Literature DB >> 20448065

Identification of GDNF gene sequence variations in patients with medullary sponge kidney disease.

Rossella Torregrossa1, Franca Anglani, Antonia Fabris, Alessia Gozzini, Annalisa Tanini, Dorella Del Prete, Rosalba Cristofaro, Lina Artifoni, Cataldo Abaterusso, Nicola Marchionna, Antonio Lupo, Angela D'Angelo, Giovanni Gambaro.   

Abstract

BACKGROUND AND OBJECTIVES: Medullary sponge kidney (MSK) is a rare nephropathy characterized by cystic anomalies of precalyceal ducts, nephrocalcinosis, renal stones, and tubule dysfunctions. Its association with various malformations and cases of familial aggregation supports the conviction that genetic factors are involved, but no genetic studies have been conducted to date. It is hypothesized that MSK is due to a disruption at the "ureteric bud/metanephric blastema" interface caused by critical developmental genes functioning abnormally. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: Fifty-five apparently sporadic MSK patients were analyzed by direct DNA sequencing of all exons and exon-intron boundaries of glial cell-derived neurotrophic factor (GDNF) gene and rearranged during transfection (RET) gene, which have a leading role in renal development.
RESULTS: Two novel variants were found in heterozygosity in the MSK case population: GDNF{ENST00000344622}:c.-45G>C and c.-27+18G>A in a putative binding domain for paired-box 2 transcription factor. As a whole, eight patients showed these variations: four patients carried the c.[-45G>C; -27+18G>A] complex allele, and the others had the c.-27+18G>A alone. A case-control study revealed that these two alleles were significantly associated with MSK. Five of the eight cases were found to be familial, and the allele variants cosegregated with the disease in a seemingly dominant pattern of inheritance. Patients revealed no mutations in the RET gene.
CONCLUSIONS: This is the first report identifying GDNF gene sequence variations in patients with MSK and suggesting a role for this gene in the pathogenesis of some cases of the disease.

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Year:  2010        PMID: 20448065      PMCID: PMC2893072          DOI: 10.2215/CJN.07551009

Source DB:  PubMed          Journal:  Clin J Am Soc Nephrol        ISSN: 1555-9041            Impact factor:   8.237


  23 in total

Review 1.  Medullary sponge kidney (Lenarduzzi-Cacchi-Ricci disease): a Padua Medical School discovery in the 1930s.

Authors:  G Gambaro; G P Feltrin; A Lupo; L Bonfante; A D'Angelo; A Antonello
Journal:  Kidney Int       Date:  2006-02       Impact factor: 10.612

2.  Renal agenesis and the absence of enteric neurons in mice lacking GDNF.

Authors:  M P Sánchez; I Silos-Santiago; J Frisén; B He; S A Lira; M Barbacid
Journal:  Nature       Date:  1996-07-04       Impact factor: 49.962

3.  An unusual association of contralateral congenital small kidney, reduced renal function and hyperparathyroidism in sponge kidney patients: on the track of the molecular basis.

Authors:  Giovanni Gambaro; Antonia Fabris; Lorenzo Citron; Enrica Tosetto; Franca Anglani; Francesco Bellan; Marilena Conte; Luciana Bonfante; Antonio Lupo; Angela D'Angelo
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4.  Glial cell line-derived neurotrophic factor (GDNF) is expressed in the human kidney and is a growth factor for human mesangial cells.

Authors:  S R Orth; E Ritz; C Suter-Crazzolara
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5.  Medullary sponge kidney in three generations.

Authors:  J J Kuiper
Journal:  N Y State J Med       Date:  1971-11

6.  Medullary sponge kidney associated with distal renal tubular acidosis in a 5-year-old girl.

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7.  Common variants of the glial cell-derived neurotrophic factor gene do not influence kidney size of the healthy newborn.

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8.  GDNF is expressed in two forms in many tissues outside the CNS.

Authors:  C Suter-Crazzolara; K Unsicker
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9.  Defects in the kidney and enteric nervous system of mice lacking the tyrosine kinase receptor Ret.

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10.  Renal aplasia in humans is associated with RET mutations.

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4.  New non-renal congenital disorders associated with medullary sponge kidney (MSK) support the pathogenic role of GDNF and point to the diagnosis of MSK in recurrent stone formers.

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6.  Spontaneous calcification process in primary renal cells from a medullary sponge kidney patient harbouring a GDNF mutation.

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9.  Efficacy of Multi-Detector Computed Tomography for the Diagnosis of Medullary Sponge Kidney.

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Review 10.  Recent advances in managing and understanding nephrolithiasis/nephrocalcinosis.

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