Evidence map›Paper›PMID 41026355›Full record

ArticleBrain imaging and behavior2025

Characterizing Gray matter atrophy patterns associated with accelerometer-measured sedentary behavior: a population-based study.

Minle Tian, Xiaolei Han, Ming Mao, Xiaomeng Li, Yi Dong, Jiahao Ding, Qinghua Zhang, Shi Tang, Xiaojuan Han, Lin Song and 5 more

Abstract read
In one paragraph

Article in Brain imaging and behavior, 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

15 authors.

Minle Tian *Key Laboratory of Endocrine Glucose & Lipids Metabolism and Brain Aging, Department of Neurology, Ministry of Education, Shandong Povincial Hospital, Shandong First Medical University, No. 324 Jingwuweiqi Road, Jinan, Shandong, 250021, P.R. China.
Xiaolei Han *Key Laboratory of Endocrine Glucose & Lipids Metabolism and Brain Aging, Department of Neurology, Ministry of Education, Shandong Povincial Hospital, Shandong First Medical University, No. 324 Jingwuweiqi Road, Jinan, Shandong, 250021, P.R. China.
Ming MaoKey Laboratory of Endocrine Glucose & Lipids Metabolism and Brain Aging, Department of Neurology, Ministry of Education, Shandong Povincial Hospital, Shandong First Medical University, No. 324 Jingwuweiqi Road, Jinan, Shandong, 250021, P.R. China.
Xiaomeng LiKey Laboratory of Endocrine Glucose & Lipids Metabolism and Brain Aging, Department of Neurology, Ministry of Education, Shandong Povincial Hospital, Shandong First Medical University, No. 324 Jingwuweiqi Road, Jinan, Shandong, 250021, P.R. China.
Yi DongKey Laboratory of Endocrine Glucose & Lipids Metabolism and Brain Aging, Department of Neurology, Ministry of Education, Shandong Povincial Hospital, Shandong First Medical University, No. 324 Jingwuweiqi Road, Jinan, Shandong, 250021, P.R. China.
Jiahao DingShandong Institute of Brain Science and Brain-inspired Research, Medical Science and Technology Innovation Center, Shandong First Medical University & Shandong Academy of Medical Sciences, Jinan, Shandong, P.R. China.
Qinghua ZhangKey Laboratory of Endocrine Glucose & Lipids Metabolism and Brain Aging, Department of Neurology, Ministry of Education, Shandong Povincial Hospital, Shandong First Medical University, No. 324 Jingwuweiqi Road, Jinan, Shandong, 250021, P.R. China.
Shi TangKey Laboratory of Endocrine Glucose & Lipids Metabolism and Brain Aging, Department of Neurology, Ministry of Education, Shandong Povincial Hospital, Shandong First Medical University, No. 324 Jingwuweiqi Road, Jinan, Shandong, 250021, P.R. China.
Xiaojuan HanKey Laboratory of Endocrine Glucose & Lipids Metabolism and Brain Aging, Department of Neurology, Ministry of Education, Shandong Povincial Hospital, Shandong First Medical University, No. 324 Jingwuweiqi Road, Jinan, Shandong, 250021, P.R. China.
Lin SongKey Laboratory of Endocrine Glucose & Lipids Metabolism and Brain Aging, Department of Neurology, Ministry of Education, Shandong Povincial Hospital, Shandong First Medical University, No. 324 Jingwuweiqi Road, Jinan, Shandong, 250021, P.R. China.
Tingting HouKey Laboratory of Endocrine Glucose & Lipids Metabolism and Brain Aging, Department of Neurology, Ministry of Education, Shandong Povincial Hospital, Shandong First Medical University, No. 324 Jingwuweiqi Road, Jinan, Shandong, 250021, P.R. China.
Lin CongKey Laboratory of Endocrine Glucose & Lipids Metabolism and Brain Aging, Department of Neurology, Ministry of Education, Shandong Povincial Hospital, Shandong First Medical University, No. 324 Jingwuweiqi Road, Jinan, Shandong, 250021, P.R. China.
Yifeng DuKey Laboratory of Endocrine Glucose & Lipids Metabolism and Brain Aging, Department of Neurology, Ministry of Education, Shandong Povincial Hospital, Shandong First Medical University, No. 324 Jingwuweiqi Road, Jinan, Shandong, 250021, P.R. China.
Chengxuan QiuKey Laboratory of Endocrine Glucose & Lipids Metabolism and Brain Aging, Department of Neurology, Ministry of Education, Shandong Povincial Hospital, Shandong First Medical University, No. 324 Jingwuweiqi Road, Jinan, Shandong, 250021, P.R. China.
Yongxiang WangKey Laboratory of Endocrine Glucose & Lipids Metabolism and Brain Aging, Department of Neurology, Ministry of Education, Shandong Povincial Hospital, Shandong First Medical University, No. 324 Jingwuweiqi Road, Jinan, Shandong, 250021, P.R. China. yongxiang.wang@ki.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evidence has linked self-reported sedentary behaviors with dementia and cognitive impairment; however, the underlying mechanisms remain poorly understood. We investigated the associations of accelerometer-measured sedentary behavior patterns with gray matter atrophy patterns in rural-dwelling older adults, while taking into account the manner in which sedentary time is accrued (in short or long bouts). This community-based study involved 911 dementia-free older adults (age ≥ 60 years, 59% women) who participated in both ActiGraph and brain MRI substudies within MIND-China (2018-2020). Sedentary behavior parameters (total sedentary time, mean sedentary bout duration, and sedentary breaks) were recorded with accelerometers. Regional gray matter volumes (GMV) were measured using voxel-based morphometry (VBM) methods. Data were analyzed using the general linear regression models, restricted cubic spline curves, and VBM analysis. There was an inverted U-shaped association between daily sedentary time and GMV in temporal, cingulate, and medial temporal cortex, while longer mean sedentary bout duration was linearly related to decreased GMV in total, frontal, temporal, insula, cingulate, and medial temporal cortex. Greater daily time spent in light or moderate-to-vigorous physical activity (LPA and MVPA) was correlated with larger insula GMV. The VBM analysis suggested that prolonged daily total sedentary time and mean sedentary bout duration were significantly associated with smaller GMV in extensive brain regions, especially in thalamus and insula. In conclusion, gray matter atrophy associated with sedentary behavior in older adults is characterized by reduced GMV in global, frontal, temporal, medial temporal, and cingulate cortex, especially in the insula and thalamus regions.

Indexed as

Brain DiseasesGray MatterSedentary BehaviorAccelerometryAgedAging in PlaceAtrophyBrainChinaCross-Sectional StudiesFemaleHumansLinear ModelsMagnetic Resonance ImagingMaleMiddle AgedAccelerometerGray matterPopulation-based studySedentary behaviorVoxel-based morphometry

Identifiers

PMID41026355
PMCPMC12831676

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