Evidence map›Paper›PMID 26849374›Full record

ArticleBrain imaging and behavior2017

Frequency specific brain networks in Parkinson's disease and comorbid depression.

Long Qian, Yi Zhang, Li Zheng, Xuemei Fu, Weiguo Liu, Yuqing Shang, Yaoyu Zhang, Yuanyuan Xu, Yijun Liu, Huaiqiu Zhu and 1 more

Open access · hybridAbstract read
In one paragraph

Article in Brain imaging and behavior, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 17% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 24 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 5 institutions in 2 countries.

Long QianDepartment of Biomedical Engineering, Peking University, Beijing, 100871, China.
Yi ZhangSchool of Life Science and Technology, Xidian University, Xi'an, Shaanxi, 710071, China. zhangyiuf@gmail.com.
Li ZhengDepartment of Biomedical Engineering, Peking University, Beijing, 100871, China.
Xuemei FuDepartment of Biomedical Engineering, Peking University, Beijing, 100871, China.
Weiguo LiuDepartment of Neurology, Affiliated Brain Hospital of Nanjing Medical University, Nanjing, 210029, China.
Yuqing ShangDepartment of Biological Sciences, National University of Singapore, Singapore, 119077, Singapore.
Yaoyu ZhangCenter for MRI Research, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, 100871, China.
Yuanyuan XuDepartment of Neurology, Affiliated Brain Hospital of Nanjing Medical University, Nanjing, 210029, China.
Yijun LiuDepartment of Biomedical Engineering, Peking University, Beijing, 100871, China.
Huaiqiu ZhuDepartment of Biomedical Engineering, Peking University, Beijing, 100871, China.
Jia-Hong GaoCenter for MRI Research, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing, 100871, China. jgao@pku.edu.cn.
Peking University · CNNanjing Brain Hospital · CNNanjing Medical University · CNNational University of Singapore · SGXidian University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The topological organization underlying the human brain was extensively investigated using resting-state functional magnetic resonance imaging, focusing on a low frequency of signal oscillation from 0.01 to 0.1 Hz. However, the frequency specificities with regard to the topological properties of the brain networks have not been fully revealed. In this study, a novel complementary ensemble empirical mode decomposition (CEEMD) method was used to separate the fMRI time series into five characteristic oscillations with distinct frequencies. Then, the small world properties of brain networks were analyzed for each of these five oscillations in patients (n = 67) with depressed Parkinson's disease (DPD, n = 20) , non-depressed Parkinson's disease (NDPD, n = 47) and healthy controls (HC, n = 46). Compared with HC, the results showed decreased network efficiency in characteristic oscillations from 0.05 to 0.12 Hz and from 0.02 to 0.05 Hz for the DPD and NDPD patients, respectively. Furthermore, compared with HC, the most significant inter-group difference across five brain oscillations was found in the basal ganglia (0.01 to 0.05 Hz) and paralimbic-limbic network (0.02 to 0.22 Hz) for the DPD patients, and in the visual cortex (0.02 to 0.05 Hz) for the NDPD patients. Compared with NDPD, the DPD patients showed reduced efficiency of nodes in the basal ganglia network (0.01 to 0.05 Hz). Our results demonstrated that DPD is characterized by a disrupted topological organization in large-scale brain functional networks. Moreover, the CEEMD analysis suggested a prominent dissociation in the topological organization of brain networks between DPD and NDPD in both space and frequency domains. Our findings indicated that these characteristic oscillatory activities in different functional circuits may contribute to distinct motor and non-motor components of clinical impairments in Parkinson's disease.

Indexed as

BrainBrain MappingComorbidityDepressive DisorderFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedNeural PathwaysNeuropsychological TestsParkinson DiseaseRestBrain NetworkComplementary Ensemble Empirical Mode DecompositionDepressionFrequency SpecificityParkinson’s Disease

Identifiers

PMID26849374
PMCPMC5415593
OpenAlexW2302089840

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.