Endocrine disorders in mitochondrial disease
- PMID: 23769710
- PMCID: PMC3820028
- DOI: 10.1016/j.mce.2013.06.004
Endocrine disorders in mitochondrial disease
Abstract
Endocrine dysfunction in mitochondrial disease is commonplace, but predominantly restricted to disease of the endocrine pancreas resulting in diabetes mellitus. Other endocrine manifestations occur, but are relatively rare by comparison. In mitochondrial disease, neuromuscular symptoms often dominate the clinical phenotype, but it is of paramount importance to appreciate the multi-system nature of the disease, of which endocrine dysfunction may be a part. The numerous phenotypes attributable to pathogenic mutations in both the mitochondrial (mtDNA) and nuclear DNA creates a complex and heterogeneous catalogue of disease which can be difficult to navigate for novices and experts alike. In this article we provide an overview of the endocrine disorders associated with mitochondrial disease, the way in which the underlying mitochondrial disorder influences the clinical presentation, and how these factors influence subsequent management.
Keywords: Diabetes; Endocrine; Mitochondrial disease; m.3243A>G; mtDNA.
Copyright © 2013 The Authors. Published by Elsevier Ireland Ltd.. All rights reserved.
Similar articles
-
Mitochondrial disease and endocrine dysfunction.Nat Rev Endocrinol. 2017 Feb;13(2):92-104. doi: 10.1038/nrendo.2016.151. Epub 2016 Oct 7. Nat Rev Endocrinol. 2017. PMID: 27716753 Review.
-
Immunometabolism in Endocrine Disorders Leads to a High Frequency of Diabetes Mellitus Caused by Heteroplasmic mtDNA Mutations.Obes Surg. 2024 Oct;34(10):3927-3929. doi: 10.1007/s11695-024-07503-y. Epub 2024 Sep 15. Obes Surg. 2024. PMID: 39279001 No abstract available.
-
Resolving complexity in mitochondrial disease: Towards precision medicine.Mol Genet Metab. 2019 Sep-Oct;128(1-2):19-29. doi: 10.1016/j.ymgme.2019.09.003. Epub 2019 Sep 14. Mol Genet Metab. 2019. PMID: 31648942 Review.
-
[Mitochondrial diabetes: clinical features, diagnosis and management].Rev Med Interne. 2010 Mar;31(3):216-21. doi: 10.1016/j.revmed.2008.11.017. Epub 2009 Mar 18. Rev Med Interne. 2010. PMID: 19299044 Review. French.
-
The non-syndromic clinical spectrums of mtDNA 3243A>G mutation.Neurosciences (Riyadh). 2021 Apr;26(2):128-133. doi: 10.17712/nsj.2021.2.20200145. Neurosciences (Riyadh). 2021. PMID: 33814365 Free PMC article. Review.
Cited by
-
Cardiac complications in inherited mitochondrial diseases.Heart Fail Rev. 2021 Mar;26(2):391-403. doi: 10.1007/s10741-020-10009-1. Heart Fail Rev. 2021. PMID: 32728985 Review.
-
Not quite type 1 or type 2, what now? Review of monogenic, mitochondrial, and syndromic diabetes.Rev Endocr Metab Disord. 2018 Mar;19(1):35-52. doi: 10.1007/s11154-018-9446-3. Rev Endocr Metab Disord. 2018. PMID: 29777474 Review.
-
Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits.Am J Hum Genet. 2019 Jan 3;104(1):112-138. doi: 10.1016/j.ajhg.2018.12.001. Epub 2018 Dec 27. Am J Hum Genet. 2019. PMID: 30595373 Free PMC article.
-
Mitochondrial disease: an uncommon but important cause of diabetes mellitus.Endocrinol Diabetes Metab Case Rep. 2018 Sep 25;2018:18-0091. doi: 10.1530/EDM-18-0091. Endocrinol Diabetes Metab Case Rep. 2018. PMID: 30306776 Free PMC article.
-
Impaired mitochondrial complex I function as a candidate driver in the biological stress response and a concomitant stress-induced brain metabolic reprogramming in male mice.Transl Psychiatry. 2020 Jun 1;10(1):176. doi: 10.1038/s41398-020-0858-y. Transl Psychiatry. 2020. PMID: 32488052 Free PMC article.
References
-
- Abad M.M., Cotter P.D., Fodor F.H., Larson S., Ginsberg-Fellner F., Desnick R.J. Screening for the mitochondrial DNA A3243G mutation in children with insulin-dependent diabetes mellitus. Metabolism. 1997;46:445–449. - PubMed
-
- Adler A.I., Stevens R.J., Manley S.E., Bilous R.W., Cull C.A., Holman R.R. Development and progression of nephropathy in Type 2 diabetes: the United Kingdom Prospective Diabetes Study (UKPDS 64) Kidney Int. 2003;63:225–232. - PubMed
-
- Anderson S., Bankier A.T., Barrell B.G., de Bruijn M.H., Coulson A.R., Drouin J. Sequence and organization of the human mitochondrial genome. Nature. 1981;290:457–465. - PubMed
-
- Austin S., Vriesendorp F., Thandroyen F., Hecht J., Jones O., Johns D. Expanding the phenotype of the 8344 transfer RNA lysine mitochondrial DNA mutation. Neurology. 1998;51:1447–1450. - PubMed
-
- Balestri P., Grosso S. Endocrine disorders in two sisters affected by MELAS syndrome. J. Child Neurol. 2000;15:755–758. - PubMed
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical