Batlle Daniel, Moorthi K M L S T, Schlueter William, Kurtzman Neil
Division of Nephrology/Hypertension, Northwestern University Feinberg School of Medicine, Chicago, IL 60611-3008, USA.
Semin Nephrol. 2006 Nov;26(6):471-8. doi: 10.1016/j.semnephrol.2006.12.001.
Severe hypokalemia is a central feature of the classic type of distal renal tubular acidosis (RTA), both in hereditary and acquired forms. In the past decade, many of the genetic defects associated with the hereditary types of distal RTA have been identified and have been the subject of a number of reviews. These genetic advances have expanded our understanding of the molecular mechanisms that lead to distal RTA. In this article, we review data published in the literature on plasma potassium from patients with inherited forms of distal RTA. The degree of hypokalemia varies depending on whether the disease is autosomal autosomal-recessive or dominant, but, interestingly, it occurs in defects caused by mutations in genes encoding the AE-1 exchanger, the carbonic anhydrase II gene, and genes encoding different subunits of the H+ adenosine triphosphatase. This shows that a unique defect involving the H+/K+-adenosine triphosphatase leading to renal potassium wastage cannot explain the hypokalemia seen in virtually all types of classic distal RTA.
严重低钾血症是经典型远端肾小管酸中毒(RTA)的核心特征,无论是遗传性还是获得性形式。在过去十年中,许多与遗传性远端RTA相关的基因缺陷已被识别,并且成为多篇综述的主题。这些遗传学进展扩展了我们对导致远端RTA的分子机制的理解。在本文中,我们回顾了文献中发表的关于遗传性远端RTA患者血浆钾的资料。低钾血症的程度因疾病是常染色体隐性还是显性而有所不同,但有趣的是,它发生在由编码AE-1交换体的基因突变、碳酸酐酶II基因以及编码H+三磷酸腺苷酶不同亚基的基因突变所导致的缺陷中。这表明,涉及H+/K+-三磷酸腺苷酶导致肾脏钾流失的独特缺陷并不能解释几乎所有类型经典远端RTA中出现的低钾血症。