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DOI 10.1210/jc.2019-00721

Медицинская библиотека · The Journal of clinical endocrinology and metabolism · 2019

Hydroxylated Long-Chain Acylcarnitines are Biomarkers of Mitochondrial Myopathy.

Vissing Christoffer Rasmus, Dunø Morten, Wibrand Flemming, Christensen Mette, Vissing John

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Аннотация

CONTEXT: Plasma acylcarnitines are biomarkers of β-oxidation and are useful in diagnosing several inborn errors of metabolism but have never been investigated systematically in patients with mitochondrial myopathy.

OBJECTIVE

We hypothesized that acylcarnitines can also be biomarkers of mitochondrial myopathy and sought to investigate the prevalence and pattern of elevated acylcarnitines.

DESIGN

This was a prospective cohort study of patients with confirmed mitochondrial myopathy followed at Copenhagen Neuromuscular Center, Rigshospitalet, Copenhagen, Denmark.

PATIENTS: We included 35 patients (44 ± 15 years, 15 women) with mitochondrial myopathy caused by single, large-scale deletions of mitochondrial DNA (n = 17), pathogenic variants in mitochondrial transfer RNA (n = 13), or in proteins of the respiratory chain complexes (n = 5).Concentrations of 35 acylcarnitines were measured using ultra-HPLC and tandem mass-spectrometry. Findings were compared with muscle mutation load in all patients and to respiratory chain activity in 26 patients.

MAIN OUTCOME MEASURES: Prevalence of elevated concentrations of acylcarnitines related to acyl-coenzyme A (CoA) dehydrogenases in patients with mitochondrial myopathy and relation to genotypes/phenotypes.

RESULTS

In total, 27 (77%) patients had elevated concentrations of acylcarnitines related to acyl-CoA dehydrogenases. Elevated concentrations of seven acylcarnitine species were more common in patients compared with a control cohort of >900 individuals, and a specific pattern involving hydroxylated long-chain acylcarnitines occurred in 22 (63%) patients. Severity of derangements was correlated with muscle mutation load and genotypes/phenotypes.

CONCLUSION

In conclusion, elevated concentrations of acylcarnitines is common in patients with mitochondrial myopathy and shows a specific pattern affecting hydroxylated long-chain acylcarnitines, which can have implications for future diagnostic workup of patients.

Для цитирования: Vissing Christoffer Rasmus, Dunø Morten, Wibrand Flemming, Christensen Mette, Vissing John. Hydroxylated Long-Chain Acylcarnitines are Biomarkers of Mitochondrial Myopathy.. The Journal of clinical endocrinology and metabolism. 2019. DOI: 10.1210/jc.2019-00721.

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