Islek Ali, Ilhan Derya, Ozturk Nurinnisa, Guven Burcu, Sag Elif
Departments of Pediatric Gastroenterology.
Pediatrics.
J Pediatr Hematol Oncol. 2021 Oct 1;43(7):e951-e956. doi: 10.1097/MPH.0000000000002038.
BACKGROUND/AIM: This study was concerned with whether vWF (von Willebrand factor) and a disintegrin and metalloprotease with a thrombospondin type 1 motif, member 13 (ADAMTS13) has altered in patients with cirrhosis and extrahepatic portal hypertension (EPH). We aimed to investigate changes to vWF and ADAMTS13 in children with cirrhosis and EPH.
This study was conducted between January and October 2019 with both cirrhosis and EPH patients and with healthy volunteers. The von Willebrand factor antigen (vWF:Ag), von Willebrand Ristocetin cofactor (vWF:RCo), and ADAMTS13 antigen and activity were studied.
Twenty-eight children with cirrhosis, 16 children with EPH, and 20 healthy controls were included in the study. vWF:Ag and vWF:RCo levels were higher in patients with cirrhosis than in healthy controls (171.65±101.67 vs. 85.86±30.58, P<0.01 and 121.62±55.83 vs. 61.52±27.03, P<0.01, respectively). vWF:Ag and vWF:RCo levels were higher in patients with EPH than in healthy controls (133.93±80.13 vs. 85.86±30.58, P<0.01 and 103.18±58.55 vs. 61.52±27.03, P=0.02, respectively). The ADAMTS13 antigen and activity levels were lower in patients with cirrhosis than in healthy controls (0.58±0.23 vs. 0.97±0.15, P<0.01 and 49.91±22.43 vs. 86.51±22.07, P=0.02, respectively). The ADAMTS13 antigen and activity levels were lower in patients with EPH than in healthy controls (0.69±0.11 vs. 0.97±0.15, P=0.03; and 68.50±13.29 vs. 86.51±22.07, P=0.02, respectively). The increase in vWF and the decrease in ADAMTS13 were more pronounced in cirrhotic patients with autoimmune hepatitis (AIH) than in non-AIH patients.
While levels of vWF:Ag and vWF:RCo increased in children with cirrhosis and EPH, levels of the ADAMTS13 antigen and ADAMTS13 activity decreased. These alterations were more pronounced in patients with AIH-derived cirrhosis.
背景/目的:本研究关注肝硬化合并肝外门静脉高压(EPH)患者的血管性血友病因子(vWF)和含血小板反应蛋白基序的解聚素样金属蛋白酶13(ADAMTS13)是否发生改变。我们旨在研究肝硬化合并EPH儿童患者中vWF和ADAMTS13的变化情况。
本研究于2019年1月至10月对肝硬化合并EPH患者及健康志愿者进行。研究了血管性血友病因子抗原(vWF:Ag)、血管性血友病因子瑞斯托霉素辅因子(vWF:RCo)以及ADAMTS13抗原和活性。
本研究纳入了28例肝硬化儿童、16例EPH儿童以及20例健康对照。肝硬化患者的vWF:Ag和vWF:RCo水平高于健康对照(分别为171.65±101.67 vs. 85.86±30.58,P<0.01;121.62±55.83 vs. 61.52±27.03,P<0.01)。EPH患者的vWF:Ag和vWF:RCo水平高于健康对照(分别为133.93±80.13 vs. 85.86±30.58,P<0.01;103.18±58.55 vs. 61.52±27.03,P=0.02)。肝硬化患者的ADAMTS13抗原和活性水平低于健康对照(分别为0.58±0.23 vs. 0.97±0.15,P<0.01;49.91±22.43 vs. 86.51±22.07,P=0.02)。EPH患者的ADAMTS13抗原和活性水平低于健康对照(分别为0.69±0.11 vs. 0.97±0.15,P=0.03;68.50±13.29 vs. 86.51±22.07,P=0.02)。与非自身免疫性肝炎(AIH)患者相比,自身免疫性肝炎(AIH)所致肝硬化患者的vWF升高及ADAMTS13降低更为明显。
肝硬化合并EPH儿童患者的vWF:Ag和vWF:RCo水平升高,而ADAMTS13抗原和ADAMTS13活性水平降低。这些改变在AIH所致肝硬化患者中更为明显。