@article {Leejrheum.180761, author = {Jung Sun Lee and Jebum Won and Oh Chan Kwon and Seung Soo Lee and Ji Seon Oh and Yong-Gil Kim and Chang-Keun Lee and Bin Yoo and Seokchan Hong}, title = {Hepatic Safety of Febuxostat Compared with Allopurinol in Gout Patients with Fatty Liver Disease}, elocation-id = {jrheum.180761}, year = {2018}, doi = {10.3899/jrheum.180761}, publisher = {The Journal of Rheumatology}, abstract = {Objective Febuxostat has superior renal safety to allopurinol, but data on its hepatic safety are limited. Thus we compared the hepatotoxicity of febuxostat and allopurinol, and the clinical factors associated with hepatotoxicity, in patients with gout and fatty liver disease (FLD). Methods We included gout patients treated with allopurinol or febuxostat who were diagnosed with fatty liver based on ultrasonography or computed tomography. Hepatotoxicity was defined as follows: (1) elevation of aspartate aminotransferase (AST)/alanine aminotransferase (ALT) at least 3{\texttimes} the upper limit of normal, when the baseline AST/ALT was normal; or (2) doubling of the baseline AST/ALT, when the baseline AST/ALT was elevated. The factors associated with hepatotoxicity were evaluated by Cox regression analysis. Results Of 134 patients identified with gout and FLD, 32 (23.9\%) received febuxostat and 102 (76.1\%) received allopurinol. There were no significant differences in age, body mass index, comorbidity, or disease severity between the groups; however, the incidence of hepatotoxicity was significantly lower in the febuxostat group (3/32, 9.4\%) than in the allopurinol group (36/102, 35.3\%, p = 0.005). Diabetes (HR 3.549, 95\% CI 1.374{\textendash}9.165, p = 0.009) and colchicine use (HR 11.518, 95\% CI 5.515{\textendash}24.054, p \< 0.001) were associated with a higher risk of hepatotoxicity, whereas febuxostat use was associated with a lower risk of hepatotoxicity (HR 0.282, 95\% CI 0.086{\textendash}0.926, p = 0.037). Conclusion In the 32 patients studied, febuxostat was well tolerated in patients with gout and FLD. However, the presence of diabetes and colchicine use may increase the risk of hepatotoxicity.}, issn = {0315-162X}, URL = {https://www.jrheum.org/content/early/2018/11/12/jrheum.180761}, eprint = {https://www.jrheum.org/content/early/2018/11/12/jrheum.180761.full.pdf}, journal = {The Journal of Rheumatology} }