1. Metabolic Acidosis in CKD: Core Curriculum 2019
Kalani L. Raphael 
American Journal of Kidney Diseases 
Volume 74, Issue 2, Pages (August 2019)
DOI: /j.ajkd
Copyright © 2019 National Kidney Foundation, Inc. Terms and Conditions

2. Figure 1
Acid loading in healthy individuals increases urinary ammonia and titratable acid excretion; however, the increase in ammonia excretion is greater. Reproduced from Weiner et al (Clin J Am Soc Nephrol. 2015;10(8): ) with permission of the American Society of Nephrology (ASN); original image ©2015 ASN.
American Journal of Kidney Diseases  , DOI: ( /j.ajkd )
Copyright © 2019 National Kidney Foundation, Inc. Terms and Conditions

3. Figure 2
Acid loading with ammonium chloride (NH4Cl) over 4 days increases urinary ammonium (NH4+) excretion in healthy individuals, which maintains serum total carbon dioxide (tCO2) level in the normal range. In chronic kidney disease (CKD), ammonium excretion fails to increase, resulting in metabolic acidosis. Adapted from Welbourne et al (J Clin Invest. 1972;51(7): ) with permission of the American Society for Clinical Investigation.
American Journal of Kidney Diseases  , DOI: ( /j.ajkd )
Copyright © 2019 National Kidney Foundation, Inc. Terms and Conditions

4. Figure 3
Urinary (B) ammonium, (C) titratable acid, and consequently (D) net acid excretion (NAE) are lower with lower measured glomerular filtration rates (mGFRs). However, (E) net endogenous acid production (NEAP) is largely unchanged. (F) The positive acid balance with lower GFR leads to (A) reduced serum total carbon dioxide (tCO2) concentration. Reproduced from Vallet et al (Kidney Int. 2015;88(1): ) with permission of the International Society of Nephrology (ISN); original image ©2015 ISN.
American Journal of Kidney Diseases  , DOI: ( /j.ajkd )
Copyright © 2019 National Kidney Foundation, Inc. Terms and Conditions

5. Figure 4
Mechanisms of acid-mediated tubulointerstitial fibrosis in chronic kidney disease (CKD). Abbreviations: ET-A, endothelin-A; ET-B, endothelin-B; NH4+, ammonium ion; RAS, renin-angiotensin system. Reproduced from Loniewski and Wesson (Kidney Int. 2014;85(3): ) with permission of the International Society of Nephrology (ISN); original image ©2013 ISN.
American Journal of Kidney Diseases  , DOI: ( /j.ajkd )
Copyright © 2019 National Kidney Foundation, Inc. Terms and Conditions

6. Figure 5
Author's approach to the management of chronic metabolic acidosis (MA) in chronic kidney disease using sodium bicarbonate (NaHCO3). The NaHCO3 dose should be reduced if total carbon dioxide (tCO2) is > 26 mEq/L. The dose of HCO3− in mEq/day is shown in parentheses; the dose of citrate-based formulations can be approximated using these values. Adapted from Raphael (Am J Kidney Dis. 2016;67(4): ) with permission of the National Kidney Foundation.
American Journal of Kidney Diseases  , DOI: ( /j.ajkd )
Copyright © 2019 National Kidney Foundation, Inc. Terms and Conditions

7. Figure 6
Estimated potential renal acid load (PRAL) of common foods per 100-g serving. Reproduced from Scialla et al (Adv Chronic Kidney Dis. 2013;20(2): ) with permission of the National Kidney Foundation.
American Journal of Kidney Diseases  , DOI: ( /j.ajkd )
Copyright © 2019 National Kidney Foundation, Inc. Terms and Conditions

8. Figure 7
Rationale to target serum total carbon dioxide (tCO2) concentration of 24 to 26 mEq/L in chronic kidney disease (CKD). The optimum serum bicarbonate concentration in CKD is unknown. tCO2 levels < 22 mEq/L are associated with bone demineralization, skeletal muscle catabolism, CKD progression, and mortality, while tCO2 levels > 26 mEq/L are associated with higher risk for incident heart failure, and levels ≥ 30 mEq/L are associated with higher mortality. Targeting levels above the normal range may predisopose to kidney and cardiovascular calcification.
American Journal of Kidney Diseases  , DOI: ( /j.ajkd )
Copyright © 2019 National Kidney Foundation, Inc. Terms and Conditions