Ginger for Prevention of Antituberculosis-induced Gastrointestinal Adverse Reactions Including Hepatotoxicity: A Randomized Pilot Clinical Trial

被引:12
作者
Emrani, Zahra [1 ]
Shojaei, Esphandiar [2 ]
Khalili, Hossein [1 ]
机构
[1] Univ Tehran Med Sci, Dept Clin Pharm, Fac Pharm, Enghelab Ave, Tehran, Iran
[2] Univ Tehran Med Sci, Dept Infect Dis, Fac Med, Tehran, Iran
关键词
ginger; antituberculosis; gastrointestinal adverse reactions; hepatotoxicity; DRUG-INDUCED HEPATOTOXICITY; RIFAMPICIN-INDUCED HEPATOTOXICITY; ZINGIBER-OFFICINALE; INDUCED NAUSEA; LIVER-INJURY; SUBSTANCE-P; TUBERCULOSIS; RATS; EXPRESSION; THERAPY;
D O I
10.1002/ptr.5607
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
In this study, the potential benefits of ginger in preventing antituberculosis drug-induced gastrointestinal adverse reactions including hepatotoxicity have been evaluated in patients with tuberculosis. Patients in the ginger and placebo groups (30 patients in each group) received either 500mg ginger (Zintoma)((R)) or placebo one-half hour before each daily dose of antituberculosis drugs for 4weeks. Patients' gastrointestinal complaints (nausea, vomiting, dyspepsia, and abdominal pain) and antituberculosis drug-induced hepatotoxicity were recorded during the study period. In this cohort, nausea was the most common antituberculosis drug-induced gastrointestinal adverse reactions. Forty eight (80%) patients experienced nausea. Nausea was more common in the placebo than the ginger group [27 (90%) vs 21 (70%), respectively, p=0.05]. During the study period, 16 (26.7%) patients experienced antituberculosis drug-induced hepatotoxicity. Patients in the ginger group experienced less, but not statistically significant, antituberculosis drug-induced hepatotoxicity than the placebo group (16.7% vs 36.7%, respectively, p=0.07). In conclusion, ginger may be a potential option for prevention of antituberculosis drug-induced gastrointestinal adverse reactions including hepatotoxicity. Copyright (c) 2016 John Wiley & Sons, Ltd.
引用
收藏
页码:1003 / 1009
页数:7
相关论文
共 39 条
[11]   Effect of vitamin C on oxidative liver injury due to isoniazid in rats [J].
Ergul, Yakup ;
Erkan, Tulay ;
Uzun, Hafize ;
Genc, Habibe ;
Altug, Tuncay ;
Erginoz, Ethem .
PEDIATRICS INTERNATIONAL, 2010, 52 (01) :69-74
[12]  
Farazi A, 2014, TUBERC RES TREAT, V2014
[13]   Carnitine for prevention of antituberculosis drug- induced hepatotoxicity: A randomized, clinical trial [J].
Hatamkhani, Shima ;
Khalili, Hossein ;
Karimzadeh, Iman ;
Dashti-Khavidaki, Simin ;
Abdollahi, Alireza ;
Jafari, Sirous .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2014, 29 (05) :997-1004
[14]  
Khalili H, 2008, DARU, V16, P47
[15]  
Khalili H, 2009, DARU, V17, P163
[16]  
Langner E, 1998, ADV THER, V15, P25
[17]   Drugs and herbs given to prevent hepatotoxicity of tuberculosis therapy: systematic review of ingredients and evaluation studies [J].
Liu, Qin ;
Garner, Paul ;
Wang, Yang ;
Huang, Binghua ;
Smith, Helen .
BMC PUBLIC HEALTH, 2008, 8 (1)
[18]  
Mahesh R, 2005, PHARMAZIE, V60, P83
[19]   Zingiber officinale acts as a nutraceutical agent against liver fibrosis [J].
Motawi, Tarek K. ;
Hamed, Manal A. ;
Shabana, Manal H. ;
Hashem, Reem M. ;
Naser, Asmaa F. Aboul .
NUTRITION & METABOLISM, 2011, 8
[20]   A METHOD FOR ESTIMATING THE PROBABILITY OF ADVERSE DRUG-REACTIONS [J].
NARANJO, CA ;
BUSTO, U ;
SELLERS, EM ;
SANDOR, P ;
RUIZ, I ;
ROBERTS, EA ;
JANECEK, E ;
DOMECQ, C ;
GREENBLATT, DJ .
CLINICAL PHARMACOLOGY & THERAPEUTICS, 1981, 30 (02) :239-245