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Volume 90, Issue 1, Pages 39-43 (January 2010)


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GSTT1 and GSTM1 null mutations and adverse reactions induced by antituberculosis drugs in Koreans

Sang-Heon Kimaemail address, Sang-Hoon Kimbemail address, Ho Joo Yoonaemail address, Dong Ho Shinaemail address, Sung Soo Parkaemail address, Youn-Seup Kimcemail address, Jae-Seuk Parkcemail address, Young Koo JeecCorresponding Author Informationemail address

Received 24 August 2009; received in revised form 27 November 2009; accepted 9 December 2009. published online 28 December 2009.

Summary 

Adverse reactions induced by antituberculosis drugs (ATD) often result in serious morbidities, impeding scheduled treatment and cure. In the development of ATD-induced adverse reactions, glutathione S-transferase has been suggested to play a protective role as an intracellular scavenger by conjugating toxic reactive metabolites of ATD. This study examined the association of null mutations in GST enzyme genes (GSTT1 and GSTM1) with the development of ATD-induced hepatitis and cutaneous reactions. We compared the frequencies of GSTT1 and GSTM1 null mutations in 57 patients with hepatitis, 94 patients with cutaneous adverse reactions, and 190 ATD-tolerant controls. The frequency of null mutations in GSTT1 and GSTM1 in patients with ATD-induced hepatitis was not significantly different from that of controls (59.6% vs. 54.2% and 45.6% vs. 54.7%, respectively). Additionally, no significant difference was observed in the frequency of either null mutation in patients with ATD-induced cutaneous reactions, including maculopapular eruption, compared with controls (58.5% vs. 54.1% for GSTT1 and 59.6% vs. 54.6% for GSTM1). These findings indicate that GSTT1 and GSTM1 null mutations are not associated with the development of ATD-induced hepatitis or cutaneous reactions in this Korean population, and suggest that glutathione S-transferase enzymes do not play important roles in the pathogenesis of these conditions.

a Department of Internal Medicine, Hanyang University College of Medicine, Haengdang-dong 17, Seongdong-gu, Seoul 133-792, Korea

b Department of Internal Medicine, Eulji University College of Medicine, Hagye-dong 280-1, Nowon-gu, Seoul 139-872, Korea

c Department of Internal Medicine, Dankook University College of Medicine, Anseo-dong San 16-5, Cheonan 330-715, Korea

Corresponding Author InformationCorresponding author. Tel.: +82 41 550 3923; fax: +82 41 556 3256.

PII: S1472-9792(09)00120-6

doi:10.1016/j.tube.2009.12.001


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