Treatment of 5-oxyproline Anion Gap Acidosis with N-acetylcysteine

Introduction: Over 60 million Americans use acetaminophen (APAP) weekly. Mitochondrial APAP metabolism requires the consumption of glutathione which is produced by the glutathione cycle (GC) consuming the amino acid, cystine. 5-oxoproline anion gap (AG) metabolic acidosis occurs when high dose APAP therapy combined with inadequate protein intake leads to depletion of cystine. Low cystine levels block the GC causing accumulation of 5 oxyproline. N-Acetylcysteine, used to threat APAP overdose, restores the GC and should reduce 5-oxoproline production. Case Description: 81 y.o. woman with past Roux-n-Y gastric bypass, leukemia s/p bone marrow transplant, cervical vertebral collapse s/p surgeries was admitted for cervical and abdominal pain and anorexia and found to have UTI and severe constipation. Her pain does not respond to narcotics: she took APAP 650 BID and 2 tablets of Fioricet (APAP 600 mg) q 8 hours at home. She received IV APAP 1000 mg BID and 2 Fioricet BID in hospital. Her baseline normal gap metabolic acidosis is treated with Ca citrate, but on admission patient had mixed non-gap and AG metabolic acidosis with normal ketones, lactate, eGFR. Urine electrolytes showed sodium 35 mEq/L but chloride was undetectable, suggesting anion drag. On Day 2 riifaxamin was started for presumed bacterial overgrowth AG acidosis. She refused to stop APAP, but reduced to ~ 2200 mg daily and N acetyl cysteine 35 mg/kg BID stared day 5. AG normalized day 8. Samples obtained day 2 showed serum d-lactate normal and urine organic a 5-oxoproline was 44-fold top of normal range with no other organic acid elevated more than 6-fold (lactate 4-fold). Discussion: Clinical recognition of 5-oxoproline metabolic acidosis is important given delays in urinary organic acid results. Treatment is discontinuing APAP and feeding protein. This first report of N-acetylcysteine treatment may provide an option if APAP cannt be discontinued when adequate protein intake is not possible.

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Journal
Journal of the American Society of Nephrology
Published
2024-10-01
DOI
https://doi.org/10.1681/asn.2024y95km4xb
Citations
1
Primary Topic
Metabolism and Genetic Disorders
Type
article
Field-Weighted Citation Impact
0.38
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article

Treatment of 5-oxyproline Anion Gap Acidosis with N-acetylcysteine

Harold A. Franch, Ryan C. Fields
1 citations
Journal of the American Society of Nephrology
Metabolism and Genetic Disorders
0.38
article

Treatment of 5-oxyproline Anion Gap Acidosis with N-acetylcysteine

Harold A. Franch, Ryan C. Fields
article en
1 citations

Abstract

Introduction: Over 60 million Americans use acetaminophen (APAP) weekly. Mitochondrial APAP metabolism requires the consumption of glutathione which is produced by the glutathione cycle (GC) consuming the amino acid, cystine. 5-oxoproline anion gap (AG) metabolic acidosis occurs when high dose APAP therapy combined with inadequate protein intake leads to depletion of cystine. Low cystine levels block the GC causing accumulation of 5 oxyproline. N-Acetylcysteine, used to threat APAP overdose, restores the GC and should reduce 5-oxoproline production. Case Description: 81 y.o. woman with past Roux-n-Y gastric bypass, leukemia s/p bone marrow transplant, cervical vertebral collapse s/p surgeries was admitted for cervical and abdominal pain and anorexia and found to have UTI and severe constipation. Her pain does not respond to narcotics: she took APAP 650 BID and 2 tablets of Fioricet (APAP 600 mg) q 8 hours at home. She received IV APAP 1000 mg BID and 2 Fioricet BID in hospital. Her baseline normal gap metabolic acidosis is treated with Ca citrate, but on admission patient had mixed non-gap and AG metabolic acidosis with normal ketones, lactate, eGFR. Urine electrolytes showed sodium 35 mEq/L but chloride was undetectable, suggesting anion drag. On Day 2 riifaxamin was started for presumed bacterial overgrowth AG acidosis. She refused to stop APAP, but reduced to ~ 2200 mg daily and N acetyl cysteine 35 mg/kg BID stared day 5. AG normalized day 8. Samples obtained day 2 showed serum d-lactate normal and urine organic a 5-oxoproline was 44-fold top of normal range with no other organic acid elevated more than 6-fold (lactate 4-fold). Discussion: Clinical recognition of 5-oxoproline metabolic acidosis is important given delays in urinary organic acid results. Treatment is discontinuing APAP and feeding protein. This first report of N-acetylcysteine treatment may provide an option if APAP cannt be discontinued when adequate protein intake is not possible.

Journal of the American Society of NephrologyVol. 35(10S)
Emory University (US)
Openalex Percentile: Top 34%
Metabolism and Genetic Disorders
0.38
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