Literature DB >> 11007676

Evidence that chronicity of hyponatremia contributes to the high urate clearance observed in the syndrome of inappropriate antidiuretic hormone secretion.

G Decaux1, F Prospert, A Soupart, W Musch.   

Abstract

The high fractional excretion (FE) of uric acid observed in hyponatremia associated with the syndrome of inappropriate secretion of antidiuretic hormone (SIADH) is commonly attributed to the volume-expanded state, although volume expansion in normonatremic volunteers is unable to increase urate clearance to a degree similar to that in SIADH. The goal of the present study is to analyze whether hyponatremia by itself could influence the FE of uric acid, as well as the effects of intravascular volume and glomerular filtration rate on FE of uric acid in SIADH. This study examines the effects of a 2-L infusion of isotonic saline over 24 hours on FE of uric acid in 9 normonatremic volunteers and 17 hyponatremic patients with SIADH. We also studied the FE of uric acid in 6 patients with SIADH with only mild water retention and the urate and creatinine clearances in 18 hyponatremic patients with SIADH before and after normalization of serum sodium levels by water restriction. When infusing 2 L of isotonic saline over 24 hours in healthy subjects, there was a decrease in plasma protein concentration of 8%, suggesting a similar degree of volume expansion than in patients with SIADH. The FE of uric acid did not increase to the same extent (9% +/- 1.5% versus 17% +/- 1.5%; P: < 0.01). Conversely, in 6 hyponatremic patients with mild water retention (1 L), the FE of uric acid was still high despite indirect signs of only a small increase in plasma volume. The mainstay of these observations is that chronicity of hyponatremia by itself could affect urate excretion. We also observed that in the patients with SIADH, high FE of uric acid inversely correlated with glomerular filtration rate (r = -0.66; P: < 0.01) only during the hyponatremic state. These data suggest that hyponatremia by itself, combined with mild volume expansion and glomerular filtration rate, has a role in the high FE of uric acid in the SIADH.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 11007676     DOI: 10.1053/ajkd.2000.17623

Source DB:  PubMed          Journal:  Am J Kidney Dis        ISSN: 0272-6386            Impact factor:   8.860


  6 in total

1.  Renal physiology: Prostaglandins in thiazide-induced hyponatraemia: do they hold water?

Authors:  Ewout J Hoorn; Jack F M Wetzels
Journal:  Nat Rev Nephrol       Date:  2017-09-25       Impact factor: 28.314

2.  Utility and limitations of biochemical parameters in the evaluation of hyponatremia in the elderly.

Authors:  W Musch; G Decaux
Journal:  Int Urol Nephrol       Date:  2001       Impact factor: 2.370

3.  More on renal salt wasting without cerebral disease: response to saline infusion.

Authors:  Solomon Bitew; Louis Imbriano; Nobuyuki Miyawaki; Steven Fishbane; John K Maesaka
Journal:  Clin J Am Soc Nephrol       Date:  2009-02       Impact factor: 8.237

4.  Application of established pathophysiologic processes brings greater clarity to diagnosis and treatment of hyponatremia.

Authors:  John K Maesaka; Louis J Imbriano; Nobuyuki Miyawaki
Journal:  World J Nephrol       Date:  2017-03-06

5.  Determining Fractional Urate Excretion Rates in Hyponatremic Conditions and Improved Methods to Distinguish Cerebral/Renal Salt Wasting From the Syndrome of Inappropriate Secretion of Antidiuretic Hormone.

Authors:  John K Maesaka; Louis J Imbriano; Nobuyuki Miyawaki
Journal:  Front Med (Lausanne)       Date:  2018-11-30

Review 6.  Differentiating SIADH from Cerebral/Renal Salt Wasting: Failure of the Volume Approach and Need for a New Approach to Hyponatremia.

Authors:  John K Maesaka; Louis Imbriano; Joseph Mattana; Dympna Gallagher; Naveen Bade; Sairah Sharif
Journal:  J Clin Med       Date:  2014-12-08       Impact factor: 4.241

  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.