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Remission of Proteinuria May Protect against Progression to Chronic Kidney Disease in Pediatric-Onset IgA Nephropathy

Authors
Suh, Jin-SoonJang, Kyung MiHyun, HyesunCho, Myung HyunLee, Joo HoonPark, Young SeoOh, Jae HyukKim, Ji HongYoo, Kee HwanChung, Woo YeongKim, Seong HeonKim, KeehyuckLee, Dae YeolLee, Jung WonCho, Min HyunPark, HyewonKoo, Ja WookHan, Kyoung HeeYang, Eun MiLee, Keum HwaShin, Jae IlCho, HeeyeonKim, Kyo SoonHa, Il-SooPark, Yong HoonKang, Hee Gyung
Issue Date
Jul-2020
Publisher
MDPI
Keywords
children; IgA nephropathy; long-term outcome; remission of proteinuria
Citation
JOURNAL OF CLINICAL MEDICINE, v.9, no.7
Indexed
SCIE
SCOPUS
Journal Title
JOURNAL OF CLINICAL MEDICINE
Volume
9
Number
7
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/54495
DOI
10.3390/jcm9072058
ISSN
2077-0383
Abstract
Immunoglobulin A nephropathy (IgAN) is one of the most common primary glomerulopathies diagnosed in children and adolescents. This study aimed to evaluate the clinical features in and outcomes of pediatric IgAN over the last 30 years. Patients who were diagnosed before age of 18 at 20 centers in Korea were evaluated retrospectively. Of the 1154 patients (768 males, 386 females) with a median follow-up of 5 years, 5.6% (n= 65) progressed to stage 3-5 chronic kidney disease (CKD). The 10- and 20-year CKD-free survival rates were 91.2% and 75.6%, respectively. Outcomes did not differ when comparing those in Korea who were diagnosed prior to versus after the year 2000. On multivariate analysis, combined asymptomatic hematuria and proteinuria as presenting symptoms and decreased renal function at the time of biopsy were associated with progression to CKD, while remission of proteinuria was negatively associated with this outcome. Patients who presented with gross hematuria or nephrotic syndrome tended toward positive outcomes, especially if they ultimately achieved remission. While remission of proteinuria might imply that the disease is inherently less aggressive, it also can be achieved by management. Therefore, more aggressive management might be required for pediatric-onset IgAN.
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