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Case Reports
. 2024 Jan 26:38:101061.
doi: 10.1016/j.ymgmr.2024.101061. eCollection 2024 Mar.

Stealthy progression of type 2 diabetes mellitus due to impaired ketone production in an adult patient with multiple acyl-CoA dehydrogenase deficiency

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Case Reports

Stealthy progression of type 2 diabetes mellitus due to impaired ketone production in an adult patient with multiple acyl-CoA dehydrogenase deficiency

Nodoka Ikeda et al. Mol Genet Metab Rep. .

Abstract

Background: Multiple acyl-CoA dehydrogenase deficiency (MADD) is an inherited metabolic disorder caused by biallelic pathogenic variants in genes related to the flavoprotein complex. Dysfunction of the complex leads to impaired fatty acid oxidation and ketone body production which can cause hypoketotic hypoglycemia with prolonged fasting. Patients with fatty acid oxidation disorders (FAODs) such as MADD are treated primarily with a dietary regimen consisting of high-carbohydrate foods and avoidance of prolonged fasting. However, information on the long-term sequelae associated with this diet have not been accumulated. In general, high-carbohydrate diets can induce diseases such as type 2 diabetes mellitus (T2DM), although few patients with both MADD and T2DM have been reported.

Case: We present the case of a 32-year-old man with MADD who was on a high-carbohydrate diet for >30 years and exhibited symptoms resembling diabetic ketoacidosis. He presented with polydipsia, polyuria, and weight loss with a decrease in body mass index from 31 to 25 kg/m2 over 2 months. Laboratory tests revealed a HbA1c level of 13.9%; however, the patient did not show metabolic acidosis but only mild ketosis.

Discussion/conclusion: This report emphasizes the potential association between long-term adherence to high-carbohydrate dietary therapy and T2DM development. Moreover, this case underscores the difficulty of detecting diabetic ketosis in patients with FAODs such as MADD due to their inability to produce ketone bodies. These findings warrant further research of the long-term complications associated with this diet as well as warning of the potential progression of diabetes in patients with FAODs such as MADD.

Keywords: Diabetic ketoacidosis; Multiple acyl-CoA dehydrogenase deficiency; Type 2 diabetes mellitus.

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Conflict of interest statement

None.

Figures

Fig. 1
Fig. 1
Temporal changes in AST, ALT, GGT, HbA1c, and BMI preceding and following the described episode.
Fig. 2
Fig. 2
Axial CT scans of the liver. A) 12 years prior to the episode. B) Near the time of the episode.

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References

    1. Frank F.E., Stephen G.I. In: The Online Metabolic and Molecular Bases of Inherited Disease. Valle David L., Antonarakis Stylianos, Ballabio Andrea, Beaudet Arthur L., Mitchell Grant A., editors. McGraw-Hill Education; New York, NY: 2019. Defects of electron transfer flavoprotein and electron transfer flavoprotein-ubiquinone oxidoreductase: Glutaric acidemia Type II.http://ommbid.mhmedical.com/content.aspx?aid=1170091187
    1. Henriques B.J., Olsen R.K.J. Katrine Jentoft, Gomes C.M., Bross P. Electron transfer flavoprotein and its role in mitochondrial energy metabolism in health and disease. Gene. 2021;776:145407. doi: 10.1016/j.gene.2021.145407. - DOI - PMC - PubMed
    1. Ghisla S., Thorpe C. Acyl-CoA dehydrogenases. A mechanistic overview. Eur. J. Biochem. 2004;271:494–508. doi: 10.1046/j.1432-1033.2003.03946.x. - DOI - PubMed
    1. Houten S.M., Violante S., Ventura F.V., Wanders R.J.A. The biochemistry and physiology of mitochondrial fatty acid β-oxidation and its genetic disorders. Annu. Rev. Physiol. 2015;78:1–22. doi: 10.1146/annurev-physiol-021115-105045. - DOI - PubMed
    1. Prasun . In: Multiple acyl-CoA dehydrogenase deficiency. Adam M.P., Mirzaa G.M., GeneReviews [Internet], editors. University of Washington; Seattle (WA: 2020. - PubMed

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