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Erschienen in: Neuroradiology 8/2017

30.06.2017 | Paediatric Neuroradiology

Cortical venous disease severity in MELAS syndrome correlates with brain lesion development

verfasst von: M. T. Whitehead, M. Wien, B. Lee, N. Bass, A. Gropman

Erschienen in: Neuroradiology | Ausgabe 8/2017

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Abstract

Purpose

MELAS syndrome is a mitochondrial disorder typified by recurrent stroke-like episodes, seizures, and progressive brain injury. Abnormal mitochondria have been found in arterial walls implicating a vasculogenic etiology. We have observed abnormal cortical vein T2/FLAIR signal in MELAS patients, potentially representing wall thickening and sluggish flow. We sought to examine the relationship of hyperintense veins and brain lesions in MELAS.

Methods

Imaging databases at two children’s hospitals were searched for brain MRIs from MELAS patients. Artifact, sedated exams, and lack of 2D–T2/FLAIR sequences were exclusion criteria. Each exam was assigned a venous score based on number of T2/FLAIR hyperintense veins: 1 = <10, 2 = 10 to 20, 3 = >20. Cumulative brain lesions and venous score in MELAS and aged-matched normal exams were compared by Mann-Whitney test.

Results

A total of 106 exams from 14 unique MELAS patients (mean 16 ± 3 years) and 30 exams from normal aged-matched patients (mean 15 ± 3 years) were evaluated. Median venous score between MELAS and control patients significantly differed (3 versus 1; p < 0.001). In the MELAS group, venous score correlated with presence (median = 3) or absence (median = 1) of cumulative brain lesions. In all 8 MELAS patients who developed lesions, venous hyperintensity was present prior to, during, and after lesion onset. Venous score did not correlate with brain lesion acuity.

Conclusion

Abnormal venous signal correlates with cumulative brain lesion severity in MELAS syndrome. Cortical venous stenosis, congestion, and venous ischemia may be mechanisms of brain injury. Identification of cortical venous pathology may aid in diagnosis and could be predictive of lesion development.
Literatur
1.
Zurück zum Zitat Goto T, Nonaka I, Harai S (1990) A mutation in the tRNA leu (UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature 348:651–653CrossRefPubMed Goto T, Nonaka I, Harai S (1990) A mutation in the tRNA leu (UUR) gene associated with the MELAS subgroup of mitochondrial encephalomyopathies. Nature 348:651–653CrossRefPubMed
3.
Zurück zum Zitat Demarest ST, Whitehead MT, Turnacioglu S, Pearl PL, Gropman AL (2014) Phenotypic analysis of epilepsy in the mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes-associated mitochondrial DNA A3243G mutation. J Child Neurol 29(9):1249–1256CrossRefPubMed Demarest ST, Whitehead MT, Turnacioglu S, Pearl PL, Gropman AL (2014) Phenotypic analysis of epilepsy in the mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes-associated mitochondrial DNA A3243G mutation. J Child Neurol 29(9):1249–1256CrossRefPubMed
4.
Zurück zum Zitat Hirano RE, Koenigsberger MR, Defendini R, Pavlakis SG, DeVivo DC, DiMauro S, Rowland LP (1992) MELAS: an original case and clinical criteria for diagnosis. Neuromuscul Disord 2:125–135CrossRefPubMed Hirano RE, Koenigsberger MR, Defendini R, Pavlakis SG, DeVivo DC, DiMauro S, Rowland LP (1992) MELAS: an original case and clinical criteria for diagnosis. Neuromuscul Disord 2:125–135CrossRefPubMed
5.
Zurück zum Zitat Yatsuga S, Povalko N, Nishioka J, Katayama K, Kakimoto N, Matsuishi T, Kakuma T, Koga Y, Taro Matsuoka for MELAS Study Group in Japan (2012) MELAS: a nationwide prospective cohort study of 96 patients in Japan. Biochim Biophys Acta 1820:619–624CrossRefPubMed Yatsuga S, Povalko N, Nishioka J, Katayama K, Kakimoto N, Matsuishi T, Kakuma T, Koga Y, Taro Matsuoka for MELAS Study Group in Japan (2012) MELAS: a nationwide prospective cohort study of 96 patients in Japan. Biochim Biophys Acta 1820:619–624CrossRefPubMed
7.
Zurück zum Zitat Tschampa HJ, Urbach H, Greschus S, Kunz WS, Kornblum C (2013) Neuroimaging characteristics in mitochondrial encephalopathies associated with the m.3243A>G MTTL1 mutation. J Neurol 260(4):1071–1080CrossRefPubMed Tschampa HJ, Urbach H, Greschus S, Kunz WS, Kornblum C (2013) Neuroimaging characteristics in mitochondrial encephalopathies associated with the m.3243A>G MTTL1 mutation. J Neurol 260(4):1071–1080CrossRefPubMed
8.
Zurück zum Zitat Lorenzoni PJ, Werneck LC, Kay CS, Silvado CE, Scola RH (2015) When should MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) be the diagnosis? Arq Neuropsiquiatr 73(11):959–967CrossRefPubMed Lorenzoni PJ, Werneck LC, Kay CS, Silvado CE, Scola RH (2015) When should MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes) be the diagnosis? Arq Neuropsiquiatr 73(11):959–967CrossRefPubMed
9.
Zurück zum Zitat Kaufmann P, Engelstad K, Wei Y et al (2011) Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype. Neurology 77(22):1965–1971CrossRefPubMedPubMedCentral Kaufmann P, Engelstad K, Wei Y et al (2011) Natural history of MELAS associated with mitochondrial DNA m.3243A>G genotype. Neurology 77(22):1965–1971CrossRefPubMedPubMedCentral
10.
Zurück zum Zitat Barkovich AJ, Good WV, Koch TK, Berg BO (1993) Mitochondrial disorders: analysis of their clinical and imaging characteristics. AJNR Am J Neuroradiol 14:1119–1137PubMed Barkovich AJ, Good WV, Koch TK, Berg BO (1993) Mitochondrial disorders: analysis of their clinical and imaging characteristics. AJNR Am J Neuroradiol 14:1119–1137PubMed
11.
Zurück zum Zitat Friedman SD, Shaw DW, Ishak G, Gropman AL, Saneto RP (2010) The use of neuroimaging in the diagnosis of mitochondrial disease. Dev Disabil Res Rev 16(2):129–135CrossRefPubMed Friedman SD, Shaw DW, Ishak G, Gropman AL, Saneto RP (2010) The use of neuroimaging in the diagnosis of mitochondrial disease. Dev Disabil Res Rev 16(2):129–135CrossRefPubMed
12.
Zurück zum Zitat Matthews PM, Tampieri D, Berkovic SF et al (1991) Magnetic resonance imaging shows specific abnormalities in the MELAS syndrome. Neurology 41:1043–1046CrossRefPubMed Matthews PM, Tampieri D, Berkovic SF et al (1991) Magnetic resonance imaging shows specific abnormalities in the MELAS syndrome. Neurology 41:1043–1046CrossRefPubMed
13.
Zurück zum Zitat Kim JH, Lim MK, Jeon TY et al (2011) Diffusion and perfusion characteristics of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode) in thirteen patients. Korean J Radiol 12(1):15–24CrossRefPubMedPubMedCentral Kim JH, Lim MK, Jeon TY et al (2011) Diffusion and perfusion characteristics of MELAS (mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episode) in thirteen patients. Korean J Radiol 12(1):15–24CrossRefPubMedPubMedCentral
14.
Zurück zum Zitat Li R, Xiao HF, Lyu JH, Wang, JJD, Ma L, Lou X (2016) Differential diagnosis of mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) and ischemic stroke using 3D pseudocontinuous arterial spin labeling. J Magn Reson Imaging Li R, Xiao HF, Lyu JH, Wang, JJD, Ma L, Lou X (2016) Differential diagnosis of mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) and ischemic stroke using 3D pseudocontinuous arterial spin labeling. J Magn Reson Imaging
15.
Zurück zum Zitat Wang Z, Xiao J, Xie S, Zhao D et al (2012) MR evaluation of cerebral oxygen metabolism and blood flow in stroke-like episodes of MELAS. J Neurol Sci 323(1–2):173–177CrossRefPubMed Wang Z, Xiao J, Xie S, Zhao D et al (2012) MR evaluation of cerebral oxygen metabolism and blood flow in stroke-like episodes of MELAS. J Neurol Sci 323(1–2):173–177CrossRefPubMed
16.
Zurück zum Zitat Ohama E, Ohara S, Ikuta F, Tanaka K, Nishizawa M, Miyatake T (1987) Mitochondrial angiopathy in cerebral blood vessels of mitochondrial encephalomyopathy. Acta Neuropathol 74(3):226–233CrossRefPubMed Ohama E, Ohara S, Ikuta F, Tanaka K, Nishizawa M, Miyatake T (1987) Mitochondrial angiopathy in cerebral blood vessels of mitochondrial encephalomyopathy. Acta Neuropathol 74(3):226–233CrossRefPubMed
17.
Zurück zum Zitat Mizukami K, Sasaki M, Suzuki T et al (1992) Central nervous system changes in mitochondrial encephalomyopathy: light and electron microscopic study. Acta Neuropathol 83(4):449–452CrossRefPubMed Mizukami K, Sasaki M, Suzuki T et al (1992) Central nervous system changes in mitochondrial encephalomyopathy: light and electron microscopic study. Acta Neuropathol 83(4):449–452CrossRefPubMed
18.
Zurück zum Zitat Gilchrist JM, Sikirica M, Stopa E, Shanske S (1996) Adult-onset MELAS. Evidence for involvement of neurons as well as cerebral vasculature in strokelike episodes. Stroke 27(8):1420–1423CrossRefPubMed Gilchrist JM, Sikirica M, Stopa E, Shanske S (1996) Adult-onset MELAS. Evidence for involvement of neurons as well as cerebral vasculature in strokelike episodes. Stroke 27(8):1420–1423CrossRefPubMed
19.
Zurück zum Zitat Sparaco M, Simonati A, Cavallaro T et al (2003) MELAS: clinical phenotype and morphological brain abnormalities. Acta Neuropathol 106(3):202–212CrossRefPubMed Sparaco M, Simonati A, Cavallaro T et al (2003) MELAS: clinical phenotype and morphological brain abnormalities. Acta Neuropathol 106(3):202–212CrossRefPubMed
20.
Zurück zum Zitat Bonneville F (2014) Imaging of cerebral venous thrombosis. Diagn Interv Imaging 12:1145–1150CrossRef Bonneville F (2014) Imaging of cerebral venous thrombosis. Diagn Interv Imaging 12:1145–1150CrossRef
21.
Zurück zum Zitat Toyoda K, Ida M, Fukuda K (2001) Fluid-attenuated inversion recovery intraarterial signal: an early sign of hyperacute cerebral ischemia. AJNR Am J Neuroradiol 22(6):1021–1029PubMed Toyoda K, Ida M, Fukuda K (2001) Fluid-attenuated inversion recovery intraarterial signal: an early sign of hyperacute cerebral ischemia. AJNR Am J Neuroradiol 22(6):1021–1029PubMed
Metadaten
Titel
Cortical venous disease severity in MELAS syndrome correlates with brain lesion development
verfasst von
M. T. Whitehead
M. Wien
B. Lee
N. Bass
A. Gropman
Publikationsdatum
30.06.2017
Verlag
Springer Berlin Heidelberg
Erschienen in
Neuroradiology / Ausgabe 8/2017
Print ISSN: 0028-3940
Elektronische ISSN: 1432-1920
DOI
https://doi.org/10.1007/s00234-017-1866-3

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