Effect of dipeptidyl peptidase-4 inhibitors on cisplatin-induced acute nephrotoxicity in cancer patients with diabetes mellitus: A retrospective study

被引:12
作者
Iwakura, Takamasa [1 ]
Fukasawa, Hirotaka [1 ]
Kitamura, Atsushi [1 ]
Ishibuchi, Kento [1 ]
Yasuda, Hideo [2 ]
Furuya, Ryuichi [1 ]
机构
[1] Iwata City Hosp, Dept Internal Med, Renal Div, Iwata, Japan
[2] Hamamatsu Univ Sch Med, Div Nephrol, Internal Med 1, Hamamatsu, Shizuoka, Japan
来源
PLOS ONE | 2020年 / 15卷 / 02期
关键词
DPP-4; INHIBITORS; KIDNEY; INJURY; LINAGLIPTIN; PROTECTION; STATEMENT; THERAPY; DISEASE; STRESS; CELLS;
D O I
10.1371/journal.pone.0229377
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Background Cisplatin is a highly effective chemotherapeutic agent. However, acute kidney injury (AKI) limits its subsequent use, resulting in poor cancer prognosis. Dipeptidyl peptidase-4 (DPP-4) inhibitors have been reported to attenuate cisplatin-induced AKI in animal models, but the effect in human patients remains to be clarified. We hypothesized that DPP-4 inhibitors can prevent cisplatin-induced AKI in diabetic-cancer patients. Methods We retrospectively reviewed all consecutive cancer patients who were treated with a first cycle of cisplatin-containing regimen between January 2011 and October 2019. We analysed data of diabetic-cancer patients treated with high-dose cisplatin (> 50 mg/m(2))-containing regimens. The change of estimated glomerular filtration rate (eGFR) within 2 weeks after cisplatin treatment was compared between the patients treated with DPP-4 inhibitors and those treated without DPP-4 inhibitors. Results A total of 455 patients were treated with cisplatin during the period. Of these, 34 patients were eligible for the analysis. The change of eGFR was significantly less in the patients treated with DPP-4 inhibitors, compared to those without DPP-4 inhibitors [the percentages of eGFR decline (mean +/- SD) was 23.6 +/- 20.3% vs 43.1 +/- 20.1%, respectively; P = 0.010]. Furthermore, the incidence of AKI was significantly less in the patients treated with DPP-4 inhibitors (25% vs 64%, respectively; P = 0.026). Conclusions DPP-4 inhibitors may decrease the risk of cisplatin-induced AKI in diabetic patients.
引用
收藏
页数:11
相关论文
共 43 条
  • [1] Effect of dipeptidyl peptidase-4 inhibitors on circulating tumor necrosis factor-α concentrations: A systematic review and meta-analysis of controlled trials
    Atkin, Stephen L.
    Katsiki, Niki
    Banach, Maciej
    Mikhailidis, Dimitri P.
    Pirro, Matteo
    Sahebkar, Amirhossein
    [J]. JOURNAL OF DIABETES AND ITS COMPLICATIONS, 2017, 31 (09) : 1458 - 1464
  • [2] Effects of a DPP4 inhibitor on cisplatin-induced acute kidney injury: study protocol for a randomized controlled trial
    Baek, Seon Ha
    Kim, Se Hyun
    Kim, Jin Won
    Kim, Yu Jung
    Lee, Keun-Wook
    Na, Ki Young
    [J]. TRIALS, 2015, 16
  • [3] Options for Combination Therapy in Type 2 Diabetes: Comparison of the ADA/EASD Position Statement and AACE/ACE Algorithm
    Bailey, Timothy
    [J]. AMERICAN JOURNAL OF MEDICINE, 2013, 126 (09) : S10 - S20
  • [4] The effects of metformin in type 1 diabetes mellitus
    Beysel, Selvihan
    Unsal, Ilknur Ozturk
    Kizilgul, Muhammed
    Caliskan, Mustafa
    Ucan, Bekir
    Cakal, Erman
    [J]. BMC ENDOCRINE DISORDERS, 2018, 18
  • [5] Antioxidant agents for delaying diabetic kidney disease progression: A systematic review and meta-analysis
    Bolignano, Davide
    Cernaro, Valeria
    Gembillo, Guido
    Baggetta, Rossella
    Buemi, Michele
    D'Arrigo, Graziella
    [J]. PLOS ONE, 2017, 12 (06):
  • [6] Proximal tubule-targeted heme oxygenase-1 in cisplatin-induced acute kidney injury
    Bolisetty, Subhashini
    Traylor, Amie
    Joseph, Reny
    Zarjou, Abolfazl
    Agarwal, Anupam
    [J]. AMERICAN JOURNAL OF PHYSIOLOGY-RENAL PHYSIOLOGY, 2016, 310 (05) : F385 - F394
  • [7] GLP-1 treatment protects endothelial cells from oxidative stress-induced autophagy and endothelial dysfunction
    Cai, Xiangsheng
    She, Miaoqin
    Xu, Mingyu
    Chen, Huiying
    Li, Jingjing
    Chen, Xinglu
    Zheng, Dianpeng
    Liu, Jun
    Chen, Shangliang
    Zhu, Jianbin
    Xu, Xiaosong
    Li, Ruiying
    Li, Jinlong
    Chen, Shaolian
    Yang, Xiaorong
    Li, Hongwei
    [J]. INTERNATIONAL JOURNAL OF BIOLOGICAL SCIENCES, 2018, 14 (12): : 1696 - 1708
  • [8] Exendin-4 and sitagliptin protect kidney from ischemia-reperfusion injury through suppressing oxidative stress and inflammatory reaction
    Chen, Yen-Ta
    Tsai, Tzu-Hsien
    Yang, Chih-Chau
    Sun, Cheuk-Kwan
    Chang, Li-Teh
    Chen, Hung-Hwa
    Chang, Chia-Lo
    Sung, Pei-Hsun
    Zhen, Yen-Yi
    Leu, Steve
    Chang, Hsueh-Wen
    Chen, Yung-Lung
    Yip, Hon-Kan
    [J]. JOURNAL OF TRANSLATIONAL MEDICINE, 2013, 11
  • [9] Kidney Disease End Points in a Pooled Analysis of Individual Patient-Level Data From a Large Clinical Trials Program of the Dipeptidyl Peptidase 4 Inhibitor Linagliptin in Type 2 Diabetes
    Cooper, Mark E.
    Perkovic, Vlado
    McGill, Janet B.
    Groop, Per-Henrik
    Wanner, Christoph
    Rosenstock, Julio
    Hehnke, Uwe
    Woerle, Hans-Juergen
    von Eynatten, Maximilian
    [J]. AMERICAN JOURNAL OF KIDNEY DISEASES, 2015, 66 (03) : 441 - 449
  • [10] Exploring the effects of DPP-4 inhibitors on the kidney from the bench to clinical trials
    Coppolino, Giuseppe
    Leporini, Christian
    Rivoli, Laura
    Ursini, Francesco
    di Paola, Eugenio Donato
    Cernaro, Valeria
    Arturi, Franco
    Bolignano, Davide
    Russo, Emilio
    De Sarro, Giovambattista
    Andreucci, Michele
    [J]. PHARMACOLOGICAL RESEARCH, 2018, 129 : 274 - 294