Literature DB >> 27231520

Mitochondrial vasculopathy.

Josef Finsterer1, Sinda Zarrouk-Mahjoub1.   

Abstract

Mitochondrial disorders (MIDs) are usually multisystem disorders (mitochondrial multiorgan disorder syndrome) either on from onset or starting at a point during the disease course. Most frequently affected tissues are those with a high oxygen demand such as the central nervous system, the muscle, endocrine glands, or the myocardium. Recently, it has been shown that rarely also the arteries may be affected (mitochondrial arteriopathy). This review focuses on the type, diagnosis, and treatment of mitochondrial vasculopathy in MID patients. A literature search using appropriate search terms was carried out. Mitochondrial vasculopathy manifests as either microangiopathy or macroangiopathy. Clinical manifestations of mitochondrial microangiopathy include leukoencephalopathy, migraine-like headache, stroke-like episodes, or peripheral retinopathy. Mitochondrial macroangiopathy manifests as atherosclerosis, ectasia of arteries, aneurysm formation, dissection, or spontaneous rupture of arteries. The diagnosis relies on the documentation and confirmation of the mitochondrial metabolic defect or the genetic cause after exclusion of non-MID causes. Treatment is not at variance compared to treatment of vasculopathy due to non-MID causes. Mitochondrial vasculopathy exists and manifests as micro- or macroangiopathy. Diagnosing mitochondrial vasculopathy is crucial since appropriate treatment may prevent from severe complications.

Entities:  

Keywords:  Angiopathy; Arteriopathy; Genotype; Mitochondrial disorder; MtDNA; Multisystem; Phenotype; Vasculopathy

Year:  2016        PMID: 27231520      PMCID: PMC4877362          DOI: 10.4330/wjc.v8.i5.333

Source DB:  PubMed          Journal:  World J Cardiol


  57 in total

1.  Carotid dissection in mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes.

Authors:  Robin C C Ryther; Yoon Andrew Cho-Park; Jong Woo Lee
Journal:  J Neurol       Date:  2010-11-13       Impact factor: 4.849

Review 2.  [Comparison of clinical pictures of mitochondrial encephalomyopathy with tRNA(Leu(UUR)) mutation in 3243 with that in 3254].

Authors:  T Mitsuoka; T Kawarai; C Watanabe; S Katayama; S Nakamura
Journal:  No To Shinkei       Date:  1998-12

3.  Dilation of the aortic root in mitochondrial disease patients.

Authors:  Nicola Brunetti-Pierri; Ricardo Pignatelli; Negin Fouladi; Jeffrey A Towbin; John W Belmont; William J Craigen; Lee-Jun Wong; John L Jefferies; Fernando Scaglia
Journal:  Mol Genet Metab       Date:  2011-02-18       Impact factor: 4.797

4.  Diffusion and perfusion characteristics of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode) in thirteen patients.

Authors:  Ji Hye Kim; Myung Kwan Lim; Tae Yeon Jeon; Joung Ho Rha; Jung Ho Rha; Hong Eo; So-Young Yoo; Chang Hae Shu
Journal:  Korean J Radiol       Date:  2011-01-03       Impact factor: 3.500

5.  Endothelial dysfunction in MELAS improved by l-arginine supplementation.

Authors:  Y Koga; Y Akita; N Junko; S Yatsuga; N Povalko; R Fukiyama; M Ishii; T Matsuishi
Journal:  Neurology       Date:  2006-06-13       Impact factor: 9.910

6.  Multisystem disorder in late-onset chronic progressive external ophthalmoplegia.

Authors:  Gerald Pfeffer; Sandra Sirrs; N Kevin Wade; Michelle M Mezei
Journal:  Can J Neurol Sci       Date:  2011-01       Impact factor: 2.104

7.  Endothelial dysfunction and increased oxidative stress in mitochondrial diseases.

Authors:  Pietro Minuz; Cristiano Fava; Gaetano Vattemi; Guido Arcaro; Matteo Riccadonna; Paola Tonin; Alessandra Meneguzzi; Maurizio Degan; Valeria Guglielmi; Alessandro Lechi; Giuliano Tomelleri
Journal:  Clin Sci (Lond)       Date:  2012-03       Impact factor: 6.124

Review 8.  [Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes (MELAS) with chronic renal failure: report of mother-child cases].

Authors:  M Ihara; H Tanaka; M Yashiro; Y Nishimura
Journal:  Rinsho Shinkeigaku       Date:  1996-09

9.  A mutational hot spot in the mitochondrial ND6 gene in patients with Leber's hereditary optic neuropathy.

Authors:  Janina Luberichs; Beate Leo-Kottler; Dorothea Besch; Sascha Fauser
Journal:  Graefes Arch Clin Exp Ophthalmol       Date:  2002-02       Impact factor: 3.117

10.  Aortic rupture in mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes.

Authors:  Stacey H K Tay; Douglas R Nordli; Eduardo Bonilla; Edward Null; Sara Monaco; Michio Hirano; Salvatore DiMauro
Journal:  Arch Neurol       Date:  2006-02
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  17 in total

1.  Late onset MELAS with m.3243A > G mutation and its association with aneurysm formation.

Authors:  Kun Zhu; Shuang Li; Huan Chen; Yao Wang; Miao Yu; Hongyan Wang; Weijie Zhao; Yunpeng Cao
Journal:  Metab Brain Dis       Date:  2017-03-21       Impact factor: 3.584

2.  Macroangiopathy is a typical phenotypic manifestation of MELAS.

Authors:  Josef Finsterer; Sinda Zarrouk-Mahjoub
Journal:  Metab Brain Dis       Date:  2017-05-02       Impact factor: 3.584

3.  Secondary manifestations of mitochondrial disorders.

Authors:  Josef Finsterer
Journal:  J Zhejiang Univ Sci B       Date:  2020-07       Impact factor: 3.066

4.  Cerebral involvement in mitochondrial disorders on imaging.

Authors:  Josef Finsterer; Sinda Zarrouk-Mahjoub
Journal:  Childs Nerv Syst       Date:  2016-09-09       Impact factor: 1.475

5.  Diagnosing MELAS requires not only an mtDNA variant but also an appropriate phenotype.

Authors:  Josef Finsterer; Sinda Zarrouk-Mahjoub
Journal:  Doc Ophthalmol       Date:  2019-03-28       Impact factor: 2.379

Review 6.  Mitophagy in Human Diseases.

Authors:  Laura Doblado; Claudia Lueck; Claudia Rey; Alejandro K Samhan-Arias; Ignacio Prieto; Alessandra Stacchiotti; Maria Monsalve
Journal:  Int J Mol Sci       Date:  2021-04-09       Impact factor: 5.923

7.  Arterioectatic Spinal Angiopathy of Childhood: Clinical, Imaging, Laboratory, Histologic, and Genetic Description of a Novel CNS Vascular Pathology.

Authors:  T Abruzzo; R van den Berg; S Vadivelu; S W Hetts; M Dishop; P Cornejo; V Narayanan; K E Ramsey; C Coopwood; E G Medici-van den Herik; S D Roosendaal; M Lawton; S Bernes
Journal:  AJNR Am J Neuroradiol       Date:  2022-06-30       Impact factor: 4.966

Review 8.  Cardiac complications in inherited mitochondrial diseases.

Authors:  Mohaddeseh Behjati; Mohammad Reza Sabri; Masood Etemadi Far; Majid Nejati
Journal:  Heart Fail Rev       Date:  2021-03       Impact factor: 4.214

Review 9.  Functional Mitochondria in Health and Disease.

Authors:  Patries M Herst; Matthew R Rowe; Georgia M Carson; Michael V Berridge
Journal:  Front Endocrinol (Lausanne)       Date:  2017-11-03       Impact factor: 5.555

10.  Mitochondrial vasculopathy due to the m.3243A > G mutation is not restricted to the carotid artery.

Authors:  Josef Finsterer; Sinda Zarrouk-Mahjoub
Journal:  Mol Genet Metab Rep       Date:  2016-10-08
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