Mitochondrial DNA as a Factor of Glaucomous Optic Neuropathy’s Development Mechanism

Currently, the mitochondrial component is becoming increasingly significant in the development and progression of glaucoma optic neuropathy. Since mitochondria have their own genetic apparatus, the study of qualitative and quantitative changes in mitochondrial DNA (mtDNA) becomes part of the disease...

Full description

Saved in:
Bibliographic Details
Main Authors: I. R. Gazizova, I. O. Mazunin, T. N. Malishevskaya, O. A. Kiseleva, A. M. Gadzhiev, Al.-M. Rindzhibal
Format: Article
Language:Russian
Published: Ophthalmology Publishing Group 2019-12-01
Series:Oftalʹmologiâ
Subjects:
Online Access:https://www.ophthalmojournal.com/opht/article/view/1081
Tags: Add Tag
No Tags, Be the first to tag this record!
_version_ 1850039720871985152
author I. R. Gazizova
I. O. Mazunin
T. N. Malishevskaya
O. A. Kiseleva
A. M. Gadzhiev
Al.-M. Rindzhibal
author_facet I. R. Gazizova
I. O. Mazunin
T. N. Malishevskaya
O. A. Kiseleva
A. M. Gadzhiev
Al.-M. Rindzhibal
author_sort I. R. Gazizova
collection DOAJ
description Currently, the mitochondrial component is becoming increasingly significant in the development and progression of glaucoma optic neuropathy. Since mitochondria have their own genetic apparatus, the study of qualitative and quantitative changes in mitochondrial DNA (mtDNA) becomes part of the disease diagnosis, in addition to studying the functional characteristics of the organelles alone. Moreover, the inability to explain the nature of the disease by known mutations of nuclear DNA contributes to the the study of mtDNA. In this review, we briefly discuss the mitochondrial genetics and the role of mitochondrial haplogroups in the diseases manifestation. We summarize the accumulated data on the qualitative and quantitative changes in mtDNA in patients with glaucoma. We discuss the approach to prevent the inheritance of mutant mtDNA as a part of assisted reproductive technologies, as well as the first steps towards the mtDNA heteroplasmy level manipulation and direct mtDNA editing.
format Article
id doaj-art-33d554669aef44a4bedb0e4e6290906e
institution DOAJ
issn 1816-5095
2500-0845
language Russian
publishDate 2019-12-01
publisher Ophthalmology Publishing Group
record_format Article
series Oftalʹmologiâ
spelling doaj-art-33d554669aef44a4bedb0e4e6290906e2025-08-20T02:56:15ZrusOphthalmology Publishing GroupOftalʹmologiâ1816-50952500-08452019-12-0116447948610.18008/1816-5095-2019-4-479-486582Mitochondrial DNA as a Factor of Glaucomous Optic Neuropathy’s Development MechanismI. R. Gazizova0I. O. Mazunin1T. N. Malishevskaya2O. A. Kiseleva3A. M. Gadzhiev4Al.-M. Rindzhibal5Institute of Experimental MedicineCenter for Genomic Research, Immanuel Kant Baltic Federal UniversityHelmholtz National medical center of Eye DiseasesHelmholtz National medical center of Eye DiseasesState instituition of health care of Leningrad region “Vsevolozhsk clinical interdistrict hospital”Institute of Experimental MedicineCurrently, the mitochondrial component is becoming increasingly significant in the development and progression of glaucoma optic neuropathy. Since mitochondria have their own genetic apparatus, the study of qualitative and quantitative changes in mitochondrial DNA (mtDNA) becomes part of the disease diagnosis, in addition to studying the functional characteristics of the organelles alone. Moreover, the inability to explain the nature of the disease by known mutations of nuclear DNA contributes to the the study of mtDNA. In this review, we briefly discuss the mitochondrial genetics and the role of mitochondrial haplogroups in the diseases manifestation. We summarize the accumulated data on the qualitative and quantitative changes in mtDNA in patients with glaucoma. We discuss the approach to prevent the inheritance of mutant mtDNA as a part of assisted reproductive technologies, as well as the first steps towards the mtDNA heteroplasmy level manipulation and direct mtDNA editing.https://www.ophthalmojournal.com/opht/article/view/1081glaucoma optic neuropathyprimary open-angle glaucomamitochondrial dysfunctionmitochondrial geneticsmitochondrial dna (mtdna)mitochondrial haplogroupsmtdna mutations correctionmitochondrial oxidative stress
spellingShingle I. R. Gazizova
I. O. Mazunin
T. N. Malishevskaya
O. A. Kiseleva
A. M. Gadzhiev
Al.-M. Rindzhibal
Mitochondrial DNA as a Factor of Glaucomous Optic Neuropathy’s Development Mechanism
Oftalʹmologiâ
glaucoma optic neuropathy
primary open-angle glaucoma
mitochondrial dysfunction
mitochondrial genetics
mitochondrial dna (mtdna)
mitochondrial haplogroups
mtdna mutations correction
mitochondrial oxidative stress
title Mitochondrial DNA as a Factor of Glaucomous Optic Neuropathy’s Development Mechanism
title_full Mitochondrial DNA as a Factor of Glaucomous Optic Neuropathy’s Development Mechanism
title_fullStr Mitochondrial DNA as a Factor of Glaucomous Optic Neuropathy’s Development Mechanism
title_full_unstemmed Mitochondrial DNA as a Factor of Glaucomous Optic Neuropathy’s Development Mechanism
title_short Mitochondrial DNA as a Factor of Glaucomous Optic Neuropathy’s Development Mechanism
title_sort mitochondrial dna as a factor of glaucomous optic neuropathy s development mechanism
topic glaucoma optic neuropathy
primary open-angle glaucoma
mitochondrial dysfunction
mitochondrial genetics
mitochondrial dna (mtdna)
mitochondrial haplogroups
mtdna mutations correction
mitochondrial oxidative stress
url https://www.ophthalmojournal.com/opht/article/view/1081
work_keys_str_mv AT irgazizova mitochondrialdnaasafactorofglaucomousopticneuropathysdevelopmentmechanism
AT iomazunin mitochondrialdnaasafactorofglaucomousopticneuropathysdevelopmentmechanism
AT tnmalishevskaya mitochondrialdnaasafactorofglaucomousopticneuropathysdevelopmentmechanism
AT oakiseleva mitochondrialdnaasafactorofglaucomousopticneuropathysdevelopmentmechanism
AT amgadzhiev mitochondrialdnaasafactorofglaucomousopticneuropathysdevelopmentmechanism
AT almrindzhibal mitochondrialdnaasafactorofglaucomousopticneuropathysdevelopmentmechanism