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益髓生血颗粒治疗156例重型β地中海贫血的临床观察及分子机制研究

Clinical observation on YiSuiShengXueGranule on treating 156 patients with beta-thalassemia major and the molecular mechanism study.

作者信息

Fang Suping, Wu Zhikui, Zhang Xinhua, Liu Yongmei, Wang Wenjuan, Chai Limin, Cai Huiguo, Yi Jie, Wang Lei, Chen Yuying, Lv Xinxia, Huang Youwen, Wang Rongxin, Chen Peizhen

机构信息

Department of Molecular-Biology, Guang'AnMen Hospital, China Academy of Traditional Chinese Medicine, Beijing, P.R. China.

出版信息

Biol Pharm Bull. 2007 Nov;30(11):2084-7. doi: 10.1248/bpb.30.2084.

Abstract

OBJECTIVE

To investigate the clinical effects and security of YiSuiShengXueGranule (YSSXG) on treating 156 patients with beta-thalassemia major.

METHODS

YSSXG was given orally to 156 patients with beta-thalassemia in GuangXi Autonomous Region (the high incidence area of beta-thalassemia in China) for 3 months as one therapeutic course, 3 times a day, 10 g each time (for children, the dose should be reduced properly according to their body weight and age), and no blood transfusion used during the course. Clinical symptoms and levels of hemoglobin (Hb), red blood cell (RBC), reticulocyte (Ret) and hemoglobin F (HbF) were observed before and after treatment, and side-effects were observed during the course. A 3-6 months follow up study was performed after withdrawal of YSSXG. And systemic gene analysis was conducted with PCR, SSCP-PCR, RT-PCR and DNA sequences analysis and mRNA differently expression technique, in order to study the molecular mechanism from the relationships between genetic mutation and clinical efficacy, gene expression and its regulation.

RESULTS

Levels of Hb, RBC, Ret and HbF obviously elevated, and clinical symptoms markedly ameliorated in patients after treated with YSSXG from the 1st to 3rd month (all p<0.01). Dynamical observation showed that the improvement of symptoms kept accordance with the elevation of hemorrheological indexes. The treatment was effective in 145 patients and ineffective in 11, and the total effective rate was 92.9%, without any adverse reaction founded. Follow-up studies showed the therapeutic effect could sustain for 3 to 4 months after drug-withdrawal. The molecular mechanism study showed: YSSXG did not change the genetic mutation type, but could obviously increase gamma/(beta+gamma) globin ratio, both gamma-globin mRNA and GM-CSF mRNA expression were significantly enhanced so as to induce HbF synthesis increasing after treated with YSSXG.

CONCLUSION

YSSXG had obvious effects in treating beta-thalassemia by unlocking gamma-gene, increasing the gamma-globin expression and enhancing HbF synthesis so as to compensate for the gene defect. This study has provided a new path for the treatment of beta-thalassemia with Traditional Chinese Medicine.

摘要

目的

探讨益髓生血颗粒(YSSXG)治疗156例重型β地中海贫血患者的临床疗效及安全性。

方法

对广西壮族自治区(中国β地中海贫血高发区)的156例β地中海贫血患者口服YSSXG,3个月为1个疗程,每日3次,每次10 g(儿童根据体重和年龄适当减量),疗程中不输血。观察治疗前后的临床症状及血红蛋白(Hb)、红细胞(RBC)、网织红细胞(Ret)和血红蛋白F(HbF)水平,并观察疗程中的不良反应。停药后进行3 - 6个月的随访研究。采用聚合酶链反应(PCR)、单链构象多态性 - 聚合酶链反应(SSCP - PCR)、逆转录 - 聚合酶链反应(RT - PCR)和DNA序列分析以及mRNA差异表达技术进行系统基因分析,从基因突变与临床疗效、基因表达及其调控的关系研究分子机制。

结果

YSSXG治疗后1至3个月患者的Hb、RBC、Ret和HbF水平明显升高,临床症状明显改善(均p < 0.01)。动态观察表明症状改善与血液流变学指标升高一致。治疗有效145例,无效11例,总有效率为92.9%,未发现任何不良反应。随访研究表明停药后治疗效果可维持3至4个月。分子机制研究表明:YSSXG未改变基因突变类型,但可明显提高γ/(β + γ)珠蛋白比值,γ珠蛋白mRNA和粒细胞 - 巨噬细胞集落刺激因子(GM - CSF)mRNA表达均显著增强,从而使YSSXG治疗后HbF合成增加。

结论

YSSXG通过开启γ基因、增加γ珠蛋白表达和增强HbF合成以弥补基因缺陷,对治疗β地中海贫血有明显效果。本研究为中医药治疗β地中海贫血提供了新途径。

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