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  1. 1
    دورية أكاديمية

    المصدر: Neurology, Neuropsychiatry, Psychosomatics; Vol 13, No 1S (2021): Спецвыпуск: рассеянный склероз; 62-68 ; Неврология, нейропсихиатрия, психосоматика; Vol 13, No 1S (2021): Спецвыпуск: рассеянный склероз; 62-68 ; 2310-1342 ; 2074-2711 ; 10.14412/2074-2711-2021-1S

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High concentrations of procoagulant microparticles in the cerebrospinal fluid and peripheral blood of patients with acute basal ganglia hemorrhage are associated with poor outcome. Surg Neurol. 2009;72(5):481-9. doi:10.1016/j.surneu.2008.12.016; Marcos-Ramiro B, Oliva Nacarino P, Serrano-Pertierra E, et al. Microparticles in multiple sclerosis and clinically isolated syndrome: effect on endothelial barrier function. BMC Neurosci. 2014;15:110. doi:10.1186/1471-2202-15-110; Jy W, Jimenez JJ, Mauro LM, et al. Endothelial microparticles induce formation of platelet aggregates via a von Willebrand factor/ristocetin dependent pathway, rendering them resistant to dissociation. J Thromb Haemost. 2005;3(6):1301-8. doi:10.1111/j.1538-7836.2005.01384.x; Scharpfenecker M, Fiedler U, Reiss Y, Augustin HG. The Tie-2 ligand angiopoietin-2 destabilizes quiescent endothelium through an internal autocrine loop mechanism. J Cell Sci. 2005;118(4):771-80. doi:10.1242/jcs.01653; Starke RD, Ferraro F, Paschalaki KE, et al. Endothelial von Willebrand factor regulates angiogenesis. Blood. 2011;117(3):1071-80. doi:10.1182/blood-2010-01-264507; Li Z, Korhonen EA, Merlini A, et al. Angiopoietin-2 blockade ameliorates autoimmune neuroinflammation by inhibiting leukocyte recruitment into the CNS. J Clin Invest. 2020;130(4):1977-90. doi:10.1172/JCI130308; Qin F, Impeduglia T, Schaffer P, Dardik H. Overexpression of von Willebrand factor is an independent risk factor for pathogenesis of intimal hyperplasia: Preliminary studies. J Vasc Surg. 2003;37(2):433-9. doi:10.1067/mva.2003.63; Zhang X, Meng H, Blaivas M, et al. Von Willebrand Factor Permeates Small Vessels in CADASIL and Inhibits Smooth Muscle Gene Expression. Transl Stroke Res. 2012;3(1):138-45. doi:10.1007/s12975-011-0112-2; Michaux G, Pullen TJ, Haberichter SL, Cutler DF. P-selectin binds to the D'-D3 domains of von Willebrand factor in WeibelPalade bodies. Blood. 2006;107(10):3922-4. doi:10.1182/blood-2005-09-3635; Denis CV, Andre P, Saffaripour S, Wagner DD. Defect in regulated secretion of P-selectin affects leukocyte recruitment in von Willebrand factor-deficient mice. Proc Natl Acad Sci USA. 2001;98(7):4072-7. doi:10.1073/pnas.061307098; Gragnano F, Sperlongano S, Golia E, et al. The Role of von Willebrand Factor in Vascular Inflammation: From Pathogenesis to Targeted Therapy. Mediators Inflamm. 2017;2017:5620314. doi:10.1155/2017/5620314; Khan MM, Motto DG, Lentz SR, Chauhan AK. ADAMTS13 reduces VWF-mediated acute inflammation following focal cerebral ischemia in mice. J Thromb Haemost. 2012;10(8):1665-71. doi:10.1111/j.1538-7836.2012.04822.x; Pendu R, Terraube V, Christophe OD, et al. P-selectin glycoprotein ligand 1 and beta 2integrins cooperate in the adhesion of leukocytes to von Willebrand factor. Blood. 2006;108(12):3746-52. doi:10.1182/blood-2006-03-010322; Fuchs TA, Brill A, Duerschmied D, et al. Extracellular DNA traps promote thrombosis. Proc Natl Acad Sci USA. 2010;107(36):15880-5. doi:10.1073/pnas.1005743107; Rondaij MG, Bierings R, Kragt A, et al. Dynamics and Plasticity of Weibel-Palade Bodies in Endothelial Cells. Arterioscler Thromb Vasc Biol. 2006;26(5):1002-7. doi:10.1161/01.ATV.0000209501.56852.6c; Bierings R, van den Biggelaar M, Kragt A, et al. Efficiency of von Willebrand factor-mediated targeting of interleukin-8 into Weibel-Palade bodies. J Thromb Haemost. 2007;5(12):2512-9. doi:10.1111/j.1538-7836.2007.02768.x; Bernardo A, Ball C, Nolasco L, et al. Effects of inflammatory cytokines on the release and cleavage of the endothelial cell-derived ultralarge von Willebrand factor multimers under flow. Blood. 2004;104(1):100-6. doi:10.1182/blood-2004-01-0107; Knipe L, Meli A, Hewlett L, et al. A revised model for the secretion of tPA and cytokines from cultured endothelial cells. Blood. 2010;116(12):2183-91. doi:10.1182/blood-2010-03-276170; Arumugam TV, Woodruff TM, Lathia JD, et al. Neuroprotection in Stroke by Complement Inhibition and Immunoglobulin Therapy. Neuroscience. 2009;158(3):1074-89. doi:10.1016/j.neuro-science.2008.07.015; Turner NA, Moake J. Assembly and Activation of Alternative Complement Components on Endothelial Cell-Anchored Ultra-Large Von Willebrand Factor Links Complement and Hemostasis-Thrombosis. Plos One. 2013;8(3):e59372. doi:10.1371/journal.pone.0059372; Feng S, Liang X, Cruz MA, et al. The Interaction between Factor H and Von Willebrand Factor. Plos One. 2013;8(8):e73715. doi:10.1371/journal.pone.0073715; Feng S, Liang X, Kroll MH, et al. Von Willebrand factor is a cofactor in complement regulation. Blood. 2015;125(6):1034-7. doi:10.1182/blood-2014-06-585430; Ingram G, Hakobyan S, Robertson NP, Morgan BP. 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Low ADAMTS13 activity is associated with an increased risk of ischemic stroke. Blood. 2015;126(25):2739-46. doi:10.1182/blood-2015-05643338; Blann AD, Naqvi T, Waite M, Mccollum CN. Von Willebrand factor and endothelial damage in essential hypertension. J Hum Hypertens. 1993;7(2):107-11.; Brandes RP. Endothelial Dysfunction and Hypertension. Hypertension. 2014;64(5):924-8. doi:10.1161/HYPERTENSIONAHA.114.03575; Frankel DS, Meigs JB, Massaro JM, et al. Von Willebrand Factor, Type 2 Diabetes and Risk of Cardiovascular Disease: The Framingham Offspring Study. Circulation. 2008;118(24):2533-9. doi:10.1161/CIRCULATIONAHA.108.792986; Van Galen KPM, Tuinenburg A, Smeets EM, Schutgens REG. Von Willebrand factor deficiency and atherosclerosis. Blood Rev. 2012;26(5):189-96. doi:10.1016/j.blre.2012.05.002; Gandhi C, Ahmad A, Wilson KM, Chauhan AK. ADAMTS13 modulates atherosclerotic plaque progression in mice via a VWF-dependent mechanism. J Thromb Haemost. 2014;12(2):255-60. doi:10.1111/jth.12456; Sonneveld MAH, van Dijk AC, van den Herik EG, et al. Relationship of Von Willebrand Factor with carotid artery and aortic arch calcification in ischemic stroke patients. Atherosclerosis. 2013;230(2):210-5. doi:10.1016/j.atherosclerosis.2013.07.046; Malek AM, Alper SL, Izumo S. Hemodynamic shear stress and its role in atherosclerosis. Jama-J Am Med Assoc. 1999;282(21):2035-42. doi:10.1001/jama.282.21.2035; Van Agtmaal EL, Bierings R, Dragt BS, et al. The Shear Stress-Induced Transcription Factor KLF2 Affects Dynamics and Angiopoietin-2 Content of Weibel-Palade Bodies. Plos One. 2012;7(6):e38399. doi:10.1371/journal.pone.0038399; Van Thienen JV, Fledderus JO, Dekker RJ, et al. Shear stress sustains atheroprotective endothelial KLF2 expression more potently than statins through mRNA stabilization. Cardiovasc Res. 2006;72(2):231-40. doi:10.1016/j.cardiores.2006.07.008; Scridon A, Girerd N, Rugeri L, et al. Progressive endothelial damage revealed by multilevel von Willebrand factor plasma concentrations in atrial fibrillation patients. Europace. 2013;15(11):1562-6. doi:10.1093/europace/eut121; Conway DSG, Pearce LA, Chin BSP, et al. Plasma von Willebrand factor and soluble P-selectin as indices of endothelial damage and platelet activation in 1321 patients with nonvalvular atrial fibrillation – Relationship to stroke risk factors. Circulation. 2002;106(15):1962-7. doi:10.1161/01.CIR.0000033220.97592.9A; Cortes GM, Sandoval MEV, Martinez CAA, et al. Von Willebrand Factor plasma levels variability in nonvalvular Atrial Fibrillation. J Atr Fibrillation. 2014;7(4):99-105. doi:10.4022/jafib.1124; Rewiuk K, Grodzicki T. Correlations of C-reactive protein, von Willebrand factor, and carotid artery intima-media thickness with CHA2DS2-VASc in patients with acute atrial fibrillation. Pol Arch Med Wewn. 2015;125(11):835-44. doi:10.20452/pamw.3162; Kraft P, Drechsler C, Gunreben I, et al. 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Rare Variants in the ADAMTS13 Von Willebrand Factor-Binding Domain Contribute to Pediatric Stroke. Circ-Cardiovasc Genet. 2016;9(4):357-67. doi:10.1161/CIRCGENETICS.115.001184; Bath PMW, Blann A, Smith N, Butterworth RJ. Von Willebrand factor, P-selectin and fibrinogen levels in patients with acute ischaemic and haemorrhagic stroke, and their relationship with stroke sub-type and functional outcome. Platelets. 1998;9(3-4):155-9. doi:10.1080/09537109876618; Zhu X, Cao Y, Wei L, et al. Von Willebrand factor contributes to poor outcome in a mouse model of intracerebral haemorrhage. Sci Rep. 2016;6:35901. doi:10.1038/srep35901; Гусев ЕИ, Мартынов МЮ, Кольцов ИА и др. Прогностическое значение дисфункции эндотелия и фактора фон Виллебранда в остром и отдаленном периодах геморрагического инсульта полушарной локализации. Журнал неврологии и психиатрии им. C.С. Корсакова. 2019;119(8-2):46-52. doi:10.17116/jnevro201911908246; Boluijt J, Meijers JCM, Rinkel GJE, Vergouwen MDI. 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Фактор фон Виллебранда и молекулы адгезии у пациентов с рассеянным склерозом. Журнал неврологии и психиатрии им. С.С. Корсакова. 2014;114(2-2):35-9.; Saenz-Cuesta M, Osorio-Querejeta I, Otaegui D. Extracellular Vesicles in Multiple Sclerosis: What are They Telling Us? Front Cell Neurosci. 2014;8:100. doi:10.3389/fncel.2014.00100; Lu K, Liu L, Xu X, et al. ADAMTS13 ameliorates inflammatory responses in experimental autoimmune encephalomyelitis. J Neuroinflammation. 2020;17(1):67. doi:10.1186/s12974-020-1713-z; Ziliotto N, Bernardi F, Jakimovski D, et al. Hemostasis biomarkers in multiple sclerosis. Eur J Neurol. 2018;25(9):1169-76. doi:10.1111/ene.13681; https://nnp.ima-press.net/nnp/article/view/1651Test

  2. 2
    دورية أكاديمية

    المساهمون: The investigation has been conducted under Russian Foundation for Basic Research Grants No. 20-07-00537 and No. 19-07-00356., Исследование выполнено по теме грантов Российского фонда фундаментальных исследований № 20-07-00537 и № 1907-00356.

    المصدر: Neurology, Neuropsychiatry, Psychosomatics; Vol 12, No 4 (2020); 91-99 ; Неврология, нейропсихиатрия, психосоматика; Vol 12, No 4 (2020); 91-99 ; 2310-1342 ; 2074-2711 ; 10.14412/2074-2711-2020-4

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