Cardiovascular Complications and Indoxyl Sulfate Are Related to Longer Duration of End Stage Renal Disease in Children

Fatina I. Fadel, N. El-Anwar, Fatma Abdel Maksoud, N. Mohamed, Yasmin Ramadan
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Abstract

Background: Indoxyl sulfate (IS) is a non-dialyzable gut-derived uremic toxin that is reported to be cardiotoxic in patients with advanced chronic kidney disease stages. Aim of the Work: The aim of this study was to investigate the role of IS as a risk factor for cardiovascular complications in children with end stage kidney disease (ESKD) on regular HD. Patients and Methods: This is a cross-sectional analytical study that included children with ESKD on regular hemodialysis (HD) for at least 6 months following at Nephrology Unit of Cairo University Pediatric Hospitals. Serum IS level was measured for all patients by the enzymelinked immunosorbent assay (ELISA). Cardiac complications was assessed using the M mode and 2D transthoracic echocardiography. Results: The study comprised 88 children with ESKD on regular HD for a mean ± SD of 31.94 ± 26.05 months, with a mean age ± SD of 9 ± 3.2 years (range 3.314 years). Of them 52 (59.1%) were males. Obstructive uropathy (28.4%), and focal segmental glomerulosclerosis (20.5%), were the main causes of ESKD in the study group. Cardiovascular complications were identified in 48 (54.5%) patients in the form of dilated cardiomyopathy in 44 (50%) children with decreased fractional shortening <30% and moderate to severe left ventricular hypertrophy above 95th for age and gender in 10 (11.4%). Cardiovascular affection correlated with duration of HD, hypertension, and IS serum level (p=<0.001 for each). Hypertension was reported in 55 (62.5%) of patients, and vascular access related complications were evident in 40 (45.4%) patients with thrombosis being the commonest complication in 16 (18.1%). The mean IS was 29.14 ± 17.43 μg/ml in ESKD patients with normal cardiac function, and 77 ± 15.18 μg/ml among those with cardiac compromise (p < 0.001). The IS level correlated with longer duration of HD (p= 0.002), and older age (p= 0.043). IS level and duration of HD did not predict cardiomyopathy, (p=0.192), and (p=0.760) respectively. Conclusion: Cardiac complications are common among children on HD. Both cardiovascular complications and IS accumulation correlated positively with longer duration of HD, and age of children with ESKD. IS is non-dialysable and there is a need to control its production from the gut. Level of Evidence of Study: IV (1).
心血管并发症和硫酸吲哚酚与儿童终末期肾病持续时间延长有关
背景:硫酸吲哚酚(IS)是一种不可透析的肠源性尿毒症毒素,据报道对晚期慢性肾病患者具有心脏毒性。工作目的:本研究的目的是调查IS作为常规HD患者终末期肾病(ESKD)儿童心血管并发症的危险因素的作用。患者和方法:这是一项横断面分析研究,纳入了在开罗大学儿科医院肾内科接受常规血液透析(HD)治疗至少6个月的ESKD患儿。采用酶联免疫吸附试验(ELISA)检测所有患者血清IS水平。采用M模式和二维经胸超声心动图评估心脏并发症。结果:本研究纳入88例ESKD患儿,平均±SD为31.94±26.05个月,平均年龄±SD为9±3.2岁(范围3.314岁)。其中男性52例(59.1%)。梗阻性尿路病变(28.4%)和局灶节段性肾小球硬化(20.5%)是研究组ESKD的主要原因。48例(54.5%)以扩张型心肌病的形式出现心血管并发症,44例(50%)儿童分数缩短<30%,10例(11.4%)年龄和性别大于95分,中度至重度左室肥厚。心血管疾病与HD病程、高血压和IS血清水平相关(p=<0.001)。高血压55例(62.5%),血管通路相关并发症40例(45.4%),血栓形成是16例(18.1%)中最常见的并发症。心功能正常ESKD患者的IS平均值为29.14±17.43 μg/ml,心功能受损ESKD患者的IS平均值为77±15.18 μg/ml (p < 0.001)。IS水平与HD持续时间较长(p= 0.002)和年龄较大(p= 0.043)相关。HD的IS水平和持续时间不能预测心肌病(p=0.192)和(p=0.760)。结论:心脏并发症在HD患儿中较为常见。心血管并发症和IS积累与HD病程延长和ESKD患儿年龄呈正相关。IS是不可透析的,需要控制其从肠道产生。研究证据水平:IV(1)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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