Publications by authors named "Peong Gang Park"

Introduction: The inflammatory phenotype of acute kidney injury (AKI), characterized by interstitial infiltration of immune cells, arises due to nephrotoxic agents. However, it does not pose the same risk of occurrence and progression for everyone, suggesting that the amplification or attenuation of disease depends on the unique immunological status of each kidney. Here, our study investigated the regulatory role of kidney-resident macrophages (KRMs) in the induction and progression of toxin-induced AKI.

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Objective: Growing concerns exist about the potential adverse effects of early antibiotic exposure on neurodevelopmental outcomes. However, large-scale studies exploring these implications in early childhood are rare.

Design: A nationwide, population-based retrospective cohort study using data from the Korean National Health Insurance System and the National Health Screening Program for Infants and Children (NHSPIC) between 2015 and 2022.

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Background: Acute kidney injury (AKI) is commonly observed in critically ill neonates; however, early identification of AKI in the first week of life is challenging due to the influence of maternal serum creatinine (SCr). An alternative criterion proposed by Gupta et al. based on SCr decline may identify additional infants at risk beyond the KDIGO definition.

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Background: Urinary tract infections (UTI) are the leading cause of severe bacterial infection in children under 24 months. Increasing antimicrobial resistance, particularly to third-generation cephalosporins, is a growing concern. This study examines recent resistance trends in young children with UTI in Korea.

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Background: Persistent hyperparathyroidism after kidney transplantation (KT) has been reported in up to 50% of adult recipients, but pediatric data remain limited. We evaluated the prevalence, skeletal manifestations, and risk factors for persistent hyperparathyroidism in children following KT.

Methods: In this retrospective cohort study, 107 pediatric KT recipients (58% male; median age 10.

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Background: The International IgA nephropathy (IgAN) Prediction Tool was recently updated to predict the risk of a 30% decline in estimated glomerular filtration rate (eGFR) or kidney failure in children with IgAN. We aimed to evaluate the clinical performance of this tool in a Korean cohort of children with IgAN.

Methods: We calculated the predicted risk for biopsy-proven IgAN children from 20 Korean centers.

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Background: This study assessed the clinical features, prevalence of kidney and urinary manifestations, and progression of chronic kidney disease (CKD) in patients with Kabuki syndrome (KS).

Methods: This retrospective cohort study enrolled patients with KS who visited a single tertiary center from 2003 to 2023.

Results: Sixty-five patients (28 boys) were diagnosed with KS at a median age of 2.

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Background: This study investigates whether intrarenal reflux (pyelotubular backflow) is associated with kidney scarring in children with urinary tract infection (UTI).

Methods: We retrospectively reviewed 441 children diagnosed with UTI who underwent voiding cystourethrography (VCUG) and a technetium-99 m dimercaptosuccinic acid (DMSA) scan more than 3 months after the UTI. Intrarenal reflux was identified on VCUG.

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Background: Due to the limited availability of therapeutic agents for type 2 diabetic kidney disease (T2DKD), there is a need for further knowledge derived from experimental models and innovative techniques. In addressing this issue, single-cell RNA sequencing (scRNA-seq) has been exclusively applied to a genetically modified diabetic kidney disease model, but not to an induced model representing T2DKD. Herein, we analyzed scRNA-seq and other experiments from an induced T2DKD model and validated the results in human-derived biospecimens.

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Background: Coenzyme Q10 (CoQ10) nephropathy is a well-known cause of hereditary steroid-resistant nephrotic syndrome, primarily impacting podocytes. This study aimed to elucidate variations in individual cell-level gene expression in CoQ10 nephropathy using single-cell transcriptomics.

Methods: We conducted single-cell sequencing of a kidney biopsy specimen from a 5-year-old boy diagnosed with a CoQ10 nephropathy caused by a compound heterozygous COQ2 mutation complicated with immune complex-mediated glomerulonephritis.

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Objective: To assess the relationship between breastfeeding and the risk of developing nephrotic syndrome using a population-based nationwide birth cohort in Korea.

Study Design: This nationwide cohort study utilized data from the National Health Information Database and the National Health Screening Program for Infants and Children. The study included all children born between January 1, 2010, and December 31, 2018, who underwent their first health screening, which included a specific questionnaire on breastfeeding between 4 and 6 months of age.

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Article Synopsis
  • Dapagliflozin, typically used for treating chronic kidney disease in adults, was studied in 22 children with kidney disease and proteinuria to evaluate its effects.
  • The treatment lasted over 3 months, with children being around 15.6 years old, and all had prior treatment with specific kidney medications.
  • Results showed no significant changes in kidney function or protein levels; however, there was a notable decrease in kidney function at the latest follow-up, indicating the need for further research to establish dapagliflozin's safety and effectiveness in this age group.
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Aim: Peritonitis is the most common complication of peritoneal dialysis (PD). This study aimed to investigate changes in the incidence, risk factors, microbiology, and clinical outcomes of PD-associated peritonitis in the past decades.

Methods: This was a retrospective study that included children who initiated chronic PD at our institution between 2000 and 2017.

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Article Synopsis
  • The study focused on understanding the genotype-phenotype relationships in children with Gitelman syndrome (GS) by analyzing genetic variations in the SLC12A3 gene in 50 Korean children.
  • The median age for diagnosis was 10.5 years, with 68% having biallelic variants; those with truncating variants experienced more severe electrolyte imbalances compared to those without.
  • Findings suggest that children with monoallelic SLC12A3 variants exhibited similar clinical symptoms and treatment responses as those with biallelic variants.
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Background: The purpose of this study was to examine the prevalence of hypertension in Korean adolescents, its long-term trends, and factors associated with the development of hypertension.

Methods: Data of the Korea National Health and Nutrition Examination Survey (KNHANES) from 2007 to 2020 were combined into three time periods (2007-2011, 2012-2016, and 2017-2020). A total of 11,146 Korean adolescents aged 10-18 were included in the analysis.

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Background: Although various childhood illnesses are known to influence growth status, the impact of urinary tract infections (UTI) on subsequent childhood growth remains unclear. This study was conducted to examine the association between UTI during infancy and growth status at 30-36 months.

Methods: Nationwide population-based matched cohort study was done using data from the Korean National Health Insurance System (NHIS) and the Korean National Health Screening Program for Infants and Children (NHSPIC) between January 2018 and December 2020.

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Background: We developed the KoreaN cohort study for Outcomes in patients With Pediatric Chronic Kidney Disease (KNOW-Ped CKD) as a subcohort of KNOW-CKD to investigate the different characteristics of pediatric CKD between countries and races.

Methods: Children aged younger than 18 years with stage 1 ~ 5 CKD were recruited at seven major pediatric nephrology centers in Korea. Blood and urine samples, as well as demographic and clinical data, were collected.

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Article Synopsis
  • X-linked hypophosphatemia (XLH) is a common type of rickets caused by gene mutations, with a study analyzing the effects of these mutations in 81 patients.
  • The research grouped patients into nontruncating and truncating mutation categories and found no significant differences in early symptoms or test results between the two groups.
  • However, over time, patients with truncating mutations had lower phosphate levels, higher rates of nephrocalcinosis, and more frequent orthopedic surgeries than those with nontruncating mutations, suggesting potential genotype-phenotype correlations in disease outcomes.
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Bioimpedance spectroscopy (BIS) is a noninvasive method used to evaluate body fluid volume status in dialysis patients, but reports on its effectiveness in pediatrics are scarce. We investigated the correlation between BIS and clinical characteristics and identified the changes in patients whose dialysis prescription was modified based on BIS. The medical records of children on maintenance dialysis who had undergone BIS between 2017 and 2019 were reviewed.

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The outbreak of Coronavirus Disease 2019 (COVID-19) caused a worldwide pandemic. Less than 6 weeks after the first confirmed cases in Korea, the patient number exceeded 5,000, which overcrowded limited hospital resources and forced confirmed patients to stay at home. To allocate medical resources efficiently, Korea implemented a novel institution for the purpose of treating patients with cohort isolation out of hospital, namely the Community Treatment Center (CTC).

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Background: Acute kidney injury (AKI) is a critical issue in cancer patients because it is not only a morbid complication but also able to interrupt timely diagnostic evaluation or planned optimal treatment. However, the impact of AKI on overall mortality in cancer patients remains unclear.

Methods: We conducted a retrospective cohort study of 67 986 cancer patients, from 2004 to 2013 to evaluate the relationship between AKI and all-cause mortality.

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Objective: To analyze the incidence of acute kidney injury (AKI) in the first year after cancer diagnosis in children and to evaluate the short-term and long-term effects on renal function and proteinuria.

Study Design: Retrospective review of medical records was done on children who were diagnosed and treated for cancer at Seoul National University Hospital between 2004 and 2013. AKI was defined according to the Kidney Disease: Improving Global Outcomes criteria.

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Article Synopsis
  • Recent genetic studies show that Schimmelpenning-Feuerstein-Mims syndrome (SFMS), which features sebaceous nevi, is a mosaic RASopathy caused by mutations in specific genes in some patients.
  • A case report describes a girl with extensive nevus sebaceous and hypophosphatemic rickets, identified as cutaneous skeletal hypophosphatemia syndrome (CSHS), which involved a mutation in the gene found only in her skin tissue.
  • The findings suggest that more research is necessary to understand how Ras activation may contribute to skeletal issues in CSHS, likely linked to overproduction of fibroblast growth factor 23.
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Background: Multicentric carpotarsal osteolysis syndrome (MCTO) is characterized by progressive destruction and disappearance of the carpal and tarsal bones associated with nephropathy. MCTO is caused by loss-of-function mutations in the MAF bZIP transcription factor B (MAFB) gene.

Case Presentation: This report describes three unrelated patients with MAFB mutations, including two male and one female patient.

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