{"id":{"repo_id":"cape-town","oai_identifier":"oai:open.uct.ac.za:11427/27336"},"canonical_url":"https://search.dev.ndltd.org/etd/cape-town/oai:open.uct.ac.za:11427/27336","repository":{"repo_id":"cape-town","name":"University of Cape Town","base_url":"https://open.uct.ac.za/oai/request"},"display":{"title":"A study of event-related electrocortical oscillatory dynamics associated with cued motor-response inhibition during performance of the Go/NoGo task within a sample of prenatally alcohol-exposed children and age-matched controls","abstract":"Fetal alcohol spectrum disorders (FASDs) are a spectrum of disorders that occur due to prenatal alcohol exposure (PAE). Response inhibition refers to the ability to inhibit/suppress a prepotent behavioural tendency set in motion during an experimental task. Our research explored neocortical processing in heavy-exposed children from Cape Town, South Africa, performing the Go/NoGo response inhibition task. We utilised event-related electroencephalographic methodologies to examine event-related potentials (ERP) and eventrelated changes in induced oscillatory power - event-related desynchronisation (ERD)/eventrelated synchronisation (ERS). Across visual and auditory Go/NoGo tasks, we observed equivalent levels of inhibitory control between heavy-exposed (HE) participants and normally-developing controls; however, HEs demonstrated significantly slower reaction times relative to the control group. In an auditory ERP study, we observed a number of alcohol-related changes in ERP waveform morphology, such as decreased P2 amplitude, reduced P3 amplitude, and longer P3 peak latency. In addition, within the HE group, late in the trials, a slow-wave component was observed in both experimental conditions. A significant difference in N2 amplitude across conditions that has consistently been observed in normally-developing samples was not observed in the HE group. We extended previous research findings in the visual domain by analysing induced oscillatory responses. We observed within the normally-developing sample: (1) in both experimental conditions, a frontal induced beta-band ERS related to decision-making; and (2) in the NoGo-condition, a frontal gamma-band ERS related to cognitive-control. Within the HE group, the beta-ERS was not observed in either of the experimental conditions, neither was the gamma-ERS observed in the NoGo-condition. Frontal induced beta-power was predictive of performance accuracy in the HE group, but not in the control group. The observed alcohol-related effects were not explained and/or mediated by IQ (WISC-IQ), socio-economic circumstances, comorbid ADHD, or teratogenic effects related to postnatal lead exposure and prenatal cigarette-smoke exposure. Our results point to alterations in scalp-measured event-related neocortical oscillatory dynamics and slower processing of task demands due to heavy PAE. These alcohol-related effects are observable on ERP component measures, primarily related to conflict-monitoring and attention-based processing. PAE also affects induced classes of neocortical oscillatory dynamics related to decision-making and cognitive-control processes required to inhibit a prepotent motor-response.","abstract_html":"Fetal alcohol spectrum disorders (FASDs) are a spectrum of disorders that occur due to prenatal alcohol exposure (PAE). Response inhibition refers to the ability to inhibit/suppress a prepotent behavioural tendency set in motion during an experimental task. Our research explored neocortical processing in heavy-exposed children from Cape Town, South Africa, performing the Go/NoGo response inhibition task. We utilised event-related electroencephalographic methodologies to examine event-related potentials (ERP) and eventrelated changes in induced oscillatory power - event-related desynchronisation (ERD)/eventrelated synchronisation (ERS). Across visual and auditory Go/NoGo tasks, we observed equivalent levels of inhibitory control between heavy-exposed (HE) participants and normally-developing controls; however, HEs demonstrated significantly slower reaction times relative to the control group. In an auditory ERP study, we observed a number of alcohol-related changes in ERP waveform morphology, such as decreased P2 amplitude, reduced P3 amplitude, and longer P3 peak latency. In addition, within the HE group, late in the trials, a slow-wave component was observed in both experimental conditions. A significant difference in N2 amplitude across conditions that has consistently been observed in normally-developing samples was not observed in the HE group. We extended previous research findings in the visual domain by analysing induced oscillatory responses. We observed within the normally-developing sample: (1) in both experimental conditions, a frontal induced beta-band ERS related to decision-making; and (2) in the NoGo-condition, a frontal gamma-band ERS related to cognitive-control. Within the HE group, the beta-ERS was not observed in either of the experimental conditions, neither was the gamma-ERS observed in the NoGo-condition. Frontal induced beta-power was predictive of performance accuracy in the HE group, but not in the control group. The observed alcohol-related effects were not explained and/or mediated by IQ (WISC-IQ), socio-economic circumstances, comorbid ADHD, or teratogenic effects related to postnatal lead exposure and prenatal cigarette-smoke exposure. Our results point to alterations in scalp-measured event-related neocortical oscillatory dynamics and slower processing of task demands due to heavy PAE. These alcohol-related effects are observable on ERP component measures, primarily related to conflict-monitoring and attention-based processing. PAE also affects induced classes of neocortical oscillatory dynamics related to decision-making and cognitive-control processes required to inhibit a prepotent motor-response.","abstract_has_math":false,"creators":["Gerhold, Mathew Michael"],"institution":"Division of Biomedical Engineering","degree_name":null,"degree_level":null,"degree_discipline":null,"degree_department":null,"school":null,"contributors":[],"advisors":["Meintjes, Ernesta M","Andrew, Colin"],"committee_chairs":[],"committee_members":[],"year":2017,"date_issued":"2017","date_published":"2017","updated_at":"2026-07-22T22:23:33Z","subjects":[],"languages":["eng"],"rights":[],"rights_urls":[],"identifier_entries":[]},"links":{"outbound_url":"http://hdl.handle.net/11427/27336","outbound_label":"Handle","outbound_source":"dc:identifier.uri"},"metadata_groups":[{"id":"people","label":"People","entries":[{"key":"dc:contributor.advisor","label":"Advisor","values":["Meintjes, Ernesta M","Andrew, Colin"]},{"key":"dc:creator","label":"Author","values":["Gerhold, Mathew Michael"]}]},{"id":"academic_context","label":"Academic Context","entries":[{"key":"dc:date.accessioned","label":"Dc Date Accessioned","values":["2018-02-06T14:16:13Z"]},{"key":"dc:date.available","label":"Dc Date Available","values":["2018-02-06T14:16:13Z"]},{"key":"dc:date.issued","label":"Date","values":["2017"]},{"key":"dc:publisher.department","label":"Dc Publisher Department","values":["Division of Biomedical Engineering"]},{"key":"dc:publisher.institution","label":"Dc Publisher Institution","values":["University of Cape Town"]},{"key":"dc:type","label":"Dc Type","values":["Doctoral Thesis"]},{"key":"dc:type.qualificationlevel","label":"Dc Type Qualificationlevel","values":["Doctoral"]},{"key":"dc:type.qualificationname","label":"Dc Type Qualificationname","values":["PhD"]}]},{"id":"language_rights","label":"Language and Rights","entries":[{"key":"dc:language.iso","label":"Language (ISO)","values":["eng"]}]},{"id":"identifiers","label":"Identifiers","entries":[{"key":"dc:identifier.uri","label":"Identifier URI","values":["http://hdl.handle.net/11427/27336"]}]},{"id":"additional","label":"Additional Metadata","entries":[{"key":"dc:description.abstract","label":"Abstract","values":["Fetal alcohol spectrum disorders (FASDs) are a spectrum of disorders that occur due to prenatal alcohol exposure (PAE). Response inhibition refers to the ability to inhibit/suppress a prepotent behavioural tendency set in motion during an experimental task. Our research explored neocortical processing in heavy-exposed children from Cape Town, South Africa, performing the Go/NoGo response inhibition task. We utilised event-related electroencephalographic methodologies to examine event-related potentials (ERP) and eventrelated changes in induced oscillatory power - event-related desynchronisation (ERD)/eventrelated synchronisation (ERS). Across visual and auditory Go/NoGo tasks, we observed equivalent levels of inhibitory control between heavy-exposed (HE) participants and normally-developing controls; however, HEs demonstrated significantly slower reaction times relative to the control group. In an auditory ERP study, we observed a number of alcohol-related changes in ERP waveform morphology, such as decreased P2 amplitude, reduced P3 amplitude, and longer P3 peak latency. In addition, within the HE group, late in the trials, a slow-wave component was observed in both experimental conditions. A significant difference in N2 amplitude across conditions that has consistently been observed in normally-developing samples was not observed in the HE group. We extended previous research findings in the visual domain by analysing induced oscillatory responses. We observed within the normally-developing sample: (1) in both experimental conditions, a frontal induced beta-band ERS related to decision-making; and (2) in the NoGo-condition, a frontal gamma-band ERS related to cognitive-control. Within the HE group, the beta-ERS was not observed in either of the experimental conditions, neither was the gamma-ERS observed in the NoGo-condition. Frontal induced beta-power was predictive of performance accuracy in the HE group, but not in the control group. The observed alcohol-related effects were not explained and/or mediated by IQ (WISC-IQ), socio-economic circumstances, comorbid ADHD, or teratogenic effects related to postnatal lead exposure and prenatal cigarette-smoke exposure. Our results point to alterations in scalp-measured event-related neocortical oscillatory dynamics and slower processing of task demands due to heavy PAE. These alcohol-related effects are observable on ERP component measures, primarily related to conflict-monitoring and attention-based processing. PAE also affects induced classes of neocortical oscillatory dynamics related to decision-making and cognitive-control processes required to inhibit a prepotent motor-response."]},{"key":"dc:title","label":"Title","values":["A study of event-related electrocortical oscillatory dynamics associated with cued motor-response inhibition during performance of the Go/NoGo task within a sample of prenatally alcohol-exposed children and age-matched controls"]}]}],"canonical_facts":{"dc:contributor.advisor":["Meintjes, Ernesta M","Andrew, Colin"],"dc:creator":["Gerhold, Mathew Michael"],"dc:date.accessioned":["2018-02-06T14:16:13Z"],"dc:date.available":["2018-02-06T14:16:13Z"],"dc:date.issued":["2017"],"dc:description.abstract":["Fetal alcohol spectrum disorders (FASDs) are a spectrum of disorders that occur due to prenatal alcohol exposure (PAE). Response inhibition refers to the ability to inhibit/suppress a prepotent behavioural tendency set in motion during an experimental task. Our research explored neocortical processing in heavy-exposed children from Cape Town, South Africa, performing the Go/NoGo response inhibition task. We utilised event-related electroencephalographic methodologies to examine event-related potentials (ERP) and eventrelated changes in induced oscillatory power - event-related desynchronisation (ERD)/eventrelated synchronisation (ERS). Across visual and auditory Go/NoGo tasks, we observed equivalent levels of inhibitory control between heavy-exposed (HE) participants and normally-developing controls; however, HEs demonstrated significantly slower reaction times relative to the control group. In an auditory ERP study, we observed a number of alcohol-related changes in ERP waveform morphology, such as decreased P2 amplitude, reduced P3 amplitude, and longer P3 peak latency. In addition, within the HE group, late in the trials, a slow-wave component was observed in both experimental conditions. A significant difference in N2 amplitude across conditions that has consistently been observed in normally-developing samples was not observed in the HE group. We extended previous research findings in the visual domain by analysing induced oscillatory responses. We observed within the normally-developing sample: (1) in both experimental conditions, a frontal induced beta-band ERS related to decision-making; and (2) in the NoGo-condition, a frontal gamma-band ERS related to cognitive-control. Within the HE group, the beta-ERS was not observed in either of the experimental conditions, neither was the gamma-ERS observed in the NoGo-condition. Frontal induced beta-power was predictive of performance accuracy in the HE group, but not in the control group. The observed alcohol-related effects were not explained and/or mediated by IQ (WISC-IQ), socio-economic circumstances, comorbid ADHD, or teratogenic effects related to postnatal lead exposure and prenatal cigarette-smoke exposure. Our results point to alterations in scalp-measured event-related neocortical oscillatory dynamics and slower processing of task demands due to heavy PAE. These alcohol-related effects are observable on ERP component measures, primarily related to conflict-monitoring and attention-based processing. PAE also affects induced classes of neocortical oscillatory dynamics related to decision-making and cognitive-control processes required to inhibit a prepotent motor-response."],"dc:identifier.uri":["http://hdl.handle.net/11427/27336"],"dc:language.iso":["eng"],"dc:publisher.department":["Division of Biomedical Engineering"],"dc:publisher.institution":["University of Cape Town"],"dc:title":["A study of event-related electrocortical oscillatory dynamics associated with cued motor-response inhibition during performance of the Go/NoGo task within a sample of prenatally alcohol-exposed children and age-matched controls"],"dc:type":["Doctoral Thesis"],"dc:type.qualificationlevel":["Doctoral"],"dc:type.qualificationname":["PhD"]},"updated_at":"2026-07-22T22:23:33Z"}