved.

                开放获取 (Open access):本文遵循知识共享许可协议,允许第三方用户按照署名-非商业性使用-禁止演绎4.0(CC BY-NC-ND 4.0)的方式,在任何媒介以任何形式复制、传播本作品( https://creativecommons.org/licenses/by-nc-nd/4.0/)。

                History
                : 24 June 2023
                Funding
                Funded by: 湖南省医学会医学科研基金
                Award ID: HNA202101002┫。This work was supported by the Medical Research Fund of Hunan Medical Association
                Award ID: China ┣HNA202101002
                Categories
                Articles

                动脉阻塞性疾病,骨形态发生蛋白-4,炎症,血管损伤,arterial occlusive disease,bone morphogenetic protein-4,inflammation,vascular injury

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