Reduction of higher-order occipital GABA and impaired visual perception in acute major depressive disorder

Major depressive disorder (MDD) is a complex state-dependent psychiatric illness for which biomarkers linking psychophysical, biochemical, and psychopathological changes remain yet elusive, though. Earlier studies demonstrate reduced GABA in lower-order occipital cortex in acute MDD leaving open its...

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Published inMolecular psychiatry Vol. 26; no. 11; pp. 6747 - 6755
Main Authors Song, Xue Mei, Hu, Xi-Wen, Li, Zhe, Gao, Yuan, Ju, Xuan, Liu, Dong-Yu, Wang, Qian-Nan, Xue, Chuang, Cai, Yong-Chun, Bai, Ruiliang, Tan, Zhong-Lin, Northoff, Georg
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LanguageEnglish
Published London Nature Publishing Group UK 01.11.2021
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Abstract Major depressive disorder (MDD) is a complex state-dependent psychiatric illness for which biomarkers linking psychophysical, biochemical, and psychopathological changes remain yet elusive, though. Earlier studies demonstrate reduced GABA in lower-order occipital cortex in acute MDD leaving open its validity and significance for higher-order visual perception, though. The goal of our study is to fill that gap by combining psychophysical investigation of visual perception with measurement of GABA concentration in middle temporal visual area (hMT+) in acute depressed MDD. Psychophysically, we observe a highly specific deficit in visual surround motion suppression in a large sample of acute MDD subjects which, importantly, correlates with symptom severity. Both visual deficit and its relation to symptom severity are replicated in the smaller MDD sample that received MRS. Using high-field 7T proton Magnetic resonance spectroscopy ( 1 H-MRS), acute MDD subjects exhibit decreased GABA concentration in visual MT+ which, unlike in healthy subjects, no longer correlates with their visual motion performance, i.e., impaired SI. In sum, our combined psychophysical-biochemical study demonstrates an important role of reduced occipital GABA for altered visual perception and psychopathological symptoms in acute MDD. Bridging the gap from the biochemical level of occipital GABA over visual-perceptual changes to psychopathological symptoms, our findings point to the importance of the occipital cortex in acute depressed MDD including its role as candidate biomarker.
AbstractList Major depressive disorder (MDD) is a complex state-dependent psychiatric illness for which biomarkers linking psychophysical, biochemical, and psychopathological changes remain yet elusive, though. Earlier studies demonstrate reduced GABA in lower-order occipital cortex in acute MDD leaving open its validity and significance for higher-order visual perception, though. The goal of our study is to fill that gap by combining psychophysical investigation of visual perception with measurement of GABA concentration in middle temporal visual area (hMT+) in acute depressed MDD. Psychophysically, we observe a highly specific deficit in visual surround motion suppression in a large sample of acute MDD subjects which, importantly, correlates with symptom severity. Both visual deficit and its relation to symptom severity are replicated in the smaller MDD sample that received MRS. Using high-field 7T proton Magnetic resonance spectroscopy ( 1 H-MRS), acute MDD subjects exhibit decreased GABA concentration in visual MT+ which, unlike in healthy subjects, no longer correlates with their visual motion performance, i.e., impaired SI. In sum, our combined psychophysical-biochemical study demonstrates an important role of reduced occipital GABA for altered visual perception and psychopathological symptoms in acute MDD. Bridging the gap from the biochemical level of occipital GABA over visual-perceptual changes to psychopathological symptoms, our findings point to the importance of the occipital cortex in acute depressed MDD including its role as candidate biomarker.
Major depressive disorder (MDD) is a complex state-dependent psychiatric illness for which biomarkers linking psychophysical, biochemical, and psychopathological changes remain yet elusive, though. Earlier studies demonstrate reduced GABA in lower-order occipital cortex in acute MDD leaving open its validity and significance for higher-order visual perception, though. The goal of our study is to fill that gap by combining psychophysical investigation of visual perception with measurement of GABA concentration in middle temporal visual area (hMT+) in acute depressed MDD. Psychophysically, we observe a highly specific deficit in visual surround motion suppression in a large sample of acute MDD subjects which, importantly, correlates with symptom severity. Both visual deficit and its relation to symptom severity are replicated in the smaller MDD sample that received MRS. Using high-field 7T proton Magnetic resonance spectroscopy (1H-MRS), acute MDD subjects exhibit decreased GABA concentration in visual MT+ which, unlike in healthy subjects, no longer correlates with their visual motion performance, i.e., impaired SI. In sum, our combined psychophysical-biochemical study demonstrates an important role of reduced occipital GABA for altered visual perception and psychopathological symptoms in acute MDD. Bridging the gap from the biochemical level of occipital GABA over visual-perceptual changes to psychopathological symptoms, our findings point to the importance of the occipital cortex in acute depressed MDD including its role as candidate biomarker.
Major depressive disorder (MDD) is a complex state-dependent psychiatric illness for which biomarkers linking psychophysical, biochemical, and psychopathological changes remain yet elusive, though. Earlier studies demonstrate reduced GABA in lower-order occipital cortex in acute MDD leaving open its validity and significance for higher-order visual perception, though. The goal of our study is to fill that gap by combining psychophysical investigation of visual perception with measurement of GABA concentration in middle temporal visual area (hMT+) in acute depressed MDD. Psychophysically, we observe a highly specific deficit in visual surround motion suppression in a large sample of acute MDD subjects which, importantly, correlates with symptom severity. Both visual deficit and its relation to symptom severity are replicated in the smaller MDD sample that received MRS. Using high-field 7T proton Magnetic resonance spectroscopy (1H-MRS), acute MDD subjects exhibit decreased GABA concentration in visual MT+ which, unlike in healthy subjects, no longer correlates with their visual motion performance, i.e., impaired SI. In sum, our combined psychophysical-biochemical study demonstrates an important role of reduced occipital GABA for altered visual perception and psychopathological symptoms in acute MDD. Bridging the gap from the biochemical level of occipital GABA over visual-perceptual changes to psychopathological symptoms, our findings point to the importance of the occipital cortex in acute depressed MDD including its role as candidate biomarker.Major depressive disorder (MDD) is a complex state-dependent psychiatric illness for which biomarkers linking psychophysical, biochemical, and psychopathological changes remain yet elusive, though. Earlier studies demonstrate reduced GABA in lower-order occipital cortex in acute MDD leaving open its validity and significance for higher-order visual perception, though. The goal of our study is to fill that gap by combining psychophysical investigation of visual perception with measurement of GABA concentration in middle temporal visual area (hMT+) in acute depressed MDD. Psychophysically, we observe a highly specific deficit in visual surround motion suppression in a large sample of acute MDD subjects which, importantly, correlates with symptom severity. Both visual deficit and its relation to symptom severity are replicated in the smaller MDD sample that received MRS. Using high-field 7T proton Magnetic resonance spectroscopy (1H-MRS), acute MDD subjects exhibit decreased GABA concentration in visual MT+ which, unlike in healthy subjects, no longer correlates with their visual motion performance, i.e., impaired SI. In sum, our combined psychophysical-biochemical study demonstrates an important role of reduced occipital GABA for altered visual perception and psychopathological symptoms in acute MDD. Bridging the gap from the biochemical level of occipital GABA over visual-perceptual changes to psychopathological symptoms, our findings point to the importance of the occipital cortex in acute depressed MDD including its role as candidate biomarker.
Major depressive disorder (MDD) is a complex state-dependent psychiatric illness for which biomarkers linking psychophysical, biochemical, and psychopathological changes remain yet elusive, though. Earlier studies demonstrate reduced GABA in lower-order occipital cortex in acute MDD leaving open its validity and significance for higher-order visual perception, though. The goal of our study is to fill that gap by combining psychophysical investigation of visual perception with measurement of GABA concentration in middle temporal visual area (hMT+) in acute depressed MDD. Psychophysically, we observe a highly specific deficit in visual surround motion suppression in a large sample of acute MDD subjects which, importantly, correlates with symptom severity. Both visual deficit and its relation to symptom severity are replicated in the smaller MDD sample that received MRS. Using high-field 7T proton Magnetic resonance spectroscopy ( H-MRS), acute MDD subjects exhibit decreased GABA concentration in visual MT+ which, unlike in healthy subjects, no longer correlates with their visual motion performance, i.e., impaired SI. In sum, our combined psychophysical-biochemical study demonstrates an important role of reduced occipital GABA for altered visual perception and psychopathological symptoms in acute MDD. Bridging the gap from the biochemical level of occipital GABA over visual-perceptual changes to psychopathological symptoms, our findings point to the importance of the occipital cortex in acute depressed MDD including its role as candidate biomarker.
Major depressive disorder (MDD) is a complex state-dependent psychiatric illness for which biomarkers linking psychophysical, biochemical, and psychopathological changes remain yet elusive, though. Earlier studies demonstrate reduced GABA in lower-order occipital cortex in acute MDD leaving open its validity and significance for higher-order visual perception, though. The goal of our study is to fill that gap by combining psychophysical investigation of visual perception with measurement of GABA concentration in middle temporal visual area (hMT+) in acute depressed MDD. Psychophysically, we observe a highly specific deficit in visual surround motion suppression in a large sample of acute MDD subjects which, importantly, correlates with symptom severity. Both visual deficit and its relation to symptom severity are replicated in the smaller MDD sample that received MRS. Using high-field 7T proton Magnetic resonance spectroscopy (.sup.1H-MRS), acute MDD subjects exhibit decreased GABA concentration in visual MT+ which, unlike in healthy subjects, no longer correlates with their visual motion performance, i.e., impaired SI. In sum, our combined psychophysical-biochemical study demonstrates an important role of reduced occipital GABA for altered visual perception and psychopathological symptoms in acute MDD. Bridging the gap from the biochemical level of occipital GABA over visual-perceptual changes to psychopathological symptoms, our findings point to the importance of the occipital cortex in acute depressed MDD including its role as candidate biomarker.
Audience Academic
Author Gao, Yuan
Hu, Xi-Wen
Li, Zhe
Song, Xue Mei
Northoff, Georg
Ju, Xuan
Wang, Qian-Nan
Tan, Zhong-Lin
Liu, Dong-Yu
Xue, Chuang
Bai, Ruiliang
Cai, Yong-Chun
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/33863994$$D View this record in MEDLINE/PubMed
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ScalabriniAVaiBPolettiSDamianiSMucciCColomboCAll roads lead to the default-mode network—global source of DMN abnormalities in major depressive disorderNeuropsychopharmacology.2020452058691:CAS:528:DC%2BB3cXhsFyit7jP10.1038/s41386-020-0785-x
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Born RT, Bradley DC. Structure and function of visual area MT. Annu Rev Neurosci. 2005;28:157–89.
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SanacoraGMasonGFRothmanDLHyderFCiarciaJJOstroffRBIncreased cortical GABA concentrations in depressed patients receiving ECTAm J Psychiatry2003160577910.1176/appi.ajp.160.3.577
GruetterRAutomatic, localizedin Vivo adjustment of all first-and second-order shim coilsMagn Reson Med199329804111:STN:280:DyaK3szlsVSktQ%3D%3D10.1002/mrm.1910290613
GolombJDMcDavittJRBRufBMChenJISaricicekAMaloneyKHEnhanced Visual Motion Perception in Major Depressive DisorderJ Neurosci200929907271:CAS:528:DC%2BD1MXovFegurc%3D10.1523/JNEUROSCI.1003-09.2009
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NortonDJMcBainRKPizzagalliDACronin-GolombAChenYDysregulation of visual motion inhibition in major depressionPsychiatry Res20162402142110.1016/j.psychres.2016.04.028
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NorthoffGMagioncaldaPMartinoMLeeH-CTsengY-CLaneTToo Fast or Too Slow? Time and Neuronal Variability in Bipolar Disorder—A Combined Theoretical and Empirical InvestigationSchizophr Bull201844546410.1093/schbul/sbx050
ZhangZZhangHXieC-MZhangMShiYSongRTask-related functional magnetic resonance imaging-based neuronavigation for the treatment of depression by individualized repetitive transcranial magnetic stimulation of the visual cortexSci China Life Sci202164961061:CAS:528:DC%2BB3cXhtFKgtrrK10.1007/s11427-020-1730-5
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SchallmoMPKaleAMMillinRFlevarisAVBrkanacZEddenRAESuppression and facilitation of human neural responsesElife.2018712310.7554/eLife.30334
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NorthoffGSibilleECortical GABA neurons and self-focus in depression: a model linking cellular, biochemical and neural network findingsMol Psychiatry2014199591:CAS:528:DC%2BC2cXhsFyltrfN10.1038/mp.2014.108
SerièsPLorenceauJFrégnacYThe “silent” surround of V1 receptive fields: theory and experimentsJ Physiol20039745374
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1090_CR1
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Z Zhang (1090_CR5) 2021; 64
JDG Watson (1090_CR22) 1993; 3
I Tkáč (1090_CR25) 1999; 41
HE Jones (1090_CR36) 2002; 88
G Sanacora (1090_CR6) 2004; 61
R Gruetter (1090_CR26) 1993; 29
G Sanacora (1090_CR14) 2002; 159
PJ Magistretti (1090_CR29) 1999; 283
H Adesnik (1090_CR35) 2012; 490
A Scalabrini (1090_CR2) 2020; 45
DP Auer (1090_CR10) 2000; 47
P Seriès (1090_CR34) 2003; 97
JH Foss-Feig (1090_CR19) 2013; 33
X Chen (1090_CR27) 2019; 29
G Hasler (1090_CR9) 2007; 64
D Tadin (1090_CR15) 2003; 424
J Frahm (1090_CR24) 1989; 9
A Rosenberg (1090_CR20) 2015; 112
JD Golomb (1090_CR21) 2009; 29
RH Kaiser (1090_CR3) 2015; 72
J Allman (1090_CR33) 1985; 8
M Carandini (1090_CR30) 2012; 13
MP Schallmo (1090_CR16) 2018; 7
G Sanacora (1090_CR13) 2006; 59
V Truong (1090_CR8) 2021; 308
1090_CR17
G Northoff (1090_CR31) 2014; 19
H Ozeki (1090_CR38) 2009; 62
SO Dumoulin (1090_CR28) 2000; 10
G Sanacora (1090_CR12) 2003; 160
SG Solomon (1090_CR37) 2004; 24
RR Schür (1090_CR11) 2016; 37
DJ Norton (1090_CR32) 2016; 240
G Northoff (1090_CR4) 2018; 44
Z Bhagwagar (1090_CR7) 2007; 61
DH Brainard (1090_CR23) 1997; 10
D Tadin (1090_CR18) 2006; 26
References_xml – reference: FrahmJBruhnHGyngellMLMerboldtKDHänickeWSauterRLocalized high-resolution proton NMR spectroscopy using stimulated echoes: Initial applications to human brainin vivoMagn Reson Med1989979931:CAS:528:DyaL1MXhs12mu70%3D10.1002/mrm.1910090110
– reference: TkáčIStarčukZChoiIYGruetterRIn vivo 1H NMR spectroscopy of rat brain at 1 ms echo timeMagn Reson Med1999416495610.1002/(SICI)1522-2594(199904)41:4<649::AID-MRM2>3.0.CO;2-G
– reference: KaiserRHAndrews-HannaJRWagerTDPizzagalliDALarge-Scale Network Dysfunction in Major Depressive DisorderJAMA Psychiatry20157260310.1001/jamapsychiatry.2015.0071
– reference: TadinDLappinJSGilroyLABlakeRPerceptual consequences of centre-surround antagonism in visual motion processingNature.200342431251:CAS:528:DC%2BD3sXlsVGjsLw%3D10.1038/nature01800
– reference: DumoulinSOA New Anatomical Landmark for Reliable Identification of Human Area V5/MT: a Quantitative Analysis of Sulcal PatterningCereb Cortex200010454631:STN:280:DC%2BD3cvhsl2htQ%3D%3D10.1093/cercor/10.5.454
– reference: BrainardDHThe Psychophysics ToolboxSpat Vis19971043361:STN:280:DyaK2szitVSlug%3D%3D10.1163/156856897X00357
– reference: CarandiniMHeegerDJNormalization as a canonical neural computationNat Rev Neurosci20121351621:CAS:528:DC%2BC3MXhsFWqtLrL10.1038/nrn3136
– reference: SatoTKHaiderBHäusserMCarandiniMAn excitatory basis for divisive normalization in visual cortexNat Neurosci201619568701:CAS:528:DC%2BC28XisFKhtrg%3D10.1038/nn.4249
– reference: MagistrettiPJNEUROSCIENCE:energy on demandScience (80-)199928349671:CAS:528:DyaK1MXoslagsw%3D%3D10.1126/science.283.5401.496
– reference: American Psychiatric Association. Diagnostic and statistical mental disorders (DSM 5); American Psychiatric Publishing; Washington; 2013.
– reference: SchallmoMPKaleAMMillinRFlevarisAVBrkanacZEddenRAESuppression and facilitation of human neural responsesElife.2018712310.7554/eLife.30334
– reference: BhagwagarZWylezinskaMJezzardPEvansJAshworthFSuleAReduction in occipital cortex gamma-aminobutyric acid concentrations in medication-free recovered unipolar depressed and bipolar subjectsBiol Psychiatry200761806121:CAS:528:DC%2BD2sXisVWhtbk%3D10.1016/j.biopsych.2006.08.048
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– reference: ChenXFanXHuYZuoCWhitfield-GabrieliSHoltDRegional GABA Concentrations Modulate Inter-network Resting-state Functional ConnectivityCereb Cortex20192916071810.1093/cercor/bhy059
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– reference: HaslerGvan der VeenJWTumonisTMeyersNShenJDrevetsWCReduced Prefrontal Glutamate/Glutamine and γ-Aminobutyric Acid Levels in Major Depression Determined Using Proton Magnetic Resonance SpectroscopyArch Gen Psychiatry2007641931:CAS:528:DC%2BD2sXisFylsLY%3D10.1001/archpsyc.64.2.193
– reference: AdesnikHBrunsWTaniguchiHHuangZJScanzianiMA neural circuit for spatial summation in visual cortexNature.2012490226311:CAS:528:DC%2BC38XhsVyktbjK10.1038/nature11526
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– reference: ZhangZZhangHXieC-MZhangMShiYSongRTask-related functional magnetic resonance imaging-based neuronavigation for the treatment of depression by individualized repetitive transcranial magnetic stimulation of the visual cortexSci China Life Sci202164961061:CAS:528:DC%2BB3cXhtFKgtrrK10.1007/s11427-020-1730-5
– reference: AllmanJStimulus Specific Responses from Beyond the Classical Receptive Field: Neurophysiological Mechanisms for Local-Global Comparisons in Visual NeuronsAnnu Rev Neurosci19858407301:STN:280:DyaL2M7ntlSrtA%3D%3D10.1146/annurev.ne.08.030185.002203
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– reference: SerièsPLorenceauJFrégnacYThe “silent” surround of V1 receptive fields: theory and experimentsJ Physiol20039745374
– reference: RosenbergAPattersonJSAngelakiDEA computational perspective on autismProc Natl Acad Sci20151129158651:CAS:528:DC%2BC2MXhtFGktrjI10.1073/pnas.1510583112
– reference: GruetterRAutomatic, localizedin Vivo adjustment of all first-and second-order shim coilsMagn Reson Med199329804111:STN:280:DyaK3szlsVSktQ%3D%3D10.1002/mrm.1910290613
– reference: SanacoraGMasonGFRothmanDLHyderFCiarciaJJOstroffRBIncreased cortical GABA concentrations in depressed patients receiving ECTAm J Psychiatry2003160577910.1176/appi.ajp.160.3.577
– reference: Foss-FeigJHTadinDSchauderKBCascioCJA Substantial and Unexpected Enhancement of Motion Perception in AutismJ Neurosci201333824391:CAS:528:DC%2BC3sXns1Ggsr8%3D10.1523/JNEUROSCI.1608-12.2013
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– reference: ScalabriniAVaiBPolettiSDamianiSMucciCColomboCAll roads lead to the default-mode network—global source of DMN abnormalities in major depressive disorderNeuropsychopharmacology.2020452058691:CAS:528:DC%2BB3cXhsFyit7jP10.1038/s41386-020-0785-x
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Snippet Major depressive disorder (MDD) is a complex state-dependent psychiatric illness for which biomarkers linking psychophysical, biochemical, and...
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Behavioral Sciences
Biological Psychology
Biomarkers
Depression
Depressive Disorder, Major
GABA
gamma-Aminobutyric Acid
Health aspects
Humans
Magnetic resonance spectroscopy
Major depressive disorder
Medicine
Medicine & Public Health
Mental depression
Motion detection
Neurosciences
Neurotransmitters
Occipital lobe
Occipital Lobe - chemistry
Pharmacotherapy
Physiological aspects
Proton Magnetic Resonance Spectroscopy
Psychiatry
Psychological aspects
Psychophysics
Temporal cortex
Visual Perception
γ-Aminobutyric acid
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Title Reduction of higher-order occipital GABA and impaired visual perception in acute major depressive disorder
URI https://link.springer.com/article/10.1038/s41380-021-01090-5
https://www.ncbi.nlm.nih.gov/pubmed/33863994
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Volume 26
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