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成纤维细胞生长因子21与血管钙化关系研究进展

Research progress on the relationship between fibroblast growth factor 21 and vascular calcification
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摘要 成纤维细胞生长因子21(FGF21)是成纤维细胞生长因子家族的一员,具有降脂、抗炎、抗氧化等生物学作用。近年来研究发现,FGF21能够有效抑制血管钙化,降低心血管事件的发生,被视为心血管系统新的保护因素,有望成为临床上防治血管钙化的新靶点。本文就FGF21与血管钙化关系的最新研究进展做一综述。 Fibroblast growth factor 21(FGF21)is a member of the fibroblast growth factor family,which has biological effects such as lipid-lowering,anti-inflammation and anti-oxidation.In recent years,studies have found that FGF21 can effectively inhibit vascular calcification and reduce the occurrence of cardiovascular events.So,it has been regarded as a new protective factor for the cardiovascular system,and is expected to become a new clinical target for the prevention and treatment of vascular calcification.This article reviewed the latest research progress on the relationship between FGF21 and vascular calcification.
作者 夏庆玲 欧三桃 Qingling Xia;Santao Ou(Department of Nephrology,Affiliated Hospital of Southwest Medical University,Sichuan Clinical Research Center for Nephrology,Luzhou 646000,Sichuan Province,China)
出处 《中华肾病研究电子杂志》 2022年第4期231-234,共4页 Chinese Journal of Kidney Disease Investigation(Electronic Edition)
基金 四川省肾脏疾病临床医学研究中心2020年开放课题重点项目(2019YFS0537-3)
关键词 成纤维细胞生长因子21 血管钙化 血管平滑肌细胞 Fibroblast growth factor 21 Vascular calcification Vascular smooth muscle cells
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  • 1Daisuke Usuda,Tsugiyasu Kanda.Peroxisome proliferator-activated receptors for hypertension[J].World Journal of Cardiology,2014,6(8):744-754. 被引量:19
  • 2Valdivielso JM.Vascular calcification:types and mechanisms.Nefrologia,2011;31(2):142-147.
  • 3Nakagawa Y,Ikeda K,Akakabe Y,et al.Paracrine osteogenic signals via bone morphogenetic protein-2 accelerate the atherosclerotic intimal calcification in vivo.Arterioscler Thromb Vasc Biol,2010;30(10):1908-1915.
  • 4Yao Y,Bennett BJ,Wang X,et al.Inhibition of bone morphogenetic proteins protects against atherosclerosis and vascular calcification.Circ Res,2010;107(4):485-494.
  • 5Ankeny RF,Thourani VH,Weiss D,et al.Preferential activation of SMAD1/5/8 on the fibrosa endothelium in calcified human aortic valves--association with low BMP antagonists and SMAD6.PLoS One,2011;6(6):e20969.doi:10 .1371/journal pone.0020969.
  • 6Sun Y,Byon CH,Yuan K,et al.Smooth muscle cell-specific runx2deficiency inhibits vascular calcification.Circ Res,2012;111(5):543-552.
  • 7Roseman DA,Hwang SJ,Manders ES,et al.Renal artery calcium,cardiovascular risk factors and indices of renal function.Am J Cardiol,2014;113(1):156-161.
  • 8Tolkin L,Bursztyn M,Ben-Dov IZ,et al.Incidental renal artery calcifications:a study of 350 consecutive abdominal computed tomography scans,Nephrol Dial Transplant,2009;24(7):2170-2175.
  • 9Chiu YW,Adler S,Budoff M,et al.Prevalence and prognostic significance of renal artery calcification in patients with diabetes and proteinuria,Clin J Am Soc Nephrol,2010;5(11):2093-2100.
  • 10Speer MY,Li X,Hiremath PG,et al.Runx2/Cbfa1,but not loss of myocardin,is required for smooth muscle cell lineage reprogramming toward osteochondrogenesis.J Cell Biochem,2010;110(4):935-947.

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