• Childhood Kidney Diseases
• /
• 제21권2호
• /
• pp.53-60
• /
• 2017

Proteinuria is common in pediatric and adolescent patients. Proteinuria is defined as urinary protein excretion at levels higher than $100-150mg/m^2/day$ in children. It can be indicative of normal or benign conditions as well as numerous types of severe underlying renal or systemic disease. The school urine screening program has been conducted in Korea since 1998. Since then, numerous patients with normal or benign proteinuria as well as early stage renal diseases have been referred to the hospital. Benign proteinuria includes orthostatic proteinuria and transient proteinuria. Most causes of proteinuria can be categorized into 3 types: 1) overflow, 2) tubular, and 3) glomerular. Although treatment should be directed at the underlying cause of the proteinuria, prompt evaluation, diagnosis, and long-term monitoring of these pediatric patients can prevent potential progression of the underlying disease process. This article provides an overview of proteinuria: its causes, methods of assessment, and algorithmic suggestions to differentiate benign from pathologic renal disease.

• Childhood Kidney Diseases
• /
• 제21권2호
• /
• pp.152-155
• /
• 2017

Orthostatic or postural proteinuria is the most common cause of asymptomatic proteinuria in children. As orthostatic proteinuria (OP) is a benign disease with relatively good prognosis, it has no specific management, and patients only need to be observed. However, if OP shows a persistently high level of proteinuria, in theory, glomerular changes can occur. An 11-year-old girl was referred to the hospital due to asymptomatic proteinuria and was diagnosed as having OP based on the results of clinical and laboratory examinations, urinalysis, and protein/creatinine (TP/Cr) ratio at both supine and erect positions. During follow-up observation, the 24-hour TP/Cr ratio was persistently higher than 1.5 mg/mg for 2 years. We performed renal biopsy, which showed mesangial proliferative glomerular lesions with focal effacement of the podocyte foot processes, but without immune depositions. OP can be accompanied by glomerular lesions if moderate to severe proteinuria persists.

• Childhood Kidney Diseases
• /
• 제10권2호
• /
• pp.119-124
• /
• 2006

Purpose : The prognosis of acute poststreptococcal glomerulonephritis(APSGN) has been reported to be favorable. However, several studies have reported that patients with nephrotic range proteinuria in the acute phase or persistent proteinuria may progress to chronic renal failure. To elucidate this further, we analyzed the features of proteinuria and its prognosis in pediatric patients with APSGN. Methods : A total of 48 children with APSGN admitted to our hospital between Jan. 2000 and Dec. 2004 were included. After discharge from the hospital, patients were regularly followed up every month by clinical evaluations and laboratory tests including routine urinalysis and quantification of proteinuria. Results : Age of the patients ranged from 3 to 15 years(median 5.8 years) at the time of disease onset. Proteinuria was present in 34(70.8%) patients and 5 of them showed heavy proteinuria. Proteinuria normalized within one month in most patients(82.3%) and there was no one with proteinuria after 6 months. Cyclosporine A(5 mg/kg/day in two divided doses) was given to 3 patients with massive proteinuria that lasted longer than 2 months and the result was complete remission within 4 months. Conclusions : Our data indicated that the prognosis of APSGN during childhood is excellent. Children with severe proteinuria or subnormal renal function in poststreptococcal glomerulonephritis had favorable prognosis without chronic renal failure, and children with crescentic formation also had favorable prognosis. Three patients who continued to have heavy proteinuria for more than 2 months received cyclosporine A and remission of proteinuria was achieved within a couple of months.

• 한국임상약학회지
• /
• 제30권4호
• /
• pp.234-242
• /
• 2020

Background: Bevacizumab-induced proteinuria is known to occur when vascular endothelial cell receptors are blocked, which leads to decreased protein filtration. Although several studies have analyzed the correlation between therapeutic effect of bevacizumab and proteinuria, no conclusion has been established. Methods: In this retrospective study, colorectal cancer patients who received bevacizumab and urinary protein check from January 2015 to December 2016, were included. The incidence of proteinuria and the grade according to Common Terminology Criteria for Adverse Events (CTCAE) 4.0 were evaluated after bevacizumab administration. The primary objective was to correlate proteinuria with overall response rate (ORR) and time to progression (TTP). Primary lesion, metastasized organs, surgery or radiation therapy, chemotherapy were investigated for analysis of risk factors for proteinuria development. Results: A total of 149 patients included in the analysis. Proteinuria occurred 19.5% (n=29) in the study patients; 20 in grade 1, 7 in grade 2, and 2 in grade 3. ORR was 55.2% in the proteinuria group and 51.7% in the non-proteinuria group. There was no difference between two groups (p=0.89). The TTP through the survival curve was similar in both groups (10 months, p=0.97). The risk of proteinuria was high in patients who had liver metastasis (p=0.02) and no surgery (p=0.01). Conclusions: These result indicates that bevacizumab-induced proteinuria expression was not correlated with the therapeutic effect on patients with colorectal cancer. Further analysis is required to find out the correlation between proteinuria and therapeutic effects. The risk of proteinuria was increased from patients who had liver metastasis, and no surgery.

• 사상체질의학회지
• /
• 제15권3호
• /
• pp.170-176
• /
• 2003

This is to report the result of the clinical treatment of One Proteinuria patient who has been hospitalized from January 2003 to August 2003 in Kwangdong Oriental Medicine Hospital. Proteinuria is an important sign of renal disease. It is very useful to estimate the patterns of proteinuria in differential diagnosis of renal disease. One patient have been diagnosed as the determination of the protein creatinine ratio when properly interpreted can replace the total urine collection for 24 hours in the clinical question of proteinuria when hospitalized. Therefore, We met One patient having Proteinuria and acquired good result by treatment with Taeyeumin Jowesungcheongtang plus jejo and bupeong for 4months. This paper describe the process and contents about the patient was cured.

• 대한한방내과학회지
• /
• 제39권6호
• /
• pp.1290-1295
• /
• 2018

Objectives: This case reports a certain level of improvement for asymptomatic proteinuria with short-term administration of herbal medicine. Methods: In the first treatment phase, the patient was treated with Dangguisu-san (DGSS) for his rib fracture. In the second treatment phase, the patient was treated with a herbal formulation of Astragali and Angelicae Sinensis (A&As particle) for asymptomatic proteinuria. Results: Treatment with herbal medicine resulted in a decrease in the patient's complaints regarding symptoms. Also, proteinuria-related items in hematology and urinalysis were improved. Conclusions: Herbal medicine therapy may be effective for proteinuria treatment.

• Childhood Kidney Diseases
• /
• 제27권1호
• /
• pp.19-25
• /
• 2023

Proteinuria is an important risk factor for renal and cardiovascular disease. It is associated with a risk for glomerulonephritis, chronic kidney disease, and end-stage renal disease. Therefore, if persistent proteinuria is detected, kidney biopsy is considered to diagnose and treat the underlying disease. Recently, variants in the cubilin (CUBN) gene, which is associated with albuminuria, have been reported. This gene encodes cubilin, a membrane glycoprotein receptor expressed in the renal proximal tubules. Cubilin is a component of the megalin and cubilin-amnionless complex that mediates albumin reabsorption into the proximal tubules through endocytosis. A defect in cubilin leads to a reduction in albumin reuptake, resulting in albumin-dominant proteinuria. Although numerous controversies exist, several reports suggest that cubilin defects lead to proteinuria with a high portion of albuminuria but may not impair renal filtration function. If albuminuria due to reduced cubilin function is confirmed as a benign condition, we can consider using genetic studies to detect CUBN mutations in patients with proteinuria and they may not require any treatment or kidney biopsy. Here, we review recent papers on CUBN mutations and discuss the prognosis and management of individuals with this mutation.

• Childhood Kidney Diseases
• /
• 제6권1호
• /
• pp.61-67
• /
• 2002

목 적 : 학교 신체검사에서 우연히 발견된 단독 단백뇨를 가진 학생들의 정밀검사와 추적 관찰 결과를 분석하여 단독 단백뇨의 원인을 규명하고 향후 치료와 추적관찰에 도움을 주고자 하였다. 대상 및 방법 : 1990년 1월부터 2001년 7월까지 학교 신체검사에서 발견된 단백뇨를 주소로 서울 아산병원 소아과 외래를 방문한 학생 중 단독 단백뇨로 진단받은 초, 중, 고등학생 114명을 대상으로 하여 후향적으로 의무기록을 검토하였다. 곁 과 : 114명의 대상 학생들의 단백뇨 정량에서 일시적 단백뇨가 36례($32\%$), 기립성 단백뇨가 74례($65\%$), 지속성 단백뇨가 4례($3\%$)였다. 기립성 단백뇨군에서는 주간 단백뇨 $319.2{\pm}189.1\;mg/dL$, 야간 단백뇨 $56.5{\pm}56.1\;mg/dL$였고, 지속성 단백뇨에서는 주간단백뇨 $1140.0{\pm}540.5\;mg/dL$, 야간 단백뇨 $289.0{\pm}58\;mg/dL$였다. 모든 대상 학생들에게서 혈청 크레아티닌, 혈청 알부민, 혈청 보체 수치가 정상 범위였다. 추적 관찰결과 기립성 단백뇨군 74례 중 44례가 6개월에 추적 관찰 되었다. 이중 14례는 단백뇨가 소실되어 더 이상 추적 관찰하지 않았고, 28례는 기립성 단백뇨 소견이 지속되었다. 이중 13례가 18개월에 추적 되었으며 12례는 계속 기립성 단백뇨로 분류되었고 1례가 지속성 단백뇨 소견을 보였으나, 30개월 추적에서는 다시 기립성 단백뇨 소견을 보였다. 6개월 추적에서 2례에서 지속성 단백뇨의 소견을 보였고, 이중 1례는 30개월 까지 단백뇨가 지속되어 신 조직검사를 시행하였으나 곁과는 정상이었다. 지속성 단백뇨를 보인 4례 중 2례가 30개월에 추적 관찰되었고, 1례는 기립성 단백뇨 소견을 보였으나 1례는 지속성 단백뇨 소견을 보여 신장 조직 검사를 시행하였고, 조직 검사 결과 국소 분절성 사구체 신염(focal segmental glomerulosclerosis)으로 진단되었다. 결 론 : 학교 신체검사에서 발견된 단독 단백뇨의 대부분은 일시적인 단백뇨이거나 기립성 단백뇨이기 때문에 초기 검진시 과다한 검사는 불필요하며 정량적인 단백뇨 검사의 정기적인 추적관찰이 필요할 것으로 생각된다.

• Journal of Preventive Medicine and Public Health
• /
• 제39권5호
• /
• pp.427-432
• /
• 2006

Objectives: This study was to investigate if the dipstick proteinuria can predict cardiovascular mortality in a population of Korean men. Methods: We measured urine protein and other cardiovascular risk factors in 100059 Korean men, aged between 35-59 years in 1990 and 1992. Levels of proteinuria measured by dipstick method were trace or less, 1+, 2+, and 3+ or greater. The primary outcomes were deaths from all causes, cardiovascular disease, cancer, and others in a 12 year follow-up from 1993 to 2004. Results: The multivariate-adjusted relative risks (95% CI) for cardiovascular death according to the level of proteinuria (1+, 2+, 3+ and more) in 1990 examination were 2.18 (1.36-3.48), 2.55 (1.37-4.78), and 4.57 (2.16-9.66) respectively. The corresponding relative risks according to the level of proteinuria in 1992 examination were 2.49 (1.71-3.64), 2.64 (1.53-4.58), and 2.78 (1.15-6.73). The relative risks for cardiovascular death of men with proteinuria (1+ or greater) once and twice among the examinations were 2.18 (1.63-2.92) and 3.75 (2.27-6.18), compared with men without proteinuria in 1990 and 1992 examinations. Conclusions: Our results showed that dipstick proteinuria is associated with cardiovascular mortality in Korean men. Dipstick proteinuria could be a predictor for cardiovascular mortality.

• Childhood Kidney Diseases
• /
• 제28권2호
• /
• pp.74-79
• /
• 2024

Purpose: To compare the Doppler sonographic findings of the left renal vein (LRV) of children diagnosed with nutcracker syndrome with and without orthostatic proteinuria. Methods: Fifty and 53 consecutive children with and without orthostatic proteinuria, respectively, underwent renal Doppler ultrasonography examinations. The peak velocity (PV) was measured at the hilar portion of the LRV and between the aorta and superior mesenteric artery. Renal Doppler ultrasonography findings and clinical data including urine protein-to-creatinine ratio (UPCR) were compared according to the presence or absence of orthostatic proteinuria. Results: Between the two groups, no significant differences were observed in terms of age or sex. The PV ratio between the aortomesenteric and hilar portions was 7.79±2.65 and 6.32±3.01 in children with and without orthostatic proteinuria, respectively (P=0.009). No significant differences were observed between the two groups in terms of the UPCR in the first morning urine sample. However, the UPCR in the afternoon urine sample was significantly higher in children with orthostatic proteinuria than in those without orthostatic proteinuria (0.49±0.46 mg/mg vs. 0.11±0.04 mg/mg, P<0.001). Furthermore, the PV ratio between the aortomesenteric and hilar portions revealed a positive correlation with the ratio of UPCR of the afternoon to that of first morning urine samples (R=0.21, P=0.034). Conclusions: This study suggests that there can be a significant correlation of the PV ratio between the aortomesenteric and hilar portion of the LRV with orthostatic proteinuria in pediatric patients with nutcracker syndrome.