Chronic Renal Failure Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Department of Pediatric Nephrology, Iran University of Medical Sciences, Tehran, Iran.
J Pediatr Urol. 2019 Apr;15(2):165.e1-165.e4. doi: 10.1016/j.jpurol.2018.11.003. Epub 2018 Nov 10.
Hematuria, either macroscopic or microscopic, is an incidental finding of multiple nephrologic or urologic disorders. Disturbances of urine inhibitors or promotors have been suggested as the potential causes of isolated idiopathic hematuria in children and its recurrence. Meanwhile, appropriate treatment of these risk factors might improve secondary asymptomatic or macroscopic hematuria.
The aim of this study was to identify contribution of urinary biochemical abnormalities in children with isolated idiopathic hematuria.
About 522 children with isolated hematuria were evaluated in a prospective cross-sectional study. Data such as clinical manifestations, family history, laboratory examinations, structural anomalies, and urine biochemistry were obtained. Patients with nephrolithiasis, nephrocalcinosis, tubulointerstitial disorder, genitourinary abnormality, urinary tract infection, and glomerular disorder were excluded from the study. Variables such as calcium, citrate, oxalate, phosphate, uric acid, cystine, and magnesium were measured in 24-h urine collection. In addition, serum levels of electrolytes, urea, creatinine, parathyroid hormone, and bicarbonate were identified.
Mean age at diagnosis was 5.9 years, and females outnumbered males (2/1). Of those, 88.5% had microscopic hematuria, and 12.6% experienced episodes of gross hematuria. Abdominal pain was the most common clinical manifestations. Urinary tract infection occurred in 30% of cases. Totally, 94% of patients had single or multiple metabolic abnormalities in 24-h urine excretion including hypocitraturia, 60.7%; hypomagnesuria, 58.2%; hyperuricosuria, 35.8%; hypercalciuria, 33.7%; hyperoxaluria, 33.7%; and cystinuria, 0.76%, respectively. About 8% of cases had mixed urine metabolic disturbances. Most patients had mild hematuria (red blood cell <10/high power field (hpf)), and 18% had significant hematuria (>30/hpf), with no statistical correlation to urine metabolic abnormalities. About 80% of patients had a history of nephrolithiasis in their relatives.
Decreased urinary inhibitor concentration followed by increased stimulator concentration were the most common abnormalities in patients with idiopathic hematuria. Accordingly, measurement of urinary biochemical concentration is highly recommended in children with isolated hematuria. In addition, investigating the therapeutic effect of potassium citrate supplements is highly recommended in these patients to prevent future stone formation and treatment of hematuria.
血尿,无论是肉眼血尿还是镜下血尿,都是多种肾脏或泌尿系统疾病的偶发表现。尿液抑制剂或促进剂的紊乱被认为是儿童孤立性特发性血尿及其复发的潜在原因。同时,适当治疗这些危险因素可能会改善继发性无症状或肉眼血尿。
本研究旨在确定尿液生化异常在儿童孤立性特发性血尿中的作用。
对 522 例孤立性血尿患儿进行前瞻性横断面研究。收集临床症状、家族史、实验室检查、结构异常和尿液生化等数据。排除肾结石、肾钙质沉着症、肾小管间质疾病、泌尿生殖系统异常、尿路感染和肾小球疾病的患者。在 24 小时尿液收集物中测量钙、柠檬酸盐、草酸盐、磷酸盐、尿酸、胱氨酸和镁等变量。此外,还检测血清电解质、尿素、肌酐、甲状旁腺激素和碳酸氢盐水平。
诊断时的平均年龄为 5.9 岁,女性多于男性(2/1)。其中 88.5%为镜下血尿,12.6%出现肉眼血尿。腹痛是最常见的临床表现。30%的病例发生尿路感染。总共,94%的患者在 24 小时尿液排泄中有单种或多种代谢异常,包括低柠檬酸尿症(94%)、低镁尿症(58.2%)、高尿酸尿症(35.8%)、高钙尿症(33.7%)、高草酸尿症(33.7%)和胱氨酸尿症(0.76%)。约 8%的病例有混合性尿液代谢紊乱。大多数患者血尿较轻(红细胞<10/高倍视野(hpf)),18%血尿较重(>30/hpf),但与尿液代谢异常无统计学相关性。约 80%的患者有肾结石家族史。
特发性血尿患者最常见的异常是尿抑制剂浓度降低,随后刺激剂浓度升高。因此,建议对孤立性血尿患儿进行尿液生化浓度检测。此外,建议对这些患者进行枸橼酸钾补充治疗效果的调查,以预防结石形成和血尿治疗。