河南中医药大学第一附属医院,河南省郑州市金水区人民路19号,450046
13838119371@163.com
收稿:2025-06-21,
修回:2025-08-15,
纸质出版:2025-11-17
移动端阅览
卫佳豪,张子玥,刘如歌等.健脾补肾益气方辅助治疗重症肌无力脾肾两虚证患者的随机对照试验[J].中医杂志,2025,66(22):2353-2359.
WEI Jiahao,ZHANG Ziyue,LIU Ruge,et al.Jianpi Bushen Yiqi Formula (健脾补肾益气方) as an Adjuvant Therapy in the Treatment of Myasthenia Gravis with Spleen-Kidney Deficiency Syndrome:A Randomized Controlled Trial[J].Journal of Traditional Chinese Medicine,2025,66(22):2353-2359.
卫佳豪,张子玥,刘如歌等.健脾补肾益气方辅助治疗重症肌无力脾肾两虚证患者的随机对照试验[J].中医杂志,2025,66(22):2353-2359. DOI: 10.13288/j.11-2166/r.2025.22.011.
WEI Jiahao,ZHANG Ziyue,LIU Ruge,et al.Jianpi Bushen Yiqi Formula (健脾补肾益气方) as an Adjuvant Therapy in the Treatment of Myasthenia Gravis with Spleen-Kidney Deficiency Syndrome:A Randomized Controlled Trial[J].Journal of Traditional Chinese Medicine,2025,66(22):2353-2359. DOI: 10.13288/j.11-2166/r.2025.22.011.
目的
2
观察健脾补肾益气方辅助治疗重症肌无力脾肾两虚证患者的临床疗效及安全性,并初步阐明其可能作用机制。
方法
2
将54例重症肌无力脾肾两虚证患者随机分为对照组28例、治疗组26例。两组均予溴吡斯的明片和醋酸泼尼松片口服,治疗组同时口服健脾补肾益气方,疗程均为12周。评估主要结局指标为定量重症肌无力评分量表(QMG)评分、中医证候积分和临床疗效;次要结局指标为重症肌无力日常活动评定量表(MG-ADL)评分、治疗后最小症状表达(MSE)情况、重症肌无力患者干预后状态(MGFA-PIS)分级情况、美国重症肌无力基金会(MGFA)分型情况、基础西药使用剂量情况以及血清抗乙酰胆碱受体抗体(AChR-Ab)水平;并进行安全性评价。
结果
2
治疗组脱落2例,对照组脱落4例,最终两组各纳入分析24例。治疗组临床总有效率87.50%(21/24)高于对照组的25.00%(6/24,
P
<0.01)。与本组治疗前比较,治疗后两组QMG评分、MG-ADL评分、血清AChR-Ab水平、溴吡斯的明及醋酸泼尼松使用剂量均降低,治疗组中医证候积分降低,MGFA分型中Ⅰ型增多,Ⅱ型、Ⅲ型、Ⅳ型减少(
P
<0.05)。治疗组治疗后QMG评分、中医证候积分、MG-ADL评分、溴吡斯的明及醋酸泼尼松使用剂量均低于对照组,
且上述各指标的治疗前后差值均高于对照组(
P
<0.05或
P
<0.01)。治疗组达到MSE的患者为18例(75.00%),对照组为11例(45.83%),两组比较差异具有统计学意义(
P
<0.05)。治疗组治疗后MGFA-PIS分级情况与对照组比较差异无统计学意义(
P
>0.05)。治疗组不良事件2例、对照组5例,均非严重不良事件。
结论
2
健脾补肾益气方可改善重症肌无力脾肾两虚证患者肌无力症状和中医证候,提升日常活动能力,促进向稳定状态转变并减少基础西药的使用剂量,其机制可能与降低血清AChR-Ab水平而调节免疫有关,且具有良好的安全性。
Objective
2
To investigate the efficacy and safety of
Jianpi Bushen Yiqi Formula
(健脾补肾益气方, JBYF) as an adjuvant treatment for myasthenia gravis(MG)patients with spleen-kidney deficiency syndrome and to preliminarily clarify its possible mechanism.
Methods
2
A total of 54 MG patients with spleen-kidney deficiency syndrome were randomly assigned to either control group (28 cases) or treatment group (26 cases). Both groups received oral pyridostigmine bromide and prednisone acetate tablets, while the treatment group additionally received JBYF. The treatment course for both groups was 12 weeks. Primary outcomes included Quantitative Myasthenia Gravis (QMG) score, traditional Chinese medicine (TCM) syndrome score, and overall clinical efficacy; secondary outcomes included Myasthenia Gravis Activities of Daily Living (MG-ADL) score, the rate of minimal symptom expression (MSE) after treatment, the Myasthenia Gravis Foundation of America Post-Intervention Status (MGFA-PIS) classification, MGFA clinical classification, baseline western medicine dosage, and serum anti-acetylcholine receptor antibody (AChR-Ab) levels. Safety evaluations were also performed.
Results
2
Two cases in the treatment group and four in the control group withdrew from the study, therefore, 24 cases in each group were included in the final analysis. The total clinical effective rate in the treatment group was 87.50% (21/24), significantly higher than 25.00% (6/24) in the control group (
P
<0.01). After tr
eatment, both groups showed significant reductions in QMG scores, MG-ADL scores, serum AChR-Ab level and the dosages of pyridostigmine bromide and prednisone acetate (
P
<0.05). In the treatment group, the TCM syndrome score also decreased, and MGFA classification showed an increase in class Ⅰ and a decrease in classes Ⅱ, Ⅲ, and Ⅳ (
P
<0.05). The treatment group demonstrated significantly lower QMG score, TCM syndrome score, MG-ADL score, and western medication dosages compared to the control group, with more changes from baseline (
P
<0.05 or
P
<0.01). The proportion of patients achieving MSE was 75.00% (18/24) in the treatment group, significantly higher 45.83% (11/24) in the control group (
P
<0.05). No significant difference was observed in MGFA-PIS classification between groups after treatment (
P
>0.05). There were 2 cases mild adverse events in the treatment group and 5 cases in the control group, none of which were serious.
Conclusion
2
JBYF can improve muscle weakness symptoms and TCM syndrome manifestations in MG patients with spleen-kidney deficiency, enhance daily living ability, promote transition to a stable disease state, and reduce the required doses of baseline western medications. Its mechanism may be related to the modulation of immune function by reducing serum AChR-Ab levels. The treatment demonstrates good safety and tolerability.
GILHUS NE , VERSCHUUREN JJ . Myasthenia gravis: subgroup classification and therapeutic strategies [J]. Lancet Neurol , 2015 , 14 ( 10 ): 1023 - 1036 .
中国免疫学会神经免疫分会 . 中国重症肌无力诊断和治疗指南(2020版) [J]. 中国神经免疫学和神经病学杂志 , 2021 , 28 ( 1 ): 1 - 12 .
JACKSON K , PARTHAN A , LAUHER-CHAREST M , et al . Understanding the symptom burden and impact of myasthenia gravis from the patient's perspective: a qualitative study [J]. Neurol Ther , 2023 , 12 ( 1 ): 107 - 128 .
张伯礼 , 吴勉华 . 中医内科学 [M]. 4版 . 北京 : 中国中医药出版社 , 2017 : 554 - 555 .
刘蔚 . 弃杖汤联合免疫球蛋白治疗重症肌无力疗效及作用机制分析 [J]. 中华中医药学刊 , 2018 , 36 ( 9 ): 2295 - 2297 .
黄春华 , 刘丽婷 , 饶旺福 . 中医药治疗重症肌无力系统评价/Meta分析的再评价 [J]. 中医杂志 , 2019 , 60 ( 15 ): 1294 - 1298,1335 .
杨俊红 , 樊飞燕 . 李发枝教授运用龟鹿二仙胶治疗神经内科疑难杂病经验 [J]. 中医研究 , 2020 , 33 ( 6 ): 31 - 34 .
JARETZKI A 3 RD, BAROHN RJ, ERNSTOFF RM, et al.Myasthenia gravis:recommendations for clinical research standa rds.Task Force of the Medical Scientific Advisory Board of the Myasthenia Gravis Foundation of America[J]. Ann Thorac Surg ,2000, 70 ( 1 ): 327 - 334 .
中华中医药学会 . 中医内科临床诊疗指南(第一册) [M]. 北京 : 中国中医药出版社 , 2020 : 5 - 19 .
NARAYANASWAMI P , SANDERS DB , WOLFE G , et al . International consensus guidance for managementof myasthenia gravis:2020 update [J]. Neurology , 2021 , 96 ( 3 ): 114 - 122 .
郑筱萸 . 中药新药临床研究指导原则(试行) [M]. 北京 : 中国医药科技出版社 , 2002 : 364 - 387 .
王秀云 , 许贤豪 , 孙宏 , 等 . 重症肌无力病人的临床绝对评分法和相对评分法 [J]. 中华神经科杂志 , 1997 , 30 ( 2 ): 87 - 90 .
DEWILDE S , QI CZ , PHILLIPS G , et al . Association between myasthenia gravis-activities of daily living (MG-ADL) and EQ-5D-5L utility values: the additional effect of efgartigimod on utilities [J]. Adv Ther , 2023 , 40 ( 4 ): 1818 - 1829 .
RUZHANSKY K , LI Y , WOLFE GI , et al . Standardization of myasthenia gravis outcome measures in clinical practice: a report of the MGFA task force [J]. Muscle Nerve , 2025 , 72 ( 1 ): 56 - 65 .
王家慧 , 刘如歌 , 刘韩彬 , 等 . 基于Agrin/LRP4/MuSK信号通路探讨健脾补肾益气方促进AChR聚集改善EAMG小鼠神经-肌肉接头功能的机制研究 [J]. 中国中药杂志 , 2025 , 50 ( 15 ): 4325 - 4332 .
SABATINO JJ JR , PRÖBSTEL AK , ZAMVIL SS . B cells in autoimmune and neurodegenerative central nervous system diseases [J]. Nat Rev Neurosci , 2019 , 20 ( 12 ): 728 - 745 .
THIRUPPATHI M , ROWIN J , GANESH B , et al . Impaired regulatory function in circulating CD4(+)CD25(high)CD127(low/-) T cells in patients with myasthenia gravis [J]. Clin Immunol , 2012 , 145 ( 3 ): 209 - 223 .
CAVALCANTE P , MANTEGAZZA R , ANTOZZI C . Targeting autoimmune mechanisms by precision medicine in myasthenia gravis [J]. Front Immunol , 2024 , 15 : 1404191 . doi: 10.3389/fimmu.2024.1404191 http://dx.doi.org/10.3389/fimmu.2024.1404191 .
0
浏览量
0
下载量
0
CSCD
关联资源
相关文章
相关作者
相关机构
京公网安备11010102007558号