MTP deficiency caused by HADHB mutations: Pathophysiology and clinical manifestations.

Robin Dagher, Rami Massie, Benoit J Gentil

Molecular genetics and metabolism 2021 May

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Mutations in the HADHB gene lead to Mitochondrial Trifunctional Protein (MTP) deficiency. MTP deficiency is a rare autosomal recessive disorder affecting long-chain fatty acid oxidation. Patients affected by MTP deficiency are unable to metabolize long-chain fatty-acids and suffer a variety of symptoms exacerbated during fasting. The three phenotypes associated with complete MTP deficiency are an early-onset cardiomyopathy and early death, an intermediate form with recurrent hypoketotic hypoglycemia and a sensorimotor neuropathy with episodic rhabdomyolysis with small amount of residual enzyme activities. This review aims to discuss the pathophysiological mechanisms and clinical manifestations of each phenotype, which appears different and linked to HADHB expression levels. Notably, the pathophysiology of the sensorimotor neuropathy is relatively unknown and we provide a hypothesis on the qualitative aspect of the role of acylcarnitine buildup in Schwann cells in MTP deficiency patients. We propose that acylcarnitine may exit the Schwann cell and alter membrane properties of nearby axons leading to axonal degeneration based on recent findings in different metabolic disorders. Copyright © 2021. Published by Elsevier Inc.

Citation

Robin Dagher, Rami Massie, Benoit J Gentil. MTP deficiency caused by HADHB mutations: Pathophysiology and clinical manifestations. Molecular genetics and metabolism. 2021 May;133(1):1-7