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维生素K环氧化物还原酶复合体亚基1()多态性是结节病中肾结石形成的危险因素吗?

Is a Vitamin K Epoxide Reductase Complex Subunit 1 () Polymorphism a Risk Factor for Nephrolithiasis in Sarcoidosis?

作者信息

Drent Marjolein, Wijnen Petal, Bekers Otto, Bast Aalt

机构信息

ILD Center of Excellence, Department of Respiratory Medicine, St. Antonius Hospital, 3435 CM Nieuwegein, The Netherlands.

Department of Pharmacology and Toxicology, Faculty of Health, Medicine, and Life Science, Maastricht University, 6200 MD Maastricht, The Netherlands.

出版信息

Int J Mol Sci. 2024 Apr 18;25(8):4448. doi: 10.3390/ijms25084448.

Abstract

Sarcoidosis is a systemic inflammatory disorder characterized by granuloma formation in various organs. It has been associated with nephrolithiasis. The vitamin K epoxide reductase complex subunit 1 () gene, which plays a crucial role in vitamin K metabolism, has been implicated in the activation of proteins associated with calcification, including in the forming of nephrolithiasis. This study aimed to investigate the C1173T polymorphism (rs9934438) in a Dutch sarcoidosis cohort, comparing individuals with and without a history of nephrolithiasis. Retrospectively, 424 patients with sarcoidosis were divided into three groups: those with a history of nephrolithiasis (Group I: = 23), those with hypercalcemia without nephrolithiasis (Group II: = 38), and those without nephrolithiasis or hypercalcemia (Group III: = 363). Of the 424 sarcoidosis patients studied, 5.4% had a history of nephrolithiasis (Group I), only two of whom possessed no polymorphisms (OR = 7.73; 95% CI 1.79-33.4; = 0.001). The presence of a C1173T variant allele was found to be a substantial risk factor for the development of nephrolithiasis in sarcoidosis patients. This study provides novel insights into the genetic basis of nephrolithiasis in sarcoidosis patients, identifying C1173T as a potential contributor. Further research is warranted to elucidate the precise mechanisms and explore potential therapeutic interventions based on these genetic findings.

摘要

结节病是一种全身性炎症性疾病,其特征是在各个器官中形成肉芽肿。它与肾结石有关。维生素K环氧化物还原酶复合体亚基1()基因在维生素K代谢中起关键作用,与包括肾结石形成在内的钙化相关蛋白的激活有关。本研究旨在调查荷兰结节病队列中的C1173T多态性(rs9934438),比较有和没有肾结石病史的个体。回顾性地,424例结节病患者被分为三组:有肾结石病史的患者(第一组: = 23)、有高钙血症但无肾结石的患者(第二组: = 38)和无肾结石或高钙血症的患者(第三组: = 363)。在研究的424例结节病患者中,5.4%有肾结石病史(第一组),其中只有两人没有多态性(OR = 7.73;95% CI 1.79 - 33.4; = 0.001)。发现C1173T变异等位基因的存在是结节病患者发生肾结石的一个重要危险因素。本研究为结节病患者肾结石的遗传基础提供了新的见解,确定C1173T为一个潜在因素。有必要进行进一步研究以阐明确切机制,并基于这些遗传发现探索潜在的治疗干预措施。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6637/11050420/fca7037c538f/ijms-25-04448-g001.jpg

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