Suppr超能文献

非诺贝特引起的肾功能障碍,是与否?

Fenofibrate-induced renal dysfunction, yes or no?

作者信息

Emami Fatemeh, Hariri Amirali, Matinfar Mohammad, Nematbakhsh Mehdi

机构信息

Water and Electrolytes Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.

Isfahan Kidney Diseases Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.

出版信息

J Res Med Sci. 2020 Apr 13;25:39. doi: 10.4103/jrms.JRMS_772_19. eCollection 2020.

Abstract

In the treatment process of hypertriglyceridemia and diabetic nephropathy in type 2 diabetes, fenofibrate (FEN) is a well-known medication. FEN is from fibrate class drugs that using orally; however, as a side effect, it is associated with serum creatinine level increasing. The aim of this review was to determine the real effect of FEN therapy on renal functions based on both experimental and clinical studies. For this review, using the keywords of "fenofibrate" and "renal" and "function," a variety of sources of information banks, including PubMed, Google Scholar, and Scopus, were used, and the published articles were considered and interpreted. Followed by searching in databases, 45 articles were collected. After screening these articles, based on the study source, they were devided into two parts: 23 articles on animal experiments and 22 articles clinical experiments. Based on this information, it seems that the protective mechanism of FEN is related to vascular endothelial functions. The increased creatinine by FEN is related to different sensitivities to FEN effects caused by a polymorphism in different patients. In patients with normal renal function, follow-up of serum creatinine would be necessary after FEN, but the discontinuation of FEN is not recommended. In addition, in diabetic patients with hypertriglyceridemia, FEN treatment would be suggested for protecting the kidney from diabetes-induced renal injury.

摘要

在2型糖尿病合并高甘油三酯血症和糖尿病肾病的治疗过程中,非诺贝特(FEN)是一种知名药物。FEN属于口服的贝特类药物;然而,作为一种副作用,它与血清肌酐水平升高有关。本综述的目的是基于实验和临床研究确定FEN治疗对肾功能的实际影响。为了进行本综述,使用了包括PubMed、谷歌学术和Scopus在内的各种信息库来源,以“非诺贝特”、“肾脏”和“功能”为关键词,并对已发表的文章进行了考量和解读。在数据库搜索之后,收集了45篇文章。在筛选这些文章后,根据研究来源将它们分为两部分:23篇关于动物实验的文章和22篇关于临床试验的文章。基于这些信息,FEN的保护机制似乎与血管内皮功能有关。FEN导致的肌酐升高与不同患者因基因多态性而对FEN作用的不同敏感性有关。在肾功能正常的患者中,服用FEN后有必要监测血清肌酐,但不建议停用FEN。此外,在患有高甘油三酯血症的糖尿病患者中,建议使用FEN治疗以保护肾脏免受糖尿病引起的肾损伤。

相似文献

1
Fenofibrate-induced renal dysfunction, yes or no?
J Res Med Sci. 2020 Apr 13;25:39. doi: 10.4103/jrms.JRMS_772_19. eCollection 2020.
2
Protective effect of peroxisome proliferator activator receptor (PPAR)-α and -γ ligands against methotrexate-induced nephrotoxicity.
Immunopharmacol Immunotoxicol. 2014 Apr;36(2):130-7. doi: 10.3109/08923973.2014.884135. Epub 2014 Feb 13.
3
Fenofibrate raises plasma homocysteine levels in the fasted and fed states.
Atherosclerosis. 2001 Apr;155(2):455-62. doi: 10.1016/s0021-9150(00)00584-0.
4
Fenofibrate pre-treatment suppressed inflammation by activating phosphoinositide 3 kinase/protein kinase B (PI3K/Akt) signaling in renal ischemia-reperfusion injury.
J Huazhong Univ Sci Technolog Med Sci. 2015 Feb;35(1):58-63. doi: 10.1007/s11596-015-1389-2. Epub 2015 Feb 12.
5
Fibrate-induced increase in blood urea and creatinine: is gemfibrozil the only innocuous agent?
Nephrol Dial Transplant. 2000 Dec;15(12):1993-9. doi: 10.1093/ndt/15.12.1993.
6
Fenofibrate reduces intestinal damage and improves intestinal recovery following intestinal ischemia-reperfusion injury in a rat.
Pediatr Surg Int. 2016 Dec;32(12):1193-1200. doi: 10.1007/s00383-016-3979-x. Epub 2016 Sep 20.
8
Effect of Fenofibrate Medication on Renal Function.
Korean J Fam Med. 2017 Jul;38(4):192-198. doi: 10.4082/kjfm.2017.38.4.192. Epub 2017 Jul 20.
9
An Increase in Serum Creatinine after Initiation of Fenofibrate in an HIV-Infected Individual: A Case Report and Review of the Literature.
J Int Assoc Physicians AIDS Care (Chic). 2011 Jul-Aug;10(4):219-22. doi: 10.1177/1545109711404945. Epub 2011 Apr 25.

引用本文的文献

1
4
Executive summary of the Hellenic Atherosclerosis Society guidelines for the diagnosis and treatment of dyslipidemias - 2023.
Atheroscler Plus. 2024 Feb 17;55:74-92. doi: 10.1016/j.athplu.2024.01.004. eCollection 2024 Mar.
5
Fenofibrate reduces glucose-induced barrier dysfunction in feline enteroids.
Sci Rep. 2023 Dec 18;13(1):22558. doi: 10.1038/s41598-023-49874-9.
7
Can coenzyme Q10 alleviate the toxic effect of fenofibrate on skeletal muscle?
Histochem Cell Biol. 2023 Aug;160(2):147-158. doi: 10.1007/s00418-023-02205-5. Epub 2023 Jun 4.
8
Factors associated with incidence of acute kidney injury: a Japanese regional population-based cohort study, the Shizuoka study.
Clin Exp Nephrol. 2023 Apr;27(4):321-328. doi: 10.1007/s10157-022-02310-0. Epub 2022 Dec 27.
9
The role of metabolic reprogramming in tubular epithelial cells during the progression of acute kidney injury.
Cell Mol Life Sci. 2021 Aug;78(15):5731-5741. doi: 10.1007/s00018-021-03892-w. Epub 2021 Jun 29.
10
Efficacy of a micronized, nanocrystal fenofibrate formulation in treatment of hyperlipidemia in dogs.
J Vet Intern Med. 2021 Jul;35(4):1733-1742. doi: 10.1111/jvim.16190. Epub 2021 Jun 6.

本文引用的文献

3
Effect of Fenofibrate Medication on Renal Function.
Korean J Fam Med. 2017 Jul;38(4):192-198. doi: 10.4082/kjfm.2017.38.4.192. Epub 2017 Jul 20.
4
Fenofibrate/simvastatin fixed-dose combination in the treatment of mixed dyslipidemia: safety, efficacy, and place in therapy.
Vasc Health Risk Manag. 2017 Feb 16;13:29-41. doi: 10.2147/VHRM.S95044. eCollection 2017.
5
Delayed treatment with fenofibrate protects against high-fat diet-induced kidney injury in mice: the possible role of AMPK autophagy.
Am J Physiol Renal Physiol. 2017 Feb 1;312(2):F323-F334. doi: 10.1152/ajprenal.00596.2015. Epub 2016 Jul 27.
6
PPARα agonist, fenofibrate, ameliorates age-related renal injury.
Exp Gerontol. 2016 Aug;81:42-50. doi: 10.1016/j.exger.2016.04.021. Epub 2016 Apr 27.
7
Fenofibrate attenuates diabetic nephropathy in experimental diabetic rat's model via suppression of augmented TGF-β1/Smad3 signaling pathway.
Arch Physiol Biochem. 2016 Oct;122(4):186-194. doi: 10.3109/13813455.2016.1164186. Epub 2016 Apr 5.
10
Fenofibrate pre-treatment suppressed inflammation by activating phosphoinositide 3 kinase/protein kinase B (PI3K/Akt) signaling in renal ischemia-reperfusion injury.
J Huazhong Univ Sci Technolog Med Sci. 2015 Feb;35(1):58-63. doi: 10.1007/s11596-015-1389-2. Epub 2015 Feb 12.

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验