机构地区:[1]联勤保障部队第九八〇医院中医科,石家庄050000 [2]联勤保障部队第九八〇医院疾病预防控制科,石家庄050000 [3]河北以岭医院风湿病二科,石家庄050000 [4]正定二五六医院中医科,石家庄050800
出 处:《中国药物应用与监测》2025年第1期51-55,共5页Chinese Journal of Drug Application and Monitoring
基 金:河北省中医药管理局科研计划项目(2021213)。
摘 要:目的探究雷公藤周期用药治疗育龄期女性类风湿性关节炎(RA)的效果、机制及安全性。方法将2021年1月至2023年10月联勤保障部队第九八〇医院中医科门诊治疗的200例育龄期女性RA患者,以随机数字表法分为4组,各50例。连续组雷公藤持续用药,1月组雷公藤间隔1月周期用药,2月组雷公藤间隔2月周期用药,3月组雷公藤间隔3月周期用药,各组育龄期女性RA患者疗程均为12个月。比较各组育龄期女性RA患者疗效、28个关节疾病活动度(DAS28)评分、血管生成因子[血管内皮生长因子(VEGF)mRNA、血管生成素2(Ang-2)]、生殖毒性及其他不良反应。结果3月组美国风湿病学会(ACR)RA治疗缓解指标ACR20、ACR50、ACR70分别为70.00%(35/50)、34.00%(17/50)、4.00%(2/50),低于1月组的84.00%(42/50)、56.00%(28/50)、24.00%(12/50)和2月组的80.00%(40/50)、52.00%(26/50)、20.00%(10/50)(χ^(2)=10.027、8.724、13.000,均P<0.05),1月组、2月组与连续组比较差异无统计学意义(均P>0.05)。3月组3、6、9、12个月后DAS28评分[分别为(6.42±2.13)分,(5.04±1.59)分,(4.40±1.31)分、(3.84±1.220)分],高于1月组[分别为(5.28±1.75)分,(3.75±1.20)分,(2.17±0.70)分、(1.88±0.61)分]、2月组[分别为(5.41±1.80)分、(3.81±1.18)分、(2.22±0.73)分、(1.97±0.58)分](均P<0.05),1月组、2月组与连续组比较差异无统计学意义(均P>0.05)。3月组3、6、9、12个月后VEGF mRNA[分别为(800.94±101.85)、(714.52±84.66)、(620.51±97.82)、(573.30±111.26)]和Ang-2[分别为(0.40±0.11)ng·mL^(-1)、(0.35±0.10)ng·mL^(-1)、(0.30±0.09)ng·mL^(-1)、(0.28±0.06)ng·mL^(-1)]高于1月组VEGF mRNA[分别为(614.86±98.57)、(528.49±108.64)、(470.35±112.61)、(414.28±90.78)]和Ang-2[分别为(0.33±0.11)ng·mL^(-1)、(0.28±0.09)ng·mL^(-1)、(0.21±0.07)ng·mL^(-1)、(0.17±0.05)ng·mL^(-1)],亦高于2月组VEGF mRNA[分别为(621.35±113.04)、(537.11±85.59)、(482.67±109.34)、(419.56±93.45)]和Ang-2[(0.34±0.12)ng·mL^(-1)、(0.2Objective To explore the efficacy,mechanism,and safety of cyclical treatment with tripterygium wilfordii(TW)for rheumatoid arthritis(RA)in women of childbearing age.Methods A total of 200 female RA patients of childbearing age treated in 980th Hospital of Joint Logistics Support Force from January 2021 to October 2023 were divided into four groups using a random number table method,with 50 in each group.TW was administered continuously in the continuous group.Meanwhile,TW was given at 1-month intervals in the 1-month group,at 2-month intervals in the 2-month group and at 3-month intervals in the 3-month group.The duration of treatment was 12 months in all the four groups.The efficacy,disease activity score indicated by 28 joint counts(DAS28)score,changes in angiogenic factors(vascular endothelial growth fac tor(VEGF)mRNA,angiopoietin-2(Ang-2)),reproductive toxicity and other adverse reactions were compared among the four groups.Results The ACR20,ACR50 and ACR70 in the 3-month group were 70.00%(35/50),34.00%(17/50)and 4.00%(2/50),respectively,which were lower than those in the 1-month group(84.00%(42/50),56.00%(28/50)and 24.00%(12/50))and the 2-month group(80.00%(40/50),52.00%(26/50)and 20.00%(10/50))(χ^(2)=10.027,8.724,13.000,P<0.05).There was no significant difference between the 1-month group and the continuous group as well as between the 2-month group and the continuous group(P>0.05).The DAS28 scores after 3,6,9,and 12 months in the 3-month group were(6.42±2.13)points,(5.04±1.59)points,(4.40±1.31)points and(3.84±1.220)points,respectively,which were higher than those in the 1-month group((5.28±1.75) points,(3.75±1.20)points,(2.17±0.70)points and(1.88±0.61)points)and the 2-month group((5.41±1.80)points,(3.81±1.18)points,(2.22±0.73)points and(1.97±0.58)points)(P<0.05).There was no significant difference between the 1-month group and the continuous group as well as between the 2-month group and the continuous group(P>0.05).After 3,6,9,and 12 months of treatment,the VEGF mRNA was(800.94±101.85),(714.
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