Circulating anions usually associated with the Krebs cycle in patients with metabolic acidosis

Forni, Lui G, McKinnon, William, Lord, Gwyn A, Treacher, David F, Peron, Jean-Marie R and Hilton, Philip J (2005) Circulating anions usually associated with the Krebs cycle in patients with metabolic acidosis. Critical Care (Online), 9(5), R591-R595. ISSN (online) 1466-609X

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Abstract

Introduction Acute metabolic acidosis of non-renal origin is usually a result of either lactic or ketoacidosis, both of which are associated with a high anion gap. There is increasing recognition, however, of a group of acidotic patients who have a large anion gap that is not explained by either keto- or lactic acidosis nor, in most cases, is inappropriate fluid resuscitation or ingestion of exogenous agents the cause. Methods Plasma ultrafiltrate from patients with diabetic ketoacidosis, lactic acidosis, acidosis of unknown cause, normal anion gap metabolic acidosis, or acidosis as a result of base loss were examined enzymatically for the presence of low molecular weight anions including citrate, isocitrate, ?-ketoglutarate, succinate, malate and d-lactate. The results obtained from the study groups were compared with those obtained from control plasma from normal volunteers. Results In five patients with lactic acidosis, a significant increase in isocitrate (0.71 ± 0.35 mEq l-1), ?-ketoglutarate (0.55 ± 0.35 mEq l-1), malate (0.59 ± 0.27 mEq l-1), and d-lactate (0.40 ± 0.51 mEq l-1) was observed. In 13 patients with diabetic ketoacidosis, significant increases in isocitrate (0.42 ± 0.35 mEq l-1), ?-ketoglutarate (0.41 ± 0.16 mEq l-1), malate (0.23 ± 0.18 mEq l-1) and d-lactate (0.16 ± 0.07 mEq l-1) were seen. Neither citrate nor succinate levels were increased. Similar findings were also observed in a further five patients with high anion gap acidosis of unknown origin with increases in isocitrate (0.95 ± 0.88 mEq l-1), ?-ketoglutarate (0.65 ± 0.20 mEq l-1), succinate (0.34 ± 0.13 mEq l-1), malate (0.49 ± 0.19 mEq l-1) and d-lactate (0.18 ± 0.14 mEq l-1) being observed but not in citrate concentration. In five patients with a normal anion gap acidosis, no increases were observed except a modest rise in d-lactate (0.17 ± 0.14 mEq l-1). Conclusion The levels of certain low molecular weight anions usually associated with intermediary metabolism were found to be significantly elevated in the plasma ultrafiltrate obtained from patients with metabolic acidosis. Our results suggest that these hitherto unmeasured anions may significantly contribute to the generation of the anion gap in patients with lactic acidosis and acidosis of unknown aetiology and may be underestimated in diabetic ketoacidosis. These anions are not significantly elevated in patients with normal anion gap acidosis. © 2005 Forni et al.; licensee BioMed Central Ltd.

Item Type: Article
Additional Information: About the authors: 1) Consultant Physician & Intensivist, Department of Critical Care, Worthing Hospital, Worthing, West Sussex, UK; 2) Research Fellow, Renal Laboratory, St Thomas' Hospital, London, UK; 3) MRC Scientist, MRC Toxicology Unit, Birkbeck College, London, UK; 4) Consultant Physician & Intensivist, Renal Laboratory, St Thomas' Hospital, London, UK; 5) Research Fellow, Department of Chemistry, Kingston University, Surrey, UK; 6) Consultant Physician & Research Director, Renal Laboratory, St Thomas' Hospital, London, UK
Uncontrolled Keywords: Circulating anions; Krebs cycle; patients; metabolic acidosis; lactic acidosis; ketoacidosis; high anion gap
Research Area: Chemistry
Other hospital based clinical subjects
Other laboratory based clinical subjects
Faculty, School or Research Centre: Faculty of Science (until 2011) > School of Pharmacy and Chemistry
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Depositing User: Jean-Marie Peron
Date Deposited: 15 Dec 2009 15:03
Last Modified: 16 Jul 2012 21:48
URI: http://eprints.kingston.ac.uk/id/eprint/7385

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