TY - JOUR
T1 - Association between blood mitochondrial DNA copy number and cognitive function
T2 - A cross-sectional study based on the Yakumo Study
AU - Teshigawara, Atsushi
AU - Mizuno, Genki
AU - Yamada, Hiroya
AU - Tsuboi, Yoshiki
AU - Munetsuna, Eiji
AU - Hattori, Yuji
AU - Yamazaki, Mirai
AU - Ando, Yoshitaka
AU - Kageyama, Itsuki
AU - Wakasugi, Takuya
AU - Ichikawa, Hayato
AU - Okumiyama, Hiroshi
AU - Fujii, Ryosuke
AU - Iwahara, Akihiko
AU - Hatta, Takeshi
AU - Ishikawa, Hiroaki
AU - Ohashi, Koji
AU - Suzuki, Koji
N1 - Publisher Copyright:
Copyright © 2026 Atsushi Teshigawara, MHSc et al. This is an Open access article distributed under the Terms of Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author(s) and source are credited.
PY - 2026
Y1 - 2026
N2 - Objectives: Mitochondrial dysfunction has been implicated in neurodegenerative diseases, but evidence regarding its association with cognitive performance in the general population remains limited. This study aimed to examine the association between peripheral blood mitochondrial DNA copy number (mtDNA-CN) and cognitive function in the general Japanese population. Methods: We conducted a cross-sectional analysis of 282 participants (134 men and 148 women) from the Yakumo Study, a population-based health examination in Hokkaido, Japan. Peripheral blood mtDNA-CN was measured by quantitative real-time PCR and categorized into tertiles. Cognitive function was assessed using the short version of the Mini-Mental State Examination (SMMSE), the Logical Memory Test (LMT), and the Digit Cancellation Test (D-CAT). Logistic regression analyses were performed to evaluate the association between mtDNA-CN levels and cognitive performance, with adjustments for relevant demographic and clinical factors. Results: Lower mtDNA-CN was significantly associated with poorer SMMSE scores in women and with reduced DCAT3 performance—reflecting attention and executive function—in men. No significant associations were observed for LMT scores in either sex. These domain- and sex-specific associations remained consistent after adjustment for potential confounders. Conclusions: Lower mtDNA-CN was associated with poorer cognitive performance in the general Japanese population, in a cognitive domain- and sex-specific manner. mtDNA-CN thus has potential as a non-invasive biomarker for the early identification of individuals at increased risk of cognitive decline. Longitudinal studies are necessary to evaluate its predictive utility and potential application in dementia prevention strategies.
AB - Objectives: Mitochondrial dysfunction has been implicated in neurodegenerative diseases, but evidence regarding its association with cognitive performance in the general population remains limited. This study aimed to examine the association between peripheral blood mitochondrial DNA copy number (mtDNA-CN) and cognitive function in the general Japanese population. Methods: We conducted a cross-sectional analysis of 282 participants (134 men and 148 women) from the Yakumo Study, a population-based health examination in Hokkaido, Japan. Peripheral blood mtDNA-CN was measured by quantitative real-time PCR and categorized into tertiles. Cognitive function was assessed using the short version of the Mini-Mental State Examination (SMMSE), the Logical Memory Test (LMT), and the Digit Cancellation Test (D-CAT). Logistic regression analyses were performed to evaluate the association between mtDNA-CN levels and cognitive performance, with adjustments for relevant demographic and clinical factors. Results: Lower mtDNA-CN was significantly associated with poorer SMMSE scores in women and with reduced DCAT3 performance—reflecting attention and executive function—in men. No significant associations were observed for LMT scores in either sex. These domain- and sex-specific associations remained consistent after adjustment for potential confounders. Conclusions: Lower mtDNA-CN was associated with poorer cognitive performance in the general Japanese population, in a cognitive domain- and sex-specific manner. mtDNA-CN thus has potential as a non-invasive biomarker for the early identification of individuals at increased risk of cognitive decline. Longitudinal studies are necessary to evaluate its predictive utility and potential application in dementia prevention strategies.
KW - Biomarker
KW - Cognitive function
KW - Mitochondria
KW - Mitochondrial DNA copy number
KW - Peripheral blood
UR - https://www.scopus.com/pages/publications/105048150336
UR - https://www.scopus.com/pages/publications/105048150336#tab=citedBy
U2 - 10.20407/fmj.2025-038
DO - 10.20407/fmj.2025-038
M3 - Article
AN - SCOPUS:105048150336
SN - 2189-7247
VL - 12
SP - 151
EP - 158
JO - Fujita Medical Journal
JF - Fujita Medical Journal
IS - 2
ER -