Chanchlani Rahul, Parekh Rulan S
Division of Pediatric Nephrology, Hospital for Sick Children, Toronto, ON, Canada; Child Health Evaluative Sciences, Research Institute, Hospital for Sick Children, Toronto, ON, Canada; Division of Pediatric Nephrology, McMaster Children's Hospital, Hamilton, ON, Canada.
Division of Pediatric Nephrology, Hospital for Sick Children, Toronto, ON, Canada; Child Health Evaluative Sciences, Research Institute, Hospital for Sick Children, Toronto, ON, Canada; Department of Medicine, Division of Nephrology, University Health Network, Toronto, ON, Canada.
Front Pediatr. 2016 Apr 19;4:39. doi: 10.3389/fped.2016.00039. eCollection 2016.
Nephrotic syndrome is a common glomerular disease in children with significant variability in both incidence and steroid responsiveness among various ethnic groups. The average incidence of nephrotic syndrome is 2-16.9 per 100,000 children worldwide. Understanding the variability by ethnicity may point to potential factors leading to nephrotic syndrome, which remains elusive, and may highlight factors accounting for differences in medication response. The emerging role of genetic factors associated with steroid responsive and steroid-resistant forms of nephrotic syndrome within an ethnic group can provide insight into potential biological mechanisms leading to disease. For example, among African-Americans, the risk variants in APOL1 are associated with a more than 10-fold increase in risk of focal segmental glomerulosclerosis and high-risk carriers have a twofold greater risk of progression to end-stage renal disease. Ongoing collaborative studies should consider capturing data on self-reported ethnicity to understand differences in incidence and outcomes. In the future, the availability of whole-genome data will provide an excellent opportunity for new clinical and translational research in childhood nephrotic syndrome and lead to a better understanding of the disease.
肾病综合征是儿童常见的肾小球疾病,不同种族之间的发病率和类固醇反应性差异很大。全球范围内,肾病综合征的平均发病率为每10万名儿童中有2至16.9例。了解种族差异可能会揭示导致肾病综合征的潜在因素(这些因素仍不明确),并可能突出解释药物反应差异的因素。种族群体中与类固醇反应性和类固醇抵抗性肾病综合征相关的遗传因素的新作用,可以为导致该疾病的潜在生物学机制提供见解。例如,在非裔美国人中,APOL1基因的风险变异与局灶节段性肾小球硬化症的风险增加10倍以上有关,高危携带者进展至终末期肾病的风险则高出两倍。正在进行的合作研究应考虑收集自我报告的种族数据,以了解发病率和预后的差异。未来,全基因组数据的可用性将为儿童肾病综合征的新临床和转化研究提供绝佳机会,并有助于更好地理解该疾病。