Literature DB >> 23349334

Simultaneous sequencing of 24 genes associated with steroid-resistant nephrotic syndrome.

Hugh J McCarthy1, Agnieszka Bierzynska, Matt Wherlock, Milos Ognjanovic, Larissa Kerecuk, Shivaram Hegde, Sally Feather, Rodney D Gilbert, Leah Krischock, Caroline Jones, Manish D Sinha, Nicholas J A Webb, Martin Christian, Margaret M Williams, Stephen Marks, Ania Koziell, Gavin I Welsh, Moin A Saleem.   

Abstract

BACKGROUND AND OBJECTIVES: Up to 95% of children presenting with steroid-resistant nephrotic syndrome in early life will have a pathogenic single-gene mutation in 1 of 24 genes currently associated with this disease. Others may be affected by polymorphic variants. There is currently no accepted diagnostic algorithm for clinical genetic testing. The hypothesis was that the increasing reliability of next generation sequencing allows comprehensive one-step genetic investigation of this group and similar patient groups. DESIGN, SETTING, PARTICIPANTS, & MEASUREMENTS: This study used next generation sequencing to screen 446 genes, including the 24 genes known to be associated with hereditary steroid-resistant nephrotic syndrome. The first 36 pediatric patients collected through a national United Kingdom Renal Registry were chosen with comprehensive phenotypic detail. Significant variants detected by next generation sequencing were confirmed by conventional Sanger sequencing.
RESULTS: Analysis revealed known and novel disease-associated variations in expected genes such as NPHS1, NPHS2, and PLCe1 in 19% of patients. Phenotypically unexpected mutations were also detected in COQ2 and COL4A4 in two patients with isolated nephropathy and associated sensorineural deafness, respectively. The presence of an additional heterozygous polymorphism in WT1 in a patient with NPHS1 mutation was associated with earlier-onset disease, supporting modification of phenotype through genetic epistasis.
CONCLUSIONS: This study shows that next generation sequencing analysis of pediatric steroid-resistant nephrotic syndrome patients is accurate and revealing. This analysis should be considered part of the routine genetic workup of diseases such as childhood steroid-resistant nephrotic syndrome, where the chance of genetic mutation is high but requires sequencing of multiple genes.

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Year:  2013        PMID: 23349334      PMCID: PMC3613958          DOI: 10.2215/CJN.07200712

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


  30 in total

1.  Novel mutations in NPHS2 detected in both familial and sporadic steroid-resistant nephrotic syndrome.

Authors:  Stephanie M Karle; Barbara Uetz; Vera Ronner; Lisa Glaeser; Friedhelm Hildebrandt; Arno Fuchshuber
Journal:  J Am Soc Nephrol       Date:  2002-02       Impact factor: 10.121

2.  INF2 Is a WASP homology 2 motif-containing formin that severs actin filaments and accelerates both polymerization and depolymerization.

Authors:  Ekta Seth Chhabra; Henry N Higgs
Journal:  J Biol Chem       Date:  2006-07-03       Impact factor: 5.157

3.  Mutational analysis of the PLCE1 gene in steroid resistant nephrotic syndrome.

Authors:  Olivia Boyer; Geneviève Benoit; Olivier Gribouval; Fabien Nevo; Audrey Pawtowski; Ilmay Bilge; Zelal Bircan; Georges Deschênes; Lisa M Guay-Woodford; Michelle Hall; Marie-Alice Macher; Kenza Soulami; Constantinos J Stefanidis; Robert Weiss; Chantal Loirat; Marie-Claire Gubler; Corinne Antignac
Journal:  J Med Genet       Date:  2010-07       Impact factor: 6.318

4.  Arhgap24 inactivates Rac1 in mouse podocytes, and a mutant form is associated with familial focal segmental glomerulosclerosis.

Authors:  Shreeram Akilesh; Hani Suleiman; Haiyang Yu; M Christine Stander; Peter Lavin; Rasheed Gbadegesin; Corinne Antignac; Martin Pollak; Jeffrey B Kopp; Michelle P Winn; Andrey S Shaw
Journal:  J Clin Invest       Date:  2011-09-12       Impact factor: 14.808

5.  Genotype/phenotype correlations of NPHS1 and NPHS2 mutations in nephrotic syndrome advocate a functional inter-relationship in glomerular filtration.

Authors:  Ania Koziell; Victor Grech; Sagair Hussain; Gary Lee; Ulla Lenkkeri; Karl Tryggvason; Peter Scambler
Journal:  Hum Mol Genet       Date:  2002-02-15       Impact factor: 6.150

6.  Schimke immunoosseous dysplasia: suggestions of genetic diversity.

Authors:  J Marietta Clewing; Helen Fryssira; David Goodman; Sarah F Smithson; Emily A Sloan; Shu Lou; Yan Huang; Kunho Choi; Thomas Lücke; Harika Alpay; Jean-Luc André; Yumi Asakura; Nathalie Biebuyck-Gouge; Radovan Bogdanovic; Dominique Bonneau; Caterina Cancrini; Pierre Cochat; Sandra Cockfield; Laure Collard; Isabel Cordeiro; Valerie Cormier-Daire; Karlien Cransberg; Karel Cutka; Georges Deschenes; Jochen H H Ehrich; Stefan Fründ; Helen Georgaki; Encarna Guillen-Navarro; Barbara Hinkelmann; Maria Kanariou; Belde Kasap; Sara Sebnem Kilic; Guiliana Lama; Petra Lamfers; Chantal Loirat; Silvia Majore; David Milford; Denis Morin; Nihal Ozdemir; Bertram F Pontz; Willem Proesmans; Stavroula Psoni; Herbert Reichenbach; Silke Reif; Cristina Rusu; Jorge M Saraiva; Onur Sakallioglu; Beate Schmidt; Lawrence Shoemaker; Sabine Sigaudy; Graham Smith; Flora Sotsiou; Natasa Stajic; Anja Stein; Asbjørg Stray-Pedersen; Doris Taha; Sophie Taque; Jane Tizard; Michel Tsimaratos; Newton A C S Wong; Cornelius F Boerkoel
Journal:  Hum Mutat       Date:  2007-03       Impact factor: 4.878

7.  UK Renal Registry 13th Annual Report (December 2010): Chapter 5: demography of the UK paediatric renal replacement therapy population in 2009.

Authors:  Manish D Sinha; Clare Castledine; Dirk van Schalkwyk; Farida Hussain; Malcolm Lewis; Carol Inward
Journal:  Nephron Clin Pract       Date:  2011-08-26

8.  Clinical and epidemiological assessment of steroid-resistant nephrotic syndrome associated with the NPHS2 R229Q variant.

Authors:  Eduardo Machuca; Aurélie Hummel; Fabien Nevo; Jacques Dantal; Frank Martinez; Essam Al-Sabban; Véronique Baudouin; Laurent Abel; Jean-Pierre Grünfeld; Corinne Antignac
Journal:  Kidney Int       Date:  2009-01-14       Impact factor: 10.612

9.  Bigenic heterozygosity and the development of steroid-resistant focal segmental glomerulosclerosis.

Authors:  Marije Löwik; Elena Levtchenko; Dineke Westra; Patricia Groenen; Eric Steenbergen; Jan Weening; Marc Lilien; Leo Monnens; Lambert van den Heuvel
Journal:  Nephrol Dial Transplant       Date:  2008-04-28       Impact factor: 5.992

10.  MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness.

Authors:  Marco Seri; Alessandro Pecci; Filomena Di Bari; Roberto Cusano; Maria Savino; Emanuele Panza; Alessandra Nigro; Patrizia Noris; Simone Gangarossa; Bianca Rocca; Paolo Gresele; Nicola Bizzaro; Paola Malatesta; Pasi A Koivisto; Ilaria Longo; Roberto Musso; Carmine Pecoraro; Achille Iolascon; Umberto Magrini; Juan Rodriguez Soriano; Alessandra Renieri; Gian Marco Ghiggeri; Roberto Ravazzolo; Carlo L Balduini; Anna Savoia
Journal:  Medicine (Baltimore)       Date:  2003-05       Impact factor: 1.889

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  83 in total

1.  Improving mutation screening in familial hematuric nephropathies through next generation sequencing.

Authors:  Vincent Morinière; Karin Dahan; Pascale Hilbert; Marieline Lison; Said Lebbah; Alexandra Topa; Christine Bole-Feysot; Solenn Pruvost; Patrick Nitschke; Emmanuelle Plaisier; Bertrand Knebelmann; Marie-Alice Macher; Laure-Hélène Noel; Marie-Claire Gubler; Corinne Antignac; Laurence Heidet
Journal:  J Am Soc Nephrol       Date:  2014-05-22       Impact factor: 10.121

2.  Retrospective mutational analysis of NPHS1, NPHS2, WT1 and LAMB2 in children with steroid-resistant focal segmental glomerulosclerosis - a single-centre experience.

Authors:  Agnieszka Bińczak-Kuleta; Jacek Rubik; Mieczysław Litwin; Małgorzata Ryder; Klaudyna Lewandowska; Olga Taryma-Leśniak; Jeremy S Clark; Ryszard Grenda; Andrzej Ciechanowicz
Journal:  Bosn J Basic Med Sci       Date:  2014-05       Impact factor: 3.363

3.  Heterogeneous genetic alterations in sporadic nephrotic syndrome associate with resistance to immunosuppression.

Authors:  Sabrina Giglio; Aldesia Provenzano; Benedetta Mazzinghi; Francesca Becherucci; Laura Giunti; Giulia Sansavini; Fiammetta Ravaglia; Rosa Maria Roperto; Silvia Farsetti; Elisa Benetti; Mario Rotondi; Luisa Murer; Elena Lazzeri; Laura Lasagni; Marco Materassi; Paola Romagnani
Journal:  J Am Soc Nephrol       Date:  2014-07-24       Impact factor: 10.121

4.  GeneVetter: a web tool for quantitative monogenic assessment of rare diseases.

Authors:  Christopher E Gillies; Catherine C Robertson; Matthew G Sampson; Hyun Min Kang
Journal:  Bioinformatics       Date:  2015-07-23       Impact factor: 6.937

Review 5.  Genetic causes of proteinuria and nephrotic syndrome: impact on podocyte pathobiology.

Authors:  Oleh Akchurin; Kimberly J Reidy
Journal:  Pediatr Nephrol       Date:  2014-03-02       Impact factor: 3.714

6.  Mutations in EMP2 cause childhood-onset nephrotic syndrome.

Authors:  Heon Yung Gee; Shazia Ashraf; Xiaoyang Wan; Virginia Vega-Warner; Julian Esteve-Rudd; Svjetlana Lovric; Humphrey Fang; Toby W Hurd; Carolin E Sadowski; Susan J Allen; Edgar A Otto; Emine Korkmaz; Joseph Washburn; Shawn Levy; David S Williams; Sevcan A Bakkaloglu; Anna Zolotnitskaya; Fatih Ozaltin; Weibin Zhou; Friedhelm Hildebrandt
Journal:  Am J Hum Genet       Date:  2014-05-08       Impact factor: 11.025

7.  Novel NPHS2 variant in patients with familial steroid-resistant nephrotic syndrome with early onset, slow progression and dominant inheritance pattern.

Authors:  Maija Suvanto; Jaakko Patrakka; Timo Jahnukainen; Pia-Maria Sjöström; Matti Nuutinen; Pekka Arikoski; Janne Kataja; Marjo Kestilä; Hannu Jalanko
Journal:  Clin Exp Nephrol       Date:  2016-08-29       Impact factor: 2.801

Review 8.  Treatment of steroid-resistant nephrotic syndrome in the genomic era.

Authors:  Adam R Bensimhon; Anna E Williams; Rasheed A Gbadegesin
Journal:  Pediatr Nephrol       Date:  2018-10-02       Impact factor: 3.714

9.  Altered expression of Crb2 in podocytes expands a variation of CRB2 mutations in steroid-resistant nephrotic syndrome.

Authors:  Tomohiro Udagawa; Tohaku Jo; Takeshi Yanagihara; Akira Shimizu; Jun Mitsui; Shoji Tsuji; Shinichi Morishita; Reiko Onai; Kenichiro Miura; Shoichiro Kanda; Yuko Kajiho; Haruko Tsurumi; Akira Oka; Motoshi Hattori; Yutaka Harita
Journal:  Pediatr Nephrol       Date:  2016-12-10       Impact factor: 3.714

Review 10.  Genetic bases and clinical manifestations of coenzyme Q10 (CoQ 10) deficiency.

Authors:  Maria Andrea Desbats; Giada Lunardi; Mara Doimo; Eva Trevisson; Leonardo Salviati
Journal:  J Inherit Metab Dis       Date:  2014-08-05       Impact factor: 4.982

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