Jessica S. Flannery , Ashley C. Parr , Kristen A. Lindquist , Eva H. Telzer
{"title":"多巴胺相关神经生理学的发育变化及其与青少年物质使用和激励促进的认知控制的关联","authors":"Jessica S. Flannery , Ashley C. Parr , Kristen A. Lindquist , Eva H. Telzer","doi":"10.1016/j.dcn.2025.101594","DOIUrl":null,"url":null,"abstract":"<div><div>When substance use begins during adolescence, it is associated with a greater long-term vulnerability to substance use disorders. Developmental changes in dopaminergic functioning may be involved in substance use initiation and escalation during adolescence. We thus used estimates of tissue iron as a noninvasive, indirect measure of dopamine-related neurophysiology to examine associations between basal ganglia tissue iron development, substance use, and incentive-boosted cognitive control in a longitudinal neuroimaging study. Adolescent participants (N = 168; 51.8 % female) underwent an fMRI scan up to four times across 6th to 11th grade (age range: 11.9–18.6 years old) resulting in 469 fMRI timepoints. Time-averaged and normalized T2*-weighted indices were extracted from basal ganglia subregions at each timepoint. Participants self-reported their past year substance use at each timepoint and completed an incentivized cognitive control task at the final time point (n = 76). In confirmation of prior studies, we show developmental increases in tissue iron at the group level. Adolescents who reported substance use showed attenuated age-related increases in tissue iron in comparison to non-users. Additionally, larger incentive-related modulation of cognitive control was associated with lower iron accumulation across adolescence, although tissue iron was not significantly associated with incentive-related changes in brain activity. Overall, findings suggest that adolescents with diminished age-related increases in basal ganglia tissue iron may have a greater propensity toward substance use. These same individuals may also require greater incentive-driven motivation to reach the same cognitive control performance as their peers. These findings suggest a potential developmental neurophysiological phenotype underlying different incentive-driven behaviors during adolescence.</div></div>","PeriodicalId":49083,"journal":{"name":"Developmental Cognitive Neuroscience","volume":"75 ","pages":"Article 101594"},"PeriodicalIF":4.9000,"publicationDate":"2025-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Developmental changes in dopamine-related neurophysiology and associations with adolescent substance use and incentive-boosted cognitive control\",\"authors\":\"Jessica S. Flannery , Ashley C. Parr , Kristen A. Lindquist , Eva H. Telzer\",\"doi\":\"10.1016/j.dcn.2025.101594\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>When substance use begins during adolescence, it is associated with a greater long-term vulnerability to substance use disorders. Developmental changes in dopaminergic functioning may be involved in substance use initiation and escalation during adolescence. We thus used estimates of tissue iron as a noninvasive, indirect measure of dopamine-related neurophysiology to examine associations between basal ganglia tissue iron development, substance use, and incentive-boosted cognitive control in a longitudinal neuroimaging study. Adolescent participants (N = 168; 51.8 % female) underwent an fMRI scan up to four times across 6th to 11th grade (age range: 11.9–18.6 years old) resulting in 469 fMRI timepoints. Time-averaged and normalized T2*-weighted indices were extracted from basal ganglia subregions at each timepoint. Participants self-reported their past year substance use at each timepoint and completed an incentivized cognitive control task at the final time point (n = 76). In confirmation of prior studies, we show developmental increases in tissue iron at the group level. Adolescents who reported substance use showed attenuated age-related increases in tissue iron in comparison to non-users. Additionally, larger incentive-related modulation of cognitive control was associated with lower iron accumulation across adolescence, although tissue iron was not significantly associated with incentive-related changes in brain activity. Overall, findings suggest that adolescents with diminished age-related increases in basal ganglia tissue iron may have a greater propensity toward substance use. These same individuals may also require greater incentive-driven motivation to reach the same cognitive control performance as their peers. These findings suggest a potential developmental neurophysiological phenotype underlying different incentive-driven behaviors during adolescence.</div></div>\",\"PeriodicalId\":49083,\"journal\":{\"name\":\"Developmental Cognitive Neuroscience\",\"volume\":\"75 \",\"pages\":\"Article 101594\"},\"PeriodicalIF\":4.9000,\"publicationDate\":\"2025-07-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Developmental Cognitive Neuroscience\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1878929325000891\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"NEUROSCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Developmental Cognitive Neuroscience","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1878929325000891","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"NEUROSCIENCES","Score":null,"Total":0}
Developmental changes in dopamine-related neurophysiology and associations with adolescent substance use and incentive-boosted cognitive control
When substance use begins during adolescence, it is associated with a greater long-term vulnerability to substance use disorders. Developmental changes in dopaminergic functioning may be involved in substance use initiation and escalation during adolescence. We thus used estimates of tissue iron as a noninvasive, indirect measure of dopamine-related neurophysiology to examine associations between basal ganglia tissue iron development, substance use, and incentive-boosted cognitive control in a longitudinal neuroimaging study. Adolescent participants (N = 168; 51.8 % female) underwent an fMRI scan up to four times across 6th to 11th grade (age range: 11.9–18.6 years old) resulting in 469 fMRI timepoints. Time-averaged and normalized T2*-weighted indices were extracted from basal ganglia subregions at each timepoint. Participants self-reported their past year substance use at each timepoint and completed an incentivized cognitive control task at the final time point (n = 76). In confirmation of prior studies, we show developmental increases in tissue iron at the group level. Adolescents who reported substance use showed attenuated age-related increases in tissue iron in comparison to non-users. Additionally, larger incentive-related modulation of cognitive control was associated with lower iron accumulation across adolescence, although tissue iron was not significantly associated with incentive-related changes in brain activity. Overall, findings suggest that adolescents with diminished age-related increases in basal ganglia tissue iron may have a greater propensity toward substance use. These same individuals may also require greater incentive-driven motivation to reach the same cognitive control performance as their peers. These findings suggest a potential developmental neurophysiological phenotype underlying different incentive-driven behaviors during adolescence.
期刊介绍:
The journal publishes theoretical and research papers on cognitive brain development, from infancy through childhood and adolescence and into adulthood. It covers neurocognitive development and neurocognitive processing in both typical and atypical development, including social and affective aspects. Appropriate methodologies for the journal include, but are not limited to, functional neuroimaging (fMRI and MEG), electrophysiology (EEG and ERP), NIRS and transcranial magnetic stimulation, as well as other basic neuroscience approaches using cellular and animal models that directly address cognitive brain development, patient studies, case studies, post-mortem studies and pharmacological studies.