Evidence map›Paper›PMID 35936769›Full record

ArticleFrontiers in aging neuroscience2022

Dysfunction of Emotion Regulation in Mild Cognitive Impairment Individuals Combined With Depressive Disorder: A Neural Mechanism Study.

Meng Liu, Jing Ma, Chang-Yong Fu, Janelle Yeo, Sha-Sha Xiao, Wei-Xin Xiao, Ren-Ren Li, Wei Zhang, Zeng-Mai Xie, Ying-Jie Li and 1 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.5field-weighted citation impact, top 11% of its field
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

11 citing papers in PubMed, 21 citations in OpenAlex.

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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

11 authors at 4 institutions in 2 countries.

Meng LiuDepartment of Neurology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Jing MaDepartment of Neurology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Chang-Yong FuDepartment of Neurology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Janelle YeoDepartment of Neurology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Sha-Sha XiaoSchool of Communication and Information Engineering, Shanghai University, Shanghai, China.
Wei-Xin XiaoDepartment of Neurology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Ren-Ren LiDepartment of Neurology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Wei ZhangDepartment of Neurology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Zeng-Mai XieDepartment of Neurology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Ying-Jie LiSchool of Communication and Information Engineering, Shanghai University, Shanghai, China.
Yun-Xia LiDepartment of Neurology, Tongji Hospital, School of Medicine, Tongji University, Shanghai, China.
Tongji University · CNTongji Hospital · CNShanghai University · CNUniversity of Sydney · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Depression increases the risk of progression from mild cognitive impairment (MCI) to dementia, where impaired emotion regulation is a core symptom of depression. However, the neural mechanisms underlying the decreased emotion regulation in individuals with MCI combined with depressive symptoms are not precise. We assessed the behavioral performance by emotion regulation tasks and recorded event-related electroencephalography (EEG) signals related to emotion regulation tasks simultaneously. EEG analysis, including event-related potential (ERP), event-related spectral perturbation (ERSP), functional connectivity and graph theory, was used to compare the difference between MCI individuals and MCI depressed individuals in behavioral performance, the late positive potential (LPP) amplitudes, neural oscillations and brain networks during the processing of emotional stimuli. We found that MCI depressed individuals have negative preferences and are prone to allocate more attentional resources to negative stimuli. Results suggested that theta and alpha oscillations activity is increased, and gamma oscillations activity is decreased during negative stimulus processing in MCI depressed individuals, thus indicating that the decreased emotion regulation in MCI depressed individuals may be associated with enhanced low-frequency and decreased high-frequency oscillations activity. Functional connectivity analysis revealed a decrease in functional connectivity in the left cerebral hemisphere of the alpha band and an increase in functional connectivity in the right cerebral hemisphere of the alpha band in MCI depressed individuals. Graph theory analysis suggested that global network metrics, including clustering coefficients and disassortative, decreased, while nodal and modular network metrics regarding local nodal efficiency, degree centrality, and betweenness centrality were significantly increased in the frontal lobe and decreased in the parieto-occipital lobe, which was observed in the alpha band, further suggesting that abnormal alpha band network connectivity may be a potential marker of depressive symptoms. Correlational analyses showed that depressive symptoms were closely related to emotion regulation, power oscillations and functional connectivity. In conclusion, the dominant processing of negative stimuli, the increased low-frequency oscillations activity and decreased high-frequency activity, so as the decrease in top-down information processing in the frontal parieto-occipital lobe, results in the abnormality of alpha-band network connectivity. It is suggested that these factors, in turn, contribute to the declined ability of MCI depressed individuals in emotion regulation.

Indexed as

depressive symptomsemotion regulationfunctional connectivitymild cognitive impairmentneural oscillations

Identifiers

PMID35936769
PMCPMC9354008
OpenAlexW4286716499

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.