首页|血府逐瘀口服液对狼疮性肾炎患者疗效和安全性评估及血清胸腺肽β4的影响

血府逐瘀口服液对狼疮性肾炎患者疗效和安全性评估及血清胸腺肽β4的影响

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目的 探究血府逐瘀口服液(XZOL)对狼疮性肾炎(LN)患者临床疗效和安全性及血清胸腺肽β4 的影响.方法 纳入 2021 年 10 月至 2022 年 10 月河北北方学院附属第二医院诊治的患者为研究对象.采用随机数字表法,将LN患者分为对照组[泼尼松(PDN)+环磷酰胺(CTX)]和血府逐瘀组(XZOL联合PDN+CTX),连续治疗 6个月.比较两组治疗有效率、系统性红斑狼疮疾病活动指数(SLEDAI)评分、免疫指标[抗双链DNA抗体(dsDNA)、血清免疫球蛋白(Ig)G和血清补体C3 水平]、肾功能指标[血肌酐(Scr)、白蛋白(ALB)、红细胞沉降率(ESR)、谷丙转氨酶(ALT)、24 h尿蛋白和C-反应蛋白(CRP)水平]、血清胸腺肽β4 水平和不良反应发生率.结果 研究共纳入 60 例LN患者,每组各 30 例.血府逐瘀组治疗总有效率明显高于对照组(P<0.05).治疗前,两组SLEDAI评分、血清胸腺肽β4、IgG、C3、抗dsDNA抗体、血清Scr、ALB、ALT、24 h尿蛋白和CRP水平差异无统计学意义(P>0.05).治疗 6个月后,两组患者SLEDAI评分、血清IgG、抗dsDNA抗体、血清Scr、ALT、24 h尿蛋白和CRP水平均较治疗前显著下降(P<0.05);而血清胸腺肽β4 水平、血清C3 水平和血清ALB水平显著上升(P<0.05).且血府逐瘀组SSLEDAI评分、血清IgG、抗dsDNA抗体、血清Scr、ALT、24 h尿蛋白和CRP水平低于对照组(P<0.05);血清胸腺肽β4、C3 和ALB水平高于对照组(P<0.05).此外,两组不良反应发生率差异无统计学分析(P>0.05).结论 XZOL治疗LN临床效果显著,未见明显不良反应,值得在临床推广使用.
Evaluation of the efficacy and safety of Xuefu Zhuyu oral liquid on patients with lupus nephritis and the effect of serum thymosin β4
Objective To investigate the clinical efficacy and safety of Xuefu Zhuyu oral liquid(XZOL)on patients with lupus nephritis(LN)and the effect of serum thymosin β4.Methods Patients treated in the Second Hospital Affiliated to Hebei North College from October 2021 to October 2022 were included in the study.Using the random number method,the LN patients were divided into the control group[prednisone(PDN)+cyclophosphamide(CTX)]and the blood-focused group(XZOL combined with PDN+CTX),and were treated continuously for 6 months.The two groups were compared in terms of treatment efficiency,systemic lupus erythematosus disease activity index(SLEDAI)score,immune indexes[anti-double-stranded DNA(dsDNA)antibody,serum immunoglobulin(Ig)G and serum complement C3 levels]and renal function indexes(Scr,ALB,ESR,ALT,24h urine protein and CRP levels),serum thymidine β4 levels and safety(incidence of adverse reactions).Results A total of 60 LN patients were included in the study,30 in each group.The total effective rate of treatment in the Xuefu Zhuyu group was significantly higher than that in the control group(P<0.05).Before treatment,there was no statistically significant difference in SLEDAI score,serum thymidine β4,IgG,C3,anti-dsDNA antibody,serum Scr,ALB,ALT,24 h urine protein and CRP levels between the two groups(P>0.05).After 6 months of treatment,SLEDAI score,serum IgG,anti-dsDNA antibody,serum Scr,ALT,24 h urine protein and CRP levels of patients in both groups decreased significantly compared with those before treatment(P<0.05),while serum thymosin β4 level,serum C3 level and serum ALB level increased significantly(P<0.05);the SSLEDAI score,serum IgG,anti-dsDNA antibody,serum Scr,ALT,24 h urine protein and CRP levels were lower in the Xuefu Zhuyu group than in the control group(P<0.05),and serum thymosin β4,C3 and ALB levels were higher than in the control group(P<0.05).In addition,there was no difference in the incidence of adverse reactions between the two groups(P>0.05).Conclusion XZOL is clinically effective in the treatment of LN,with fewer adverse reactions,and is worth promoting its use in the clinic.

Xuefu Zhuyu oral liquidLupus nephritisClinical efficacySafetythymosin β4

徐娜、韩梅、封锦慧、孙垚、任占芬、杨悦

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河北北方学院附属第二医院药剂科(河北张家口 075100)

河北北方学院附属第二医院手术室(河北张家口 075100)

河北北方学院附属第一医院风湿免疫科(河北张家口 075100)

血府逐瘀口服液 狼疮性肾炎 临床疗效 安全性 胸腺肽β4

张家口市重点研发计划

2121133D

2024

中国药师
国家药品监督管理局高级研修学院,武汉医药(集团)股份有限公司

中国药师

CSTPCD
影响因子:0.944
ISSN:1008-049X
年,卷(期):2024.27(3)
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