Institute of Physiology, University of Zurich, Zurich, Switzerland; and
Institute for Biomedicine, Eurac Research, Affiliated Institute of the University of Lübeck, Bolzano, Italy.
J Am Soc Nephrol. 2018 Mar;29(3):713-726. doi: 10.1681/ASN.2017070716. Epub 2017 Nov 27.
The identification of genetic factors associated with kidney disease has the potential to provide critical insights into disease mechanisms. Genome-wide association studies have uncovered genomic regions associated with renal function metrics and risk of CKD. is among the most outstanding loci associated with CKD in the general population, because it has a large effect on eGFR and CKD risk that is consistent across different ethnic groups. The relevance of for CKD is clear, because the encoded protein, uromodulin (Tamm-Horsfall protein), is exclusively produced by the kidney tubule and has specific biochemical properties that mediate important functions in the kidney and urine. Rare mutations in are the major cause of autosomal dominant tubulointerstitial kidney disease, a condition that leads to CKD and ESRD. In this brief review, we use the paradigm to describe how population genetic studies can yield insight into the pathogenesis and prognosis of kidney diseases.
与肾脏疾病相关的遗传因素的鉴定有可能为疾病机制提供重要的见解。全基因组关联研究已经揭示了与肾功能指标和 CKD 风险相关的基因组区域。 UMOD 是与普通人群中 CKD 相关的最显著的基因座之一,因为它对 eGFR 和 CKD 风险的影响在不同的种族群体中是一致的。UMOD 对于 CKD 的相关性是明确的,因为其编码的蛋白,尿调蛋白(Tamm-Horsfall 蛋白),是由肾小管专门产生的,具有特定的生化特性,介导肾脏和尿液中的重要功能。 UMOD 中的罕见突变是常染色体显性遗传性肾小管间质性肾病的主要原因,这种疾病会导致 CKD 和终末期肾病。在这篇简短的综述中,我们使用 UMOD 范例来描述群体遗传学研究如何深入了解肾脏疾病的发病机制和预后。