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花生四烯酸代谢环氧合酶途径中的基因变异与类二十烷酸水平及糖尿病肾病风险相关。

Genetics Variants in the Epoxygenase Pathway of Arachidonic Metabolism Are Associated with Eicosanoids Levels and the Risk of Diabetic Nephropathy.

作者信息

Mota-Zamorano Sonia, Robles Nicolás R, González Luz M, Valdivielso José M, Lopez-Gomez Juan, Cancho Bárbara, García-Pino Guadalupe, Gervasini Guillermo

机构信息

Department of Medical and Surgical Therapeutics, Division of Pharmacology, Medical School, University of Extremadura, 06071 Badajoz, Spain.

Service of Nephrology, Badajoz University Hospital, 06071 Badajoz, Spain.

出版信息

J Clin Med. 2021 Sep 2;10(17):3980. doi: 10.3390/jcm10173980.

Abstract

Genes in the epoxygenase pathway of arachidonic acid metabolism leading to vasoactive eicosanoids, mainly 20-hydroxyeicosatetraenoic (20-HETE) and epoxyeicosatrienoic (EETs) acids, have been related to glucose-induced renal damage in preclinical reports. We genotyped 1088 diabetic kidney disease (DKD) patients and controls for seven polymorphisms in five genes (, , , , and ) along this metabolic route and evaluated their effect on DKD risk, clinical outcomes, and the plasma/urine levels of eicosanoids measured by LC/MS/MS and immunoenzymatic assays. The 433M variant allele was associated with lower incidence of DKD (OR = 0.65 (0.48-0.90), = 0.008), whilst the genotype was related to increased risk (OR = 3.21 (1.05-9.87), = 0.036). Patients carrying the 433M allele also showed lower eGFR [median and interquartile range vs. wildtype carriers: 30.8 (19.8) and 33.0 (23.2) mL/min/1.73 m, = 0.037). Finally, the 433VM/MM variant genotypes were associated with lower urinary levels of 20-HETE compared with 433VV (3.14 (0.86) vs. 8.45 (3.69) ng/mg Creatinine, = 0.024). Our results indicate that the V433M polymorphism, by decreasing 20-HETE levels, may play an important role in DKD.

摘要

在临床前报告中,花生四烯酸代谢的环氧合酶途径中的基因会产生血管活性类二十烷酸,主要是20-羟基二十碳四烯酸(20-HETE)和环氧二十碳三烯酸(EETs),这些基因与葡萄糖诱导的肾脏损伤有关。我们对1088例糖尿病肾病(DKD)患者和对照者进行了该代谢途径中五个基因(、、、和)的七个多态性位点的基因分型,并评估了它们对DKD风险、临床结局以及通过液相色谱/串联质谱法(LC/MS/MS)和免疫酶法测定的类二十烷酸血浆/尿液水平的影响。433M变异等位基因与DKD的较低发病率相关(OR = 0.65(0.48 - 0.90),= 0.008),而基因型与风险增加相关(OR = 3.21(1.05 - 9.87),= 0.036)。携带433M等位基因的患者的估算肾小球滤过率(eGFR)也较低[中位数和四分位间距与野生型携带者相比:30.8(19.8)和33.0(23.2)mL/min/1.73 m²,= 0.037]。最后,与433VV相比,433VM/MM变异基因型与较低的20-HETE尿液水平相关(3.14(0.86)对8.45(3.69)ng/mg肌酐,= 0.024)。我们的结果表明,V433M多态性通过降低20-HETE水平,可能在DKD中起重要作用。

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