Evidence map›Paper›PMID 41105621›Full record

ArticlePloS one2025

Mitochondrial dysfunction-related metabolite methylmalonic acid is associated with decreased cognitive performance.

Yige Liu, Jiaxin Wang, Pengyan Wu, Fan Tang, Wanlu Guo, Ruishan Li, Xinran Wang, Yiying Zhang, Shaohong Fang

Abstract read
In one paragraph

Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Yige LiuDepartment of Cardiology, Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.ORCID https://orcid.org/0000-0003-0628-1344
Jiaxin WangDepartment of Cardiology, Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Pengyan WuDepartment of Cardiology, Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.
Fan TangDepartment of Epidemiology and Biostatistics, School of Public Health, Jiamusi University, Jiamusi, Heilongjiang, China.
Wanlu GuoDepartment of Epidemiology and Biostatistics, School of Public Health, Jiamusi University, Jiamusi, Heilongjiang, China.
Ruishan LiDepartment of Epidemiology and Biostatistics, School of Public Health, Jiamusi University, Jiamusi, Heilongjiang, China.
Xinran WangDepartment of Epidemiology and Biostatistics, School of Public Health, Jiamusi University, Jiamusi, Heilongjiang, China.
Yiying ZhangDepartment of Epidemiology and Biostatistics, School of Public Health, Jiamusi University, Jiamusi, Heilongjiang, China.
Shaohong FangDepartment of Cardiology, Second Affiliated Hospital of Harbin Medical University, Harbin, Heilongjiang, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMethylmalonic acid (MMA), a mitochondrial metabolite derived from propionate metabolism, has been implicated in fatal neurodegeneration in children with congenital methylmalonic acidemia. However, its clinical relevance in chronic cognitive decline remains poorly understood. This study aims to investigate the association between MMA levels, its metabolic coenzyme vitamin B12, and cognitive impairment in an elderly population. PATIENTS AND

methodsThe cohort comprised 2,762 participants aged 60 and older, who underwent assessments using the Digit Symbol Substitution Test (DSST), Animal Fluency test (AFT), Consortium to Establish a Registry for Alzheimer's disease (CERAD) Immediate Recall (CERAD-IR), CERAD Delayed Recall (CERAD-DR), with low cognitive performance defined as the bottom quartile. Generalized linear regression models were applied to explore potential associations. Additionally, differentially expressed genes (DEGs) in MMA-related propionate metabolic process were identified from the RNA expression profiles in frontal cortex from 56 Alzheimer's disease and 44 non-dementia controls.

resultsAmong the 2,762 participants, with a mean age of 69.2 years and 53.8% female, elevated MMA levels were significantly associated with an increased likelihood of low cognitive performance across multiple tests: DSST (OR = 1.95; 95% CI: 1.41-2.73), AFT (OR = 1.51; 95% CI: 1.01-2.25), CERAD-IR (OR = 1.58; 95% CI: 1.19-2.09), and CERAD-DR (OR = 1.56; 95% CI: 1.12-2.18). High serum vitamin B12 levels were associated with an increased likelihood of impaired CERAD-IR scores, although dietary B12 supplementation did not correlate with cognitive performance. Stratified analyses revealed a stronger relationship between MMA and cognitive decline in males, individuals over 75 years, and those with elevated serum and dietary vitamin B12 levels. DEG analysis identified genes related to MMA synthesis and mitochondrial function in cognitively impaired individuals, with significant enrichment in mitochondrial propionate metabolism pathways.

conclusionThe findings indicate that elevated MMA levels are linked to cognitive decline in older adults, potentially through mitochondrial dysfunction. These results underscore the clinical importance of MMA in the context of chronic cognitive impairment.

Indexed as

CognitionCognitive DysfunctionMethylmalonic AcidMitochondriaAgedAged, 80 and overAlzheimer DiseaseCohort StudiesFemaleHumansMaleMiddle AgedVitamin B 12Methylmalonic AcidVitamin B 12

Identifiers

PMID41105621
PMCPMC12533889

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.