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Elevated plasma Pim‐1 and its clinical significance in patients with pulmonary arterial hypertension

机译:肺动脉高压患者升高的血浆PIM-1及其临床意义

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Abstract This study was aimed to determine plasma Pim‐1 levels in patients with pulmonary arterial hypertension ( PAH ) and to estimate the clinical value of Pim‐1 as a biomarker of PAH . This was a single‐centre retrospective study in 111 patients with congenital heart disease ( CHD ) and idiopathic PAH ( IPAH ). Those CHD patients were divided into two groups: PAH associated with CHD ( PAH ‐ CHD ) and CHD without PAH ( nPAH ‐ CHD ). Plasma Pim‐1 levels were measured by enzyme‐linked immunosorbent assay. (a) Plasma Pim‐1 levels were significantly increased in patients with PAH ‐ CHD and IPAH compared with the healthy control group (27.81?±?11.34?ng/mL vs 13.02?±?5.30?ng/mL; 32.81?±?12.28?ng/mL vs 13.02?±?5.30?ng/mL, P? ? 0.05) and nPAH ‐ CHD (27.81?±?11.34?ng/mL vs 17.33?±?7.99?ng/mL; 32.81?±?12.28?ng/mL vs 17.33?±?7.99?ng/mL, P ??0.05). Pim‐1 levels were substantially increased in patients with severe PAH ‐ CHD compared with mild‐to‐moderate PAH ‐ CHD (19.12?±?6.70?ng/mL vs 8.54?±?3.71?ng/mL, P ??0.05). (b) Pim‐1 levels were correlated positively with the mean pulmonary artery pressure ( mPAP ) and pulmonary vascular resistance ( PVR ) ( r ?=?0.582, 0.516; P ??0.001, respectively), while negatively with tricuspid annular plane systolic excursion ( TAPSE ), tricuspid annular plane systolic velocity (S’) and right ventricular fractional area changes ( RVFAC ) ( r ?=??0.375, ?0.354, ?0.507; P ??0.05, respectively). (c) PAH ‐ CHD and severe PAH ‐ CHD was identified by plasma Pim‐1 with a cutoff value of 16.8?ng/mL ( P ??0.001) with a sensitivity of 87.3% and a specificity of 65%, and a cutoff value of 20.53?ng/mL ( P ??0.001) with a sensitivity of 87.3% and a specificity of 52%, respectively. Plasma Pim‐1 levels were significantly higher in patients with PAH ‐ CHD and IPAH . Plasma Pim‐1 may represent an effectively biomarker in patients with PAH.
机译:摘要本研究旨在确定肺动脉高血压(PAH)患者的血浆PIM-1水平,并估计PIM-1作为PAH的生物标志物的临床价值。这是111例先天性心脏病(CHD)和特发性Pah(IPAH)的111名患者的单中心回顾性研究。这些CHD患者分为两组:与CHD(PAH - CHD)和CHD相关的PAH(NPAH - CHD)。通过酶联免疫吸附测定法测量血浆PIM-1水平。 (a)与健康对照组(27.81Ω·±11.34×11.34〜13.02α≤13.02≤13.81Ω,PAH - CHD和IPAH患者血浆PIM-1水平显着增加12.28?ng / ml vs 13.02?±5.30?5.30?ng / ml,p?&?0.05)和npah - chd(27.81?±α11.34≤≤x≤7.99?ng / ml; 32.81?32.81?32.81? ±12.28?ng / ml vs17.33?αα±7.99?ng / ml,p≤≤0.05)。严重的PAH-CHD患者与轻度至中度PAH - CHD(19.12?±6.7.7.7.16.3.71≤3.71≤3.71Ω患者,PIM-1水平显着增加0.05)。 (b)PIM-1水平随着平均肺动脉压(MPAP)和肺血管阻力(PVR)(Rα= 0.582,0.516;p≤0.0.001),同时对三尖瓣环形呈正相关飞机收缩偏移(磁带),三尖瓣环形平面收缩速度(S')和右心室分数区域变化(RVFAC)(R?= ?? 0.375,Δ0.354,分别分别)。 (c)通过血浆PIM-1鉴定PAH-CHD和严重的PIM-CHD,截止值为16.8〜Ng / ml(p≤0.001),敏感性为87.3%,特异性为65%,截止值为20.53?ng / ml(p≤≤0.001),灵敏度分别为87.3%,特异性分别为52%。 PAH - CHD和IPAH患者血浆PIM-1水平显着高。血浆PIM-1可以代表PAH患者的有效生物标志物。

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