Kidney Stones are Prevalent in Individuals with Pseudoxanthoma Elasticum, a Genetic Ectopic Mineralization Disorder.

Douglas Ralph, Rina Allawh, Ian F Terry, Sharon F Terry, Jouni Uitto, Qiaoli Li
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引用次数: 2

Abstract

Pseudoxanthoma elasticum (PXE) is a rare genetic disorder caused by loss-of-function mutations in the ABCC6 gene. While PXE is characterized by ectopic mineralization of connective tissues clinically affecting the skin, eyes, and cardiovascular system, kidney stones were reported in some individuals with PXE. The aim of this study is to determine whether kidney stones are an incidental finding or a frequent manifestation of PXE. We investigated the genetic basis of two siblings diagnosed with PXE. The younger patient presented with recurrent kidney stones since age 8. To address whether kidney stones are associated with PXE, the prevalence of kidney stones in a survey cohort of 563 respondents with PXE was compared to that of a general U.S. population survey, NHANES (National Health and Nutrition Examination Survey), with 28,629 participants. Genetic analysis in both patients identified compound heterozygous mutations in ABCC6, c.2787+1G>T and c.3774_3775insC. The analysis of participants aged 20 and older revealed that 23.4% of PXE patients had previously had a kidney stone, a significant increase compared to 9.2% in the general population. In addition, 17.8% of PXE patients reported their first kidney stone episode before age 18. PXE correlates with an increased risk of developing kidney stones with considerable morbidity and health-care cost.

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肾结石普遍存在于弹性假黄瘤患者,这是一种遗传性异位矿化疾病。
弹性假黄瘤(PXE)是一种罕见的遗传性疾病,由ABCC6基因的功能缺失突变引起。虽然PXE的特点是结缔组织异位矿化,临床上影响皮肤、眼睛和心血管系统,但在一些PXE患者中有肾结石的报道。本研究的目的是确定肾结石是PXE的偶然发现还是常见表现。我们调查了两个被诊断为PXE的兄弟姐妹的遗传基础。年轻的患者自8岁起肾结石复发。为了确定肾结石是否与PXE相关,563名PXE应答者的肾结石患病率与美国普通人口调查NHANES(国家健康与营养检查调查)28,629名参与者的肾结石患病率进行了比较。两例患者的遗传分析均发现ABCC6、c.2787+1G>T和c.3774_3775insC存在复合杂合突变。对20岁及以上参与者的分析显示,23.4%的PXE患者以前患有肾结石,与普通人群的9.2%相比显着增加。此外,17.8%的PXE患者在18岁之前报告了第一次肾结石发作。PXE与患肾结石的风险增加相关,且发病率和保健费用相当高。
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