Literature DB >> 7703383

Characterization of carrier females and affected males with X-linked recessive nephrolithiasis.

S C Reinhart1, A G Norden, M Lapsley, R V Thakker, J Pang, A M Moses, P A Frymoyer, M J Favus, J A Hoepner, S J Scheinman.   

Abstract

X-linked recessive nephrolithiasis (XRN) was described in a large kindred in which nephrolithiasis; proximal tubular dysfunction, proteinuria, nephrocalcinosis, and renal failure occur only in males. Carrier females are asymptomatic, but formal studies of them have not been done. The gene for XRN has been mapped to the pericentromeric region of the X chromosome, close to the loci for several eye disease genes. We studied six affected males, 13 carrier females, and 25 normal members of this family including 7 females whose genetic haplotype predicted them to be carriers. Studies were done in the Clinical Research Unit on a diet containing 400 mg of calcium and 2 g of sodium, and by an additional outpatient urine collection was obtained on a 1-g calcium intake. Hypercalciuria occurred in five of six affected males, 4 of 12 carrier females, and three of seven predicted carriers. Significant proteinuria was present in all affected males and in no other subjects. Low-molecular-weight proteinuria was present in all affected males: the excretion of alpha 1-microglobulin exceeded normal by 3- to 14-fold, of beta 2-microglobulin exceeded normal by 100- to 400-fold, and of retinol-binding protein exceeded normal by 1,000- to 3,000-fold. The excretion of these proteins was less strikingly elevated in carrier females, but the excretion of alpha 1-microglobulin was abnormal in 9 of 15 carriers, beta 2-microglobulin was abnormal in 12 of 15, and retinolbinding protein in was abnormal 12 of 13, and this pattern was similar in predicted carriers. The urinary concentrating ability was abnormal in four affected males with renal insufficiency but normal in all other subjects. Urinary wasting of potassium, phosphorous, and glucose occurred infrequently, and no subject was hypouricemic. Formal ophthalmologic studies were normal in five affected males. Thus, the most consistent urinary abnormalities in XRN are hypercalciuria and low-molecular-weight proteinuria, the latter of which appears to be a marker for the carrier state.

Entities:  

Mesh:

Substances:

Year:  1995        PMID: 7703383     DOI: 10.1681/ASN.V571451

Source DB:  PubMed          Journal:  J Am Soc Nephrol        ISSN: 1046-6673            Impact factor:   10.121


  18 in total

1.  Family history may be misleading in the diagnosis of Dent's disease.

Authors:  F Anglani; P Bernich; E Tosetto; M Cara; A Lupo; F Nalesso; A D'Angelo; G Gambaro
Journal:  Urol Res       Date:  2006-01-14

Review 2.  Kidney stone disease.

Authors:  Fredric L Coe; Andrew Evan; Elaine Worcester
Journal:  J Clin Invest       Date:  2005-10       Impact factor: 14.808

3.  ClC-5, the chloride channel mutated in Dent's disease, colocalizes with the proton pump in endocytotically active kidney cells.

Authors:  W Günther; A Lüchow; F Cluzeaud; A Vandewalle; T J Jentsch
Journal:  Proc Natl Acad Sci U S A       Date:  1998-07-07       Impact factor: 11.205

4.  Dent disease: Same CLCN5 mutation but different phenotypes in two brothers in China.

Authors:  Hongwen Zhang; Fang Wang; Huijie Xiao; Yong Yao
Journal:  Intractable Rare Dis Res       Date:  2017-05

5.  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

6.  Hypercalciuria in patients with CLCN5 mutations.

Authors:  Michael Ludwig; Boris Utsch; Bernd Balluch; Stefan Fründ; Eberhard Kuwertz-Bröking; Arend Bökenkamp
Journal:  Pediatr Nephrol       Date:  2006-06-29       Impact factor: 3.714

7.  On the Origin of Urinary Renin: A Translational Approach.

Authors:  Lodi C W Roksnoer; Bart F J Heijnen; Daisuke Nakano; Janos Peti-Peterdi; Stephen B Walsh; Ingrid M Garrelds; Jeanette M G van Gool; Robert Zietse; Harry A J Struijker-Boudier; Ewout J Hoorn; A H Jan Danser
Journal:  Hypertension       Date:  2016-02-29       Impact factor: 10.190

8.  A patient with nephrotic-range proteinuria and focal global glomerulosclerosis.

Authors:  Fernando C Fervenza
Journal:  Clin J Am Soc Nephrol       Date:  2013-07-25       Impact factor: 8.237

9.  Dent's disease complicated by nephrotic syndrome: A case report.

Authors:  Guohua He; Hongwen Zhang; Shanshan Cao; Huijie Xiao; Yong Yao
Journal:  Intractable Rare Dis Res       Date:  2016-11

Review 10.  Hereditary causes of kidney stones and chronic kidney disease.

Authors:  Vidar O Edvardsson; David S Goldfarb; John C Lieske; Lada Beara-Lasic; Franca Anglani; Dawn S Milliner; Runolfur Palsson
Journal:  Pediatr Nephrol       Date:  2013-01-20       Impact factor: 3.714

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.