Literature DB >> 30586318

Diagnostic Utility of Exome Sequencing for Kidney Disease.

Emily E Groopman1, Maddalena Marasa1, Sophia Cameron-Christie1, Slavé Petrovski1, Vimla S Aggarwal1, Hila Milo-Rasouly1, Yifu Li1, Junying Zhang1, Jordan Nestor1, Priya Krithivasan1, Wan Yee Lam1, Adele Mitrotti1, Stacy Piva1, Byum H Kil1, Debanjana Chatterjee1, Rachel Reingold1, Drew Bradbury1, Michael DiVecchia1, Holly Snyder1, Xueru Mu1, Karla Mehl1, Olivia Balderes1, David A Fasel1, Chunhua Weng1, Jai Radhakrishnan1, Pietro Canetta1, Gerald B Appel1, Andrew S Bomback1, Wooin Ahn1, Natalie S Uy1, Shumyle Alam1, David J Cohen1, Russell J Crew1, Geoffrey K Dube1, Maya K Rao1, Sitharthan Kamalakaran1, Brett Copeland1, Zhong Ren1, Joshua Bridgers1, Colin D Malone1, Caroline M Mebane1, Neha Dagaonkar1, Bengt C Fellström1, Carolina Haefliger1, Sumit Mohan1, Simone Sanna-Cherchi1, Krzysztof Kiryluk1, Jan Fleckner1, Ruth March1, Adam Platt1, David B Goldstein1, Ali G Gharavi1.   

Abstract

BACKGROUND: Exome sequencing is emerging as a first-line diagnostic method in some clinical disciplines, but its usefulness has yet to be examined for most constitutional disorders in adults, including chronic kidney disease, which affects more than 1 in 10 persons globally.
METHODS: We conducted exome sequencing and diagnostic analysis in two cohorts totaling 3315 patients with chronic kidney disease. We assessed the diagnostic yield and, among the patients for whom detailed clinical data were available, the clinical implications of diagnostic and other medically relevant findings.
RESULTS: In all, 3037 patients (91.6%) were over 21 years of age, and 1179 (35.6%) were of self-identified non-European ancestry. We detected diagnostic variants in 307 of the 3315 patients (9.3%), encompassing 66 different monogenic disorders. Of the disorders detected, 39 (59%) were found in only a single patient. Diagnostic variants were detected across all clinically defined categories, including congenital or cystic renal disease (127 of 531 patients [23.9%]) and nephropathy of unknown origin (48 of 281 patients [17.1%]). Of the 2187 patients assessed, 34 (1.6%) had genetic findings for medically actionable disorders that, although unrelated to their nephropathy, would also lead to subspecialty referral and inform renal management.
CONCLUSIONS: Exome sequencing in a combined cohort of more than 3000 patients with chronic kidney disease yielded a genetic diagnosis in just under 10% of cases. (Funded by the National Institutes of Health and others.).

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Year:  2018        PMID: 30586318      PMCID: PMC6510541          DOI: 10.1056/NEJMoa1806891

Source DB:  PubMed          Journal:  N Engl J Med        ISSN: 0028-4793            Impact factor:   176.079


  37 in total

1.  Association of trypanolytic ApoL1 variants with kidney disease in African Americans.

Authors:  Giulio Genovese; David J Friedman; Michael D Ross; Laurence Lecordier; Pierrick Uzureau; Barry I Freedman; Donald W Bowden; Carl D Langefeld; Taras K Oleksyk; Andrea L Uscinski Knob; Andrea J Bernhardy; Pamela J Hicks; George W Nelson; Benoit Vanhollebeke; Cheryl A Winkler; Jeffrey B Kopp; Etienne Pays; Martin R Pollak
Journal:  Science       Date:  2010-07-15       Impact factor: 47.728

2.  Exome sequencing can improve diagnosis and alter patient management.

Authors:  Stacey B Gabriel; Joseph G Gleeson; Tracy J Dixon-Salazar; Jennifer L Silhavy; Nitin Udpa; Jana Schroth; Stephanie Bielas; Ashleigh E Schaffer; Jesus Olvera; Vineet Bafna; Maha S Zaki; Ghada H Abdel-Salam; Lobna A Mansour; Laila Selim; Sawsan Abdel-Hadi; Naima Marzouki; Tawfeg Ben-Omran; Nouriya A Al-Saana; F Müjgan Sonmez; Figen Celep; Matloob Azam; Kiley J Hill; Adrienne Collazo; Ali G Fenstermaker; Gaia Novarino; Naiara Akizu; Kiran V Garimella; Carrie Sougnez; Carsten Russ
Journal:  Sci Transl Med       Date:  2012-06-13       Impact factor: 17.956

Review 3.  The landscape of clinical trials in nephrology: a systematic review of Clinicaltrials.gov.

Authors:  Jula K Inrig; Robert M Califf; Asba Tasneem; Radha K Vegunta; Christopher Molina; John W Stanifer; Karen Chiswell; Uptal D Patel
Journal:  Am J Kidney Dis       Date:  2013-12-06       Impact factor: 8.860

4.  Individuals with a family history of ESRD are a high-risk population for CKD: implications for targeted surveillance and intervention activities.

Authors:  William M McClellan; Scott G Satko; Elisa Gladstone; Jenna O Krisher; Andrew S Narva; Barry I Freedman
Journal:  Am J Kidney Dis       Date:  2009-03       Impact factor: 8.860

Review 5.  The renal biopsy in the genomic era.

Authors:  Helen Liapis; Joseph P Gaut
Journal:  Pediatr Nephrol       Date:  2012-11-21       Impact factor: 3.714

6.  Clinical whole-exome sequencing for the diagnosis of mendelian disorders.

Authors:  Yaping Yang; Donna M Muzny; Jeffrey G Reid; Matthew N Bainbridge; Alecia Willis; Patricia A Ward; Alicia Braxton; Joke Beuten; Fan Xia; Zhiyv Niu; Matthew Hardison; Richard Person; Mir Reza Bekheirnia; Magalie S Leduc; Amelia Kirby; Peter Pham; Jennifer Scull; Min Wang; Yan Ding; Sharon E Plon; James R Lupski; Arthur L Beaudet; Richard A Gibbs; Christine M Eng
Journal:  N Engl J Med       Date:  2013-10-02       Impact factor: 91.245

7.  Rosuvastatin and cardiovascular events in patients undergoing hemodialysis.

Authors:  Bengt C Fellström; Alan G Jardine; Roland E Schmieder; Hallvard Holdaas; Kym Bannister; Jaap Beutler; Dong-Wan Chae; Alejandro Chevaile; Stuart M Cobbe; Carola Grönhagen-Riska; José J De Lima; Robert Lins; Gert Mayer; Alan W McMahon; Hans-Henrik Parving; Giuseppe Remuzzi; Ola Samuelsson; Sandor Sonkodi; D Sci; Gultekin Süleymanlar; Dimitrios Tsakiris; Vladimir Tesar; Vasil Todorov; Andrzej Wiecek; Rudolf P Wüthrich; Mattis Gottlow; Eva Johnsson; Faiez Zannad
Journal:  N Engl J Med       Date:  2009-03-30       Impact factor: 91.245

8.  Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 gene.

Authors:  Shay Tzur; Saharon Rosset; Revital Shemer; Guennady Yudkovsky; Sara Selig; Ayele Tarekegn; Endashaw Bekele; Neil Bradman; Walter G Wasser; Doron M Behar; Karl Skorecki
Journal:  Hum Genet       Date:  2010-07-16       Impact factor: 4.132

Review 9.  Epidemiology of chronic kidney disease in children.

Authors:  Jérôme Harambat; Karlijn J van Stralen; Jon Jin Kim; E Jane Tizard
Journal:  Pediatr Nephrol       Date:  2011-06-29       Impact factor: 3.714

10.  Copy-number disorders are a common cause of congenital kidney malformations.

Authors:  Simone Sanna-Cherchi; Krzysztof Kiryluk; Katelyn E Burgess; Monica Bodria; Matthew G Sampson; Dexter Hadley; Shannon N Nees; Miguel Verbitsky; Brittany J Perry; Roel Sterken; Vladimir J Lozanovski; Anna Materna-Kiryluk; Cristina Barlassina; Akshata Kini; Valentina Corbani; Alba Carrea; Danio Somenzi; Corrado Murtas; Nadica Ristoska-Bojkovska; Claudia Izzi; Beatrice Bianco; Marcin Zaniew; Hana Flogelova; Patricia L Weng; Nilgun Kacak; Stefania Giberti; Maddalena Gigante; Adela Arapovic; Kristina Drnasin; Gianluca Caridi; Simona Curioni; Franca Allegri; Anita Ammenti; Stefania Ferretti; Vinicio Goj; Luca Bernardo; Vaidehi Jobanputra; Wendy K Chung; Richard P Lifton; Stephan Sanders; Matthew State; Lorraine N Clark; Marijan Saraga; Sandosh Padmanabhan; Anna F Dominiczak; Tatiana Foroud; Loreto Gesualdo; Zoran Gucev; Landino Allegri; Anna Latos-Bielenska; Daniele Cusi; Francesco Scolari; Velibor Tasic; Hakon Hakonarson; Gian Marco Ghiggeri; Ali G Gharavi
Journal:  Am J Hum Genet       Date:  2012-11-15       Impact factor: 11.025

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  147 in total

1.  Decreased secretion and profibrotic activity of tubular exosomes in diabetic kidney disease.

Authors:  Jin Wen; Zhengwei Ma; Man J Livingston; Wei Zhang; Yanggang Yuan; Chunyuan Guo; Yutao Liu; Ping Fu; Zheng Dong
Journal:  Am J Physiol Renal Physiol       Date:  2020-07-27

Review 2.  Machine learning, the kidney, and genotype-phenotype analysis.

Authors:  Rachel S G Sealfon; Laura H Mariani; Matthias Kretzler; Olga G Troyanskaya
Journal:  Kidney Int       Date:  2020-04-01       Impact factor: 10.612

Review 3.  Exome Sequencing in Clinical Hepatology.

Authors:  Sílvia Vilarinho; Pramod K Mistry
Journal:  Hepatology       Date:  2019-12       Impact factor: 17.425

4.  Autosomal Recessive Alport Syndrome Unveiled by Pregnancy.

Authors:  Erika R Drury; Isaac E Stillman; Martin R Pollak; Bradley M Denker
Journal:  Nephron       Date:  2019-08-13       Impact factor: 2.847

Review 5.  Variations of type IV collagen-encoding genes in patients with histological diagnosis of focal segmental glomerulosclerosis.

Authors:  Erol Demir; Yasar Caliskan
Journal:  Pediatr Nephrol       Date:  2019-06-28       Impact factor: 3.714

6.  Filling the Gap: Drosophila Nephrocytes as Model System in Kidney Research.

Authors:  Zvonimir Marelja; Matias Simons
Journal:  J Am Soc Nephrol       Date:  2019-03-25       Impact factor: 10.121

7.  Exome-Based Rare-Variant Analyses in CKD.

Authors:  Sophia Cameron-Christie; Charles J Wolock; Emily Groopman; Slavé Petrovski; Sitharthan Kamalakaran; Gundula Povysil; Dimitrios Vitsios; Mengqi Zhang; Jan Fleckner; Ruth E March; Sahar Gelfman; Maddalena Marasa; Yifu Li; Simone Sanna-Cherchi; Krzysztof Kiryluk; Andrew S Allen; Bengt C Fellström; Carolina Haefliger; Adam Platt; David B Goldstein; Ali G Gharavi
Journal:  J Am Soc Nephrol       Date:  2019-05-13       Impact factor: 10.121

8.  Risk of Cardiovascular Disease and Mortality in Young Adults With End-stage Renal Disease: An Analysis of the US Renal Data System.

Authors:  Zubin J Modi; Yee Lu; Nan Ji; Alissa Kapke; David T Selewski; Xue Dietrich; Kevin Abbott; Brahmajee K Nallamothu; Douglas E Schaubel; Rajiv Saran; Debbie S Gipson
Journal:  JAMA Cardiol       Date:  2019-04-01       Impact factor: 14.676

9.  Clinical Genetic Screening in Adult Patients with Kidney Disease.

Authors:  Enrico Cocchi; Jordan Gabriela Nestor; Ali G Gharavi
Journal:  Clin J Am Soc Nephrol       Date:  2020-07-09       Impact factor: 8.237

Review 10.  Genetic testing for kidney disease of unknown etiology.

Authors:  Thomas Hays; Emily E Groopman; Ali G Gharavi
Journal:  Kidney Int       Date:  2020-04-24       Impact factor: 10.612

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