Evidence map›Paper›PMID 38580625›Full record

ArticleTranslational psychiatry2024

Low Functional network integrity in cognitively unimpaired and MCI subjects with depressive symptoms: results from a multi-center fMRI study.

Gabor Csukly, László Tombor, Zoltan Hidasi, Eva Csibri, Máté Fullajtár, Zsolt Huszár, Vanda Koszovácz, Orsolya Lányi, Edit Vass, Boróka Koleszár and 8 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Translational psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.4field-weighted citation impact, top 12% 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

5 citing papers in PubMed, 7 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

18 authors at 3 institutions in 1 country.

Gabor CsuklyDepartment of Psychiatry and Psychotherapy, Semmelweis University, Budapest, Hungary. csugab@yahoo.com.ORCID 0000-0002-5006-9407
László TomborDepartment of Psychiatry and Psychotherapy, Semmelweis University, Budapest, Hungary.
Zoltan HidasiDepartment of Psychiatry and Psychotherapy, Semmelweis University, Budapest, Hungary.
Eva CsibriDepartment of Psychiatry and Psychotherapy, Semmelweis University, Budapest, Hungary.
Máté FullajtárDepartment of Psychiatry and Psychotherapy, Semmelweis University, Budapest, Hungary.
Zsolt HuszárDepartment of Psychiatry and Psychotherapy, Semmelweis University, Budapest, Hungary.
Vanda KoszováczDepartment of Psychiatry and Psychotherapy, Semmelweis University, Budapest, Hungary.
Orsolya LányiDepartment of Psychiatry and Psychotherapy, Semmelweis University, Budapest, Hungary.
Edit VassDepartment of Psychiatry and Psychotherapy, Semmelweis University, Budapest, Hungary.ORCID 0000-0002-8858-7277
Boróka KoleszárDepartment of Psychiatry and Psychotherapy, Semmelweis University, Budapest, Hungary.
István KóborMedical Imaging Centre, Semmelweis University, Budapest, Hungary.
Katalin FarkasNeurocognitive Research Center, Budapest, National Institute of Mental Health, Neurology, and Neurosurgery, Budapest, Hungary.
Viktoria RosenfeldNeurocognitive Research Center, Budapest, National Institute of Mental Health, Neurology, and Neurosurgery, Budapest, Hungary.ORCID 0009-0001-3599-7803
Dalida Borbála BerenteNeurocognitive Research Center, Budapest, National Institute of Mental Health, Neurology, and Neurosurgery, Budapest, Hungary.
Gergo BollaNeurocognitive Research Center, Budapest, National Institute of Mental Health, Neurology, and Neurosurgery, Budapest, Hungary.
Mate KissSiemens Healthcare, Budapest, Hungary.
Anita KamondiNeurocognitive Research Center, Budapest, National Institute of Mental Health, Neurology, and Neurosurgery, Budapest, Hungary.ORCID 0000-0001-9860-730X
Andras Attila HorvathNeurocognitive Research Center, Budapest, National Institute of Mental Health, Neurology, and Neurosurgery, Budapest, Hungary.
Semmelweis University · HUBudapest University of Technology and Economics · HUSiemens (Hungary) · HU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Evidence suggests that depressive symptomatology is a consequence of network dysfunction rather than lesion pathology. We studied whole-brain functional connectivity using a Minimum Spanning Tree as a graph-theoretical approach. Furthermore, we examined functional connectivity in the Default Mode Network, the Frontolimbic Network (FLN), the Salience Network, and the Cognitive Control Network. All 183 elderly subjects underwent a comprehensive neuropsychological evaluation and a 3 Tesla brain MRI scan. To assess the potential presence of depressive symptoms, the 13-item version of the Beck Depression Inventory (BDI) or the Geriatric Depression Scale (GDS) was utilized. Participants were assigned into three groups based on their cognitive status: amnestic mild cognitive impairment (MCI), non-amnestic MCI, and healthy controls. Regarding affective symptoms, subjects were categorized into depressed and non-depressed groups. An increased mean eccentricity and network diameter were found in patients with depressive symptoms relative to non-depressed ones, and both measures showed correlations with depressive symptom severity. In patients with depressive symptoms, a functional hypoconnectivity was detected between the Anterior Cingulate Cortex (ACC) and the right amygdala in the FLN, which impairment correlated with depressive symptom severity. While no structural difference was found in subjects with depressive symptoms, the volume of the hippocampus and the thickness of the precuneus and the entorhinal cortex were decreased in subjects with MCI, especially in amnestic MCI. The increase in eccentricity and diameter indicates a more path-like functional network configuration that may lead to an impaired functional integration in depression, a possible cause of depressive symptomatology in the elderly.

Indexed as

Cognitive DysfunctionDepressionAgedBrainBrain MappingHumansMagnetic Resonance ImagingNeuropsychological Tests

Identifiers

PMID38580625
PMCPMC10997664
OpenAlexW4393987559

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.