Literature DB >> 18758188

The genetics of nephrolithiasis.

John A Sayer1.   

Abstract

Renal stone formation (nephrolithiasis) is a worldwide problem causing substantial morbidity and economic burden. The heritability of stone formation has long been recognized, and with the advent of the genomic era, we have the potential to define the underlying genetic defects. Renal stone formation is multifactorial, with environmental factors interacting with underlying genetic factors. Isolated genetic defects and single gene disorders which lead to stone formation have been valuable in defining renal pathophysiology, but these remain rare diseases. In this review, we examine the genetics of nephrolithiasis by considering the genetic components of defined metabolic risk factors. Hypercalciuria is the most important risk factor for calcium stone formation, although hyperoxaluria, cystinuria and other rarer defects are discussed. It is important to consider the complexity of this condition, and realize that the understanding of the genetic basis of nephrolithiasis is within our grasp. (c) 2008 S. Karger AG, Basel.

Entities:  

Mesh:

Year:  2008        PMID: 18758188     DOI: 10.1159/000151730

Source DB:  PubMed          Journal:  Nephron Exp Nephrol        ISSN: 1660-2129


  13 in total

Review 1.  Urolithiasis as an extraarticular manifestation of ankylosing spondylitis.

Authors:  Cengiz Korkmaz; Döndü Üsküdar Cansu; John A Sayer
Journal:  Rheumatol Int       Date:  2017-08-18       Impact factor: 2.631

2.  Urolithiasis in ankylosing spondylitis: Correlation with Bath ankylosing spondylitis disease activity index (BASDAI), Bath ankylosing spondylitis functional index (BASFI) and Bath ankylosing spondylitis metrology index (BASMI).

Authors:  Sasan Fallahi; Ahmad Reza Jamshidi; Farhad Gharibdoost; Mahdi I Mahmoud; Pedram Paragomi; Mohammad Hossein Nicknam; Elham Farhadi; Mostafa Qorbani
Journal:  Caspian J Intern Med       Date:  2012

3.  Decreased expression of vitamin K epoxide reductase complex subunit 1 in kidney of patients with calcium oxalate urolithiasis.

Authors:  Bo Hu; Tao Wang; Zhuo Liu; Xiaolin Guo; Jun Yang; Jihong Liu; Shaogang Wang; Zhangqun Ye
Journal:  J Huazhong Univ Sci Technolog Med Sci       Date:  2011-12-16

4.  Association of nephrolithiasis and gene for glucose transporter type 9 (SLC2A9): study of 145 patients.

Authors:  Ozren Polasek; Grgo Gunjaca; Ivana Kolcić; Lina Zgaga; Snjezana Dzijan; Robert Smolić; Martina Smolić; Jasminka Milas-Ahić; Vatroslav Serić; Josip Galić; Sandra Tucak-Zorić; Antun Tucak; Igor Rudan; Gordan Lauc
Journal:  Croat Med J       Date:  2010-02       Impact factor: 1.351

Review 5.  Pediatric stone disease.

Authors:  Stacy T Tanaka; John C Pope
Journal:  Curr Urol Rep       Date:  2009-03       Impact factor: 3.092

6.  Association study of DGKH gene polymorphisms with calcium oxalate stone in Chinese population.

Authors:  Yong Xu; Guohua Zeng; Zanlin Mai; Lili Ou
Journal:  Urolithiasis       Date:  2014-08-01       Impact factor: 3.436

7.  Mutations in SLC26A1 Cause Nephrolithiasis.

Authors:  Heon Yung Gee; Ikhyun Jun; Daniela A Braun; Jennifer A Lawson; Jan Halbritter; Shirlee Shril; Caleb P Nelson; Weizhen Tan; Deborah Stein; Ari J Wassner; Michael A Ferguson; Zoran Gucev; John A Sayer; Danko Milosevic; Michelle Baum; Velibor Tasic; Min Goo Lee; Friedhelm Hildebrandt
Journal:  Am J Hum Genet       Date:  2016-05-19       Impact factor: 11.025

Review 8.  Genetic kidney diseases.

Authors:  Friedhelm Hildebrandt
Journal:  Lancet       Date:  2010-04-10       Impact factor: 79.321

Review 9.  Progress in Understanding the Genetics of Calcium-Containing Nephrolithiasis.

Authors:  John A Sayer
Journal:  J Am Soc Nephrol       Date:  2016-12-08       Impact factor: 10.121

10.  Application of a new method for GWAS in a related case/control sample with known pedigree structure: identification of new loci for nephrolithiasis.

Authors:  Silvia Tore; Stefania Casula; Giuseppina Casu; Maria Pina Concas; Paola Pistidda; Ivana Persico; Alessandro Sassu; Giovanni Battista Maestrale; Caterina Mele; Maria Rosa Caruso; Bibiana Bonerba; Paolo Usai; Ivo Deiana; Timothy Thornton; Mario Pirastu; Paola Forabosco
Journal:  PLoS Genet       Date:  2011-01-20       Impact factor: 5.917

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