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艾司西酞普兰联合多巴丝肼治疗帕金森病患者的临床研究

郭莞莹 林熙汶 李辙 赵楠 舒可

中国临床药理学杂志2025,Vol.41Issue(3):301-305,5.
中国临床药理学杂志2025,Vol.41Issue(3):301-305,5.DOI:10.13699/j.cnki.1001-6821.2025.03.001

艾司西酞普兰联合多巴丝肼治疗帕金森病患者的临床研究

Clinical trial of escitalopram combined with levodopa and benserazide hydrochloride in the treatment of patients with Parkinson's disease

郭莞莹 1林熙汶 2李辙 2赵楠 2舒可1

作者信息

  • 1. 昆明市第一人民医院神经内科,云南 昆明 650031
  • 2. 昆明市第一人民医院神经外科,云南 昆明 650031
  • 折叠

摘要

Abstract

Objective To observe the clinical efficacy and safety of escitalopram oxalate tablets combined with levodopa and benserazide hydrochloride tablets in the treatment of patients with Parkinson's disease.Methods The patients with Parkinson's disease were randomly divided into control group and treatment group.The control group received levodopa and benserazide hydrochloride tablets 125 mg per time,tid,orally.On the basis of control group,the treatment group received escitalopram oxalate tablets 10 mg per time,qd,orally.Two groups were treated for 3 months.The clinical efficacy,Montreal cognitive assessment(MoCA)scores,Hamilton depression rating scale(HAMD)scores,unified Parkinson's disease rating scale(UPDRS)scores,the levels of interleukin-6(IL-6),tumor necrosis factor-alpha(TNF-α)and nerve growth factor(NGF),and safety were compared between two groups.Results Treatment group was enrolled 116 cases,4 cases dropped out,and 112 cases were finally included in the statistical analysis.Control group was enrolled 116 cases,2 cases dropped out,and 114 cases were finally included in the statistical analysis.After treatment,the total effective rates of treatment and control group were 82.14%(92 cases/112 cases)and 65.79%(75 cases/114 cases),with significant difference(P<0.05).After treatment,the MoCA scores of treatment and control groups were(24.89±2.87)and(19.58±2.62)points,the HAMD scores were(10.45±1.06)and(15.84±1.49)points,the UPDRS scores were(40.06±5.28)and(47.78±5.52)points,the IL-6 levels were(4.12±0.63)and(6.71±1.13)mg·L-1,the TNF-α levels were(8.71±1.64)and(11.14±2.05)mg·L-1,the NGF levels were(41.56±5.20)and(30.47±4.14)ng·mL-1,respectively.The differences of above indexes were statistically significant between two groups(all P<0.05).The adverse drug reactions of treatment group were somnolence and nausea/vomiting,while those in control group were nausea/vomiting and constipation.The total incidences of adverse drug reactions in treatment and control groups were 15.18%and 12.28%,without statistically significant difference(P>0.05).Conclusion Escitalopram oxalate tablets combined with levodopa and benserazide hydrochloride tablets significantly improves clinical efficacy in the treatment of patients with Parkinson's disease,which can significantly ameliorate the inflammatory responses and neurotrophic factor levels,without increasing the incidence of adverse drug reactions.

关键词

草酸艾司西酞普兰片/多巴丝肼片/帕金森病/认知功能/神经营养因子/安全性评价

Key words

escitalopram oxalate tablet/levodopa and benserazide hydrochloride tablet/Parkinson's disease/cognitive function/neurotrophic factor/safety evaluation

分类

医药卫生

引用本文复制引用

郭莞莹,林熙汶,李辙,赵楠,舒可..艾司西酞普兰联合多巴丝肼治疗帕金森病患者的临床研究[J].中国临床药理学杂志,2025,41(3):301-305,5.

基金项目

云南省科技厅科技计划基金资助项目(202301AY070001-286) (202301AY070001-286)

中国临床药理学杂志

OA北大核心

1001-6821

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