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Defect of Cobalamin Intracellular Metabolism Presenting as Diabetic Ketoacidosis: A Rare Manifestation

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JIMD Reports - Volume 11

Part of the book series: JIMD Reports ((JIMD,volume 11))

Abstract

Hypoglycemia is the usual feature of commonly occurring organic acidemias. Organic acidemias manifesting as hyperglycemia or diabetic ketoacidosis are rare and only a few cases have been reported. We report a 13-month-old boy who presented with vomiting, dehydration, coma, hyperglycemia, high anion gap metabolic acidosis and ketosis, mimicking diabetic ketoacidosis (DKA). Treatment with parenteral fluid, electrolytes, and insulin infusion resulted in an improvement in hyperglycemia, but persistence of metabolic acidosis and lack of improvement of neurologic status led us to suspect an organic acidemia. Urinary organic acid analysis revealed increased methylmalonic acid levels. In addition, hyperhomocysteinemia and homocystinuria were also noted in presence of normal vitamin B12 levels. This confirmed the diagnosis of cobalamin metabolism defect leading to combined methylmalonic aciduria and homocystinuria. There was some improvement in neurologic status and metabolic parameters after treatment with low-protein diet, vitamin B12, folic acid, and L-carnitine, but he ultimately succumbed to polymicrobial nosocomial sepsis. The entire MMACHC gene of the patient was sequenced and no mutations were identified. This is probably the first case report of cobalamin intracellular metabolism defect (CblC/CblD/CblF/CblJ or ABCD4) presenting as diabetic ketoacidosis.

Competing interests: None declared

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References

  • Abramowicz MJ, Andrien M et al (1994) Isodisomy of chromosome 6 in a newborn with methylmalonic acidemia and agenesis of pancreatic beta cells causing diabetes mellitus. J Clin Invest 94(1):418–421

    Article  PubMed  CAS  Google Scholar 

  • Bachynski BN, Flynn JT et al (1986) Hyperglycemic acidotic coma and death in Kearns-Sayre syndrome. Ophthalmology 93(3):391–396

    PubMed  CAS  Google Scholar 

  • Boeckx RL, Hicks JM (1982) Methylmalonic acidemia with the unusual complication of severe hyperglycemia. Clin Chem 28(8):1801–1803

    PubMed  CAS  Google Scholar 

  • Ciani F, Donati MA et al (2000) Lethal late onset cblB methylmalonic aciduria. Crit Care Med 28(6):2119–2121

    Article  PubMed  CAS  Google Scholar 

  • Coelho D, Suormala T et al (2008) Gene identification for the cblD defect of vitamin B12 metabolism. N Engl J Med 358(14):1454–1464

    Article  PubMed  CAS  Google Scholar 

  • Coelho D, Kim JC et al (2012) Mutations in ABCD4 cause a new inborn error of vitamin B12 metabolism. Nat Genet 44(10):1152–1155

    Article  PubMed  CAS  Google Scholar 

  • Dweikat IM, Naser EN et al (2011) Propionic acidemia mimicking diabetic ketoacidosis. Brain Dev 33(5):428–431

    Article  PubMed  Google Scholar 

  • Filippi L, Gozzini E, et al (2009). Insulin-resistant hyperglycaemia complicating neonatal onset of methylmalonic and propionic acidaemias. J Inherit Metab Dis 32 Suppl 1:S179–86

    Google Scholar 

  • Fowler B, Leonard JV et al (2008) Causes of and diagnostic approach to methylmalonic acidurias. J Inherit Metab Dis 31(3):350–360

    Article  PubMed  CAS  Google Scholar 

  • Froese DS, Gravel RA (2010) Genetic disorders of vitamin B(1)(2) metabolism: eight complementation groups–eight genes. Expert Rev Mol Med 12:e37

    Article  PubMed  Google Scholar 

  • Guven A, Cebeci N et al (2012) Methylmalonic acidemia mimicking diabetic ketoacidosis in an infant. Pediatr Diabetes 13(6):e22–25

    Article  PubMed  CAS  Google Scholar 

  • Henriquez H, el Din A, et al (1994) Emergency presentations of patients with methylmalonic acidemia, propionic acidemia and branched chain amino acidemia (MSUD). Brain Dev 16 Suppl: 86–93

    Google Scholar 

  • Hou JW (2004) Biotin responsive multiple carboxylase deficiency presenting as diabetic ketoacidosis. Chang Gung Med J 27(2):129–133

    PubMed  Google Scholar 

  • Imen M, Hanene B et al (2012) Methylmalonic acidemia and hyperglycemia: an unusual association. Brain Dev 34(2):113–114

    Article  PubMed  Google Scholar 

  • Kim JC, Lee NC et al (2012) Late onset of symptoms in an atypical patient with the cblJ inborn error of vitamin B12 metabolism: diagnosis and novel mutation revealed by exome sequencing. Mol Genet Metab 107(4):664–668

    Article  PubMed  CAS  Google Scholar 

  • Lerner-Ellis JP, Tirone JC et al (2006) Identification of the gene responsible for methylmalonic aciduria and homocystinuria, cblC type. Nat Genet 38(1):93–100

    Article  PubMed  CAS  Google Scholar 

  • Lerner-Ellis JP, Anastasio N et al (2009) Spectrum of mutations in MMACHC, allelic expression, and evidence for genotype-phenotype correlations. Hum Mutat 30(7):1072–1081

    Article  PubMed  CAS  Google Scholar 

  • Marles SL, Casiro OG (1998) Persistent neonatal hypoglycemia: diagnosis and management. Paediatr Child Health 3(1):16–19

    PubMed  CAS  Google Scholar 

  • Mathew PM, Hamdan JA (1988) Transient diabetes mellitus in neonatal methylmalonic aciduria. J Inherit Metab Dis 11(2):218–219

    Article  PubMed  CAS  Google Scholar 

  • Ozand PT (2000) Hypoglycemia in association with various organic and amino acid disorders. Semin Perinatol 24(2):172–193

    Article  PubMed  CAS  Google Scholar 

  • Paksu MS, Kalkan G et al (2011) Gluconeogenesis defect presenting with resistant hyperglycemia and acidosis mimicking diabetic ketoacidosis. Pediatr Emerg Care 27(12):1180–1181

    Article  PubMed  Google Scholar 

  • Rosenblatt DS, Hosack A et al (1985) Defect in vitamin B12 release from lysosomes: newly described inborn error of vitamin B12 metabolism. Science 228(4705):1319–1321

    Article  PubMed  CAS  Google Scholar 

  • Rutsch F, Gailus S et al (2009) Identification of a putative lysosomal cobalamin exporter altered in the cblF defect of vitamin B12 metabolism. Nat Genet 41(2):234–239

    Article  PubMed  CAS  Google Scholar 

  • Watkins D, Rosenblatt DS (2011) Inborn errors of cobalamin absorption and metabolism. Am J Med Genet C Semin Med Genet 157(1):33–44

    Article  PubMed  CAS  Google Scholar 

  • Worthen HG, al Ashwal A et al (1994) Comparative frequency and severity of hypoglycemia in selected organic acidemias, branched chain amino acidemia, and disorders of fructose metabolism. Brain Dev 16 Suppl: 81–85

    Google Scholar 

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Acknowledgments

We acknowledge Dr Lisa Kratz, Director, Biochemical Genetics Laboratory, Kennedy Krieger Institute, Baltimore (USA) for GCMS analysis.

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Correspondence to Savita Attri .

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Communicated by: Verena Peters

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Take-Home Message

Inborn errors of cobalamin metabolism can present with hyperglycemia and ketoacidosis, mimicking classical diabetic ketoacidosis. Testing for metabolic disorders in new onset diabetes patients should be considered, especially when response to traditional therapy is incomplete.

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Sharda, S., Angurana, S.K., Walia, M., Attri, S. (2013). Defect of Cobalamin Intracellular Metabolism Presenting as Diabetic Ketoacidosis: A Rare Manifestation. In: Zschocke, J., Gibson, K., Brown, G., Morava, E., Peters, V. (eds) JIMD Reports - Volume 11. JIMD Reports, vol 11. Springer, Berlin, Heidelberg. https://doi.org/10.1007/8904_2013_220

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  • DOI: https://doi.org/10.1007/8904_2013_220

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  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-37327-5

  • Online ISBN: 978-3-642-37328-2

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