中国基层医药
中國基層醫藥
중국기층의약
CHINESE JOURNAL OF PRIMARY MEDICINE AND PHARMACY
2009年
3期
445-446
,共2页
李明生%刘雅%郑晓璐%李济福%史利亚%曹双印%卢明友
李明生%劉雅%鄭曉璐%李濟福%史利亞%曹雙印%盧明友
리명생%류아%정효로%리제복%사리아%조쌍인%로명우
咳嗽变异性哮喘%西替利嗪%白细胞介素13%白细胞介素18
咳嗽變異性哮喘%西替利嗪%白細胞介素13%白細胞介素18
해수변이성효천%서체리진%백세포개소13%백세포개소18
Cough variant asthma%Levocitirize dihydrochloride%Interleukin-13%Interleukin-18
目的 探讨左旋西替利嗪对咳嗽变异性哮喘患者血清白细胞介素13(IL-13.)与白细胞介素18(IL-18)的影响.方法 70例咳嗽变异性哮喘患者随机分为35例用左旋西替利嗪治疗的治疗组,35例用氯苯那敏治疗的对照组.检测治疗前后IL-13与IL-18的变化.结果 治疗组治疗后患者的咳嗽评分有明显改善.治疗组治疗后IL-13与IL-18分别为(46.7±17.3)ng/L和(145.2±27.1)ng/L,对照组分别为(98.5±30.7)ng/L和(179.6±30.5)ng/L,两组比较差异有统计学意义(P<0.01).结论 左旋西替利嗪可能通过改善IL-13与IL-18而改善咳嗽变异性哮喘患者的病情.
目的 探討左鏇西替利嗪對咳嗽變異性哮喘患者血清白細胞介素13(IL-13.)與白細胞介素18(IL-18)的影響.方法 70例咳嗽變異性哮喘患者隨機分為35例用左鏇西替利嗪治療的治療組,35例用氯苯那敏治療的對照組.檢測治療前後IL-13與IL-18的變化.結果 治療組治療後患者的咳嗽評分有明顯改善.治療組治療後IL-13與IL-18分彆為(46.7±17.3)ng/L和(145.2±27.1)ng/L,對照組分彆為(98.5±30.7)ng/L和(179.6±30.5)ng/L,兩組比較差異有統計學意義(P<0.01).結論 左鏇西替利嗪可能通過改善IL-13與IL-18而改善咳嗽變異性哮喘患者的病情.
목적 탐토좌선서체리진대해수변이성효천환자혈청백세포개소13(IL-13.)여백세포개소18(IL-18)적영향.방법 70례해수변이성효천환자수궤분위35례용좌선서체리진치료적치료조,35례용록분나민치료적대조조.검측치료전후IL-13여IL-18적변화.결과 치료조치료후환자적해수평분유명현개선.치료조치료후IL-13여IL-18분별위(46.7±17.3)ng/L화(145.2±27.1)ng/L,대조조분별위(98.5±30.7)ng/L화(179.6±30.5)ng/L,량조비교차이유통계학의의(P<0.01).결론 좌선서체리진가능통과개선IL-13여IL-18이개선해수변이성효천환자적병정.
Objective To explore the effects of Levoeitirize dihydrochloride on interleukin-13(IL-13)and interleukin-18(IL-18)in the serum of the patients with cough variant asthma(CVA).Methods 70 cases with CVA were randomly devided into control group of 35 cases and treatment group of 35 cases.Control group was given Chlort rimeton and the treatment group was given Levocitirize dihydroehloride.The levels of IL-13 and IL-18 in the serum were measured before and after treatment.Results After treatment,the concentrations of IL-13 and IL-18 in patients in the treatment group were(46.7±17.3)ng/L and(145.2±27.1)ng/L,and those in the control group were(98.5±30.7)ng/L and(179.6±30.5)ne/L,which were significantly improved.Conclusion The treatmem of Levoeitirize dihydrochloride could improve the CVA through improving the production of IL-13 and IL-18.