» Articles » PMID: 38791238

Metabolic Acidosis in CKD: Pathogenesis, Adverse Effects, and Treatment Effects

Overview
Journal Int J Mol Sci
Publisher MDPI
Date 2024 May 25
PMID 38791238
Authors
Affiliations
Soon will be listed here.
Abstract

Metabolic acidosis is a frequent complication of chronic kidney disease and is associated with a number of adverse outcomes, including worsening kidney function, poor musculoskeletal health, cardiovascular events, and death. Mechanisms that prevent metabolic acidosis detrimentally promote further kidney damage, creating a cycle between acid accumulation and acid-mediated kidney injury. Disrupting this cycle through the provision of alkali, most commonly using sodium bicarbonate, is hypothesized to preserve kidney function while also mitigating adverse effects of excess acid on bone and muscle. However, results from clinical trials have been conflicting. There is also significant interest to determine whether sodium bicarbonate might improve patient outcomes for those who do not have overt metabolic acidosis. Such individuals are hypothesized to be experiencing acid-mediated organ damage despite having a normal serum bicarbonate concentration, a state often referred to as subclinical metabolic acidosis. Results from small- to medium-sized trials in individuals with subclinical metabolic acidosis have also been inconclusive. Well-powered clinical trials to determine the efficacy and safety of sodium bicarbonate are necessary to determine if this intervention improves patient outcomes.

Citing Articles

The association between anion gap and prognosis in patients myocardial infarction with congestive heart failure: a retrospective analysis of the MIMIC-IV database.

Li M, Li C, Wang J, Yuan Q Int J Emerg Med. 2025; 18(1):33.

PMID: 39994567 PMC: 11849230. DOI: 10.1186/s12245-025-00828-0.


The Effect of Renaltec on Serum Uremic Toxins in Cats with Experimentally Induced Chronic Kidney Disease.

Paschall R, Quimby J, Lourenco B, Summers S, Schmiedt C Vet Sci. 2024; 11(8).

PMID: 39195833 PMC: 11359303. DOI: 10.3390/vetsci11080379.

References
1.
Kohan D, Inscho E, Wesson D, Pollock D . Physiology of endothelin and the kidney. Compr Physiol. 2013; 1(2):883-919. PMC: 3940435. DOI: 10.1002/cphy.c100039. View

2.
Kotchen T, Luke R, Ott C, Galla J, Whitescarver S . Effect of chloride on renin and blood pressure responses to sodium chloride. Ann Intern Med. 1983; 98(5 Pt 2):817-22. DOI: 10.7326/0003-4819-98-5-817. View

3.
Moranne O, Froissart M, Rossert J, Gauci C, Boffa J, Haymann J . Timing of onset of CKD-related metabolic complications. J Am Soc Nephrol. 2008; 20(1):164-71. PMC: 2615728. DOI: 10.1681/ASN.2008020159. View

4.
Lemann J, Litzow J, Lennon E . Studies of the mechanism by which chronic metabolic acidosis augments urinary calcium excretion in man. J Clin Invest. 1967; 46(8):1318-28. PMC: 297133. DOI: 10.1172/JCI105624. View

5.
De Solis A, Gonzalez-Pacheco F, Deudero J, Neria F, Albalate M, Petkov V . Alkalinization potentiates vascular calcium deposition in an uremic milieu. J Nephrol. 2009; 22(5):647-53. View