Literature DB >> 3306417

Oxalate dynamics in chronic renal failure. Comparison with normal subjects and patients with primary hyperoxaluria.

S H Morgan, P Purkiss, R W Watts, M A Mansell.   

Abstract

In order to separate the effect of oxalate retention in primary hyperoxaluria with renal failure from that of excessive oxalate synthesis and to determine the optimum time for renal transplantation in primary hyperoxaluria, we have studied a series of patients with different degrees of renal failure due to other causes. The results were compared with those obtained in studies on 8 patients with primary hyperoxaluria at different levels of residual overall renal function. In the patients with renal failure unrelated to primary hyperoxaluria, oxalate retention increases rapidly when the glomerular filtration rate (GFR) decreases below about 20 ml X min-1. These results suggest that the reduced renal excretory contribution to oxalate accumulation in primary hyperoxaluria would be expected to be particularly important in this range of GFR. In primary hyperoxaluria, oxalate retention occurs when GFR is only a little below the reference range and measures to remove oxalate from the body should be considered when the GFR falls below 40 ml X min-1 X 1.73 m-2, with a view to their introduction when the GFR is in the range 20-25 ml X min-1 X 1.73 m-2.

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Year:  1987        PMID: 3306417     DOI: 10.1159/000184364

Source DB:  PubMed          Journal:  Nephron        ISSN: 1660-8151            Impact factor:   2.847


  15 in total

1.  Oxalate, livers, and kidneys.

Authors:  R W Watts; M A Mansell
Journal:  BMJ       Date:  1990-10-06

2.  What treatment do you advise for a small child with hyperoxaluria presenting with renal calculi?

Authors:  R W Watts
Journal:  Pediatr Nephrol       Date:  1990-01       Impact factor: 3.714

3.  End Points for Clinical Trials in Primary Hyperoxaluria.

Authors:  Dawn S Milliner; Tracy L McGregor; Aliza Thompson; Bastian Dehmel; John Knight; Ralf Rosskamp; Melanie Blank; Sixun Yang; Sonia Fargue; Gill Rumsby; Jaap Groothoff; Meaghan Allain; Melissa West; Kim Hollander; W Todd Lowther; John C Lieske
Journal:  Clin J Am Soc Nephrol       Date:  2020-03-12       Impact factor: 8.237

Review 4.  Bone impairment in primary hyperoxaluria: a review.

Authors:  Justine Bacchetta; Georges Boivin; Pierre Cochat
Journal:  Pediatr Nephrol       Date:  2015-01-29       Impact factor: 3.714

5.  Subclinical celiac disease and crystal-induced kidney disease following kidney transplant.

Authors:  Giovanna Capolongo; Sameh Abul-Ezz; Orson W Moe; Khashayar Sakhaee
Journal:  Am J Kidney Dis       Date:  2012-06-26       Impact factor: 8.860

Review 6.  Recent advances in the understanding, diagnosis and treatment of primary hyperoxaluria type 1.

Authors:  C J Danpure
Journal:  J Inherit Metab Dis       Date:  1989       Impact factor: 4.982

Review 7.  Liver transplantation for pediatric inherited metabolic disorders: Considerations for indications, complications, and perioperative management.

Authors:  Kimihiko Oishi; Ronen Arnon; Melissa P Wasserstein; George A Diaz
Journal:  Pediatr Transplant       Date:  2016-06-21

8.  Initial manifestation of primary hyperoxaluria type I in adults-- recognition, diagnosis, and management.

Authors:  J J Kuiper
Journal:  West J Med       Date:  1996-01

9.  Bone metabolism in oxalosis: a single-center study using new imaging techniques and biomarkers.

Authors:  Justine Bacchetta; Sonia Fargue; Stéphanie Boutroy; Odile Basmaison; Nicolas Vilayphiou; Ingrid Plotton; Fitsum Guebre-Egziabher; Bruno Dohin; Rémi Kohler; Pierre Cochat
Journal:  Pediatr Nephrol       Date:  2010-03-06       Impact factor: 3.714

Review 10.  Hereditary causes of kidney stones and chronic kidney disease.

Authors:  Vidar O Edvardsson; David S Goldfarb; John C Lieske; Lada Beara-Lasic; Franca Anglani; Dawn S Milliner; Runolfur Palsson
Journal:  Pediatr Nephrol       Date:  2013-01-20       Impact factor: 3.714

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