Lobe Of Brain Research Articles

Diffusion kurtosis imaging reveals abnormal gray matter and white matter development in some brain regions of children with attention-deficit/hyperactivity disorder.

In this study, we explored the application of diffusion kurtosis imaging (DKI) technology in the brains of children with attention-deficit/hyperactivity disorder (ADHD). Seventy-two children with ADHD and 79 age- and sex-matched healthy controls were included in the study. All children were examined by means of 3D T1-weighted image, DKI, and conventional sequence scanning. The volume and DKI parameters of each brain region were obtained by software postprocessing (GE ADW 4.6 workstation) and compared between the two groups of children to determine the imaging characteristics of children with ADHD. The result showed the total brain volume was lower in children with ADHD than in healthy children (p < .05). The gray and white matter volumes in the frontal lobe, temporal lobe, hippocampus, caudate nucleus, putamen, globus pallidus, and other brain regions were lower in children with ADHD than in healthy children (p < .05). The axial kurtosis (Ka), mean kurtosis (MK), fractional anisotropy (FA), and radial kurtosis(Kr) values in the frontal lobe, temporal lobe, and caudate nucleus of children with ADHD were lower than those of healthy children, while the mean diffusivity(MD) and fractional anisotropy of kurtosis (FAK) values were higher than those of healthy children (p < .05). Additionally, the Ka, MK, FA, and Kr values in the frontal lobe, caudate nucleus, and temporal lobe could be used to distinguish children with ADHD (AUC > .05, p < .05). In conclusion, DKI showed abnormal gray matter and white matter development in some brain regions of children with ADHD.

A Unique Case of Primary Subfrontal Lobe Meningioma with Intraorbital Extension

Introduction: Meningiomas, tumors originating from the meninges covering the brain, are typically considered benign. They primarily develop from arachnoid cap cells within the meninges and can manifest as primary orbital meningiomas (affecting structures like the optic nerve sheath) or secondary orbital meningiomas that extend from intracranial origins, such as the sphenoid wing and rarely from frontal lobe as in our case. Case Presentation: This report documents a very rare case where a meningioma emerged in the subfrontal lobe of the brain and subsequently spread to the orbit. The presence of such malignant variants in the orbit poses unique diagnostic challenges due to their potential to compress critical adjacent brain structures. Impact on Orbital Structures: The extension of these tumors into the orbit can have significant consequences, affecting structures like the cavernous sinus, superior orbital fissure, intraorbital contents, and the optic nerve. This further complicates their surgical management, given their proximity to essential neurological systems. Conclusion: This case study underscores the atypical growth pattern of malignant meningioma and highlights the complexities associated with identifying and treating meningioma with orbital extensions. The propensity of these tumors to impact vital brain structures necessitates a comprehensive approach to their diagnosis and management.

Clinical and neuroimaging predictors of Alzheimer’s Dementia Conversion in patients with mild cognitive impairment using 18F‐Florapronol amyloid PET by quantitative analysis over 2 years

AbstractBackgroundPatients with mild cognitive impairment(MCI) are a clinically important group because of the increased risk for the progression to Alzheimer’s dementia(AD). Amyloid positron emission tomography(PET) was useful as a predictor for identifying AD pathology in the pre‐dementia stage. We determined the rates of conversion to AD in MCI patients based on amyloid positivity by visual and quantitative analysis over 2 years. We also investigated the clinical and neuroimaging predictors for conversion to AD.MethodIndividuals aged 50 and above with MCI according to Petersen’s criteria were eligible. Subjects underwent laboratory tests including APOE genotyping, neuropsychological tests, brain magnetic resonance imaging(MRI), and amyloid PET assessed by 18F‐FC119S. Amyloid positivity was determined in each lobe of the brain and quantitatively analyzed. The follow‐up period was at least 2 years. Cox regression analysis was performed to identify prognostic factors which are independently related to time to AD conversion.ResultWe recruited 50 patients and 39 subjects were enrolled. 5 patients dropped out at 2 years, so 34 subjects were finally included. 13 of 34(38.2%) by visual analysis and 12 of 34(35.3%) by quantitative analysis of 18F‐FC119S PET showed amyloid positive. The basic demographics were not significantly different between the groups except for Korea‐Instrumental Activities of Daily Living(K‐IADL) at baseline(p = 0.004) and 1 year(p = 0.001), Mini‐mental State Examination(MMSE) at 2 years(p = 0.047) and Global Deterioration Scale(GDS) at 2 years(p = 0.029). 4 of 13(30.8%) by visual analysis, 4 of 12(66.7%) by quantitative analysis amyloid‐positive MCI patients converted to AD. Amyloid positive in posterior cingulate was marginally significant(p = 0.066). AD conversion group had a higher Clinical Dementia Rating‐Sum of box(CDR‐SOB) at baseline(p = 0.002) compared with remained MCI group. In multivariate cox regression, CDR‐SOB at baseline, MMSE at 1 year and K‐IADL at 2 years were included.ConclusionAmyloid‐positive MCI group was more likely to progress to AD. But long‐term follow‐up was required. By quantitative analysis of 18F‐FC119S PET, amyloid deposition in posterior cingulate was highly associated with the AD conversion group. CDR‐SOB at baseline, MMSE at 1 year and K‐IADL at 2 years were considered as clinically valuable prognostic predictors of disease progression. Especially, CDR‐SOB is important as a predictive biomarker in the pre‐dementia stage.

Stimulation of Cerebral Angiogenesis and Neurogenesis with Transcatheter Intracerebral Laser Photobiomodulation Therapy in Alzheimer’s Disease and Vascular Parkinsonism Aggravated by Dementia

AbstractBackgroundThe research is focused on the stimulation of cerebral angiogenesis and neurogenesis using Transcatheter Intracerebral Laser Photobiomodulation Therapy (PBMT) in patients with dementia in Alzheimer’s disease (AD) and patients with vascular parkinsonism (VP).MethodThe examination of 155 patients included assessment of CDR, The Tomography Dementia Rating scale (TDR), MMSE, cerebral CT, MRI, SG, rheoencephalography (REG) and cerebral MUGA.85 patients were selected, of whom:• 48 (30.97%) people suffering from AD, aged 34‐80 (mean age 67.5), men ‐ 17 (35.42%), women ‐ 31 (54.58%). According to dementia severity, patients were subdivided: preclinical stage (TDR‐0) ‐ 4, mild stage (TDR‐1) ‐ 16, moderately severe stage (TDR‐2) ‐ 21, severe stage (TDR‐3) ‐ 7 patients.• 37 (23.87%) people suffering from VP, aged 58‐80 (mean age 77), men 28 (75.68%), women ‐ 9 (24.32%). 19 (51.35%) had a mild dementia stage (CDR‐1).In hospital conditions, in a specialized cath lab, all patients underwent Transcatheter Intracerebral Laser Photobiomodulation Therapy (PBMT) (wavelength 632.8 nanometers).ResultAll 48 (100%) patients with AD underwent angiogenesis stimulation resulting in cerebral collateral capillary revascularization and closure of atreriovenous shunts.Simultaneously, patients showed a 10‐20% increase in cerebral temporal lobes volume, which indicates cerebral neurogenesis development and tissue regeneration. The process was accompanied by dementia level decrease and cognitive functions restoration. Consequently, patients were transferred to a milder TDR group. Depending on the initial dementia severity, the resulting positive effect was observed from 2 to 15 years.All 37 (100%) patients with VP underwent angiogenesis stimulation resulting in cerebral microcirculation improvement and cerebral involutive changes decrease, which indicates the neurogenesis development and tissue regeneration. The process was accompanied by decreased dementia and cognitive functions restoration. The resulting positive effect was observed over 10 years.ConclusionDespite the differences in AD and VP etiology, Transcatheter Intracerebral Laser Photobiomodulation Therapy (PBMT) is an effective treatment for dementia in these diseases. The method stimulates angiogenesis and improves blood supply to the brain, it stimulates neurogenesis and the restoration of normal tissue structures, which leads to improved mental and cognitive functions. The resulting effect persists for a long time.

Higher baseline cerebrospinal fluid platelet‐derived growth factor receptor‐β levels are associated with slower reductions in longitudinal cerebral blood flow among cognitively unimpaired individuals

AbstractBackgroundCerebrospinal fluid (CSF) platelet‐derived growth factor receptor‐β (PDGFR‐β) is an emerging biomarker hypothesized to reflect pericyte damage. CSF PDGFR‐β levels are increased in Alzheimer’s disease (AD), but it is unknown if pericyte injury contributes to cerebrovascular changes common in AD. We examined if PDGFR‐β relates to changes in cerebral blood flow (CBF) and white matter injury in older adults.MethodVanderbilt Memory and Aging Project participants (n = 152, baseline age 73±7 years, 43% mild cognitive impairment [MCI]) underwent baseline lumbar puncture and serial brain MRI over a 7‐year (5.5±2.3) follow‐up period. CSF PDGFR‐β concentrated was measured by immunoassay. MRI included pseudo‐continuous arterial spin‐labeling to quantify CBF, T2‐FLAIR to quantify white matter hyperintensities (WMHs), and diffusion tensor imaging (DTI) to quantify white matter microstructural integrity. Ordinary least squares regression and linear mixed‐effects models related baseline CSF PDGFR‐β to baseline and longitudinal whole brain and regional CBF, WMH, and DTI metrics, adjusting for baseline demographic variables, modified Framingham Stroke Risk Profile, cognitive status, apolipoprotein‐ε4 status, and regional tissue volume. Longitudinal models adjusted for follow‐up time. Follow‐up models tested a CSF PDGFR‐β x cognitive status interaction.ResultIn main models, higher CSF PDGFR‐β levels were cross‐sectionally associated with lower mean diffusivity (indicating better microstructural integrity) in white matter tracts in the frontal, temporal, parietal, and occipital lobes (p‐values&lt;0.03) but were unrelated to WMHs (p‐values&gt;0.18). Models investigating associations with longitudinal white matter variables were null (p‐values&gt;0.35). CSF PDGFR‐β cross‐sectionally interacted with diagnosis on temporal lobe CBF, such that higher CSF PDGFR‐β related to higher CBF in MCI participants (p = 0.01). In longitudinal models, baseline CSF PDGFR‐β interacted with cognitive status on whole brain and occipital lobe CBF (p‐values&lt;0.04). Stratified models showed higher baseline CSF PDGFR‐β related slower reductions in longitudinal CBF in whole brain (p = 0.02), frontal (p = 0.04), temporal (p = 0.02), parietal (p = 0.01), and occipital lobes (p = 0.008) in cognitively unimpaired participants only.ConclusionAmong older adults, higher CSF PDGFR‐β levels are associated with better white matter integrity at study entry and predict slower reductions in longitudinal CBF among cognitively unimpaired individuals. Results suggest that higher PDGFR‐β levels may reflect subclinical vascular remodeling that provides protection to future cerebrovascular compromise.

Associations between glymphatic function and BBB water exchange rate and perfusion in a Latinx cohort

AbstractBackgroundThe glymphatic system is thought to clear waste products from the brain by facilitating the exchange of interstitial fluid (ISF) with cerebrospinal fluid (CSF) through aquaporin‐4 (AQP4) water channels present in astrocyte endfeet. A recent non‐invasive MRI method, diffusion tensor image analysis along the perivascular space (DTI‐ALPS), has been proposed for evaluating brain clearance function and has shown reduced glymphatic function in various neurological disorders such as Alzheimer’s disease. However, the role of microvascular perfusion and blood‐brain barrier (BBB) permeability in the glymphatic system remains unclear. In this study, we used a novel diffusion‐prepared arterial spin labeling (DP‐ASL) MRI technique to measure BBB water exchange rate (kw) and cerebral blood flow (CBF) and studied their relationships with the DTI‐ALPS score.Method44 Latinx subjects (20 male; age = 65.6±5.6 years) were recruited from the USC MarkVCID study. Imaging parameters for DP‐ASL were: resolution = 3.5×3.5×8mm3, 10 slices, scan time 10 mins. kw was calculated from the ratio of intra‐ and extra‐vascular perfusion signals with total‐general‐variation (TGV) regularized single‐pass approximation (SPA) modeling and CBF was calculated from PLD = 1800ms data using one‐compartment Kety model. kw and CBF maps were normalized into the MNI space and regional analysis was performed in the frontal/temporal/parietal lobe, and subcortical regions. Association between ALPS score and CBF/kw values were studied by linear regressions. P&lt;0.05 was considered as significant.ResultFig.1 shows kw and CBF maps from three representative subjects with increasing ALPS scores (top to bottom). ALPS was significantly correlated with kw in MTL (β = 1.7e‐3,P = 0.04) and a positive trend was observed between ALPS and whole brain average kw (P = 0.11). While significant correlations were found between ALPS and CBF in multiple brain regions including frontal lobe (β = 7e‐3,P = 0.009), temporal lobe (β = 7e‐3,P = 0.002), parietal lobe (β = 4e‐3,P = 0.03), MTL (β = 8e‐3,P = 0.03), ACC (β = 6e‐3,P = 0.005), PCC (β = 4e‐3,P = 0.02), precuneus (β = 4e‐3,P = 0.04) and whole brain (β = 8e‐3,P = 0.01). Fig.2 shows scatter plots of ALPS versus kw (A) and CBF in MTL and whole brain, respectively.ConclusionThis is the first study in Latinx population demonstrating positive correlations between ALPS score and both CBF and kw, suggesting a possible involvement of blood flow and BBB water exchange rate in the glymphatic system.

Basic Science and Pathogenesis - Part 2.

Traumatic Brain Injury (TBI) is a known risk factor for developing a neurodegenerative disease later in life, including Alzheimer's Disease (AD) and other forms of tauopathy such as chronic traumatic encephalopathy (CTE) and frontal-temporal dementia (FTD). Although several studies highlight the relationship between the severity and frequency of a TBI and the development of these tauopathies, the mechanism behind this association remains unknown. Proper meningeal lymphatic function is required for clearance of waste products and protein aggregates such as amyloid beta and tau from the brain parenchyma. While post-TBI inflammation is beneficial for clearing debris and promoting tissue repair, prolonged glial activation and decreased meningeal lymphatic drainage have been linked to worsened cognitive function. A mild TBI (mTBI) was delivered to three-month-old young adult mice overexpressing P301S mutant human tau (PS19) through the skull on the right inferior temporal lobe of the brain. Sham and TBI injured mice were tested on behavioral tests at 5 months of age. At 7 months of age, brains were examined for tau pathology and neuroinflammation using confocal microscopy. Four months after mTBI, the brains of TBI PS19 mice exhibit increased levels of microglia and astrocytes, and increased P-S202/T-205-Tau in the cortex and thalamus of the ipsilateral hemisphere compared to the contralateral side and to Sham PS19 controls. These findings correlate with our behavior study showing increased hyperactivity, risk-taking behavior, and impaired short term working memory. PS19 TBI mice also present larger ventricles than their uninjured controls suggesting a potential loss of white matter in the cortex and/or hippocampus. P-S202/T-205-Tau orginated from the cortex near the injury site can aggregate and promote the formation of more toxic tau that spreads to deeper regions of the cortex and in the thalamus primarily through the thalamocortical circuit. Also, microglia and astrocyte activation and production of inflammatory mediators has been associated with synapse pruning and engulfment of damaged neurons expressing 'eat me signals' leading to neurodegeneration.

Dysfunctional cerebral glucose transport in Alzheimer’s Disease

AbstractBackgroundGlucose is the primary energy source required for the homeostatic function of the brain. Glucose transporter 1 (GLUT1) present at the blood‐brain barrier is a key regulator of glucose transport into the brain. Reduced GLUT1 expression is shown to exacerbate Alzheimer’s pathology in rodent models. Here we aimed to establish whether there are regional differences in ineffective glucose transport amongst people living with Alzheimer’s disease.Method125 participants diagnosed with Alzheimer’s dementia, with an [18F]FDG scan with atrial input were enrolled. All participants underwent 3‐tesla magnetic resonance imaging and [18F]FDG scan with continuous and discrete arterial sampling. Spectral analysis was performed to create 1‐minute input‐response function parametric maps. To produce glucose transfer maps we applied the following equation; K1 ⁎ Ca / τ (K1 = 1‐minute IRF map, Ca = Plasma glucose concentration, τ = 1.48 a lumped constant). Glucose transfer maps were then coregistered to the participants’ structural MRI and normalised to MNI space. Regional mean glucose transfer was then calculated for the anterior cingulate cortex, frontal lobe, hippocampus, parahippocampus, occipital lobe, parietal lobe, posterior cingulate cortex, striatum, temporal lobe, and thalamus. A within‐subject ANOVA was then performed to evaluate the regional differences in cerebral glucose transport.ResultThe parahippocampus exhibited the lowest rate of glucose transfer in comparison to all other regions (p &lt; 0.001), followed by the hippocampus. The striatum and occipital lobe demonstrated the regions of the highest mean glucose transportation from blood to the brain. In terms of brain lobes, the temporal lobe showed the lowest rates of glucose transfer, followed by the parietal lobe, then frontal and occipital (p &lt; 0.001).ConclusionWe demonstrate dysfunctional BBB glucose transport in Alzheimer’s disease, with prominent glucose transport abnormalities localised in the parahippocampus. Impaired glucose transport was most apparent within temporal lobe structures. Targeting glucose transfer may be an effective way of treating Alzheimer’s disease.

Convergent evolution of the sensory pits in and within flatworms

BackgroundUnlike most free-living platyhelminths, catenulids, the sister group to all remaining flatworms, do not have eyes. Instead, the most prominent sensory structures in their heads are statocysts or sensory pits. The latter, found in the family Stenostomidae, are concave depressions located laterally on the head that represent one of the taxonomically important traits of the family. In the past, the sensory pits of flatworms have been homologized with the cephalic organs of nemerteans, a clade that occupies a sister position to platyhelminths in some recent phylogenies. To test for this homology, we studied morphology and gene expression in the sensory pits of the catenulid Stenostomum brevipharyngium.ResultsWe used confocal and electron microscopy to investigate the detailed morphology of the sensory pits, as well as their formation during regeneration and asexual reproduction. The most prevalent cell type within the organ is epidermally-derived neuron-like cells that have cell bodies embedded deeply in the brain lobes and long neurite-like processes extending to the bottom of the pit. Those elongated processes are adorned with extensive microvillar projections that fill up the cavity of the pit, but cilia are not associated with the sensory pit. We also studied the expression patterns of some of the transcription factors expressed in the nemertean cephalic organs during the development of the pits. Only a single gene, pax4/6, is expressed in both the cerebral organs of nemerteans and sensory pits of S. brevipharyngium, challenging the idea of their deep homology.ConclusionsSince there is no morphological or molecular correspondence between the sensory pits of Stenostomum and the cerebral organs of nemerteans, we reject their homology. Interestingly, the major cell type contributing to the sensory pits of stenostomids shows ultrastructural similarities to the rhabdomeric photoreceptors of other flatworms and expresses ortholog of the gene pax4/6, the pan-bilaterian master regulator of eye development. We suggest that the sensory pits of stenostomids might have evolved from the ancestral rhabdomeric photoreceptors that lost their photosensitivity and evolved secondary function. The mapping of head sensory structures on plathelminth phylogeny indicates that sensory pit-like organs evolved many times independently in flatworms.

Predicting progression of white matter hyperintensity using coronary artery calcium score based on coronary CT angiography-feasibility and accuracy.

Coronary artery disease (CAD) usually coexists with subclinical cerebrovascular diseases given the systematic nature of atherosclerosis. In this study, our objective was to predict the progression of white matter hyperintensity (WMH) and find its risk factors in CAD patients using the coronary artery calcium (CAC) score. We also investigated the relationship between the CAC score and the WMH volume in different brain regions. We evaluated 137 CAD patients with WMH who underwent coronary computed tomography angiography (CCTA) and two magnetic resonance imaging (MRI) scans from March 2018 to February 2023. Patients were categorized into progressive (n = 66) and nonprogressive groups (n = 71) by the change in WMH volume from the first to the second MRI. We collected demographic, clinical, and imaging data for analysis. Independent risk factors for WMH progression were identified using logistic regression. Three models predicting WMH progression were developed and assessed. Finally, patients were divided into groups based on their total CAC score (0 to <100, 100 to 400, and > 400) to compare their WMH changes in nine brain regions. Alcohol abuse, maximum pericoronary fat attenuation index (pFAI), CT-fractional flow reserve (CT-FFR), and CAC risk grade independently predicted WMH progression (p < 0.05). The logistic regression model with all four variables performed best (training: AUC = 0.878, 95% CI: 0.790, 0.938; validation: AUC = 0.845, 95% CI: 0.734, 0.953). An increased CAC risk grade came with significantly higher WMH volume in the total brain, corpus callosum, and frontal, parietal and occipital lobes (p < 0.05). This study demonstrated the application of the CCTA-derived CAC score to predict WMH progression in elderly people (≥60 years) with CAD.

Posterior reversible encephalopathy syndrome in a patient with late postpartum eclampsia.

Posterior reversible encephalopathy syndrome (PRES) is a rare complication commonly associated with headache and acute changes in blood pressure that results from a variety of causes, culminating in vasogenic cerebral edema in the occipital and parietal lobes of the brain. We report here a woman who suffered from headache, generalized tonic-clonic seizures, and cortical blindness in the late postpartum period. Posterior reversible encephalopathy syndrome. The patient was treated with amlodipine besylate tablets for hypertension, dehydration with mannitol and glycerin fructose, and antispasmodic treatment with sodium valproate and oxcarbazepine. On day 2, the patient became conscious, headache and vision improved. One week later, symptoms and signs disappeared, blood pressure returned to normal, and brain MRI lesions disappeared in re-examination. Eclampsia associated with PRES is reversible in most cases, but it is a serious and potentially life-threatening obstetric emergency. If adequate treatment is provided in a timely manner, most women will make a full recovery. Attention needs to be paid to timely and adequate treatment, as well as appropriate follow-up and support for patients with PRES.

Abstract 17621: Acute Coronary Syndrome Due to Septic Emboli From Infective Endocarditis

Case Description: A 34-year-old female with a history of IV drug use and valvular infective endocarditis requiring multiple valve replacements presented with weakness and abdominal pain. She was found to be in septic shock requiring vasopressors and antibiotics. EKG was initially without ischemic changes. Imaging revealed multiorgan infarction including the spleen, left kidney, and parietal and temporal lobes of the brain with concomitant subarachnoid hemorrhage. TTE showed multiple masses on the mitral valve and new stenosis of the recently replaced tricuspid valve, concerning for multi-valvular involvement. LV systolic function was normal. Blood cultures were positive for MRSA and Strep agalactiae. Severe troponin elevation along with diffuse ST elevations in V3-6 prompted cardiology consultation, however intervention was deemed inappropriate due to presence of subarachnoid hemorrhage, thrombocytopenia and multiorgan failure. The patient was soon transitioned to comfort care after a discussion with family. Discussion: Acute coronary syndrome (ACS) secondary to infective endocarditis is a rarely cited phenomenon. Standardized management and treatment for ACS is difficult in the setting of co-existing multiorgan failure. In this case, our patient with infective endocarditis subsequently developed ACS secondary to septic emboli from large perivalvular vegetations. We emphasize vigilance for acute coronary events during infective endocarditis without source control.

EEG-Based Functional Connectivity Analysis for Cognitive Impairment Classification

Understanding how mild cognitive impairment affects global neural networks may explain changes in brain electrophysiology. Using graph theory and the visual oddball paradigm, we evaluated the functional connectivity of neuronal networks in brain lobes. The study involved 30 participants: 14 with mild cognitive impairment (MCI) and 16 healthy control (HC) participants. We conducted an examination using the visual oddball paradigm, focusing on electroencephalography signals with targeted stimuli. Our analysis employed functional connectivity utilizing the change point detection method. Additionally, we implemented training for linear discriminant analysis, K-nearest neighbor, and decision tree techniques to classify brain activity, distinguishing between subjects with mild cognitive impairment and those in the healthy control group. Our results demonstrate the efficacy of combining functional connectivity measurements derived from electroencephalography with machine learning for cognitive impairment classification. This research opens avenues for further exploration, including the potential for real-time detection of cognitive decline in complex real-world scenarios.

Recalling gist memory depends on CA1 hippocampal neurons for lifetime retention and CA3 neurons for memory precision

Why some of us remember events more clearly than others and why memory loses precision over time is a major focus in memory research. Here, we show that the recruitment of specific neuroanatomical pathways within the medial temporal lobe (MTL) of the brain defines the precision of the memory recalled over the lifespan. Using optogenetics, neuronal activity mapping, and studying recent to very remote memories, we report that the hippocampal subfield CA1 is necessary for retrieving the gist of events and receives maximal support from MTL cortical areas (MEC, LEC, PER, and POR) for recalling the most remote memories. In contrast, reduction of CA3's activity alone coincides with the loss of memory precision over time. We propose that a shift between specific MTL subnetworks over time might be a fundamental mechanism of memory consolidation.

Intimate Relationships Weaken Female Competition: Evidence from Phase-amplitude Coupling and Event-Related Potentials

Competition, an essential component of social interaction, frequently occurs in daily life, and the impact of intimate relationships on women's competition has not yet been revealed. In this study, the visual target paradigm was used to explore the neural mechanisms underlying the regulation of female competitiveness by intimate relationships using event-related potential (ERP) data, time–frequency analysis, and brain functional connectivity. The research results indicate that, the P1, the N4, and the LPP were sensitive to the impact of intimate relationships on competition. Compared to competition between unfamiliar opposite-gender dyads, the average amplitudes of the N4 and LPP were higher in the late stage of competition between romantic partners. Compared to competition with strangers of the opposite gender, alpha band power was significantly higher when female individuals competed with their romantic partners. In addition, there was a positive correlation between the synchronization of activity in the frontal, parietal, and right temporal lobes of a female's brain and their degree of female engagement in competition. When a female individuals focused on the competition, activity synchronization was higher. The results indicate that competition with unfamiliar individuals of the opposite gender can make female focus on the competitive task, causing synchronous activation of corresponding brain regions. When competing with a romantic partner, women's focus decreases, their willingness to compete decreases, and the synchrony of brain functional connectivity decreases. This study suggests that intimate relationship weakens women's competitiveness, which is of significant importance for understanding high-quality intimate relationship and promoting the development of healthy competition.

MRI with generalized diffusion encoding reveals damaged white matter in patients previously hospitalized for COVID-19 and with persisting symptoms at follow-up.

There is mounting evidence of the long-term effects of COVID-19 on the central nervous system, with patients experiencing diverse symptoms, often suggesting brain involvement. Conventional brain MRI of these patients shows unspecific patterns, with no clear connection of the symptomatology to brain tissue abnormalities, whereas diffusion tensor studies and volumetric analyses detect measurable changes in the brain after COVID-19. Diffusion MRI exploits the random motion of water molecules to achieve unique sensitivity to structures at the microscopic level, and new sequences employing generalized diffusion encoding provide structural information which are sensitive to intravoxel features. In this observational study, a total of 32 persons were investigated: 16 patients previously hospitalized for COVID-19 with persisting symptoms of post-COVID condition (mean age 60 years: range 41-79, all male) at 7-month follow-up and 16 matched controls, not previously hospitalized for COVID-19, with no post-COVID symptoms (mean age 58 years, range 46-69, 11 males). Standard MRI and generalized diffusion encoding MRI were employed to examine the brain white matter of the subjects. To detect possible group differences, several tissue microstructure descriptors obtainable with the employed diffusion sequence, the fractional anisotropy, mean diffusivity, axial diffusivity, radial diffusivity, microscopic anisotropy, orientational coherence (Cc) and variance in compartment's size (CMD) were analysed using the tract-based spatial statistics framework. The tract-based spatial statistics analysis showed widespread statistically significant differences (P < 0.05, corrected for multiple comparisons using the familywise error rate) in all the considered metrics in the white matter of the patients compared to the controls. Fractional anisotropy, microscopic anisotropy and Cc were lower in the patient group, while axial diffusivity, radial diffusivity, mean diffusivity and CMD were higher. Significant changes in fractional anisotropy, microscopic anisotropy and CMD affected approximately half of the analysed white matter voxels located across all brain lobes, while changes in Cc were mainly found in the occipital parts of the brain. Given the predominant alteration in microscopic anisotropy compared to Cc, the observed changes in diffusion anisotropy are mostly due to loss of local anisotropy, possibly connected to axonal damage, rather than white matter fibre coherence disruption. The increase in radial diffusivity is indicative of demyelination, while the changes in mean diffusivity and CMD are compatible with vasogenic oedema. In summary, these widespread alterations of white matter microstructure are indicative of vasogenic oedema, demyelination and axonal damage. These changes might be a contributing factor to the diversity of central nervous system symptoms that many patients experience after COVID-19.

Prevalence, Risk Factors, and Clinical Outcomes of New Cerebral Microbleeds After Intravenous Thrombolysis in Acute Ischemic Stroke: aSystematic Review and Meta-analysis.

Cerebral microbleeds (CMBs) are common in the elderly population, and are associated with an increased risk of stroke and dementia. An acute ischemic stroke event can make CMBs develop rapidly. However, the progression of CMBs after intravenous thrombolysis is not well understood. Following apreviously registered protocol, PubMed, Web of Science, and Embase databases were systematically searched to identify relevant literature up to August 2022. Cohort studies that reported new CMBs in patients with acute ischemic stroke undergoing intravenous thrombolysis were included. Random effects models were used to calculate the pooled estimates. Seven studies with 1079 patients were included in the meta-analysis. The pooled new CMBs prevalence was 7.6% (95% CI 3.9-14.3%) and 63.6% new CMBs were located in the cerebral lobes. Compared with patients without new CMBs, those with new CMBs were older, had ahigher proportion of hypertension, and had higher systolic blood pressure and baseline CMBs burden. The presence of new CMBs increased the likelihood of remote intracerebral hemorrhage (OR 28.75, 95% CI 8.58-96.38) and symptomatic intracerebral hemorrhage (OR 15.49, 95% CI 3.21-74.73) but was not related to functional outcomes or hemorrhagic transformation. The prevalence of new CMBs after intravenous thrombolysis was approximately 7.6%. The presence of new CMBs is associated with remote and symptomatic intracerebral hemorrhage following intravenous thrombolysis. Considering the potential long-term adverse effects of CMBs progression, patients at ahigh risk of developing new CMBs should be identified based on potential risk factors.

State of the Hippocampus and Frontal Brain in Rats with Experimental Hypothyroidism

Introduction. Despite the fact that today patients with hypothyroidism manage to correct their hormonal profile, perfect control is not always achieved during the course of the disease. This was noted in a study of 22 people with hypothyroidism according to medical records for 8.24±0.76 years: the average TSH level was 7.14±2.37 mIU∕l, T4 was 23.01±4.38 pmol/l, although at the start of the study TSH was 3.72±0.76 mIU∕l and T4 was 13.8±1.96 pmol/l. Ultimately, this affected cognitive functions, including attention, speech and memory, despite the fact that cognitive impairment with drug compensation of hypothyroidism is considered reversible.&#x0D; The results of a morphological study of the hippocampus and frontal lobe of the brain in rats with experimental hypothyroidism at an early stage can serve as a prototype for changes in the corresponding structures responsible for cognitive functions in individuals with hypothyroidism, even against the background of relative compensation with a long course of the disease.&#x0D; Objective. To study morphology of the brain areas responsible for cognitive functions, in particular the hippocampus and anterior-frontal cortex in rats in the early stages of experimental hypothyroidism.&#x0D; Materials and methods. The study included 12 white outbred sexually mature male rats. Hypothyroidism was modelled in 7 rats using the drug “Mercazolil” (“Zdorovye”, Ukraine). After 28 days, the animals underwent light-optical study of the histological structure of CA1, CA3 fields of the hippocampus, dentate gyrus and anterior-frontal cortex. Five animals were intact and, accordingly, served as controls.&#x0D; Results. The light-optical examination revealed the sequence and depth of the violations: the most pronounced dystrophic changes with vacuolation of structures occur in the dentate gyrus; in the hippocampus itself, the CA1 field is the most vulnerable; lateralisation of hippocampal morphological changes with left-sided dominance was detected; minor morphological changes were detected in the anterior-frontal cortex. It is important that neuro-glial changes occur in parallel with vascular disorders.&#x0D; Conclusions. Under the conditions of simulated hypothyroidism, changes occur in all studied brain components with their left-sided dominance, except for the anterior-frontal cortex.

The characteristics and risk factors of cerebrovascular events in young systemic lupus erythematosus patients: A case-control study

We clarified the characteristics and risk factors of CVEs in young SLE patients. We retrospectively reviewed the medical records of patients younger than 50 years of age diagnosed with SLE and first CVEs from 1995 to 2020 in a tertiary medical center in Taiwan. We collected data on the patient characteristics before the CVE and reviewed the laboratory data obtained during the period. At a ratio of 1:3, cases and controls were matched with sex, SLE diagnosis age, diagnosis year, and SLE duration. We enrolled 43 CVE SLE patients and matched 129 non-CVE SLE controls. The median age at the time of the CVE was 39 years. Around 70% of young-aged CVE involved the cerebral lobes of frontal (∼30%), parietal (∼20%), occipital (∼10%), and temporal (∼10%). The peak incidence period for hemorrhagic CVE was within 1st year of SLE diagnosis (37%); in contrast, during the 2nd to 5th year of SLE diagnosis (25%) for ischemia CVEs. Hyperlipidemia (odds ratio [OR]=19.36, p=0.002), anti-phospholipid syndrome (APS) (OR=41.9, p=0.0068), a lower hemoglobin level (OR=0.66, p=0.0192), and a higher SLE Disease Activity Index (SLEDAI-2k) score (OR=1.22, p=0.0019) were independent risk factors for CVEs in young SLE patients. Hyperlipidemia, APS, low Hb level, and high SLEDAI-2k significantly increase the risk of young-aged SLE patients developing CVE.

Cerebral dominance representation of directed connectivity within and between left-right hemispheres and frontal-posterior lobes in mild cognitive impairment.

Electroencephalography can assess connectivity between brain hemispheres, potentially influencing cognitive functions. Much of the existing electroencephalography research primarily focuses on undirected connectivity, leaving uncertainties about directed connectivity alterations between left-right brain hemispheres or frontal-posterior lobes in mild cognitive impairment. We analyzed resting-state electroencephalography data from 34 mild cognitive impairment individuals and 23 normal controls using directed transfer function and graph theory for directed network analysis. Concerning the dominance within left-right hemispheres or frontal-posterior lobes, the mild cognitive impairment group exhibited decreased connectivity within the frontal compared with posterior brain regions in the delta and theta bands. Regarding the dominance between the brain hemispheres or lobes, the mild cognitive impairment group showed reduced connectivity from the posterior to the frontal regions versus the reverse direction in the same bands. Among all participants, the intra-lobe frontal-posterior dominance correlated positively with executive function in the delta and alpha bands. Inter-lobe dominance between frontal and posterior regions also positively correlated with executive function, attention, and language in the delta band. Additionally, interhemispheric dominance between the left and right hemispheres positively correlated with attention in delta and theta bands. These findings suggest altered cerebral dominance in mild cognitive impairment, potentially serving as electrophysiological markers for neurocognitive disorders.