Metformin-Associated Lactic Acidosis and Relative Euglycemic Ketoacidosis Precipitated by a Glucagon-Like Peptide-1 Receptor Agonist: A Case Report and Literature Review.

Metformin-associated lactic acidosis (MALA) is an uncommon but often fatal complication of metformin therapy (incidence less than 10 per 100,000 patient-years; with a 30-50% mortality). MALA most commonly occurs with acute kidney injury, which impairs metformin excretion and inhibits mitochondrial complex I, shifting pyruvate metabolism toward lactate production. Euglycemic diabetic ketoacidosis (euDKA), classically defined as DKA with glucose below 250 mg/dL, is increasingly recognized not only with sodium-glucose cotransporter-2 (SGLT2) inhibitors but also with glucagon-like peptide-1 receptor agonists (GLP-1 RA) through appetite suppression, vomiting, and reduced intake. Concurrent MALA and ketoacidosis with relative euglycemia is exceedingly rare, with no published synthesis of such cases to guide recognition or management. We present a case of severe MALA with ketoacidosis and relative euglycemia in a 59-year-old woman with type 2 diabetes on metformin and tirzepatide, managed successfully with emergent sequential hemodialysis and high-dose continuous venovenous hemodiafiltration. We also review reported MALA cases with GLP-1 RA use to identify shared precipitants, risk factors, and outcomes. The key lesson is that, in patients on metformin and a GLP-1 RA, gastrointestinal side effects can precipitate MALA, while a disproportionately low glucose can mask the accompanying ketoacidosis. Recognizing this pattern demands early measurement of serum beta-hydroxybutyrate and prompt initiation of renal replacement therapy.

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PubMed
Published
2026-09-04
DOI
https://doi.org/10.34067/kid.0000001379
Primary Topic
Diabetes Treatment and Management
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article
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article

Metformin-Associated Lactic Acidosis and Relative Euglycemic Ketoacidosis Precipitated by a Glucagon-Like Peptide-1 Receptor Agonist: A Case Report and Literature Review.

Harsha Adnani, Ami Patel, Matthew R Weir, Melinda Lee et al.
PubMed
Diabetes Treatment and Management
article

Metformin-Associated Lactic Acidosis and Relative Euglycemic Ketoacidosis Precipitated by a Glucagon-Like Peptide-1 Receptor Agonist: A Case Report and Literature Review.

Harsha Adnani, Ami Patel, Matthew R Weir, Melinda Lee, Joshua King, Zoya Ladiwala
article en

Abstract

Metformin-associated lactic acidosis (MALA) is an uncommon but often fatal complication of metformin therapy (incidence less than 10 per 100,000 patient-years; with a 30-50% mortality). MALA most commonly occurs with acute kidney injury, which impairs metformin excretion and inhibits mitochondrial complex I, shifting pyruvate metabolism toward lactate production. Euglycemic diabetic ketoacidosis (euDKA), classically defined as DKA with glucose below 250 mg/dL, is increasingly recognized not only with sodium-glucose cotransporter-2 (SGLT2) inhibitors but also with glucagon-like peptide-1 receptor agonists (GLP-1 RA) through appetite suppression, vomiting, and reduced intake. Concurrent MALA and ketoacidosis with relative euglycemia is exceedingly rare, with no published synthesis of such cases to guide recognition or management. We present a case of severe MALA with ketoacidosis and relative euglycemia in a 59-year-old woman with type 2 diabetes on metformin and tirzepatide, managed successfully with emergent sequential hemodialysis and high-dose continuous venovenous hemodiafiltration. We also review reported MALA cases with GLP-1 RA use to identify shared precipitants, risk factors, and outcomes. The key lesson is that, in patients on metformin and a GLP-1 RA, gastrointestinal side effects can precipitate MALA, while a disproportionately low glucose can mask the accompanying ketoacidosis. Recognizing this pattern demands early measurement of serum beta-hydroxybutyrate and prompt initiation of renal replacement therapy.

PubMed
University of Maryland, Baltimore (US)
Good health and well-being
Openalex Percentile: Top 10%
Diabetes Treatment and Management
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