New prognostic markers for IgA nephropathy in children.

IF 2.6 3区 医学 Q1 PEDIATRICS
Chiara Casuscelli, Elisa Longhitano, Giovanni Conti, Veronica Maressa, Silvia Di Carlo, Claudia Spinella, Luigi Peritore, Vincenzo Calabrese, Domenico Santoro
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Abstract

IgA nephropathy (IgAN) is the most common glomerulonephritis worldwide, with significant implications for adults and children. The disease progresses variably, from asymptomatic hematuria to severe glomerulonephritis, and around 10-20% of children diagnosed in childhood develop stage 5 chronic kidney disease (CKD 5) within 20 years. Identifying reliable prognostic markers is crucial for early intervention and long-term management. The International IgAN Prediction Tool combines clinical, laboratory, and histological data and has been adapted for pediatric use. It is highly accurate in predicting CKD 5. Markers such as the Oxford MEST-C score, proteinuria, eGFR, and blood pressure assist in risk stratification. Emerging biomarkers, including the IgA/C3 ratio, galactose-deficient IgA1, soluble CD89, and urinary cytokines like IL-6 and TGF-β1, show potential for predicting disease progression. Although promising, further research is needed to validate these biomarkers in pediatric populations and refine predictive tools for IgAN progression. These advances will guide targeted therapies and improve long-term renal outcomes in children.

儿童IgA肾病的新预后指标。
IgA肾病(IgAN)是世界范围内最常见的肾小球肾炎,对成人和儿童都有重要影响。从无症状血尿到严重的肾小球肾炎,该疾病的进展是可变的,大约10-20%在儿童期诊断的儿童在20年内发展为5期慢性肾脏疾病(CKD 5)。确定可靠的预后标记对于早期干预和长期管理至关重要。国际IgAN预测工具结合了临床、实验室和组织学数据,并已适应儿科使用。预测ckd5的准确度高。诸如牛津大学MEST-C评分、蛋白尿、eGFR和血压等标志物有助于风险分层。新兴的生物标志物,包括IgA/C3比值、半乳糖缺乏的IgA1、可溶性CD89和尿细胞因子如IL-6和TGF-β1,显示出预测疾病进展的潜力。虽然很有希望,但需要进一步的研究来验证这些生物标志物在儿科人群中的有效性,并完善IgAN进展的预测工具。这些进展将指导靶向治疗并改善儿童肾脏的长期预后。
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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来源期刊
Pediatric Nephrology
Pediatric Nephrology 医学-泌尿学与肾脏学
CiteScore
4.70
自引率
20.00%
发文量
465
审稿时长
1 months
期刊介绍: International Pediatric Nephrology Association Pediatric Nephrology publishes original clinical research related to acute and chronic diseases that affect renal function, blood pressure, and fluid and electrolyte disorders in children. Studies may involve medical, surgical, nutritional, physiologic, biochemical, genetic, pathologic or immunologic aspects of disease, imaging techniques or consequences of acute or chronic kidney disease. There are 12 issues per year that contain Editorial Commentaries, Reviews, Educational Reviews, Original Articles, Brief Reports, Rapid Communications, Clinical Quizzes, and Letters to the Editors.
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