Progressive White Matter Changes in Mitochondrial Disease: A Quantitative MRI Study

dc.contributor.authorMickelsson, Nora
dc.contributor.authorHirvonen, Jussi
dc.contributor.authorMartikainen, Mika H.
dc.contributor.organizationfi=kliininen laitos|en=Department of Clinical Medicine|
dc.contributor.organizationfi=kuvantaminen ja kliininen diagnostiikka|en=Imaging and Clinical Diagnostics|
dc.contributor.organizationfi=tyks, vsshp|en=tyks, varha|
dc.contributor.organization-code1.2.246.10.2458963.20.61334543354
dc.contributor.organization-code1.2.246.10.2458963.20.69079168212
dc.converis.publication-id523754700
dc.converis.urlhttps://research.utu.fi/converis/portal/Publication/523754700
dc.date.accessioned2026-06-05T20:13:52Z
dc.description.abstract<p>Primary mitochondrial diseases frequently affect the central nervous system, yet the extent, distribution and progression of white matter hyperintensities (WMHs) remain insufficiently characterised, particularly in terms of quantitative volumetrics and longitudinal progression. Although WMHs are typically attributed to cerebral small-vessel disease, mitochondrial disorders may cause white matter injury through distinct vascular and metabolic mechanisms. We conducted a retrospective single-centre study at Turku University Hospital including 36 patients with mitochondrial disease, each with at least one brain MRI (73 images). Longitudinal data were available for 15 patients. Three-dimensional T1-weighted and FLAIR images (1.5/3 T) were analysed with the FDA-cleared cNeuro tool to obtain intracranial volume-normalised WMH and lesion volumes and an automated global Fazekas score. At baseline (median age 49 years), WMHs were present in all supratentorial regions. Over time, WMH volumes increased significantly in periventricular, deep and juxtacortical regions, while lesion progression was predominantly periventricular. Fazekas scores remained generally low and stable. In follow-up imaging, women and patients carrying the m.3243A>G variant showed a greater burden of WMHs and lesions, compared with men and those with other mitochondrial diagnoses. WMH load did not differ according to history of stroke-like episodes. Mitochondrial disease is associated with early and progressive WMH accumulation, particularly in individuals with the m.3243A>G variant, and the pattern exceeds what would be expected from conventional vascular risk factors alone. These findings support a disease-specific mechanism of white matter vulnerability and highlight the importance of quantitative MRI for monitoring progression in mitochondrial disease.<br></p>
dc.identifier.eissn2192-8312
dc.identifier.jour-issn2192-8304
dc.identifier.urihttps://www.utupub.fi/handle/11111/61623
dc.identifier.urlhttps://doi.org/10.1002/jmd2.70093
dc.identifier.urnURN:NBN:fi-fe2026060564522
dc.language.isoen
dc.okm.affiliatedauthorMickelsson, Nora
dc.okm.affiliatedauthorHirvonen, Jussi
dc.okm.affiliatedauthorMartikainen, Mika
dc.okm.affiliatedauthorDataimport, tyks, vsshp
dc.okm.discipline3112 Neurosciencesen_GB
dc.okm.discipline3112 Neurotieteetfi_FI
dc.okm.internationalcopublicationnot an international co-publication
dc.okm.typeA1 ScientificArticle
dc.publisherWiley
dc.publisher.countryGermanyen_GB
dc.publisher.countrySaksafi_FI
dc.publisher.country-codeDE
dc.relation.articlenumbere70093
dc.relation.doi10.1002/jmd2.70093
dc.relation.ispartofjournalJIMD Reports
dc.relation.issue3
dc.relation.volume67
dc.titleProgressive White Matter Changes in Mitochondrial Disease: A Quantitative MRI Study
dc.year.issued2026

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