Evidence map›Paper›PMID 40745599›Full record

ArticleBMC neurology2025

Cognitive impairment profile in patients with the m.3243A> G variant in mitochondrial DNA.

Satu Winqvist, Mikko Kärppä, Jukka S Moilanen, Kari Majamaa

Abstract read
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Article in BMC neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Satu WinqvistNeurocenter, Oulu University Hospital, Oulu, Finland.
Mikko KärppäNeurocenter, Oulu University Hospital, Oulu, Finland.ORCID http://orcid.org/0009-0003-9193-5492
Jukka S MoilanenMedical Research Center Oulu, Oulu University Hospital, Oulu, Finland.ORCID http://orcid.org/0000-0002-8041-3205
Kari MajamaaNeurocenter, Oulu University Hospital, Oulu, Finland. kari.majamaa@oulu.fi.ORCID http://orcid.org/0000-0002-9070-3791

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe m.3243A>G variant in mitochondrial DNA is associated with a wide spectrum of clinical features ranging from asymptomatic subjects to severely symptomatic patients. Cognitive involvement is one of the clinical features, but its severity and frequency are not properly known. Here we describe neuropsychological features associated with m.3243 A > G.

methodsWe studied 45 adult patients with m.3243 A > G and 45 healthy subjects. Comprehensive neuropsychological test battery was applied. Cognitive impairment was defined, if at least five out of seven cognitive domains were impaired compared to matched controls. Major cognitive impairment was diagnosed, if the impairment was general across the domains.

resultsSixteen patients (36%) with m.3243 A > G were diagnosed with cognitive impairment, and six of them (13%) had a major cognitive impairment. The median age at diagnosis of cognitive impairment was 53 years (range, 25-64). The profile consisted of impaired abstract reasoning, memory problems, motor function defects and executive problems. Executive functions were affected most, and verbal memory was affected the least. Higher variant heteroplasmy and more severe global phenotype were associated with cognitive impairment, whereas age and sex were not.

conclusionCognitive impairment is found frequently in patients with m.3243 A > G, but major cognitive impairment is not common. The impairment affects all neuropsychological domains and no specific profile could be identified.

Indexed as

Cognitive DysfunctionDNA, MitochondrialAdultFemaleHumansMaleMiddle AgedNeuropsychological TestsDNA, MitochondrialCognitive dysfunctionHeteroplasmyKaplan-Meier estimateMELAS syndromeNeuropsychological tests

Identifiers

PMID40745599
PMCPMC12315284

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