Efficacy and Safety of Sitagliptin for the Treatment of Nonalcoholic Fatty Liver Disease with Type 2 Diabetes Mellitus

被引:59
作者
Fukuhara, Takayuki [1 ]
Hyogo, Hideyuki [1 ]
Ochi, Hidenori [1 ]
Fujino, Hatsue [1 ]
Kan, Hiromi [1 ]
Naeshiro, Noriaki [1 ]
Honda, Yohji [1 ]
Miyaki, Daisuke [1 ]
Kawaoka, Tomokazu [1 ]
Tsuge, Masataka [1 ]
Hiramatsu, Akira [1 ]
Imamura, Michio [1 ]
Kawakami, Yoshiiku [1 ]
Aikata, Hiroshi [1 ]
Chayama, Kazuaki [1 ]
机构
[1] Hiroshima Univ, Dept Gastroenterol & Metab, Hiroshima, Japan
关键词
Nonalcoholic fatty liver disease; sitagliptin; type 2 diabetes mellitus; PEPTIDASE-4 INHIBITOR SITAGLIPTIN; INSULIN-RESISTANCE; NATURAL-HISTORY; SCORING SYSTEM; STEATOHEPATITIS; MONOTHERAPY; PREVALENCE; VALIDATION; PREDICTOR;
D O I
10.5754/hge13832
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background/Aims: Dipeptidyl peptidase-4 inhibitor is useful for the treatment of type 2 diabetes mellitus (DM). However, effects on liver function and glucose metabolism in nonalcoholic fatty liver disease (NAFLD) have not been established. The objective of this study was to evaluate the efficacy and safety of sitagliptin in NAFLD patients with type 2 DM. Methodology: Forty-four patients with biopsy-proven NAFLD with type 2 DM were evaluated. Patients were administered sitagliptin (50 mg/day) for 12 months. Results: Hemoglobin A1c (HbA1c) decreased by 0.7% after treatment (P <0.001). While HbA1c levels decreased by 0.4% in the low HbA1c (<7.5%) group, those decreased by 1.2% in the high HbA1c (>= 7.5%) group. Liver transaminases did not change significantly during the treatment. Improvement of HbA1c (Delta HbA1c) and that of aspartate aminotransferase (Delta AST), alanine aminotransferase (Delta ALT) was positively correlated (r = 0.425, and 0.455, respectively), especially in the high HbA1c (>= 7.5%) group before treatment (r = 0.568, and 0.501, respectively). Conclusions: Sitagliptin for the treatment of NAFLD with type2 DM was safe and showed similar antidiabetic effects as reported for type 2 DM, suggesting that tight glycemic control would contribute to the improvement of NAFLD based from the findings of correlation between the changes of HbA1c and transaminases.
引用
收藏
页码:323 / 328
页数:6
相关论文
共 42 条
[1]   The natural history of nonalcoholic fatty liver disease: A population-based cohort study [J].
Adams, LA ;
Lymp, JF ;
St Sauver, J ;
Sanderson, SO ;
Lindor, KD ;
Feldstein, A ;
Angulo, P .
GASTROENTEROLOGY, 2005, 129 (01) :113-121
[2]   How common is non-alcoholic fatty liver disease in the Asia-Pacific region and are there local differences? [J].
Amarapurkar, Deepak N. ;
Hashimoto, Estsuko ;
Lesmana, Laurentius A. ;
Sollano, Jose D. ;
Chen, Pei-Jer ;
Goh, Khean-Lee .
JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, 2007, 22 (06) :788-793
[4]   Nonalcoholic fatty liver disease [J].
Brunt, Elizabeth M. ;
Wong, Vincent W. -S. ;
Nobili, Valerio ;
Day, Christopher P. ;
Sookoian, Silvia ;
Maher, Jacquelyn J. ;
Bugianesi, Elisabetta ;
Sirlin, Claude B. ;
Neuschwander-Tetri, BrentA. ;
Rinella, Mary E. .
NATURE REVIEWS DISEASE PRIMERS, 2015, 1
[5]   Efficacy and safety in sitagliptin therapy for diabetes complicated by non-alcoholic fatty liver disease [J].
Arase, Yasuji ;
Kawamura, Yusuke ;
Seko, Yuya ;
Kobayashi, Mariko ;
Suzuki, Fumitaka ;
Suzuki, Yoshiyuki ;
Akuta, Norio ;
Kobayashi, Masahiro ;
Sezaki, Hitomi ;
Saito, Satoshi ;
Hosaka, Tetsuya ;
Ikeda, Kenji ;
Kumada, Hiromitsu ;
Ohmoto-Sekine, Yuki ;
Hsieh, Shiun Dong ;
Amakawa, Kazuhisa ;
Ogawa, Kyoko ;
Matsumoto, Naoki ;
Iwao, Akiko ;
Tsuji, Hiroshi ;
Hara, Shigeko ;
Mori, Yasumichi ;
Okubo, Minoru ;
Sone, Hirohito ;
Kobayashi, Tetsuro .
HEPATOLOGY RESEARCH, 2013, 43 (11) :1163-1168
[6]   Effect of the dipeptidyl peptidase-4 inhibitor sitagliptin as monotherapy on glycemic control in patients with type 2 diabetes [J].
Aschner, Pablo ;
Kipnes, Mark S. ;
Lunceford, Jared K. ;
Sanchez, Matilde ;
Mickel, Carolyn ;
Williams-Herman, Debora E. .
DIABETES CARE, 2006, 29 (12) :2632-2637
[7]   Cardiovascular pleiotropic actions of DPP-4 inhibitors: A step at the cutting edge in understanding their additional therapeutic potentials [J].
Balakumar, Pitchai ;
Dhanaraj, Sokkalingam A. .
CELLULAR SIGNALLING, 2013, 25 (09) :1799-1803
[8]  
Brunt EM, 1999, AM J GASTROENTEROL, V94, P2467, DOI 10.1111/j.1572-0241.1999.01377.x
[9]   NASH and insulin resistance: Insulin hypersecretion and specific association with the insulin resistance syndrome [J].
Chitturi, S ;
Abeygunasekera, S ;
Farrell, GC ;
Holmes-Walker, J ;
Hui, JM ;
Fung, C ;
Karim, R ;
Lin, R ;
Samarasinghe, D ;
Liddle, C ;
Weltman, M ;
George, J .
HEPATOLOGY, 2002, 35 (02) :373-379
[10]   Long term prognosis of fatty liver: risk of chronic liver disease and death [J].
Dam-Larsen, S ;
Franzmann, M ;
Andersen, IB ;
Christoffersen, P ;
Jensen, LB ;
Sorensen, TIA ;
Becker, U ;
Bendtsen, F .
GUT, 2004, 53 (05) :750-755