Source decomposition of the frontocentral auditory steady‐state gamma band response in schizophrenia patients and healthy subjects
Aim Gamma‐band auditory steady‐state response (ASSR) is a neurophysiologic index that is increasingly used as a translational biomarker in the development of treatments of neuropsychiatric disorders. While gamma‐band ASSR is generated by distributed networks of highly interactive temporal and fronta...
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| Published in | Psychiatry and clinical neurosciences Vol. 75; no. 5; pp. 172 - 179 |
|---|---|
| Main Authors | , , , , , , |
| Format | Journal Article |
| Language | English |
| Published |
Melbourne
John Wiley & Sons Australia, Ltd
01.05.2021
Wiley Subscription Services, Inc |
| Subjects | |
| Online Access | Get full text |
| ISSN | 1323-1316 1440-1819 1440-1819 |
| DOI | 10.1111/pcn.13201 |
Cover
| Abstract | Aim
Gamma‐band auditory steady‐state response (ASSR) is a neurophysiologic index that is increasingly used as a translational biomarker in the development of treatments of neuropsychiatric disorders. While gamma‐band ASSR is generated by distributed networks of highly interactive temporal and frontal cortical sources, the majority of human gamma‐band ASSR studies using electroencephalography (EEG) highlight activity from only a single frontocentral scalp site, Fz, where responses tend to be largest and reductions in schizophrenia patients are most evident. However, no previous study has characterized the relative source contributions to Fz, which is a necessary step to improve the concordance of preclinical and clinical EEG studies.
Methods
A novel method to back‐project the contributions of independent cortical source components was applied to assess the independent sources and their proportional contributions to Fz as well as source‐resolved responses in 432 schizophrenia patients and 294 healthy subjects.
Results
Independent contributions of gamma‐band ASSR to Fz were detected from orbitofrontal, bilateral superior/middle/inferior temporal, bilateral middle frontal, and posterior cingulate gyri in both groups. In contrast to expectations, the groups showed comparable source contribution weight to gamma‐band ASSR at Fz. While gamma‐band ASSR reductions at Fz were present in schizophrenia patients consistent with previous studies, no group differences in individual source‐level responses to Fz were detected.
Conclusion
Small differences in multiple independent sources summate to produce scalp‐level differences at Fz. The identification of independent source contributions to a single scalp sensor represents a promising methodology for measuring dissociable and homologous biomarker targets in future translational studies. |
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| AbstractList | Gamma-band auditory steady-state response (ASSR) is a neurophysiologic index that is increasingly used as a translational biomarker in the development of treatments of neuropsychiatric disorders. While gamma-band ASSR is generated by distributed networks of highly interactive temporal and frontal cortical sources, the majority of human gamma-band ASSR studies using electroencephalography (EEG) highlight activity from only a single frontocentral scalp site, Fz, where responses tend to be largest and reductions in schizophrenia patients are most evident. However, no previous study has characterized the relative source contributions to Fz, which is a necessary step to improve the concordance of preclinical and clinical EEG studies.AIMGamma-band auditory steady-state response (ASSR) is a neurophysiologic index that is increasingly used as a translational biomarker in the development of treatments of neuropsychiatric disorders. While gamma-band ASSR is generated by distributed networks of highly interactive temporal and frontal cortical sources, the majority of human gamma-band ASSR studies using electroencephalography (EEG) highlight activity from only a single frontocentral scalp site, Fz, where responses tend to be largest and reductions in schizophrenia patients are most evident. However, no previous study has characterized the relative source contributions to Fz, which is a necessary step to improve the concordance of preclinical and clinical EEG studies.A novel method to back-project the contributions of independent cortical source components was applied to assess the independent sources and their proportional contributions to Fz as well as source-resolved responses in 432 schizophrenia patients and 294 healthy subjects.METHODSA novel method to back-project the contributions of independent cortical source components was applied to assess the independent sources and their proportional contributions to Fz as well as source-resolved responses in 432 schizophrenia patients and 294 healthy subjects.Independent contributions of gamma-band ASSR to Fz were detected from orbitofrontal, bilateral superior/middle/inferior temporal, bilateral middle frontal, and posterior cingulate gyri in both groups. In contrast to expectations, the groups showed comparable source contribution weight to gamma-band ASSR at Fz. While gamma-band ASSR reductions at Fz were present in schizophrenia patients consistent with previous studies, no group differences in individual source-level responses to Fz were detected.RESULTSIndependent contributions of gamma-band ASSR to Fz were detected from orbitofrontal, bilateral superior/middle/inferior temporal, bilateral middle frontal, and posterior cingulate gyri in both groups. In contrast to expectations, the groups showed comparable source contribution weight to gamma-band ASSR at Fz. While gamma-band ASSR reductions at Fz were present in schizophrenia patients consistent with previous studies, no group differences in individual source-level responses to Fz were detected.Small differences in multiple independent sources summate to produce scalp-level differences at Fz. The identification of independent source contributions to a single scalp sensor represents a promising methodology for measuring dissociable and homologous biomarker targets in future translational studies.CONCLUSIONSmall differences in multiple independent sources summate to produce scalp-level differences at Fz. The identification of independent source contributions to a single scalp sensor represents a promising methodology for measuring dissociable and homologous biomarker targets in future translational studies. Aim Gamma‐band auditory steady‐state response (ASSR) is a neurophysiologic index that is increasingly used as a translational biomarker in the development of treatments of neuropsychiatric disorders. While gamma‐band ASSR is generated by distributed networks of highly interactive temporal and frontal cortical sources, the majority of human gamma‐band ASSR studies using electroencephalography (EEG) highlight activity from only a single frontocentral scalp site, Fz, where responses tend to be largest and reductions in schizophrenia patients are most evident. However, no previous study has characterized the relative source contributions to Fz, which is a necessary step to improve the concordance of preclinical and clinical EEG studies. Methods A novel method to back‐project the contributions of independent cortical source components was applied to assess the independent sources and their proportional contributions to Fz as well as source‐resolved responses in 432 schizophrenia patients and 294 healthy subjects. Results Independent contributions of gamma‐band ASSR to Fz were detected from orbitofrontal, bilateral superior/middle/inferior temporal, bilateral middle frontal, and posterior cingulate gyri in both groups. In contrast to expectations, the groups showed comparable source contribution weight to gamma‐band ASSR at Fz. While gamma‐band ASSR reductions at Fz were present in schizophrenia patients consistent with previous studies, no group differences in individual source‐level responses to Fz were detected. Conclusion Small differences in multiple independent sources summate to produce scalp‐level differences at Fz. The identification of independent source contributions to a single scalp sensor represents a promising methodology for measuring dissociable and homologous biomarker targets in future translational studies. Gamma-band auditory steady-state response (ASSR) is a neurophysiologic index that is increasingly used as a translational biomarker in the development of treatments of neuropsychiatric disorders. While gamma-band ASSR is generated by distributed networks of highly interactive temporal and frontal cortical sources, the majority of human gamma-band ASSR studies using electroencephalography (EEG) highlight activity from only a single frontocentral scalp site, Fz, where responses tend to be largest and reductions in schizophrenia patients are most evident. However, no previous study has characterized the relative source contributions to Fz, which is a necessary step to improve the concordance of preclinical and clinical EEG studies. A novel method to back-project the contributions of independent cortical source components was applied to assess the independent sources and their proportional contributions to Fz as well as source-resolved responses in 432 schizophrenia patients and 294 healthy subjects. Independent contributions of gamma-band ASSR to Fz were detected from orbitofrontal, bilateral superior/middle/inferior temporal, bilateral middle frontal, and posterior cingulate gyri in both groups. In contrast to expectations, the groups showed comparable source contribution weight to gamma-band ASSR at Fz. While gamma-band ASSR reductions at Fz were present in schizophrenia patients consistent with previous studies, no group differences in individual source-level responses to Fz were detected. Small differences in multiple independent sources summate to produce scalp-level differences at Fz. The identification of independent source contributions to a single scalp sensor represents a promising methodology for measuring dissociable and homologous biomarker targets in future translational studies. AimGamma‐band auditory steady‐state response (ASSR) is a neurophysiologic index that is increasingly used as a translational biomarker in the development of treatments of neuropsychiatric disorders. While gamma‐band ASSR is generated by distributed networks of highly interactive temporal and frontal cortical sources, the majority of human gamma‐band ASSR studies using electroencephalography (EEG) highlight activity from only a single frontocentral scalp site, Fz, where responses tend to be largest and reductions in schizophrenia patients are most evident. However, no previous study has characterized the relative source contributions to Fz, which is a necessary step to improve the concordance of preclinical and clinical EEG studies.MethodsA novel method to back‐project the contributions of independent cortical source components was applied to assess the independent sources and their proportional contributions to Fz as well as source‐resolved responses in 432 schizophrenia patients and 294 healthy subjects.ResultsIndependent contributions of gamma‐band ASSR to Fz were detected from orbitofrontal, bilateral superior/middle/inferior temporal, bilateral middle frontal, and posterior cingulate gyri in both groups. In contrast to expectations, the groups showed comparable source contribution weight to gamma‐band ASSR at Fz. While gamma‐band ASSR reductions at Fz were present in schizophrenia patients consistent with previous studies, no group differences in individual source‐level responses to Fz were detected.ConclusionSmall differences in multiple independent sources summate to produce scalp‐level differences at Fz. The identification of independent source contributions to a single scalp sensor represents a promising methodology for measuring dissociable and homologous biomarker targets in future translational studies. |
| Author | Miyakoshi, Makoto Koshiyama, Daisuke Joshi, Yash B. Tanaka‐Koshiyama, Kumiko Light, Gregory A. Nakanishi, Masaki Sprock, Joyce |
| Author_xml | – sequence: 1 givenname: Daisuke surname: Koshiyama fullname: Koshiyama, Daisuke organization: University of California San Diego – sequence: 2 givenname: Makoto orcidid: 0000-0002-4062-6679 surname: Miyakoshi fullname: Miyakoshi, Makoto email: mmiyakoshi@ucsd.edu organization: University of California San Diego – sequence: 3 givenname: Yash B. surname: Joshi fullname: Joshi, Yash B. organization: VA San Diego Healthcare System – sequence: 4 givenname: Masaki surname: Nakanishi fullname: Nakanishi, Masaki organization: University of California San Diego – sequence: 5 givenname: Kumiko surname: Tanaka‐Koshiyama fullname: Tanaka‐Koshiyama, Kumiko organization: University of California San Diego – sequence: 6 givenname: Joyce surname: Sprock fullname: Sprock, Joyce organization: VA San Diego Healthcare System – sequence: 7 givenname: Gregory A. surname: Light fullname: Light, Gregory A. organization: VA San Diego Healthcare System |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/33470494$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_1016_j_pneurobio_2024_102695 crossref_primary_10_1038_s41537_024_00454_4 crossref_primary_10_1111_pcn_13331 crossref_primary_10_3390_jpm12061004 crossref_primary_10_1111_pcn_13472 crossref_primary_10_1016_j_psychres_2021_114239 crossref_primary_10_1016_j_bionps_2022_100046 crossref_primary_10_1016_j_biopsych_2023_03_026 crossref_primary_10_1038_s41380_022_01572_0 crossref_primary_10_1007_s10548_023_00947_y crossref_primary_10_1016_j_compbiomed_2023_107902 |
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Gamma‐band auditory steady‐state response (ASSR) is a neurophysiologic index that is increasingly used as a translational biomarker in the development of... Gamma-band auditory steady-state response (ASSR) is a neurophysiologic index that is increasingly used as a translational biomarker in the development of... AimGamma‐band auditory steady‐state response (ASSR) is a neurophysiologic index that is increasingly used as a translational biomarker in the development of... |
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| SubjectTerms | Biomarkers EEG gamma‐band auditory steady‐state response independent component analysis Mental disorders Schizophrenia source‐level analysis Translation translational biomarker |
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| Title | Source decomposition of the frontocentral auditory steady‐state gamma band response in schizophrenia patients and healthy subjects |
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