[1]陈秋宏 王春彬 吴奇.肺动脉高压相关生物标志物的研究新进展[J].心血管病学进展,2021,(11):986-989.[doi:10.16806/j.cnki.issn.1004-3934.2021.11.000]
 CHEN Qiuhong,WANG Chunbin,WU Qi.Pulmonary Hypertension-Related Biomarkers[J].Advances in Cardiovascular Diseases,2021,(11):986-989.[doi:10.16806/j.cnki.issn.1004-3934.2021.11.000]
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肺动脉高压相关生物标志物的研究新进展()
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《心血管病学进展》[ISSN:51-1187/R/CN:1004-3934]

卷:
期数:
2021年11期
页码:
986-989
栏目:
综述
出版日期:
2021-11-25

文章信息/Info

Title:
Pulmonary Hypertension-Related Biomarkers
文章编号:
202107018
作者:
陈秋宏1 王春彬2 吴奇13
(1.成都医学院第一附属医院心血管内科,四川 成都 610500;2.西南交通大学附属医院 成都市第三人民医院心血管内科,四川 成都 610031;3.成都医学院第二附属医院·核工业四一六医院,四川 成都 610057)
Author(s):
CHEN Qiuhong1 WANG Chunbin2 WU Qi13
(1. Department of Cardiology, The First Affiliated Hospital of Chengdu Medical Colle ge, Chengdu 610500, Sichuan, China; 2. Department of Cardiology, The Third People’s Hospital of Chengdu,The Affiliated Hospital of Southwest Jiaotong University,Chengdu 610031,Sichuan,China; 3.The Second Affiliated Hospital of Chengdu Medical College·Nuclear Industry 416 Hospital,Chengdu 610057,Sichuan,China)
关键词:
肺动脉高压生物标志物MicroRNA
Keywords:
Pulmonary hypertensionPH-related biomarkersMicroRNA
DOI:
10.16806/j.cnki.issn.1004-3934.2021.11.000
摘要:
肺动脉高压(PH)目前是一种发病机制尚未完全阐明的致死性肺血管疾病,其起病隐匿,病因复杂,且发病率、致残率和致死率均较高。多数患者发现时已出现右心功能不全甚至猝死,故早诊断、早干预和预后评估分层对提高PH患者的生存率、预后以及精准治疗具有重要的临床意义。生物标志物是PH诊断、评估预后和治疗反应的非侵入性客观指标,为PH领域的诊断及治疗提供了新的策略,现对PH相关生物标志物的近年研究进展做一综述。
Abstract:
Pulmonary hypertension(PH) is a fatal pulmonary vascular disease which pathogenesis has not been fully elucidated . The onset of the disease is hidden,the cause is complex,and the incidence rate,disability rate and mortality rate are all higher. Most patients have appeared right ventricular dysfunction or even sudden death when PH was found . Therefore,early diagnosis,early intervention and prognosis evaluation are of great clinical significance to improve the survival rate,prognosis and precise treatment of PH patients. Biomarkers are non-invasive objective indicators of PH diagnosis,prognosis assessment and treatment response. This paper reviews the recent research progress of PH-related biomarkers

参考文献/References:

[1]中华医学会呼吸病学分会肺栓塞与肺血管病学组,中国医师协会呼吸医师分会肺栓塞 与肺血管病工作委员会,全国肺栓塞与肺血管病防治协作组,等. 中国肺动脉高压诊断与治疗指南(2021版)[J]. 中华医学杂志,2021,101(1):11-51.

[2]Hoeper MM,Humbert M,Souza R,et al. A global view of pulmonary hypertension[J]. Lancet Respir Med,2016,4(4):306-322.

[3]Chun HJ,Bonnet S,Chan SY. Translational advances in the field of pulmonary hypertension. Translating microRNA biology in pulmonary hypertension. It will take more than “miR” words[J]. Am J Respir Crit Care Med,2017,195(2):167-178.

[4]Daniels LB,Clopton P,Iqbal N,et al. Association of ST2 levels with cardiac structure and function and mortality in outpatients[J]. Am Heart J,2010,160(4):721-728.

[5]Simpson CE,Damico RL,Hassoun PM,et al. Noninvasive prognostic biomarkers for left-sided heart failure as predictors of survival in pulmonary arterial hypertension[J]. Chest,2020,157(6):1606-1616.

[6]Geenen LW,Baggen VJM,Kauling RM,et al. The prognostic value of soluble ST2 in adults with pulmonary hypertension[J]. J Clin Med,2019,8(10):1517.

[7]Ogita M,Miyauchi K,Jiang M,et al. Circulating soluble LR11,a novel marker of smooth muscle cell proliferation,is enhanced after coronary stenting in response to vascular injury[J]. Atherosclerosis,2014,237(1):374-378.

[8]Jiang L,Konishi H,Nurwidya F,et al. Deletion of LR11 attenuates hypoxia-induced pulmonary arterial smooth muscle cell proliferation with medial thickening in mice[J]. Arterioscler Thromb Vasc Biol,2016,36(9):1972-1979.

[9]Kikuchi N,Satoh K,Saito Y,et al. Response by Kikuchi et al Regarding Article, “Selenoprotein P Promotes the Development of Pulmonary Arterial Hypertension: A Possible Novel Therapeutic Target”[J]. Circulation,2019,139(5):724-725.

[10]Kikuchi N,Satoh K,Satoh T,et al. Diagnostic and prognostic significance of serum levels of SeP(selenoprotein P) in patients with pulmonary hypertension[J]. Arterioscler Thromb Vasc Biol,2019,39(12):2553-2562.

[11]Sun Q,Hackler J,Hilger J,et al. Selenium and copper as biomarkers for pulmonary arterial hypertension in systemic sclerosis[J]. Nutrients,2020,12(6):1894.

[12] Drab M,Verkade P,Elger M,et al. Loss of caveolae,vascular dysfunction,and pulmonary defects in caveolin-1 gene-disrupted mice[J]. Science,2001,293(5539):2449-2452.

[13]Jasmin JF,Mercier I,Dupuis J,et al. Short-term administration of a cell-permeable caveolin-1 peptide prevents the development of monocrotaline-induced pulmonary hypertension and right ventricular hypertrophy[J]. Circulation,2006,114(9):912-920.

[14]Zhao YY,Zhao YD,Mirza MK,et al. Persistent eNOS activation secondary to caveolin-1 deficiency induces pulmonary hypertension in mice and humans through PKG nitration[J]. J Clin Invest,2009,119(7):2009-2018.

[15]Wang KY,Lee MF,Ho HC,et al. Serum caveolin-1 as a novel biomarker in idiopathic pulmonary artery hypertension[J]. Biomed Res Int,2015,2015:173970.

[16]Sarrion I,Milian L,Juan G,et al. Role of circulating miRNAs as biomarkers in idiopathic pulmonary arterial hypertension:possible relevance of miR-23a[J]. Oxid Med Cell Longev,2015,2015:792846.

[17]Santos-Ferreira CA,Abreu MT,Marques CI,et al. Micro-RNA analysis in pulmonary arterial hypertension:current knowledge and challenges[J]. JACC Basic Transl Sci,2020,5(11):1149-1162.

[18]Luo Y,Dong HY,Zhang B,et al. miR-29a-3p attenuates hypoxic pulmonary hypertension by inhibiting pulmonary adventitial fibroblast activation[J]. Hypertension,2015,65(2):414-420.

[19]Wang T,Li Y,Chen J,et al. TGF-β1/Smad3 signaling promotes collagen synthesis in pulmonary artery smooth muscle by down-regulating miR-29b[J]. Int J Clin Exp Pathol,2018,11(12):5592-5601.

[20]Chen X,Talati M,Fessel JP,et al. Estrogen metabolite 16α-hydroxyestrone exacerbates bone morphogenetic protein receptor type Ⅱ-associated pulmonary arterial hypertension through microRNA-29-mediated modulation of cellular metabolism[J]. Circulation,2016,133(1):82-97.

[21]Wang D,Zhang H,Li M,et al. MicroRNA-124 controls the proliferative,migratory,and inflammatory phenotype of pulmonary vascular fibroblasts[J]. Circ Res,2014,114(1):67-78.

[22]Zhang H,Wang D,Li M,et al. Metabolic and proliferative state of vascular adventitial fibroblasts in pulmonary hypertension is regulated through a microRNA-124/PTBP1(polypyrimidine tract binding protein 1)/pyruvate kinase muscle axis[J]. Circulation,2017,136(25):2468-2485.

[23]Caruso P,Dunmore BJ,Schlosser K,et al. Identification of microRNA-124 as a major regulator of enhanced endothelial cell glycolysis in pulmonary arterial hypertension via PTBP1(polypyrimidine tract binding protein) and pyruvate kinase M2[J]. Circulation,2017,136(25):2451-2467.

[24]Kang K,Peng X,Zhang X,et al. MicroRNA-124 suppresses the transactivation of nuclear factor of activated T cells by targeting multiple genes and inhibits the proliferation of pulmonary artery smooth muscle cells[J]. J Biol Chem,2013,288(35):25414-25427.

[25]Zhu TT,Zhang WF,Yin YL,et al. MicroRNA-140-5p targeting tumor necrosis factor-α prevents pulmonary arterial hypertension[J]. J Cell Physiol,2019,234(6):9535-9550.

[26]Zhang Y,Xu J. MiR-140-5p regulates hypoxia-mediated human pulmonary artery smooth muscle cell proliferation,apoptosis and differentiation by targeting Dnmt1 and promoting SOD2 expression[J]. Biochem Biophys Res Commun,2016,473(1):342-348.

[27]Rothman AM,Arnold ND,Pickworth JA,et al. MicroRNA-140-5p and SMURF1 regulate pulmonary arterial hypertension[J]. J Clin Invest,2016,126(7):2495-2508.

[28]Zhou G,Chen T,Raj JU.MicroRNAs in pulmonary arterial hypertension[J]. Am J Respir Cell Mol Biol,2015,52(2):139-151.

[29]Courboulin A,Paulin R,Giguère NJ,et al. Role for miR-204 in human pulmonary arterial hypertension[J]. J Exp Med,2011,208(3):535-548.

[30]Meloche J,Pflieger A,Vaillancourt M,et al. Role for DNA damage signaling in pulmonary arterial hypertension[J]. Circulation,2014,129(7):786-797.

[31]Ruffenach G,Chabot S,Tanguay VF,et al. Role for Runt-related transcription factor 2 in proliferative and calcified vascular lesions in pulmonary arterial hypertension[J]. Am J Respir Crit Care Med,2016,194(10):1273-1285.

[32]Soubrier F,Chung WK,Machado R,et al. Genetics and genomics of pulmonary arterial hypertension[J]. J Am Coll Cardiol,2013,62(25 suppl):D13-D21.

[33]Morrell NW,Aldred MA,Chung WK,et al. Genetics and genomics of pulmonary arterial hypertension[J]. Eur Respir J,2019,53(1):1801899.

[34]Southgate L,Machado RD,Gr?f S,et al. Molecular genetic framework underlying pulmonary arterial hypertension[J]. Nat Rev Cardiol,2020,17(2):85-95.

[35]Rhodes CJ,Batai K,Bleda M,et al. Genetic determinants of risk in pulmonary arterial hypertension:international genome-wide association studies and meta-analysis[J]. Lancet Respir Med,2019,7(3):227-238.

[36]Gr?f S,Haimel M,Bleda M,et al. Identification of rare sequence variation underlying heritable pulmonary arterial hypertension[J]. Nat Commun,2018,9(1):1416.

[37]Zhu N,Pauciulo MW,Welch CL,et al. Novel risk genes and mechanisms implicated by exome sequencing of 2572 individuals with pulmonary arterial hypertension[J]. Genome Med,2019,11(1):69.

[38]Ventetuolo CE,Mitra N,Wan F,et al. Oestradiol metabolism and androgen receptor genotypes are associated with right ventricular function[J]. Eur Respir J,2016,47(2):553-563.

[39]Damico R,Kolb TM,Valera L,et al. Serum endostatin is a genetically determined predictor of survival in pulmonary arterial hypertension[J]. Am J Respir Crit Care Med,2015,191(2):208-218.

[40]Eyries M,Montani D,Girerd B,et al. EIF2AK4 mutations cause pulmonary veno-occlusive disease,a recessive form of pulmonary hypertension[J]. Nat Genet,2014,46(1):65-69.

[41]Liu D,Liu QQ,Eyries M,et al. Molecular genetics and clinical features of Chinese idiopathic and heritable pulmonary arterial hypertension patients[J]. Eur Respir J,2012,39(3):597-603.

[42]Evans JD,Girerd B,Montani D,et al. BMPR2 mutations and survival in pulmonary arterial hypertension:an individual participant data meta-analysis[J]. Lancet Respir Med,2016,4(2):129-137.

[43]Zhu N,Gonzaga-Jauregui C,Welch CL,et al. Exome sequencing in children with pulmonary arterial hypertension demonstrates differences compared with adults[J]. Circ Genom Precis Med,2018,11(4):e001887.

[44]Germain M,Eyries M,Montani D,et al. Genome-wide association analysis identifies a susceptibility locus for pulmonary arterial hypertension[J]. Nat Genet,2013,45(5):518-521.

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更新日期/Last Update: 2021-12-06