Literature DB >> 32739203

Genetic testing for kidney disease of unknown etiology.

Thomas Hays1, Emily E Groopman2, Ali G Gharavi3.   

Abstract

In many cases of chronic kidney disease, the cause of disease remains unknown despite a thorough nephrologic workup. Genetic testing has revolutionized many areas of medicine and promises to empower diagnosis and targeted management of such cases of kidney disease of unknown etiology. Recent studies using genetic testing have demonstrated that Mendelian etiologies account for approximately 20% of cases of kidney disease of unknown etiology. Although genetic testing has significant benefits, including tailoring of therapy, informing targeted workup, detecting extrarenal disease, counseling patients and families, and redirecting care, it also has important limitations and risks that must be considered.
Copyright © 2020 International Society of Nephrology. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  chronic kidney disease; genetic testing; kidney disease of unknown etiology

Mesh:

Year:  2020        PMID: 32739203      PMCID: PMC7784921          DOI: 10.1016/j.kint.2020.03.031

Source DB:  PubMed          Journal:  Kidney Int        ISSN: 0085-2538            Impact factor:   10.612


  97 in total

Review 1.  Exploring the genetic basis of early-onset chronic kidney disease.

Authors:  Asaf Vivante; Friedhelm Hildebrandt
Journal:  Nat Rev Nephrol       Date:  2016-01-11       Impact factor: 28.314

Review 2.  Structural variation in the human genome and its role in disease.

Authors:  Paweł Stankiewicz; James R Lupski
Journal:  Annu Rev Med       Date:  2010       Impact factor: 13.739

3.  Alport syndrome: a unified classification of genetic disorders of collagen IV α345: a position paper of the Alport Syndrome Classification Working Group.

Authors:  Clifford E Kashtan; Jie Ding; Guido Garosi; Laurence Heidet; Laura Massella; Koichi Nakanishi; Kandai Nozu; Alessandra Renieri; Michelle Rheault; Fang Wang; Oliver Gross
Journal:  Kidney Int       Date:  2018-03-16       Impact factor: 10.612

4.  Prevalence of chronic kidney disease in the United States.

Authors:  Josef Coresh; Elizabeth Selvin; Lesley A Stevens; Jane Manzi; John W Kusek; Paul Eggers; Frederick Van Lente; Andrew S Levey
Journal:  JAMA       Date:  2007-11-07       Impact factor: 56.272

5.  Prevalence of WT1 mutations in a large cohort of patients with steroid-resistant and steroid-sensitive nephrotic syndrome.

Authors:  Rainer G Ruf; Michael Schultheiss; Anne Lichtenberger; Stephanie M Karle; Isabella Zalewski; Bettina Mucha; Anne Schulze Everding; Thomas Neuhaus; Ludwig Patzer; Christian Plank; Johannes P Haas; Fatih Ozaltin; Anita Imm; Arno Fuchshuber; Aysin Bakkaloglu; Friedhelm Hildebrandt
Journal:  Kidney Int       Date:  2004-08       Impact factor: 10.612

Review 6.  Velocardiofacial syndrome, DiGeorge syndrome: the chromosome 22q11.2 deletion syndromes.

Authors:  Lisa J Kobrynski; Kathleen E Sullivan
Journal:  Lancet       Date:  2007-10-20       Impact factor: 79.321

Review 7.  Genetic testing, insurance discrimination and medical research: what the United States can learn from peer countries.

Authors:  Jean-Christophe Bélisle-Pipon; Effy Vayena; Robert C Green; I Glenn Cohen
Journal:  Nat Med       Date:  2019-08-06       Impact factor: 53.440

8.  Meta-analysis and multidisciplinary consensus statement: exome sequencing is a first-tier clinical diagnostic test for individuals with neurodevelopmental disorders.

Authors:  Siddharth Srivastava; Jamie A Love-Nichols; Kira A Dies; David H Ledbetter; Christa L Martin; Wendy K Chung; Helen V Firth; Thomas Frazier; Robin L Hansen; Lisa Prock; Han Brunner; Ny Hoang; Stephen W Scherer; Mustafa Sahin; David T Miller
Journal:  Genet Med       Date:  2019-06-11       Impact factor: 8.822

9.  Looking beyond the exome: a phenotype-first approach to molecular diagnostic resolution in rare and undiagnosed diseases.

Authors:  Loren D M Pena; Yong-Hui Jiang; Kelly Schoch; Rebecca C Spillmann; Nicole Walley; Nicholas Stong; Sarah Rapisardo Horn; Jennifer A Sullivan; Allyn McConkie-Rosell; Sujay Kansagra; Edward C Smith; Mays El-Dairi; Jane Bellet; Martha Ann Keels; Joan Jasien; Peter G Kranz; Richard Noel; Shashi K Nagaraj; Robert K Lark; Daniel S G Wechsler; Daniela Del Gaudio; Marco L Leung; Laura G Hendon; Collette C Parker; Kelly L Jones; David B Goldstein; Vandana Shashi
Journal:  Genet Med       Date:  2017-09-14       Impact factor: 8.822

10.  Using high-resolution variant frequencies to empower clinical genome interpretation.

Authors:  Nicola Whiffin; Eric Minikel; Roddy Walsh; Anne H O'Donnell-Luria; Konrad Karczewski; Alexander Y Ing; Paul J R Barton; Birgit Funke; Stuart A Cook; Daniel MacArthur; James S Ware
Journal:  Genet Med       Date:  2017-05-18       Impact factor: 8.822

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  13 in total

Review 1.  A Practical Guide to Genetic Testing for Kidney Disorders of Unknown Etiology.

Authors:  Abraham W Aron; Neera K Dahl; Whitney Besse
Journal:  Kidney360       Date:  2022-07-08

2.  Prevalence of hereditary tubulointerstitial kidney diseases in the German Chronic Kidney Disease study.

Authors:  Bernt Popp; Arif B Ekici; Karl X Knaup; Karen Schneider; Steffen Uebe; Jonghun Park; Vineet Bafna; Heike Meiselbach; Kai-Uwe Eckardt; Mario Schiffer; André Reis; Cornelia Kraus; Michael Wiesener
Journal:  Eur J Hum Genet       Date:  2022-09-13       Impact factor: 5.351

Review 3.  Novel Therapies for Alport Syndrome.

Authors:  Efren Chavez; Juanly Rodriguez; Yelena Drexler; Alessia Fornoni
Journal:  Front Med (Lausanne)       Date:  2022-04-25

Review 4.  Rare genetic causes of complex kidney and urological diseases.

Authors:  Emily E Groopman; Gundula Povysil; David B Goldstein; Ali G Gharavi
Journal:  Nat Rev Nephrol       Date:  2020-08-17       Impact factor: 28.314

5.  Study Design and Baseline Characteristics of the CARDINAL Trial: A Phase 3 Study of Bardoxolone Methyl in Patients with Alport Syndrome.

Authors:  Glenn M Chertow; Gerald B Appel; Sharon Andreoli; Sripal Bangalore; Geoffrey A Block; Arlene B Chapman; Melanie P Chin; Keisha L Gibson; Angie Goldsberry; Kazumoto Iijima; Lesley A Inker; Bertrand Knebelmann; Laura H Mariani; Colin J Meyer; Kandai Nozu; Megan O'Grady; Arnold L Silva; Peter Stenvinkel; Roser Torra; Bradley A Warady; Pablo E Pergola
Journal:  Am J Nephrol       Date:  2021-03-31       Impact factor: 3.754

Review 6.  Genetic testing for unexplained perinatal disorders.

Authors:  Thomas Hays; Ronald J Wapner
Journal:  Curr Opin Pediatr       Date:  2021-04-01       Impact factor: 2.856

7.  Genetic Testing for Chronic Kidney Diseases: Clinical Utility and Barriers Perceived by Nephrologists.

Authors:  Michal Mrug; Michelle S Bloom; Christine Seto; Meenakshi Malhotra; Hossein Tabriziani; Philippe Gauthier; Vicki Sidlow; Trudy McKanna; Paul R Billings
Journal:  Kidney Med       Date:  2021-10-05

Review 8.  Emerging Role of Clinical Genetics in CKD.

Authors:  Prasad Devarajan; Glenn M Chertow; Katalin Susztak; Adeera Levin; Rajiv Agarwal; Peter Stenvinkel; Arlene B Chapman; Bradley A Warady
Journal:  Kidney Med       Date:  2022-02-11

9.  Vignette-Based Reflections to Inform Genetic Testing Policies in Living Kidney Donors.

Authors:  Gurmukteshwar Singh; Reginald Gohh; Dinah Clark; Kartik Kalra; Manoj Das; Gitana Bradauskaite; Anthony J Bleyer; Bekir Tanriover; Alex R Chang; Prince M Anand
Journal:  Genes (Basel)       Date:  2022-03-26       Impact factor: 4.141

10.  An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease.

Authors:  Zhigang Wang; Hongen Xu; Tianchao Xiang; Danhua Liu; Fei Xu; Lixiang Zhao; Yonghua Feng; Linan Xu; Jialu Liu; Ye Fang; Huanfei Liu; Ruijun Li; Xinxin Hu; Jingyuan Guan; Longshan Liu; Guiwen Feng; Qian Shen; Hong Xu; Dmitrij Frishman; Wenxue Tang; Jiancheng Guo; Jia Rao; Wenjun Shang
Journal:  NPJ Genom Med       Date:  2021-07-02       Impact factor: 8.617

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