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作 者:拓步雄[1] 李慧[1] 李超民[1] 彭利静[1] 钟筱兰[1]
机构地区:[1]解放军第四五一医院心血管内科,陕西西安710054
出 处:《心脏杂志》2010年第5期730-732,共3页Chinese Heart Journal
摘 要:目的:观察冠状动脉慢血流现象(CSF)患者血清脂质过氧化水平的变化,并探讨CSF的影响因素。方法:采用TIM I帧计数(TFC)法作为测定CSF的指标,将入选病例分为两组:CSF组35例,正常对照组35例,均排除既往冠心病、心肌病及其他类型心脏病。采用生化法测定血清中超氧化物歧化酶(SOD),谷胱甘肽过氧化物酶(GSH-PX),丙二醛(MDA),过氧化脂质(LPO)的含量。结果:CSF组的血清MDA、LPO明显高于对照组[MDA:(18.9±2.0)μmol/Lv.s(10.5±1.3)μmol/L,P<0.01],[LPO:(2.8±0.4)μmol/Lvs.(1.9±0.2)μmol/L,P<0.01];CSF组血清GSH-PX明显高于对照组[GSH-PX:(0.22±0.04)μmol/Lvs.(0.20±0.03)μmol/L,P<0.05]。CSF组血清SOD明显低于对照组[SOD:(72±11)kU/Lv.s(79±10)kU/L,P<0.01]。在校正体质量指数、总胆固醇、尿素氮等后CSH-PX、MDA、LPO是CSF的危险因素(分别OR=3.987、4.782、3.381;分别为P<0.05、P<0.01、P<0.01)。SOD则是其保护因素(OR=0.892,P<0.05)。结论:CSF患者血清SOD下降,MDA、LPO、GSH-PX上升,体内氧化应激增强。AIM: To observe the levels of serum lipid peroxidation in patients with coronary slow flow (CSF) and to study related factors. METHODS: Thirty-five patients with documented CSF defined according to TIMI frame count method (TFC) and 35 patients with normal coronary flow were enrolled. Levels of superoxide dismutase ( SOD), glutathione peroxidase ( GSH-PX), malonyldialdehyde (MDA) and lipid peroxidation (LPO) were determined by biochemistry and logistic regression analysis was per- formed. RESULTS: Baseline data showed that compared with control group, MDA and LPO significantly increased inCSFgroup [MDA: (18.9 ±2.0) vs. (10.5±1.3) mol/L, P〈0. 01], [LPO: (2.8±0. 4) vs. ( 1.9 ±0. 2 ) tool/L, P 〈 0. 01 ]. Serum GSH-PX also increased in CSF group [ GSH-PX : (0. 22 ±0. 04) vs. (0. 20 ± 0. 03 ) tool/L, P 〈 0. 05 ], but SOD significantly decreased in CSF group [ SOD: (72 ± 11 ) vs. (79 ± 10) kU/L, P 〈 0. 01 ]. After calibration of body mass index, total cholesterol and blood urea nitrogen, analysis showed that CSF was positively correlated with GSH-PX, MDA and LPO ( [3 = 1. 768, 1. 565 and 1. 204, respectively, P 〈0. 05, P 〈0. 01, P 〈0. 01 ) but was negatively correlated with SOD (J3 =0. 115, P 〈0.05). CONCLUSION: In CSF patients, serum SOD decreases, whereas MDA, LPO and GSH-PX increase. The increased peroxide products of MDA, LPO and GSH-PX enhance oxidative stress in the body, which may result in CSF.
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