Literature DB >> 17687260

Genetics of hypercalciuric stone forming diseases.

O Devuyst1, Y Pirson.   

Abstract

With a lifetime incidence of up to 12% in man and 6% in woman, nephrolithiasis is a major health problem worldwide. Approximately, 80% of kidney stones are composed of calcium and hypercalciuria is found in up to 40% of stone-formers. Although the mechanisms resulting in precipitation and growth of calcium crystals in the urinary tract are multiple and not fully understood, hypercalciuria per se is recognized as an important and reversible risk factor in stone formation. In this brief review, we summarize the studies assessing the heritability of hypercalciuria and pinpoint recently identified human genetic disorders as well as relevant animal models that provided new insights into the segment-specific tubular handling of calcium and the pathophysiology of renal hypercalciuria and kidney stones. We also discuss novel strategies that may help to unravel the genetic bases of such complex conditions.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17687260     DOI: 10.1038/sj.ki.5002441

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  32 in total

Review 1.  The tubular epithelium in the initiation and course of intratubular nephrocalcinosis.

Authors:  Benjamin A Vervaet; Anja Verhulst; Marc E De Broe; Patrick C D'Haese
Journal:  Urol Res       Date:  2010-08-02

2.  Family history influences clinical course of idiopathic calcium nephrolithiasis: case-control study of a large cohort of Italian patients.

Authors:  Angela Guerra; Giuseppina Folesani; Antonio Nouvenne; Andrea Ticinesi; Franca Allegri; Silvana Pinelli; Beatrice Prati; Ilaria Morelli; Loredana Guida; Rosalia Aloe; Tiziana Meschi
Journal:  J Nephrol       Date:  2015-08-22       Impact factor: 3.902

Review 3.  Nephrolithiasis.

Authors:  Elaine M Worcester; Fredric L Coe
Journal:  Prim Care       Date:  2008-06       Impact factor: 2.907

4.  Suppression of intestinal calcium entry channel TRPV6 by OCRL, a lipid phosphatase associated with Lowe syndrome and Dent disease.

Authors:  Guojin Wu; Wei Zhang; Tao Na; Haiyan Jing; Hongju Wu; Ji-Bin Peng
Journal:  Am J Physiol Cell Physiol       Date:  2012-02-29       Impact factor: 4.249

Review 5.  Pediatric stone disease.

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

Review 6.  Genetic basis of renal cellular dysfunction and the formation of kidney stones.

Authors:  Saeed R Khan; Benjamin K Canales
Journal:  Urol Res       Date:  2009-06-11

Review 7.  Herbal medicines in the management of urolithiasis: alternative or complementary?

Authors:  Veronika Butterweck; Saeed R Khan
Journal:  Planta Med       Date:  2009-05-14       Impact factor: 3.352

Review 8.  History, epidemiology and regional diversities of urolithiasis.

Authors:  Michelle López; Bernd Hoppe
Journal:  Pediatr Nephrol       Date:  2010-01       Impact factor: 3.714

Review 9.  Dent's disease.

Authors:  Olivier Devuyst; Rajesh V Thakker
Journal:  Orphanet J Rare Dis       Date:  2010-10-14       Impact factor: 4.123

10.  Dissecting the genetic basis of kidney tubule response to hyperoxaluria using chromosome substitution strains.

Authors:  John H Wiessner; Michael R Garrett; Richard J Roman; Neil S Mandel
Journal:  Am J Physiol Renal Physiol       Date:  2009-06-03
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.