Literature DB >> 29237739

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

Robert Kleta1, Detlef Bockenhauer2.   

Abstract

Renal tubulopathies provide insights into the inner workings of the kidney, yet also pose therapeutic challenges. Because of the central nature of sodium in tubular transport physiology, disorders of sodium handling may affect virtually all aspects of the homeostatic functions of the kidney. Yet, owing to the rarity of these disorders, little clinical evidence regarding treatment exists. Consequently, treatment can vary widely between individual physicians and centers and is based mainly on understanding of renal physiology, reported clinical observations, and individual experiences. Salt-losing tubulopathies can affect all tubular segments, from the proximal tubule to the collecting duct. But the more frequently observed disorders are Bartter and Gitelman syndrome, which affect salt transport in the thick ascending limb of Henle's loop and/or the distal convoluted tubule, and these disorders generate the greatest controversies regarding management. Here, we review clinical and molecular aspects of salt-losing tubulopathies and discuss novel insights provided mainly by genetic investigations and retrospective clinical reviews. Additionally, we discuss controversial topics in the management of these disorders to highlight areas of importance for future clinical trials. International collaboration will be required to perform clinical studies to inform the treatment of these rare disorders.
Copyright © 2018 by the American Society of Nephrology.

Entities:  

Keywords:  Bartter-s syndrome; Cell & Transport Physiology; Gitelman-s syndrome; children; kidney tubule

Mesh:

Substances:

Year:  2017        PMID: 29237739      PMCID: PMC5827598          DOI: 10.1681/ASN.2017060600

Source DB:  PubMed          Journal:  J Am Soc Nephrol        ISSN: 1046-6673            Impact factor:   10.121


  98 in total

1.  Immunolocalization of NHE8 in rat kidney.

Authors:  Sunita Goyal; SueAnn Mentone; Peter S Aronson
Journal:  Am J Physiol Renal Physiol       Date:  2004-11-02

2.  Mistargeting of peroxisomal EHHADH and inherited renal Fanconi's syndrome.

Authors:  Enriko D Klootwijk; Markus Reichold; Amanda Helip-Wooley; Asad Tolaymat; Carsten Broeker; Steven L Robinette; Joerg Reinders; Dominika Peindl; Kathrin Renner; Karin Eberhart; Nadine Assmann; Peter J Oefner; Katja Dettmer; Christina Sterner; Josef Schroeder; Niels Zorger; Ralph Witzgall; Stephan W Reinhold; Horia C Stanescu; Detlef Bockenhauer; Graciana Jaureguiberry; Holly Courtneidge; Andrew M Hall; Anisha D Wijeyesekera; Elaine Holmes; Jeremy K Nicholson; Kevin O'Brien; Isa Bernardini; Donna M Krasnewich; Mauricio Arcos-Burgos; Yuichiro Izumi; Hiroshi Nonoguchi; Yuzhi Jia; Janardan K Reddy; Mohammad Ilyas; Robert J Unwin; William A Gahl; Richard Warth; Robert Kleta
Journal:  N Engl J Med       Date:  2014-01-09       Impact factor: 91.245

3.  Furosemide-induced urinary acidification is caused by pronounced H+ secretion in the thick ascending limb.

Authors:  Pauline I A de Bruijn; Casper K Larsen; Sebastian Frische; Nina Himmerkus; Helle A Praetorius; Markus Bleich; Jens Leipziger
Journal:  Am J Physiol Renal Physiol       Date:  2015-07-15

Review 4.  Integrated control of Na transport along the nephron.

Authors:  Lawrence G Palmer; Jürgen Schnermann
Journal:  Clin J Am Soc Nephrol       Date:  2014-08-06       Impact factor: 8.237

Review 5.  The proximal tubule and albuminuria: really!

Authors:  Landon E Dickson; Mark C Wagner; Ruben M Sandoval; Bruce A Molitoris
Journal:  J Am Soc Nephrol       Date:  2014-01-09       Impact factor: 10.121

6.  Cystinosin deficiency causes podocyte damage and loss associated with increased cell motility.

Authors:  Ekaterina A Ivanova; Fanny O Arcolino; Mohamed A Elmonem; Maria P Rastaldi; Laura Giardino; Elisabeth M Cornelissen; Lambertus P van den Heuvel; Elena N Levtchenko
Journal:  Kidney Int       Date:  2016-03-11       Impact factor: 10.612

7.  A novel compound heterozygous ROMK mutation presenting as late onset Bartter syndrome associated with nephrocalcinosis and elevated 1,25(OH)(2) vitamin D levels.

Authors:  Amita Sharma; Micheal A Linshaw
Journal:  Clin Exp Nephrol       Date:  2011-03-25       Impact factor: 2.801

8.  Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10.

Authors:  Ute I Scholl; Murim Choi; Tiewen Liu; Vincent T Ramaekers; Martin G Häusler; Joanne Grimmer; Sheldon W Tobe; Anita Farhi; Carol Nelson-Williams; Richard P Lifton
Journal:  Proc Natl Acad Sci U S A       Date:  2009-03-16       Impact factor: 11.205

9.  Fainting Fanconi syndrome clarified by proxy: a case report.

Authors:  Stephen Benedict Walsh; Robert Unwin; Robert Kleta; William Van't Hoff; Paul Bass; Khalid Hussain; Sian Ellard; Detlef Bockenhauer
Journal:  BMC Nephrol       Date:  2017-07-11       Impact factor: 2.388

10.  Proximal tubule specific knockout of the Na⁺/H⁺ exchanger NHE3: effects on bicarbonate absorption and ammonium excretion.

Authors:  Hong C Li; Zhaopeng Du; Sharon Barone; Isabelle Rubera; Alicia A McDonough; Michel Tauc; Kamyar Zahedi; Tong Wang; Manoocher Soleimani
Journal:  J Mol Med (Berl)       Date:  2013-03-19       Impact factor: 4.599

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  17 in total

1.  Regulation of NKCC2B by TNF-α in response to salt restriction.

Authors:  Shoujin Hao; Joseph Salzo; Mary Hao; Nicholas R Ferreri
Journal:  Am J Physiol Renal Physiol       Date:  2019-12-09

2.  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 3.  Long-term complications of primary distal renal tubular acidosis.

Authors:  Fernando Santos; Helena Gil-Peña
Journal:  Pediatr Nephrol       Date:  2022-05-11       Impact factor: 3.714

4.  Bartter syndrome with multiple renal and liver cysts: a case report.

Authors:  Yemei He; Yue Zhou; Weihua Wu; Yue Chen; Santao Ou
Journal:  Int Urol Nephrol       Date:  2022-06-29       Impact factor: 2.370

5.  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

Review 6.  Bartter syndrome: causes, diagnosis, and treatment.

Authors:  Tamara da Silva Cunha; Ita Pfeferman Heilberg
Journal:  Int J Nephrol Renovasc Dis       Date:  2018-11-09

7.  HNF1B Mutations Are Associated With a Gitelman-like Tubulopathy That Develops During Childhood.

Authors:  Shazia Adalat; Wesley N Hayes; William A Bryant; John Booth; Adrian S Woolf; Robert Kleta; Sandra Subtil; Rhian Clissold; Kevin Colclough; Sian Ellard; Detlef Bockenhauer
Journal:  Kidney Int Rep       Date:  2019-05-29

Review 8.  Inherited Tubulopathies of the Kidney: Insights from Genetics.

Authors:  Mallory L Downie; Sergio C Lopez Garcia; Robert Kleta; Detlef Bockenhauer
Journal:  Clin J Am Soc Nephrol       Date:  2020-04-01       Impact factor: 8.237

Review 9.  Hypokalemia: a clinical update.

Authors:  Efstratios Kardalas; Stavroula A Paschou; Panagiotis Anagnostis; Giovanna Muscogiuri; Gerasimos Siasos; Andromachi Vryonidou
Journal:  Endocr Connect       Date:  2018-03-14       Impact factor: 3.335

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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