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1.
Autism Res ; 17(7): 1328-1343, 2024 Jul.
Article in English | MEDLINE | ID: mdl-38949436

ABSTRACT

Although aversive responses to sensory stimuli are common in autism spectrum disorder (ASD), it remains unknown whether the social relevance of aversive sensory inputs affects their processing. We used functional magnetic resonance imaging (fMRI) to investigate neural responses to mildly aversive nonsocial and social sensory stimuli as well as how sensory over-responsivity (SOR) severity relates to these responses. Participants included 21 ASD and 25 typically-developing (TD) youth, aged 8.6-18.0 years. Results showed that TD youth exhibited significant neural discrimination of socially relevant versus irrelevant aversive sensory stimuli, particularly in the amygdala and orbitofrontal cortex (OFC), regions that are crucial for sensory and social processing. In contrast, ASD youth showed reduced neural discrimination of social versus nonsocial stimuli in the amygdala and OFC, as well as overall greater neural responses to nonsocial compared with social stimuli. Moreover, higher SOR in ASD was associated with heightened responses in sensory-motor regions to socially-relevant stimuli. These findings further our understanding of the relationship between sensory and social processing in ASD, suggesting limited attention to the social relevance compared with aversiveness level of sensory input in ASD versus TD youth, particularly in ASD youth with higher SOR.


Subject(s)
Autism Spectrum Disorder , Magnetic Resonance Imaging , Humans , Male , Adolescent , Child , Female , Autism Spectrum Disorder/physiopathology , Amygdala/physiopathology , Social Perception , Brain/physiopathology , Brain/diagnostic imaging , Prefrontal Cortex/physiopathology , Prefrontal Cortex/diagnostic imaging , Brain Mapping/methods
2.
BMC Psychiatry ; 24(1): 533, 2024 Jul 25.
Article in English | MEDLINE | ID: mdl-39054442

ABSTRACT

BACKGROUND: Anxious depression (AD) is a common subtype of major depressive disorder (MDD). Neuroimaging studies of AD have revealed inconsistent and heterogeneous brain alterations with the use of single-model methods. Therefore, it is necessary to explore the pathogenesis of AD using multi-model imaging analyses to obtain more homogeneous and robust results. METHODS: One hundred and eighty-two patients with MDD and 64 matched healthy controls (HCs) were recruited. Voxel-based morphometry (VBM) was used to estimate the gray matter volume (GMV) of all subjects. The GMV differences between the AD and non-anxious depression (NAD) participants were used as regions of interest (ROIs) for subsequent resting state functional connectivity (rs-FC) analyses. Correlation analysis was used to evaluate the associations between clinical symptoms and abnormal function in specific brain areas. RESULTS: Decreased GMV in the medial frontal gyrus (MFG) and the superior frontal gyrus (SFG) was observed in the AD group compared to the NAD group. Taking the MFG and SFG as ROIs, the rs-FC analysis revealed decreased FC between the left SFG and left temporal pole and between the left SFG and right MFG in the AD group compared to the NAD group. Finally, the FC between the left SFG and left temporal pole was negatively correlated with HAMD-17 scores in the AD group. CONCLUSION: By combining the GMV and rs-FC models, this study revealed that structural and functional disruption of the affective network may be an important pathophysiology underlying AD. The structural impairment may serve as the foundation of the functional impairment.


Subject(s)
Depressive Disorder, Major , Gray Matter , Magnetic Resonance Imaging , Humans , Male , Female , Depressive Disorder, Major/physiopathology , Depressive Disorder, Major/diagnostic imaging , Depressive Disorder, Major/pathology , Adult , Gray Matter/diagnostic imaging , Gray Matter/pathology , Gray Matter/physiopathology , Brain/diagnostic imaging , Brain/physiopathology , Brain/pathology , Middle Aged , Case-Control Studies , Nerve Net/physiopathology , Nerve Net/diagnostic imaging , Nerve Net/pathology , Connectome , Prefrontal Cortex/physiopathology , Prefrontal Cortex/diagnostic imaging , Prefrontal Cortex/pathology
3.
Cereb Cortex ; 34(7)2024 Jul 03.
Article in English | MEDLINE | ID: mdl-39010819

ABSTRACT

Learning how others perceive us helps us tune our behavior to form adaptive relationships. But which perceptions stick with us? And when in the learning process are they codified in memory? We leveraged a popular television series-The Office-to answer these questions. Prior to their functional magnetic resonance imaging (fMRI) session, viewers of The Office reported which characters they identified with, as well as which characters they perceived another person (i.e. counterpart) was similar to. During their fMRI scan, participants found out which characters other people thought they and the counterpart were like, and also completed rest scans. Participants remembered more feedback inconsistent with their self-views (vs. views of the counterpart). Although neural activity while encoding self-inconsistent feedback did not meaningfully predict memory, returning to the inconsistent self feedback during subsequent rest did. During rest, participants reinstated neural patterns engaged while receiving self-inconsistent feedback in the dorsomedial prefrontal cortex (DMPFC). DMPFC reinstatement also quadratically predicted self-inconsistent memory, with too few or too many reinstatements compromising memory performance. Processing social feedback during rest may impact how we remember and integrate the feedback, especially when it contradicts our self-views.


Subject(s)
Brain , Magnetic Resonance Imaging , Humans , Male , Female , Young Adult , Adult , Brain/physiology , Brain/diagnostic imaging , Memory/physiology , Rest/physiology , Social Perception , Prefrontal Cortex/physiology , Prefrontal Cortex/diagnostic imaging , Brain Mapping , Feedback, Psychological/physiology , Adolescent , Self Concept
4.
Cereb Cortex ; 34(7)2024 Jul 03.
Article in English | MEDLINE | ID: mdl-39030744

ABSTRACT

This study aimed to investigate the effect of a 12-wk extracurricular volleyball training on working memory from both behavioral and cerebral aspects. A total of 80 children were randomized assigned to (i) the experimental group, who engaged in extracurricular volleyball training for 60 min, thrice a week for 12 wk, and (ii) the control group, who maintained their regular daily routine. Working memory was evaluated in both groups using the N-back task before and after the intervention. Furthermore, functional near-infrared spectroscopy was employed to monitor the level of oxygenated hemoglobin in the prefrontal cortex. The experimental group performed better in the behavioral task than the control group, as evidenced by a shorter response time and a higher correct rate. The functional near-infrared spectroscopy results suggested that the activation of the left dorsolateral prefrontal cortex was significantly higher in the experimental group than in the control group. In addition, correlation analyses showed that the enhancement of left dorsolateral prefrontal cortex activation was significantly correlated with decreasing response time and improving response accuracy in the N-back task. These findings suggest that the left dorsolateral prefrontal cortex is likely the neural substrate for improved working memory performance elicited by 12-wk open skill exercise.


Subject(s)
Memory, Short-Term , Spectroscopy, Near-Infrared , Volleyball , Humans , Spectroscopy, Near-Infrared/methods , Memory, Short-Term/physiology , Male , Female , Volleyball/physiology , Child , Oxyhemoglobins/metabolism , Prefrontal Cortex/physiology , Prefrontal Cortex/diagnostic imaging , Reaction Time/physiology , Dorsolateral Prefrontal Cortex/physiology , Neuropsychological Tests
5.
Hippocampus ; 34(8): 438-451, 2024 Aug.
Article in English | MEDLINE | ID: mdl-39016331

ABSTRACT

Studies of the impact of brain injury on memory processes often focus on the quantity and episodic richness of those recollections. Here, we argue that the organization of one's recollections offers critical insights into the impact of brain injury on functional memory. It is well-established in studies of word list memory that free recall of unrelated words exhibits a clear temporal organization. This temporal contiguity effect refers to the fact that the order in which word lists are recalled reflects the original presentation order. Little is known, however, about the organization of recall for semantically rich materials, nor how recall organization is impacted by hippocampal damage and memory impairment. The present research is the first study, to our knowledge, of temporal organization in semantically rich narratives in three groups: (1) Adults with bilateral hippocampal damage and severe declarative memory impairment, (2) adults with bilateral ventromedial prefrontal cortex (vmPFC) damage and no memory impairment, and (3) demographically matched non-brain-injured comparison participants. We find that although the narrative recall of adults with bilateral hippocampal damage reflected the temporal order in which those narratives were experienced above chance levels, their temporal contiguity effect was significantly attenuated relative to comparison groups. In contrast, individuals with vmPFC damage did not differ from non-brain-injured comparison participants in temporal contiguity. This pattern of group differences yields insights into the cognitive and neural systems that support the use of temporal organization in recall. These data provide evidence that the retrieval of temporal context in narrative recall is hippocampal-dependent, whereas damage to the vmPFC does not impair the temporal organization of narrative recall. This evidence of limited but demonstrable organization of memory in participants with hippocampal damage and amnesia speaks to the power of narrative structures in supporting meaningfully organized recall despite memory impairment.


Subject(s)
Amnesia , Hippocampus , Mental Recall , Humans , Hippocampus/pathology , Hippocampus/diagnostic imaging , Hippocampus/physiopathology , Mental Recall/physiology , Male , Female , Middle Aged , Amnesia/physiopathology , Amnesia/pathology , Amnesia/psychology , Adult , Narration , Aged , Neuropsychological Tests , Time Factors , Prefrontal Cortex/pathology , Prefrontal Cortex/physiopathology , Prefrontal Cortex/diagnostic imaging , Prefrontal Cortex/injuries
6.
Brain Behav ; 14(7): e3622, 2024 Jul.
Article in English | MEDLINE | ID: mdl-39021241

ABSTRACT

BACKGROUND: Default mode network (DMN) is one of the most recognized resting-state networks in major depressive disorder (MDD). However, the homogeneity of this network in MDD remains incompletely explored. Therefore, this study aims to determine whether there is abnormal network homogeneity (NH) of the DMN in MDD patients. At the same time, correlations between clinical variables and brain functional connectivity are examined. METHODS: We enrolled 42 patients diagnosed with MDD and 42 HCs. A variety of clinical variables were collected, and data analysis was conducted using the NH and independent component analysis methods. RESULTS: The study shows that MDD patients have higher NH values in the left superior medial prefrontal cortex (MPFC) and left posterior cingulate cortex (PCC) compared to HCs. Additionally, there is a positive correlation between NH values of the left superior MPFC and Eysenck Personality Questionnaire values. NH values of the left PCC are positively linked to CHOL levels, LDL levels, and utilization scores. However, these correlations lose significance after the Bonferroni correction. CONCLUSION: Our findings indicate the presence of abnormal DMN homogeneity in MDD, underscoring the significance of DMN in the pathophysiology of MDD. Simultaneously, the study provides preliminary evidence for the correlation between clinical variables and brain functional connectivity.


Subject(s)
Default Mode Network , Depressive Disorder, Major , Magnetic Resonance Imaging , Personality , Prefrontal Cortex , Humans , Depressive Disorder, Major/physiopathology , Depressive Disorder, Major/diagnostic imaging , Depressive Disorder, Major/blood , Male , Female , Adult , Default Mode Network/physiopathology , Default Mode Network/diagnostic imaging , Personality/physiology , Prefrontal Cortex/physiopathology , Prefrontal Cortex/diagnostic imaging , Gyrus Cinguli/physiopathology , Gyrus Cinguli/diagnostic imaging , Gyrus Cinguli/metabolism , Middle Aged , Nerve Net/physiopathology , Nerve Net/diagnostic imaging , Lipids/blood , Connectome , Young Adult
7.
Transl Psychiatry ; 14(1): 301, 2024 Jul 23.
Article in English | MEDLINE | ID: mdl-39039061

ABSTRACT

Depressive symptoms occur commonly in Alzheimer's disease (AD). Although abnormalities in the amygdala-frontal circuit have been linked to emotional dysregulation and cognitive impairment, the neurological basis underlying these associations in AD patients with depressive symptoms (ADD) is unclear. We aimed to investigate the relationship between the amygdala-frontal circuit and depressive symptoms and cognitive function in ADD. We recruited 60 ADD, 60 AD patients without depressive symptoms (ADND), and 60 healthy controls (HC). Functional connectivity (FC) maps of the bilateral amygdala were compared. Fractional anisotropy (FA) of the amygdala-frontal circuit connected by the uncinate fasciculus (UF) was calculated using automated fiber quantification (AFQ). In addition, mediation analysis was performed to explore the effects of the amygdala-frontal circuit on the relationship between depressive symptoms and cognitive function. We found decreased bilateral amygdala FC with the inferior frontal gyrus (IFG) in the ADD group compared to the ADND and HC groups. Moreover, FA in the left frontal UF (nodes 64-97) was significantly lower in the ADD group than ADND group. Notably, amygdala-based FC with IFG and the left frontal UF FA mediated the relationship between depressive symptoms and cognitive function in ADD, with mediating effects ranging between 15 and 18%. Our study is the first to demonstrate the mediating effect of functional and microstructural abnormalities in the amygdala-frontal circuit in ADD. The findings suggest that the amygdala-frontal circuit may underlie emotional dysregulation in ADD, providing potential targets for treatment strategies.


Subject(s)
Alzheimer Disease , Amygdala , Cognition , Depression , Humans , Amygdala/physiopathology , Amygdala/diagnostic imaging , Alzheimer Disease/physiopathology , Alzheimer Disease/diagnostic imaging , Alzheimer Disease/psychology , Male , Female , Aged , Depression/physiopathology , Depression/diagnostic imaging , Middle Aged , Diffusion Tensor Imaging , Cognitive Dysfunction/physiopathology , Cognitive Dysfunction/diagnostic imaging , Cognitive Dysfunction/etiology , Frontal Lobe/physiopathology , Frontal Lobe/diagnostic imaging , Neural Pathways/physiopathology , Case-Control Studies , Magnetic Resonance Imaging , Prefrontal Cortex/diagnostic imaging , Prefrontal Cortex/physiopathology
8.
Cereb Cortex ; 34(7)2024 Jul 03.
Article in English | MEDLINE | ID: mdl-38970361

ABSTRACT

Empathy toward suffering individuals serves as potent driver for prosocial behavior. However, it remains unclear whether prosociality induced by empathy for another person's pain persists once that person's suffering diminishes. To test this, participants underwent functional magnetic resonance imaging while performing a binary social decision task that involved allocation of points to themselves and another person. In block one, participants completed the task after witnessing frequent painful stimulation of the other person, and in block two, after observing low frequency of painful stimulation. Drift-diffusion modeling revealed an increased initial bias toward making prosocial decisions in the first block compared with baseline that persisted in the second block. These results were replicated in an independent behavioral study. An additional control study showed that this effect may be specific to empathy as stability was not evident when prosocial decisions were driven by a social norm such as reciprocity. Increased neural activation in dorsomedial prefrontal cortex was linked to empathic concern after witnessing frequent pain and to a general prosocial decision bias after witnessing rare pain. Altogether, our findings show that empathy for pain elicits a stable inclination toward making prosocial decisions even as their suffering diminishes.


Subject(s)
Decision Making , Empathy , Magnetic Resonance Imaging , Humans , Empathy/physiology , Male , Female , Decision Making/physiology , Young Adult , Adult , Social Behavior , Pain/psychology , Pain/physiopathology , Brain Mapping , Prefrontal Cortex/physiology , Prefrontal Cortex/diagnostic imaging , Brain/physiology , Brain/diagnostic imaging
9.
Aging Clin Exp Res ; 36(1): 154, 2024 Jul 30.
Article in English | MEDLINE | ID: mdl-39078432

ABSTRACT

Mild cognitive impairment (MCI) is recognized as the prodromal phase of dementia, a condition that can be either maintained or reversed through timely medical interventions to prevent cognitive decline. Considerable studies using functional magnetic resonance imaging (fMRI) have indicated that altered activity in the medial prefrontal cortex (mPFC) serves as an indicator of various cognitive stages of aging. However, the impacts of intrinsic functional connectivity in the mPFC as a mediator on cognitive performance in individuals with and without MCI have not been fully understood. In this study, we recruited 42 MCI patients and 57 healthy controls, assessing their cognitive abilities and functional brain connectivity patterns through neuropsychological evaluations and resting-state fMRI, respectively. The MCI patients exhibited poorer performance on multiple neuropsychological tests compared to the healthy controls. At the neural level, functional connectivity between the mPFC and the anterior cingulate cortex (ACC) was significantly weaker in the MCI group and correlated with multiple neuropsychological test scores. The result of the mediation analysis further demonstrated that functional connectivity between the mPFC and ACC notably mediated the relationship between the MCI and semantic fluency performance. These findings suggest that altered mPFC-ACC connectivity may have a plausible causal influence on cognitive decline and provide implications for early identifications of neurodegenerative diseases and precise monitoring of disease progression.


Subject(s)
Cognitive Dysfunction , Gyrus Cinguli , Magnetic Resonance Imaging , Prefrontal Cortex , Humans , Cognitive Dysfunction/physiopathology , Cognitive Dysfunction/diagnostic imaging , Prefrontal Cortex/physiopathology , Prefrontal Cortex/diagnostic imaging , Gyrus Cinguli/physiopathology , Gyrus Cinguli/diagnostic imaging , Male , Female , Aged , Magnetic Resonance Imaging/methods , Middle Aged , Neuropsychological Tests , Case-Control Studies
10.
Nat Commun ; 15(1): 6424, 2024 Jul 30.
Article in English | MEDLINE | ID: mdl-39080250

ABSTRACT

We make decisions by comparing values, but it is not yet clear how value is represented in the brain. Many models assume, if only implicitly, that the representational geometry of value is linear. However, in part due to a historical focus on noisy single neurons, rather than neuronal populations, this hypothesis has not been rigorously tested. Here, we examine the representational geometry of value in the ventromedial prefrontal cortex (vmPFC), a part of the brain linked to economic decision-making, in two male rhesus macaques. We find that values are encoded along a curved manifold in vmPFC. This curvilinear geometry predicts a specific pattern of irrational decision-making: that decision-makers will make worse choices when an irrelevant, decoy option is worse in value, compared to when it is better. We observe this type of irrational choices in behavior. Together, these results not only suggest that the representational geometry of value is nonlinear, but that this nonlinearity could impose bounds on rational decision-making.


Subject(s)
Choice Behavior , Macaca mulatta , Prefrontal Cortex , Animals , Male , Prefrontal Cortex/physiology , Prefrontal Cortex/diagnostic imaging , Choice Behavior/physiology , Decision Making/physiology , Reward , Neurons/physiology , Magnetic Resonance Imaging , Behavior, Animal/physiology
11.
Behav Brain Res ; 471: 115138, 2024 Aug 05.
Article in English | MEDLINE | ID: mdl-38969019

ABSTRACT

Negative urgency (NU), or the tendency to act rashly when stress of negative affect is high, could be the result of an insufficient control of the ventromedial prefrontal cortex (vmPFC) over the striatum, through an impaired dopamine (DA) transmission. Therefore, we investigated in vivo human stress-induced DA release in the vmPFC, its relation with fronto-striatal functional connectivity (FC), and NU in daily life. In total, 12 female healthy participants performed a simultaneous [18 F]fallypride PET and fMRI scan during which stress was induced. Regions displaying stress-induced DA release were identified and used to investigate stress-induced changes in fronto-striatal FC. Additionally, participants enrolled in an experience sampling study, reporting on daily life stress and rash actions over a 12-month-long period. Mixed models explored whether stress-induced DA release and FC moderated NU in daily life. Stress led to a lower FC between the vmPFC and dorsal striatum, but a higher FC between the vmPFC and contralateral ventral striatum. Participants with a higher FC between the vmPFC and dorsal striatum displayed more NU in daily life. A higher stress-induced DA release in the vmPFC was related to a higher stress-induced change in FC between the vmPFC and striatum. Participants with a higher DA release in the vmPFC displayed more NU in daily life. In conclusion, stress could differentially impact fronto-striatal FC whereby the connectivity with the dorsal striatum is especially important for NU in daily life. This could be mediated by a higher, but not a lower, stress-induced DA release in the vmPFC.


Subject(s)
Corpus Striatum , Dopamine , Magnetic Resonance Imaging , Positron-Emission Tomography , Prefrontal Cortex , Stress, Psychological , Humans , Female , Prefrontal Cortex/metabolism , Prefrontal Cortex/diagnostic imaging , Adult , Dopamine/metabolism , Stress, Psychological/metabolism , Stress, Psychological/physiopathology , Stress, Psychological/diagnostic imaging , Corpus Striatum/metabolism , Corpus Striatum/diagnostic imaging , Young Adult , Benzamides , Multimodal Imaging , Impulsive Behavior/physiology , Pyrrolidines
12.
Nat Commun ; 15(1): 6283, 2024 Jul 29.
Article in English | MEDLINE | ID: mdl-39075054

ABSTRACT

Adolescence is a period of dynamic brain remodeling and susceptibility to psychiatric risk factors, mediated by the protracted consolidation of association cortices. Here, we investigated whether longitudinal variation in adolescents' resilience to psychosocial stressors during this vulnerable period is associated with ongoing myeloarchitectural maturation and consolidation of functional networks. We used repeated myelin-sensitive Magnetic Transfer (MT) and resting-state functional neuroimaging (n = 141), and captured adversity exposure by adverse life events, dysfunctional family settings, and socio-economic status at two timepoints, one to two years apart. Development toward more resilient psychosocial functioning was associated with increasing myelination in the anterolateral prefrontal cortex, which showed stabilized functional connectivity. Studying depth-specific intracortical MT profiles and the cortex-wide synchronization of myeloarchitectural maturation, we further observed wide-spread myeloarchitectural reconfiguration of association cortices paralleled by attenuated functional reorganization with increasingly resilient outcomes. Together, resilient/susceptible psychosocial functioning showed considerable intra-individual change associated with multi-modal cortical refinement processes at the local and system-level.


Subject(s)
Magnetic Resonance Imaging , Myelin Sheath , Psychosocial Functioning , Resilience, Psychological , Humans , Adolescent , Male , Female , Myelin Sheath/metabolism , Longitudinal Studies , Prefrontal Cortex/physiology , Prefrontal Cortex/diagnostic imaging , Stress, Psychological/physiopathology , Cerebral Cortex/physiology , Cerebral Cortex/diagnostic imaging
13.
Cereb Cortex ; 34(7)2024 Jul 03.
Article in English | MEDLINE | ID: mdl-39066505

ABSTRACT

Taste and health are critical factors to be considered when choosing foods. Prioritizing healthiness over tastiness requires self-control. It has also been suggested that self-control is guided by cognitive control. We then hypothesized that neural mechanisms underlying healthy food choice are associated with both self-control and cognitive control. Human participants performed a food choice task and a working memory task during functional MRI scanning. Their degree of self-control was assessed behaviorally by the value discount of delayed monetary rewards in intertemporal choice. Prioritizing healthiness in food choice was associated with greater activity in the superior, dorsolateral, and medial prefrontal cortices. Importantly, the prefrontal activity was greater in individuals with smaller delay discounting (i.e. high self-control) who preferred a delayed larger reward to an immediate smaller reward in intertemporal choice. On the other hand, working memory activity did not show a correlation with delay discounting or food choice activity, which was further supported by supplementary results that analyzed data from the Human Connectome Project. Our results suggest that the prefrontal cortex plays a critical role in healthy food choice, which requires self-control, but not working memory, for maximization of reward attainments in a remote future.


Subject(s)
Choice Behavior , Delay Discounting , Food Preferences , Magnetic Resonance Imaging , Memory, Short-Term , Prefrontal Cortex , Reward , Humans , Memory, Short-Term/physiology , Prefrontal Cortex/physiology , Prefrontal Cortex/diagnostic imaging , Male , Female , Young Adult , Adult , Choice Behavior/physiology , Food Preferences/physiology , Delay Discounting/physiology , Diet, Healthy/psychology , Self-Control , Connectome
14.
Hum Brain Mapp ; 45(11): e26766, 2024 Aug 01.
Article in English | MEDLINE | ID: mdl-39046072

ABSTRACT

Mood variability, the day-to-day fluctuation in mood, differs between individuals and develops during adolescence. Because adolescents show higher mood variability and average mood than children and adults, puberty might be a potential biological mechanism underlying this increase. The goal of this preregistered developmental study was to examine the neural and hormonal underpinnings of adolescent-specific within-person changes in mood variability, with a specific focus on testosterone, cortisol, pubertal status, and resting-state functional brain connectivity. Data from two longitudinal cohorts were used: the L-CID twin study (aged 7-13, N at the first timepoint = 258) and the accelerated Leiden Self-Concept study (SC; aged 11-21, N at the first timepoint = 138). In both studies resting-state functional magnetic resonance imaging (rs-fMRI) data was collected, as well as daily mood. Additionally, in the SC study self-reported puberty testosterone and cortisol were collected. Random intercept cross-lagged panel models (RI-CLPM) were used to study the within-person relations between these biological measures and mood variability and average mood. Mood variability and average mood peaked in adolescence and testosterone levels and self-reported puberty also showed an increase. Connectivity between prefrontal cortex (dlPFC and vmPFC) and subcortical regions (caudate, amygdala) decreased across development. Moreover, higher testosterone predicted average negative mood at the next time point, but not vice versa. Further, stronger vmPFC-amygdala functional connectivity predicted decreases in mood variability. Here, we show that brain connectivity during development is an important within-person biological mechanism of the development of mood in adolescents. PRACTITIONER POINTS: Mood variability peaks in adolescence. Within-person changes in testosterone predict within-person changes in mood. Within-person changes in vmPFC-amygdala connectivity predict within-person changes in mood variability.


Subject(s)
Affect , Hydrocortisone , Magnetic Resonance Imaging , Puberty , Testosterone , Humans , Adolescent , Child , Male , Testosterone/blood , Affect/physiology , Female , Hydrocortisone/blood , Hydrocortisone/metabolism , Longitudinal Studies , Puberty/physiology , Young Adult , Brain/diagnostic imaging , Brain/growth & development , Brain/physiology , Adult , Connectome , Prefrontal Cortex/diagnostic imaging , Prefrontal Cortex/physiology , Prefrontal Cortex/growth & development , Amygdala/diagnostic imaging , Amygdala/physiology , Amygdala/growth & development , Adolescent Development/physiology
15.
Proc Natl Acad Sci U S A ; 121(32): e2316021121, 2024 Aug 06.
Article in English | MEDLINE | ID: mdl-39078679

ABSTRACT

For the human brain to operate, populations of neurons across anatomical structures must coordinate their activity within milliseconds. To date, our understanding of such interactions has remained limited. We recorded directly from the hippocampus (HPC), posteromedial cortex (PMC), ventromedial/orbital prefrontal cortex (OFC), and the anterior nuclei of the thalamus (ANT) during two experiments of autobiographical memory processing that are known from decades of neuroimaging work to coactivate these regions. In 31 patients implanted with intracranial electrodes, we found that the presentation of memory retrieval cues elicited a significant increase of low frequency (LF < 6 Hz) activity followed by cross-regional phase coherence of this LF activity before select populations of neurons within each of the four regions increased high-frequency (HF > 70 Hz) activity. The power of HF activity was modulated by memory content, and its onset followed a specific temporal order of ANT→HPC/PMC→OFC. Further, we probed cross-regional causal effective interactions with repeated electrical pulses and found that HPC stimulations cause the greatest increase in LF-phase coherence across all regions, whereas the stimulation of any region caused the greatest LF-phase coherence between that particular region and ANT. These observations support the role of the ANT in gating, and the HPC in synchronizing, the activity of cortical midline structures when humans retrieve self-relevant memories of their past. Our findings offer a fresh perspective, with high temporal fidelity, about the dynamic signaling and underlying causal connections among distant regions when the brain is actively involved in retrieving self-referential memories from the past.


Subject(s)
Memory, Episodic , Humans , Male , Female , Adult , Hippocampus/physiology , Prefrontal Cortex/physiology , Prefrontal Cortex/diagnostic imaging , Brain/physiology , Brain/diagnostic imaging , Mental Recall/physiology , Brain Mapping , Middle Aged , Neurons/physiology , Anterior Thalamic Nuclei/physiology
16.
Cereb Cortex ; 34(7)2024 Jul 03.
Article in English | MEDLINE | ID: mdl-39073380

ABSTRACT

Disinhibition, characterized by a loss of dietary control, is a significant risk factor for diet failure and the onset of eating disorders in restrained eaters. This study employs resting-state functional connectivity and structural covariance network analyses to explore the neural associations underlying this behavior. By analyzing functional MRI data from 63 female college students, we found that increased disinhibition correlates with enhanced functional connectivity between the medial orbitofrontal cortex and key components of the inhibition system, particularly within the fronto-parietal network. Moreover, we observed a relationship between the structural covariance of the medial orbitofrontal cortex and the inferior parietal lobule and the severity of disinhibition. Importantly, the functional connectivity between the medial orbitofrontal cortex and the inferior parietal lobule predicts the severity of binge eating symptoms in these individuals. These findings indicate that imbalances in the interaction between the brain's reward and inhibition systems can lead to dietary failures and eating disorders, emphasizing the need for targeted interventions.


Subject(s)
Magnetic Resonance Imaging , Neural Pathways , Parietal Lobe , Prefrontal Cortex , Female , Humans , Magnetic Resonance Imaging/methods , Young Adult , Parietal Lobe/physiology , Parietal Lobe/diagnostic imaging , Prefrontal Cortex/physiology , Prefrontal Cortex/diagnostic imaging , Neural Pathways/physiology , Neural Pathways/diagnostic imaging , Feeding Behavior/physiology , Feeding Behavior/psychology , Adult , Inhibition, Psychological , Brain Mapping/methods , Adolescent , Feeding and Eating Disorders/diagnostic imaging , Feeding and Eating Disorders/physiopathology , Feeding and Eating Disorders/psychology
17.
J Orthop Surg Res ; 19(1): 361, 2024 Jun 18.
Article in English | MEDLINE | ID: mdl-38890731

ABSTRACT

BACKGROUND: Near infrared brain functional imaging (FNIRS) has been used for the evaluation of brain functional areas, the imaging differences of central activation of cognitive-motor dual tasks between patients with chronic lateral ankle instability (CLAI) and healthy population remain unclear. This study aimed to evaluated the role of central imaging based on FNIRS technology on the plan management in patients with CLAI, to provide insights to the clinical treatment of CLAI. METHODS: CLAI patients treated in our hospital from January 1, 2021 to June 31, 2022 were selected. Both CLAI patients and health controls were intervened with simple task and cognitive-motor dual task under sitting and walking conditions, and the changes of oxygenated hemoglobin concentration in bilateral prefrontal cortex (PFC), premotor cortex (PMC) and auxiliary motor area (SMA) were collected and compared. RESULTS: A total of 23 participants were enrolled. There were significant differences in the fNIRS ΔHbO2 of barefoot subtractive walking PFC-R and barefoot subtractive walking SMA-R between experimental and control group (all P < 0.05). There was no significant difference in ΔHbO2 between the experimental group and the control group in other states (P > 0.05). There was no significant difference in ΔHbO2 between the experimental group and the control group in each state of the brain PMC region. CONCLUSION: Adaptive alterations may occur within the relevant brain functional regions of individuals with CLAI. The differential activation observed between the PFC and the SMA could represent a compensatory mechanism emerging from proprioceptive afferent disruptions following an initial ankle sprain.


Subject(s)
Joint Instability , Spectroscopy, Near-Infrared , Humans , Female , Joint Instability/diagnostic imaging , Joint Instability/physiopathology , Male , Adult , Chronic Disease , Young Adult , Spectroscopy, Near-Infrared/methods , Ankle Joint/diagnostic imaging , Ankle Joint/physiopathology , Walking/physiology , Prefrontal Cortex/diagnostic imaging , Prefrontal Cortex/physiopathology , Motor Cortex/diagnostic imaging , Motor Cortex/physiopathology , Cognition/physiology
18.
Neuroimage ; 296: 120670, 2024 Aug 01.
Article in English | MEDLINE | ID: mdl-38848980

ABSTRACT

Humans constantly make predictions and such predictions allow us to prepare for future events. Yet, such benefits may come with drawbacks as premature predictions may potentially bias subsequent judgments. Here we examined how prediction influences our perceptual decisions and subsequent confidence judgments, on scenarios where the predictions were arbitrary and independent of the identity of the upcoming stimuli. We defined them as invalid and non-informative predictions. Behavioral results showed that, such non-informative predictions biased perceptual decisions in favor of the predicted choice, and such prediction-induced perceptual bias further increased the metacognitive efficiency. The functional MRI results showed that activities in the medial prefrontal cortex (mPFC) and subgenual anterior cingulate cortex (sgACC) encoded the response consistency between predictions and perceptual decisions. Activity in mPFC predicted the strength of this congruency bias across individuals. Moreover, the parametric encoding of confidence in putamen was modulated by prediction-choice consistency, such that activity in putamen was negatively correlated with confidence rating after inconsistent responses. These findings suggest that predictions, while made arbitrarily, orchestrate the neural representations of choice and confidence judgment.


Subject(s)
Magnetic Resonance Imaging , Metacognition , Prefrontal Cortex , Humans , Male , Female , Metacognition/physiology , Young Adult , Adult , Prefrontal Cortex/physiology , Prefrontal Cortex/diagnostic imaging , Brain Mapping/methods , Judgment/physiology , Gyrus Cinguli/physiology , Gyrus Cinguli/diagnostic imaging , Choice Behavior/physiology
19.
Sci Rep ; 14(1): 13222, 2024 06 08.
Article in English | MEDLINE | ID: mdl-38851794

ABSTRACT

When a single choice impacts on life outcomes, faculties to make ethical judgments come into play. Here we studied decisions in a real-life setting involving life-and-death outcomes that affect others and the decision-maker as well. We chose a genuine situation where prior training and expertise play a role: firefighting in life-threatening situations. By studying the neural correlates of dilemmas involving life-saving decisions, using realistic firefighting situations, allowed us to go beyond previously used hypothetical dilemmas, while addressing the role of expertise and the use of coping strategies (n = 47). We asked the question whether the neural underpinnings of deontologically based decisions are affected by expertise. These realistic life-saving dilemmas activate the same core reward and affective processing network, in particular the ventromedial prefrontal cortex, nucleus accumbens and amygdala, irrespective of prior expertise, thereby supporting general domain theories of ethical decision-making. We found that brain activity in the hippocampus and insula parametrically increased as the risk increased. Connectivity analysis showed a larger directed influence of the insula on circuits related to action selection in non-experts, which were slower than experts in non rescuing decisions. Relative neural activity related to the decision to rescue or not, in the caudate nucleus, insula and anterior cingulate cortex was negatively associated with coping strategies, in experts (firefighters) suggesting practice-based learning. This shows an association between activity and expert-related usage of coping strategies. Expertise enables salience network activation as a function of behavioural coping dimensions, with a distinct connectivity profile when facing life-rescuing dilemmas.


Subject(s)
Decision Making , Firefighters , Humans , Firefighters/psychology , Decision Making/physiology , Male , Adult , Female , Magnetic Resonance Imaging , Brain/physiology , Brain/diagnostic imaging , Adaptation, Psychological/physiology , Brain Mapping , Prefrontal Cortex/physiology , Prefrontal Cortex/diagnostic imaging
20.
PLoS One ; 19(6): e0303211, 2024.
Article in English | MEDLINE | ID: mdl-38837991

ABSTRACT

INTRODUCTION: Mental fatigue is an early and enduring symptom in persons with autoimmune disease particularly multiple sclerosis (MS). Neuromodulation has emerged as a potential treatment although optimal cortical targets have yet to be determined. We aimed to examine cortical hemodynamic responses within bilateral dorsolateral prefrontal cortex (dlPFC) and frontopolar areas during single and dual cognitive tasks in persons with MS-related fatigue compared to matched controls. METHODS: We recruited persons (15 MS and 12 age- and sex-matched controls) who did not have physical or cognitive impairment and were free from depressive symptoms. Functional near infrared spectroscopy (fNIRS) registered hemodynamic responses during the tasks. We calculated oxyhemoglobin peak, time-to-peak, coherence between channels (a potential marker of neurovascular coupling) and functional connectivity (z-score). RESULTS: In MS, dlPFC demonstrated disrupted hemodynamic coherence during both single and dual tasks, as evidenced by non-significant and negative correlations between fNIRS channels. In MS, reduced coherence occurred in left dorsolateral PFC during the single task but occurred bilaterally as the task became more challenging. Functional connectivity was lower during dual compared to single tasks in the right dorsolateral PFC in both groups. Lower z-score was related to greater feelings of fatigue. Peak and time-to-peak hemodynamic response did not differ between groups or tasks. CONCLUSIONS: Hemodynamic responses were inconsistent and disrupted in people with MS experiencing mental fatigue, which worsened as the task became more challenging. Our findings point to dlPFC, but not frontopolar areas, as a potential target for neuromodulation to treat cognitive fatigue.


Subject(s)
Cognition , Dorsolateral Prefrontal Cortex , Hemodynamics , Multiple Sclerosis , Spectroscopy, Near-Infrared , Humans , Female , Male , Adult , Multiple Sclerosis/physiopathology , Multiple Sclerosis/complications , Dorsolateral Prefrontal Cortex/physiopathology , Dorsolateral Prefrontal Cortex/diagnostic imaging , Cognition/physiology , Middle Aged , Fatigue/physiopathology , Case-Control Studies , Mental Fatigue/physiopathology , Prefrontal Cortex/physiopathology , Prefrontal Cortex/diagnostic imaging
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