摘要
目的探讨核因子-E2相关因子2(Nrf2)/血红素氧化酶(HO)-1通路在慢性阻塞性肺疾病(COPD)患者营养不良中的作用及其与肿瘤坏死因子(TNF)-α的关系。方法将60例稳定期男性COPD患者分为COPDI组(COPD伴营养不良患者)30例,COPDⅡ组(营养正常的COPD患者)30例,同期健康男性体检者30例为对照组,测量3组研究对象的白蛋白(A1b)、肱三头肌皮褶厚度(TSF)、上臂肌围(AMC)、BMI及实际体重占理想体重百分比(IBW%)等营养指标,采用酶联免疫吸附试验测定血浆Nrf2、HO-1及TNF-α浓度。结果COPDI组的TSF、A1b、AMC、BMI、IBW%均低于COPDⅡ组及对照组,COPDⅡ组的TSF、A1b、AMC明显低于对照组,差异均有统计学意义(P〈0.05);但COPDⅡ组的BMI、IBW%和对照组比较,差异无统计学意义(P〉0.05)。COPDI组血浆Nrf2、HO-1浓度低于COPDⅡ组及对照组,TNF—α浓度高于COPDⅡ组及对照组,COPDⅡ组血浆Nrf2、HO-1浓度低于对照组,TNF-α浓度高于对照组,差异均有统计学意义(P〈0.05)。COPD姐、嘲患者血浆Nr12与HO-1均呈正相关(r=0.823,P〈0.001;r=0.513,P=0.042);COPDI组、Ⅱ组患者血浆Nrf2、HO-1与TNF-α均无相关性(P〉0.05)。结论Nrf2/HO-1通路可能在一定程度上延缓男性COPD患者营养不良的进展,但与TNF-α无明显相关关系。
Objective To explore the role of nuclear factor-E2 related factor 2 (Nrf2)/Heine oxygenase-1 (HO-1) pathway in malnutrition of patients with chronic obstructive pulmonary disease (COPD) and its relationship with tumor necrosis factor(TNF)-cc Methods Sixty male patients with stable COPD were divided into COPD I group( patients with malnutrition,30 cases) and COPD Ⅱ group( patients with normal nutrition,30 cases). Thirty cases of healthy male subjects during the same period were selected as control group. Albumin ( Alb ), triceps skin-fold thickness ( TSF ) , arm muscle circumference ( AMC ), BMI and percentage of ideal body mass( IBW% ) were measured in all subjects. Concentrations of Nrf2, HO-1 and TNF-α in plasma of all subjects were detected by enzyme-linked immunosorbent assay. Results TSF,Alb,AMC,BMI and IBW% in COPD I group were significantly lower than those in COPDⅡand control group. TSF,Alb and AMC in COPDⅡ group were significantly lower than those in control group (P 〈 0. 05 ) , but BMI and IBW% were not significantly different between COPD Ⅱ group and control group( P 〉 0. 05 ). Concentrations of Nrf2 and HO-1 in plasma in COPD I group were lower and TNF-α was higher than those in COPD Ⅱ group and control group( P 〈 0.05 ). Concentrations of Nrf2 and HO-1 in plasma in COPD II group were lower and TNF-α was higher than those in control group( P 〈 0. 05 ). Nrf2 in plasma was positively correlated with HO-1 in COPD Ⅰ and COPD Ⅱgroup ( r = 0. 823, P 〈 0. 001 ; r = 0. 513, P = 0. 042). There was no significant correlation between Nrf2, HO-1 and TNF-α in COPD Ⅰ and COPD Ⅱ group ( P 〉 0. 05 ). Conclusion. Nrf2/HO-1 pathway may delay the progression of malnutrition in male COPD patients to some extent, but it has no significant correlation with TNF-α.
出处
《临床内科杂志》
CAS
2017年第9期628-630,共3页
Journal of Clinical Internal Medicine