Literature DB >> 32238367

Inherited Tubulopathies of the Kidney: Insights from Genetics.

Mallory L Downie1,2, Sergio C Lopez Garcia1,2, Robert Kleta1,2, Detlef Bockenhauer3,2.   

Abstract

The kidney tubules provide homeostasis by maintaining the external milieu that is critical for proper cellular function. Without homeostasis, there would be no heartbeat, no muscle movement, no thought, sensation, or emotion. The task is achieved by an orchestra of proteins, directly or indirectly involved in the tubular transport of water and solutes. Inherited tubulopathies are characterized by impaired function of one or more of these specific transport molecules. The clinical consequences can range from isolated alterations in the concentration of specific solutes in blood or urine to serious and life-threatening disorders of homeostasis. In this review, we focus on genetic aspects of the tubulopathies and how genetic investigations and kidney physiology have crossfertilized each other and facilitated the identification of these disorders and their molecular basis. In turn, clinical investigations of genetically defined patients have shaped our understanding of kidney physiology.
Copyright © 2021 by the American Society of Nephrology.

Entities:  

Keywords:  Bartter-s syndrome; Emotions; Genomics; Homeostasis; Kidney; Kidney Tubules; Sensation; Series; Urinary Tract Physiological Phenomena; Water; kidney; kidney tubule; magnesium wasting disorders; nephrogenic diabetes insipidus; renal tubular acidosis; tubulopathies

Mesh:

Year:  2020        PMID: 32238367      PMCID: PMC8092065          DOI: 10.2215/CJN.14481119

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


  71 in total

Review 1.  Renal vacuolar H+-ATPase.

Authors:  Carsten A Wagner; Karin E Finberg; Sylvie Breton; Vladimir Marshansky; Dennis Brown; John P Geibel
Journal:  Physiol Rev       Date:  2004-10       Impact factor: 37.312

2.  Renal apnoea: extreme disturbance of homoeostasis in a child with Bartter syndrome type IV.

Authors:  Lucy Anne Plumb; William Van't Hoff; Robert Kleta; Chris Reid; Emma Ashton; Martin Samuels; Detlef Bockenhauer
Journal:  Lancet       Date:  2016-08-06       Impact factor: 79.321

Review 3.  Transcription-factor mutations and disease.

Authors:  D S Latchman
Journal:  N Engl J Med       Date:  1996-01-04       Impact factor: 91.245

Review 4.  Salt-Losing Tubulopathies in Children: What's New, What's Controversial?

Authors:  Robert Kleta; Detlef Bockenhauer
Journal:  J Am Soc Nephrol       Date:  2017-12-13       Impact factor: 10.121

5.  Bicarbonate reabsorption and hydrogen ion excretion in children with renal tubular acidosis.

Authors:  J R Soriano; H Boichis; C M Edelmann
Journal:  J Pediatr       Date:  1967-12       Impact factor: 4.406

Review 6.  Unraveling the molecular pathogenesis of isolated proximal renal tubular acidosis.

Authors:  Takashi Igarashi; Takashi Sekine; Jun Inatomi; George Seki
Journal:  J Am Soc Nephrol       Date:  2002-08       Impact factor: 10.121

7.  High-throughput sequencing contributes to the diagnosis of tubulopathies and familial hypercalcemia hypocalciuria in adults.

Authors:  Marguerite Hureaux; Emma Ashton; Karin Dahan; Pascal Houillier; Anne Blanchard; Catherine Cormier; Eugenie Koumakis; Daniela Iancu; Hendrica Belge; Pascale Hilbert; Annelies Rotthier; Jurgen Del Favero; Franz Schaefer; Robert Kleta; Detlef Bockenhauer; Xavier Jeunemaitre; Olivier Devuyst; Stephen B Walsh; Rosa Vargas-Poussou
Journal:  Kidney Int       Date:  2019-09-16       Impact factor: 10.612

8.  A missense mutation in the Kv1.1 voltage-gated potassium channel-encoding gene KCNA1 is linked to human autosomal dominant hypomagnesemia.

Authors:  Bob Glaudemans; Jenny van der Wijst; Rosana H Scola; Paulo J Lorenzoni; Angelien Heister; Annemiete W van der Kemp; Nine V Knoers; Joost G Hoenderop; René J Bindels
Journal:  J Clin Invest       Date:  2009-03-23       Impact factor: 14.808

9.  AKAPs-PKA disruptors increase AQP2 activity independently of vasopressin in a model of nephrogenic diabetes insipidus.

Authors:  Fumiaki Ando; Shuichi Mori; Naofumi Yui; Tetsuji Morimoto; Naohiro Nomura; Eisei Sohara; Tatemitsu Rai; Sei Sasaki; Yoshiaki Kondo; Hiroyuki Kagechika; Shinichi Uchida
Journal:  Nat Commun       Date:  2018-04-12       Impact factor: 14.919

10.  Multiplex epithelium dysfunction due to CLDN10 mutation: the HELIX syndrome.

Authors:  Smail Hadj-Rabia; Gaelle Brideau; Yasser Al-Sarraj; Rachid C Maroun; Marie-Lucile Figueres; Stéphanie Leclerc-Mercier; Eric Olinger; Stéphanie Baron; Catherine Chaussain; Dominique Nochy; Rowaida Z Taha; Bertrand Knebelmann; Vandana Joshi; Patrick A Curmi; Marios Kambouris; Rosa Vargas-Poussou; Christine Bodemer; Olivier Devuyst; Pascal Houillier; Hatem El-Shanti
Journal:  Genet Med       Date:  2017-08-03       Impact factor: 8.822

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  17 in total

1.  A clinical approach to tubulopathies in children and young adults.

Authors:  Andrew Mallett; Hugh McCarthy; Rachael Kermond
Journal:  Pediatr Nephrol       Date:  2022-05-18       Impact factor: 3.714

Review 2.  Genetic diagnosis and treatment of hereditary renal tubular disease with hypokalemia and alkalosis.

Authors:  Wenkai Guo; Pengcheng Ji; Yuansheng Xie
Journal:  J Nephrol       Date:  2022-08-22       Impact factor: 4.393

3.  Clinical and Genetic Characterization of Patients with Bartter and Gitelman Syndrome.

Authors:  Viviana Palazzo; Valentina Raglianti; Samuela Landini; Luigi Cirillo; Carmela Errichiello; Elisa Buti; Rosangela Artuso; Lucia Tiberi; Debora Vergani; Elia Dirupo; Paola Romagnani; Benedetta Mazzinghi; Francesca Becherucci
Journal:  Int J Mol Sci       Date:  2022-05-18       Impact factor: 6.208

4.  The Bartter-Gitelman Spectrum: 50-Year Follow-up With Revision of Diagnosis After Whole-Genome Sequencing.

Authors:  Mark Stevenson; Alistair T Pagnamenta; Heather G Mack; Judith Savige; Edoardo Giacopuzzi; Kate E Lines; Jenny C Taylor; Rajesh V Thakker
Journal:  J Endocr Soc       Date:  2022-05-15

Review 5.  Organs-on-chip technology: a tool to tackle genetic kidney diseases.

Authors:  Marta G Valverde; João Faria; Elena Sendino Garví; Manoe J Janssen; Rosalinde Masereeuw; Silvia M Mihăilă
Journal:  Pediatr Nephrol       Date:  2022-03-14       Impact factor: 3.651

6.  Gitelman-Like Syndrome Caused by Pathogenic Variants in mtDNA.

Authors:  Daan Viering; Karl P Schlingmann; Marguerite Hureaux; Tom Nijenhuis; Andrew Mallett; Melanie M Y Chan; André van Beek; Albertien M van Eerde; Jean-Marie Coulibaly; Marion Vallet; Stéphane Decramer; Solenne Pelletier; Günter Klaus; Martin Kömhoff; Rolf Beetz; Chirag Patel; Mohan Shenoy; Eric J Steenbergen; Glenn Anderson; Ernie M H F Bongers; Carsten Bergmann; Daan Panneman; Richard J Rodenburg; Robert Kleta; Pascal Houillier; Martin Konrad; Rosa Vargas-Poussou; Nine V A M Knoers; Detlef Bockenhauer; Jeroen H F de Baaij
Journal:  J Am Soc Nephrol       Date:  2021-10-04       Impact factor: 10.121

7.  Defects in KCNJ16 Cause a Novel Tubulopathy with Hypokalemia, Salt Wasting, Disturbed Acid-Base Homeostasis, and Sensorineural Deafness.

Authors:  Karl P Schlingmann; Aparna Renigunta; Ewout J Hoorn; Anna-Lena Forst; Vijay Renigunta; Velko Atanasov; Sinthura Mahendran; Tahsin Stefan Barakat; Valentine Gillion; Nathalie Godefroid; Alice S Brooks; Dorien Lugtenberg; Jennifer Lake; Huguette Debaix; Christoph Rudin; Bertrand Knebelmann; Stephanie Tellier; Caroline Rousset-Rouvière; Daan Viering; Jeroen H F de Baaij; Stefanie Weber; Oleg Palygin; Alexander Staruschenko; Robert Kleta; Pascal Houillier; Detlef Bockenhauer; Olivier Devuyst; Rosa Vargas-Poussou; Richard Warth; Anselm A Zdebik; Martin Konrad
Journal:  J Am Soc Nephrol       Date:  2021-04-02       Impact factor: 14.978

8.  mTOR-Activating Mutations in RRAGD Are Causative for Kidney Tubulopathy and Cardiomyopathy.

Authors:  Karl P Schlingmann; François Jouret; Kuang Shen; Anukrati Nigam; Francisco J Arjona; Claudia Dafinger; Pascal Houillier; Deborah P Jones; Felix Kleinerüschkamp; Jun Oh; Nathalie Godefroid; Mehmet Eltan; Tülay Güran; Stéphane Burtey; Marie-Christine Parotte; Jens König; Alina Braun; Caro Bos; Maria Ibars Serra; Holger Rehmann; Fried J T Zwartkruis; Kirsten Y Renkema; Karin Klingel; Eric Schulze-Bahr; Bernhard Schermer; Carsten Bergmann; Janine Altmüller; Holger Thiele; Bodo B Beck; Karin Dahan; David Sabatini; Max C Liebau; Rosa Vargas-Poussou; Nine V A M Knoers; Martin Konrad; Jeroen H F de Baaij
Journal:  J Am Soc Nephrol       Date:  2021-10-04       Impact factor: 14.978

Review 9.  Bartter's syndrome: clinical findings, genetic causes and therapeutic approach.

Authors:  Flavia Cristina Carvalho Mrad; Sílvia Bouissou Morais Soares; Luiz Alberto Wanderley de Menezes Silva; Pedro Versiani Dos Anjos Menezes; Ana Cristina Simões-E-Silva
Journal:  World J Pediatr       Date:  2020-06-01       Impact factor: 2.764

Review 10.  Tubulopathy meets Sherlock Holmes: biochemical fingerprinting of disorders of altered kidney tubular salt handling.

Authors:  Detlef Bockenhauer; Robert Kleta
Journal:  Pediatr Nephrol       Date:  2021-06-18       Impact factor: 3.714

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