Tawfeek Gehan Abd-Elfatah, Kora Mahmoud Abdelaziz, Yassein Yassein Salah, Baghdadi Amal Muhammad, Elzorkany Khaled Mohamed
Clinical Pathology Department, Faculty of Medicine - Menoufia University, Egypt.
Internal Medicine Department, Faculty of Medicine - Menoufia University, Egypt.
Cytokine. 2021 Jan;137:155293. doi: 10.1016/j.cyto.2020.155293. Epub 2020 Oct 28.
Intradialytic hypertension (IDH) is a major problem of hemodialysis and it is a multifactorial disorder and need early identification and management.
Evaluate the serum concentration of endothelin-1 in patients with IDH and healthy control and the impact of pre-pro-endothelin gene polymorphism on level of endothelin-1 and susceptibility to IDH in Egyptian population.
The patient groups divided into group I, End stage renal disease (ESRD) on chronic hemodialysis with IDH (112); group II, ESRD on chronic hemodialysis without IDH (112); group III, healthy control (112). All undergone to full history, clinical examination, routine laboratory investigations, echocardiography, serum ET-1 level by ELISA and A(8002)G polymorphism detection in pre-pro-endothelin gene by PCR-RFLP.
Our results showed significantly higher concentration of Endothelin-1 (ET-1) in both patient groups than healthy control and in group with IDH than cases without IDH (p < 0.001). GG, GA and mutated G allele carry the risk of IDH (OR = 15.94, 13.5, 5.51 respectively p < 0.001). There was association between GG and GA genotypes and higher ET-1 level in both patient groups (p < 0.001) and association between GG and GA genotype and higher mean arterial pressure (MAP), delta MAP (DMAP) and increased left ventricular mass index (LVMI) in both patient groups (p = 0.001, 0.028).
Pre-pro-endothelin gene polymorphism A(8002)G is an independent risk factor for IDH through changing the level of ET-1 concentration in Egyptian population undergoing chronic hemodialysis.
透析中高血压(IDH)是血液透析的一个主要问题,它是一种多因素疾病,需要早期识别和管理。
评估IDH患者和健康对照者血清内皮素-1浓度,以及前内皮素原基因多态性对埃及人群内皮素-1水平和IDH易感性的影响。
患者分为三组,第一组为慢性血液透析伴IDH的终末期肾病(ESRD)患者(112例);第二组为慢性血液透析不伴IDH的ESRD患者(112例);第三组为健康对照者(112例)。所有患者均接受全面病史、临床检查、常规实验室检查、超声心动图检查,采用酶联免疫吸附测定法检测血清ET-1水平,并通过聚合酶链反应-限制性片段长度多态性技术检测前内皮素原基因的A(8002)G多态性。
我们的结果显示,两组患者的内皮素-1(ET-1)浓度均显著高于健康对照者,且伴IDH组高于不伴IDH组(p < 0.001)。GG、GA和突变的G等位基因携带IDH风险(OR分别为15.94、13.5、5.51,p < 0.001)。两组患者中,GG和GA基因型与较高的ET-1水平相关(p < 0.001),且GG和GA基因型与较高的平均动脉压(MAP)、平均动脉压变化值(DMAP)及左心室质量指数(LVMI)增加相关(p = 0.001,0.028)。
在前内皮素原基因多态性A(8002)G通过改变慢性血液透析埃及人群的ET-1浓度水平,是IDH的一个独立危险因素。