» Articles » PMID: 33188473

Frequency-specific Altered Global Signal Topography in Drug-naïve First-episode Patients with Adolescent-onset Schizophrenia

Overview
Publisher Springer
Date 2020 Nov 14
PMID 33188473
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Adolescent-onset schizophrenia (AOS) is a severe neuropsychiatric disease associated with frequency-specific abnormalities across distributed neural systems in a slow rhythm. Recently, functional magnetic resonance imaging (fMRI) studies have determined that the global signal. (GS) is an important source of the local neuronal activity in 0.01-0.1 Hz frequency band. However, it remains unknown whether the effects follow a specific spatially preferential pattern in different frequency bands in schizophrenia. To address this issue, resting-state fMRI data from 39 drug-naïve AOS patients and 31 healthy controls (HCs) were used to assess the changes in GS topography patterns in the slow-4 (0.027-0.073 Hz) and slow-5 bands (0.01-0.027 Hz). Results revealed that GS mainly affects the default mode network (DMN) in slow-4 and sensory regions in the slow-5 band respectively, and GS has a stronger driving effect in the slow-5 band. Moreover, significant frequency-by-group interaction was observed in the frontoparietal network. Compared with HCs, patients with AOS exhibited altered GS topography mainly located in the DMN. Our findings demonstrated that the influence of the GS on brain networks altered in a frequency-specific way in schizophrenia.

Citing Articles

Spatiotemporal dedifferentiation of the global brain signal topography along the adult lifespan.

Ao Y, Yang C, Drewes J, Jiang M, Huang L, Jing X Hum Brain Mapp. 2023; 44(17):5906-5918.

PMID: 37800366 PMC: 10619384. DOI: 10.1002/hbm.26484.


A schizophrenia study based on multi-frequency dynamic functional connectivity analysis of fMRI.

Shi Y, Shen Z, Zeng W, Luo S, Zhou L, Wang N Front Hum Neurosci. 2023; 17:1164685.

PMID: 37250690 PMC: 10213427. DOI: 10.3389/fnhum.2023.1164685.


Frequency-dependent effective connections between local signals and the global brain signal during resting-state.

Wang Y, Yang C, Li G, Ao Y, Jiang M, Cui Q Cogn Neurodyn. 2023; 17(2):555-560.

PMID: 37007197 PMC: 10050607. DOI: 10.1007/s11571-022-09831-0.


Gestational age-related changes in the fetal functional connectome: in utero evidence for the global signal.

Kim J, De Asis-Cruz J, Cook K, Limperopoulos C Cereb Cortex. 2022; 33(5):2302-2314.

PMID: 35641159 PMC: 9977380. DOI: 10.1093/cercor/bhac209.


Altered Global Signal Topography in Alcohol Use Disorders.

Duan R, Jing L, Li Y, Gong Z, Yao Y, Wang W Front Aging Neurosci. 2022; 14:803780.

PMID: 35250540 PMC: 8888878. DOI: 10.3389/fnagi.2022.803780.


References
1.
Aguirre G, Zarahn E, DEsposito M . Empirical analyses of BOLD fMRI statistics. II. Spatially smoothed data collected under null-hypothesis and experimental conditions. Neuroimage. 1997; 5(3):199-212. DOI: 10.1006/nimg.1997.0264. View

2.
Andrews-Hanna J, Reidler J, Sepulcre J, Poulin R, Buckner R . Functional-anatomic fractionation of the brain's default network. Neuron. 2010; 65(4):550-62. PMC: 2848443. DOI: 10.1016/j.neuron.2010.02.005. View

3.
Anticevic A, Cole M, Repovs G, Murray J, Brumbaugh M, Winkler A . Characterizing thalamo-cortical disturbances in schizophrenia and bipolar illness. Cereb Cortex. 2013; 24(12):3116-30. PMC: 4224238. DOI: 10.1093/cercor/bht165. View

4.
Berman R, Gotts S, McAdams H, Greenstein D, Lalonde F, Clasen L . Disrupted sensorimotor and social-cognitive networks underlie symptoms in childhood-onset schizophrenia. Brain. 2015; 139(Pt 1):276-91. PMC: 4719706. DOI: 10.1093/brain/awv306. View

5.
Braun U, Schaefer A, Betzel R, Tost H, Meyer-Lindenberg A, Bassett D . From Maps to Multi-dimensional Network Mechanisms of Mental Disorders. Neuron. 2018; 97(1):14-31. PMC: 5757246. DOI: 10.1016/j.neuron.2017.11.007. View