Clinical and Molecular Characterization of Patients with Heterozygous Mutations in Wilms Tumor Suppressor Gene 1
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Clinical and Molecular Characterization of Patients with Heterozygous Mutations in Wilms Tumor Suppressor Gene 1. / Lehnhardt, Anja; Karnatz, Nadia; Ahlenstiel-Grunow, Thurid; Benz, Kerstin; Benz, Marcus R; Budde, Klemens; Büscher, Anja K; Fehr, Thomas; Feldkötter, Markus; Graf, Norbert; Höcker, Britta; Jungraithmayr, Therese; Klaus, Günter; Koehler, Birgit; Konrad, Martin; Kranz, Birgitta; Montoya, Carmen R; Müller, Dominik; Neuhaus, Thomas J; Oh, Jun; Pape, Lars; Pohl, Martin; Royer-Pokora, Brigitte; Querfeld, Uwe; Schneppenheim, Reinhard; Staude, Hagen; Spartà, Giuseppina; Timmermann, Kirsten; Wilkening, Frauke; Wygoda, Simone; Bergmann, Carsten; Kemper, Markus J.
In: CLIN J AM SOC NEPHRO, Vol. 10, No. 5, 07.05.2015, p. 825-831.Research output: SCORING: Contribution to journal › SCORING: Journal article › Research › peer-review
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TY - JOUR
T1 - Clinical and Molecular Characterization of Patients with Heterozygous Mutations in Wilms Tumor Suppressor Gene 1
AU - Lehnhardt, Anja
AU - Karnatz, Nadia
AU - Ahlenstiel-Grunow, Thurid
AU - Benz, Kerstin
AU - Benz, Marcus R
AU - Budde, Klemens
AU - Büscher, Anja K
AU - Fehr, Thomas
AU - Feldkötter, Markus
AU - Graf, Norbert
AU - Höcker, Britta
AU - Jungraithmayr, Therese
AU - Klaus, Günter
AU - Koehler, Birgit
AU - Konrad, Martin
AU - Kranz, Birgitta
AU - Montoya, Carmen R
AU - Müller, Dominik
AU - Neuhaus, Thomas J
AU - Oh, Jun
AU - Pape, Lars
AU - Pohl, Martin
AU - Royer-Pokora, Brigitte
AU - Querfeld, Uwe
AU - Schneppenheim, Reinhard
AU - Staude, Hagen
AU - Spartà, Giuseppina
AU - Timmermann, Kirsten
AU - Wilkening, Frauke
AU - Wygoda, Simone
AU - Bergmann, Carsten
AU - Kemper, Markus J
N1 - Copyright © 2015 by the American Society of Nephrology.
PY - 2015/5/7
Y1 - 2015/5/7
N2 - BACKGROUND AND OBJECTIVES: The Wilms tumor suppressor gene 1 (WT1) plays an essential role in urogenital and kidney development. Genotype/phenotype correlations of WT1 mutations with renal function and proteinuria have been observed in world-wide cohorts with nephrotic syndrome or Wilms tumor (WT). This study analyzed mid-European patients with known constitutional heterozygous mutations in WT1, including patients without proteinuria or WT.DESIGN, SETTING, PARTICIPANTS & MEASUREMENTS: Retrospective analysis of genotype, phenotype, and treatment of 53 patients with WT1 mutation from all pediatric nephrology centers in Germany, Austria, and Switzerland performed from 2010 to 2012.RESULTS: Median age was 12.4 (interquartile range [IQR], 6-19) years. Forty-four of 53 (83%) patients had an exon mutation (36 missense, eight truncating), and nine of 53 (17%) had an intronic lysine-threonine-serine (KTS) splice site mutation. Fifty of 53 patients (94%) had proteinuria, which occurred at an earlier age in patients with missense mutations (0.6 [IQR, 0.1-1.5] years) than in those with truncating (9.7 [IQR, 5.7-11.9]; P<0.001) and splice site (4.0 [IQR, 2.6-6.6]; P=0.004) mutations. Thirteen of 50 (26%) were treated with steroids and remained irresponsive, while three of five partially responded to cyclosporine A. Seventy-three percent of all patients required RRT, those with missense mutations significantly earlier (at 1.1 [IQR, 0.01-9.3] years) than those with truncating mutations (16.5 [IQR, 16.5-16.8]; P<0.001) and splice site mutations (12.3 [IQR, 7.9-18.2]; P=0.002). Diffuse mesangial sclerosis was restricted to patients with missense mutations, while focal segmental sclerosis occurred in all groups. WT occurred only in patients with exon mutations (n=19). Fifty of 53 (94%) patients were karyotyped: Thirty-one (62%) had XY and 19 (38%) had XX chromosomes, and 96% of male karyotypes had urogenital malformations.CONCLUSIONS: Type and location of WT1 mutations have predictive value for the development of proteinuria, renal insufficiency, and WT. XY karyotype was more frequent and associated with urogenital malformations in most cases.
AB - BACKGROUND AND OBJECTIVES: The Wilms tumor suppressor gene 1 (WT1) plays an essential role in urogenital and kidney development. Genotype/phenotype correlations of WT1 mutations with renal function and proteinuria have been observed in world-wide cohorts with nephrotic syndrome or Wilms tumor (WT). This study analyzed mid-European patients with known constitutional heterozygous mutations in WT1, including patients without proteinuria or WT.DESIGN, SETTING, PARTICIPANTS & MEASUREMENTS: Retrospective analysis of genotype, phenotype, and treatment of 53 patients with WT1 mutation from all pediatric nephrology centers in Germany, Austria, and Switzerland performed from 2010 to 2012.RESULTS: Median age was 12.4 (interquartile range [IQR], 6-19) years. Forty-four of 53 (83%) patients had an exon mutation (36 missense, eight truncating), and nine of 53 (17%) had an intronic lysine-threonine-serine (KTS) splice site mutation. Fifty of 53 patients (94%) had proteinuria, which occurred at an earlier age in patients with missense mutations (0.6 [IQR, 0.1-1.5] years) than in those with truncating (9.7 [IQR, 5.7-11.9]; P<0.001) and splice site (4.0 [IQR, 2.6-6.6]; P=0.004) mutations. Thirteen of 50 (26%) were treated with steroids and remained irresponsive, while three of five partially responded to cyclosporine A. Seventy-three percent of all patients required RRT, those with missense mutations significantly earlier (at 1.1 [IQR, 0.01-9.3] years) than those with truncating mutations (16.5 [IQR, 16.5-16.8]; P<0.001) and splice site mutations (12.3 [IQR, 7.9-18.2]; P=0.002). Diffuse mesangial sclerosis was restricted to patients with missense mutations, while focal segmental sclerosis occurred in all groups. WT occurred only in patients with exon mutations (n=19). Fifty of 53 (94%) patients were karyotyped: Thirty-one (62%) had XY and 19 (38%) had XX chromosomes, and 96% of male karyotypes had urogenital malformations.CONCLUSIONS: Type and location of WT1 mutations have predictive value for the development of proteinuria, renal insufficiency, and WT. XY karyotype was more frequent and associated with urogenital malformations in most cases.
U2 - 10.2215/CJN.10141014
DO - 10.2215/CJN.10141014
M3 - SCORING: Journal article
C2 - 25818337
VL - 10
SP - 825
EP - 831
JO - CLIN J AM SOC NEPHRO
JF - CLIN J AM SOC NEPHRO
SN - 1555-9041
IS - 5
ER -