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首页> 外文期刊>Clinica chimica acta: International journal of clinical chemistry and applied molecular biology >Significantly increased concentration of soluble urokinase-type plasminogen activator receptor in the blood of patients with pelvic inflammatory disease.
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Significantly increased concentration of soluble urokinase-type plasminogen activator receptor in the blood of patients with pelvic inflammatory disease.

机译:盆腔炎性疾病患者血液中可溶性尿激酶型纤溶酶原激活因子浓度显着增加。

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To determine expression levels of urokinase-type plasminogen activator (uPA), soluble urokinase-type plasminogen activator receptor (suPAR), plasminogen activator inhibitor-1 (PAI-1) in plasma and to identify gene polymorphisms specific to patients with pelvic inflammatory disease (PID) and healthy controls.Enzyme-linked immunosorbent assay and polymerase chain reaction-restriction fragment length polymorphism were used to measure plasma levels and polymorphisms in uPA, suPAR, and PAI-1 among seventy healthy controls and 64 PID patients before and after they received routine treatment protocols.The levels of plasma uPA (ng/ml) and soluble suPAR (pg/ml) were significantly increased in PID patients (uPA: 0.57±0.03; suPAR: 1372.04±68.20) when compared to that in normal controls (uPA: 0.55±0.06, p=0.002; suPAR: 1192.46±51.98, p=0.04); moreover, suPAR decreased significantly after treatment when compared to levels noted in the same patients (1220.06±58.14; p=0.003) after they received treatment. The increased expression of suPAR was significantly correlated with WBC counts (r=0.382, p=0.002, n=64) in blood as well as the plasma levels of CRP (r=0.441, p<0.0001, n=64) and uPA (r=0.426, p<0.0001, n=64) of PID patients prior to receiving treatment.Increased plasma suPAR could be a biological marker for the diagnosis of PID and may reflect a new focus in targeted therapy for pelvic inflammatory disease.
机译:为了确定尿激酶型纤溶酶原激活剂(UPA),可溶性尿激酶型纤溶酶原激活剂受体(SUPAR),纤溶酶原激活物抑制剂-1(PAI-1)的表达水平,并鉴定对盆腔炎患者特异的基因多态性( PID)和健康对照。酶联免疫吸附测定和聚合酶链反应限制片段长度多态性用于测量七十个健康对照组和64个PID患者的UPA,SUPAR和PAI-1中的血浆水平和多态性与正常对照相比,PID患者(UPA:0.57±0.03)显着增加了血浆UPA(Ng / ml)和可溶性苏壳(PG / ml)水平的水平(UPA:0.57±68.20) :0.55±0.06,P = 0.002; SUPAR:1192.46±51.98,P = 0.04);此外,与同一患者中的水平相比,在治疗后(1220.06±58.14; p = 0.003)在接受治疗后,Supar显着降低。血液中的WBC计数(R = 0.382,P = 0.002,N = 0.002,N = 64)显着相关,以及CRP的血浆水平(r = 0.441,p <0.0001,n = 64)和upa( PID患者r = 0.426,p <0.0001,n = 64)PID患者在接受治疗前。增加的等离子体SUPAR可以是用于PID的生物学标志物,并且可以反映盆腔炎患者靶向治疗的新重点。

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