Trovato Francesca M, Catalano Daniela, Ragusa Angela, Martines G Fabio, Pirri Clara, Buccheri Maria Antonietta, Di Nora Concetta, Trovato Guglielmo M
Francesca M Trovato, Daniela Catalano, Clara Pirri, Concetta Di Nora, Guglielmo M Trovato, Department of Internal Medicine, University of Catania, 95100 Catania, Italy.
World J Nephrol. 2015 Feb 6;4(1):127-37. doi: 10.5527/wjn.v4.i1.127.
To investigate the effects of different methylenetetrahydrofolate reductase (MTHFR) 677C>T gene polymorphism and hyperhomocysteinemia for the development of renal failure and cardiovascular events, which are controversial.
We challenged the relationship, if any, of MTHFR 677C>T and MTHFR 1298A>C polymorphisms with renal and heart function. The present article is a reappraisal of these concepts, investigating within a larger population, and including a subgroup of dialysis patients, if the two most common MTHFR polymorphisms, C677T and A1298C, as homozygous, heterozygous or with a compound heterozygous state, show different association with chronic renal failure requiring hemodialysis. MTHFR polymorphism could be a favorable evolutionary factor, i.e., a protective factor for many ominous conditions, like cancer and renal failure. A similar finding was reported in fatty liver disease in which it is suggested that MTHFR polymorphisms could have maintained and maintain their persistence by an heterozygosis advantage mechanism. We studied a total of 630 Italian Caucasian subject aged 54.60 ± 16.35 years, addressing to the increased hazard of hemodialysis, if any, according to the studied MTHFR genetic polymorphisms.
A favorable association with normal renal function of MTHFR polymorphisms, and notably of MTHFR C677T is present independently of the negative effects of left ventricular hypertrophy, increased Intra-Renal arterial Resistance and hyperparathyroidism.
MTHFR gene polymorphisms could have a protective role on renal function as suggested by their lower frequency among our dialysis patients in end-stage renal failure; differently, the association with left ventricular hypertrophy and reduced left ventricular relaxation suggest some type of indirect, or concurrent mechanism.
探讨不同的亚甲基四氢叶酸还原酶(MTHFR)677C>T基因多态性和高同型半胱氨酸血症对肾衰竭和心血管事件发生发展的影响,这一问题存在争议。
我们对MTHFR 677C>T和MTHFR 1298A>C基因多态性与肾功能和心脏功能之间的关系(若存在)进行了研究。本文是对这些概念的重新评估,在更大的人群中进行调查,并纳入了一组透析患者,研究两种最常见的MTHFR基因多态性,即C677T和A1298C,处于纯合子、杂合子或复合杂合子状态时,与需要血液透析的慢性肾衰竭是否存在不同的关联。MTHFR基因多态性可能是一个有利的进化因素,即对许多严重疾病(如癌症和肾衰竭)的保护因素。在脂肪肝疾病中也有类似的发现,提示MTHFR基因多态性可能通过杂合优势机制得以维持并持续存在。我们共研究了630名年龄在54.60±16.35岁的意大利白种人受试者,根据所研究的MTHFR基因多态性,探讨其与血液透析增加的风险(若存在)之间的关系。
MTHFR基因多态性,尤其是MTHFR C677T与正常肾功能呈有利关联,且独立于左心室肥厚、肾内动脉阻力增加和甲状旁腺功能亢进的负面影响。
MTHFR基因多态性可能对肾功能具有保护作用,这一点从我们终末期肾衰竭透析患者中其较低的频率可以看出;不同的是,其与左心室肥厚和左心室舒张功能降低的关联提示存在某种间接或并发机制。