首页|左乙拉西坦联合鼠神经生长因子治疗脑卒中后癫痫对患者神经细胞因子和认知功能的影响

左乙拉西坦联合鼠神经生长因子治疗脑卒中后癫痫对患者神经细胞因子和认知功能的影响

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目的 探讨脑卒中后癫痫患者应用左乙拉西坦联合鼠神经生长因子治疗对其神经细胞因子和认知功能的影响。方法 将 2021 年 2 月至 2023 年 5 月河南省南阳市第一人民医院收治的脑卒中后癫痫90例,依据治疗方法不同分为对照组(30 例)、干预组(30 例)、试验组(30 例)。对照组实施左乙拉西坦治疗,干预组实施鼠神经生长因子治疗,试验组实施左乙拉西坦联合鼠神经生长因子治疗,治疗时间为 1 个月。对比 3 组患者临床疗效,治疗前后左大脑中动脉血流、右大脑中动脉血流、基底动脉血流、神经细胞因子[胶质纤维酸性蛋白(GFAP)、脑源性神经营养因子(BDNF)、S-100β蛋白(S-100β)、神经元特异性烯醇化酶(NSE)]水平,治疗前及治疗 2、4 周后炎症因子[微小核糖核酸-222(miR-222)、白细胞介素-6(IL-6)]水平、认知功能[蒙特利尔认知评估量表(MoCA)、简易智力状态检查量表(MMSE)]评分。结果 经过临床治疗试验组总有效率高于对照组、干预组(χ2=7。081,P<0。05),3 组治疗后左大脑中动脉血流、右大脑中动脉血流、基底动脉血流相较于治疗前升高,试验组相较于对照组、干预组更高(F=42。600、23。662、21。116,P<0。05),3 组治疗后GFAP、S-100β、NSE相较于治疗前降低,试验组比对照组更低;BDNF相较于治疗前升高,试验组相较于对照组、干预组更高(F=29。842、97。544、13。495、78。796,P<0。05),3 组治疗 2、4 周后miR-222、IL-6 水平相较于治疗前降低,试验组相较于对照组、干预组更高(F=12。572、15。907,12。286、26。380,P<0。05),3 组治疗 2、4 周后MoCA、MMSE评分相较于治疗前升高,试验组相较于对照组、干预组更高(F=12。572、15。907,12。286、26。380,P<0。05)。结论 左乙拉西坦联合鼠神经生长因子治疗应用于脑卒中后癫痫患者中,可提高疗效,促进脑部血液代谢,改善神经功能,减轻机体的炎症程度,缓解认知损伤。
Effects of levetiracetam with murine nerve growth factor for poststroke epilepsy on neural cytokines and cognitive function in patients
Objective To investigate the effect of levetiracetam combined with murine nerve growth fac-tor on neural cytokines and cognitive function in patients with epilepsy.Methods A total of 90 patients with post-stroke epilepsy admitted to Nanyang First People's Hospital from February 2021 to May 2023 were divided into control group(30 cases),intervention group(30 cases)and experimental group(30 cases)according to different treatment methods.The control group was treated with levetiracetam,the intervention group was treated with rat nerve growth factor,and the experimental group was treated with levetiracetam combined with rat nerve growth fac-tor for 1 month.The clinical efficacy of the 3 groups was compared,and the left middle cerebral artery blood flow,right middle cerebral artery blood flow,basilar artery blood flow,nerve cytokines[glial fibrillary acidic protein(GFAP),brain-derived neurotrophic factor(BDNF),S-100β protein(S-100β),neuron-specific enolase(NSE)]levels before and after treatment in 3 groups were compared.Levels of inflammatory factors[micrornA-222(miR-222),in-terleukin-6(IL-6)]and scores of cognitive functions[Montreal Cognitive Assessment Scale(MoCA),Mini Mental State Examination Scale(MMSE)]were measured before treatment and 2 and 4 weeks after treatment.Results After clinical treatment,the total effective rate of experimental group was higher than that of the control group and the intervention group(χ2=7.081,P<0.05).Left middle cerebral artery blood flow,right middle cerebral artery blood flow and basilar artery blood flow in the 3 groups after treatment were higher than before treatment,and the experimental group was higher than the control group and the intervention group(F=42.600,23.662,21.116,P<0.05).GFAP,S-100β and NSE in the 3 groups after treatment were lower than those before treatment.BDNF was higher than before treatment,the test group was lower than control group,and higher in test group than control group and intervention group(F=29.842,97.544,13.495,78.796,P<0.05).After 2 and 4 weeks of treatment,the levels of miR-222 and IL-6 in the 3 groups were lower than those before treatment,and the test group was higher than the control group and the intervention group(F=12.572,15.907,12.286,26.380,P<0.05).After 2 and 4 weeks of treatment,the scores of MoCA and MMSE in the three groups were higher than those before treatment,and the scores in the test group were higher than those in the control group and the intervention group(F=12.572,15.907,12.286,26.380,P<0.05).Conclusion Levetiracetam combined with rat nerve growth factor can improve the therapeutic effect,promote brain blood metabolism,improve nerve function,reduce the degree of inflammation and alleviate cognitive impairment in patients with post-stroke epilepsy.

StrokeEpliepsyLevetiracetamNerve growth factorNeural cytokinesCognition function

程棵、王叶琳

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南阳市第一人民医院西药科,河南南阳 473000

卒中 癫痫 左乙拉西坦 神经生长因子 神经细胞因子 认知

2024

中国药物与临床
中国医院协会

中国药物与临床

影响因子:0.846
ISSN:1671-2560
年,卷(期):2024.24(9)