Brain Correlates of Persistent Postural-Perceptual Dizziness: A Review of Neuroimaging Studies

Persistent postural-perceptual dizziness (PPPD), defined in 2017, is a vestibular disorder characterized by chronic dizziness that is exacerbated by upright posture and exposure to complex visual stimuli. This review focused on recent neuroimaging studies that explored the pathophysiological mechanisms underlying PPPD and three conditions that predated it. The emerging picture is that local activity and functional connectivity in multimodal vestibular cortical areas are decreased in PPPD, which is potentially related to structural abnormalities (e.g., reductions in cortical folding and grey-matter volume). Additionally, connectivity between the prefrontal cortex, which regulates attentional and emotional responses, and primary visual and motor regions appears to be increased in PPPD. These results complement physiological and psychological data identifying hypervigilant postural control and visual dependence in patients with PPPD, supporting the hypothesis that PPPD arises from shifts in interactions among visuo-vestibular, sensorimotor, and emotional networks that overweigh visual over vestibular inputs and increase the effects of anxiety-related mechanisms on locomotor control and spatial orientation.

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Structural Brain Correlates of Creative Personality

10.1101/2021.01.06.425561 ◽

2021 ◽

Author(s):

Divya Sadana ◽

Rajnish Kumar Gupta ◽

S Senthil Kumaran ◽

Sanjeev Jain ◽

Jamuna Rajeswaran

Keyword(s):

Grey Matter ◽

Inferior Frontal Gyrus ◽

Anterior Cingulate ◽

Grey Matter Volume ◽

Voxel Based Morphometry ◽

Creative Personality ◽

Brain Correlates ◽

The Right ◽

Creative Artists ◽

Age Range

Creative individuals and their enigmatic personalities have always been a subject of fascination. The current study explored the neuroanatomical basis of creative personality using voxel-based morphometry. The sample comprised of two groups - Creative (CR) group (professional creative artists) and matched controls with no demonstrated artistic creativity (NC) with 20 participants in each group, in the age range of 20-40 years, right-handed, and had minimum average intelligence (IQ > 90). Participants in CR were selected using the creativity achievement questionnaire, creativity was assessed using the Wallach & Kogan test of creativity, and personality was administered using NEO-FFI. Results indicated significantly higher openness to new experiences in CR which positively correlates with the right middle frontal gyrus. An increased grey matter volume in the inferior frontal gyrus, anterior cingulate gyrus in CR, pointing towards the integration of cognitive and imaginative processes that might be implicated in creative personality.

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Structural abnormalities in gyri of the prefrontal cortex in individuals with schizophrenia and their unaffected siblings

The British Journal of Psychiatry ◽

10.1192/bjp.bp.109.067314 ◽

2010 ◽

Vol 196 (2) ◽

pp. 150-157 ◽

Cited By ~ 48

Author(s):

Michael P. Harms ◽

Lei Wang ◽

Carolina Campanella ◽

Kristina Aldridge ◽

Amanda J. Moffitt ◽

...

Keyword(s):

Prefrontal Cortex ◽

Cortical Thickness ◽

Grey Matter ◽

Genetic Factors ◽

Inferior Frontal Gyrus ◽

Familial Risk ◽

Grey Matter Volume ◽

Genetic Contribution ◽

Matter Volume ◽

Structural Abnormalities

BackgroundThe relatives of individuals with schizophrenia exhibit deficits of overall frontal lobe volume, consistent with a genetic contribution to these deficits.AimsTo quantify the structure of gyral-defined subregions of prefrontal cortex in individuals with schizophrenia and their siblings.MethodGrey matter volume, cortical thickness, and surface area of the superior, middle and inferior frontal gyri were measured in participants with schizophrenia and their unaffected (non-psychotic) siblings (n = 26 pairs), and controls and their siblings (n = 40 pairs).ResultsGrey matter volume was reduced in the middle and inferior frontal gyri of individuals with schizophrenia, relative to controls. However, only inferior frontal gyrus volume was also reduced in the unaffected siblings of those with schizophrenia, yielding a volume intermediate between their affected siblings and controls.ConclusionsThe structure of subregions of the prefrontal cortex may be differentially influenced by genetic factors in schizophrenia, with inferior frontal gyrus volume being most related to familial risk.

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Larger right inferior frontal gyrus volume and surface area in participants at genetic risk for bipolar disorders

Psychological Medicine ◽

10.1017/s0033291718001903 ◽

2018 ◽

Vol 49 (08) ◽

pp. 1308-1315 ◽

Cited By ~ 8

Author(s):

V. Drobinin ◽

C. Slaney ◽

J. Garnham ◽

L. Propper ◽

R. Uher ◽

...

Keyword(s):

Surface Area ◽

Genetic Risk ◽

Grey Matter ◽

Inferior Frontal Gyrus ◽

Bipolar Disorders ◽

Group Differences ◽

Grey Matter Volume ◽

Cortical Folding ◽

Matter Volume ◽

Pars Triangularis

AbstractBackgroundLarger grey matter volume of the inferior frontal gyrus (IFG) is among the most replicated biomarkers of genetic risk for bipolar disorders (BD). However, the IFG is a heterogeneous prefrontal region, and volumetric findings can be attributable to changes in cortical thickness (CT), surface area (SA) or gyrification. Here, we investigated the morphometry of IFG in participants at genetic risk for BD.MethodsWe quantified the IFG cortical grey matter volume in 29 affected, 32 unaffected relatives of BD probands, and 42 controls. We then examined SA, CT, and cortical folding in subregions of the IFG.ResultsWe found volumetric group differences in the right IFG, with the largest volumes in unaffected high-risk and smallest in control participants (F2,192 = 3.07, p = 0.01). The volume alterations were localized to the pars triangularis of the IFG (F2,97 = 4.05, p = 0.02), with no differences in pars opercularis or pars orbitalis. Pars triangularis volume was highly correlated with its SA [Pearson r(101) = 0.88, p < 0.001], which significantly differed between the groups (F2,97 = 4.45, p = 0.01). As with volume, the mean SA of the pars triangularis was greater in unaffected (corrected p = 0.02) and affected relatives (corrected p = 0.05) compared with controls. We did not find group differences in pars triangularis CT or gyrification.ConclusionsThese findings strengthen prior knowledge about the volumetric findings in this region and provide a new insight into the localization and topology of IFG alterations. The unique nature of rIFG morphology in BD, with larger volume and SA early in the course of illness, could have practical implications for detection of participants at risk for BD.

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The relationship of symptom dimensions and grey matter volume in a transdiagnostic cohort: Results from the DFG FOR2107

10.1055/s-0039-1679161 ◽

2019 ◽

Author(s):

F Stein ◽

G Lemmer ◽

S Schmitt ◽

K Brosch ◽

E Fischer ◽

...

Keyword(s):

Grey Matter ◽

Grey Matter Volume ◽

Symptom Dimensions ◽

Matter Volume ◽

Relationship Of ◽

The Relationship

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Social cognition and brain organization in chimpanzees (Pan troglodytes) and bonobos (Pan paniscus)

10.1093/oso/9780198728511.003.0014 ◽

2018 ◽

Author(s):

William D. Hopkins ◽

Cheryl D. Stimpson ◽

Chet C. Sherwood

Keyword(s):

Social Cognition ◽

Social Behaviour ◽

Grey Matter ◽

Species Differences ◽

Pan Paniscus ◽

Grey Matter Volume ◽

Evolutionary Models ◽

Brain Organization ◽

Matter Volume ◽

Cognition Sociale

Bonobos and chimpanzees are two closely relates species of the genus Pan, yet they exhibit marked differences in anatomy, behaviour and cognition. For this reason, comparative studies on social behaviour, cognition and brain organization between these two species provide important insights into evolutionary models of human origins. This chapter summarizes studies on socio-communicative competencies and social cognition in chimpanzees and bonobos from the authors’ laboratory in comparison to previous reports. Additionally, recent data on species differences and similarities in brain organization in grey matter volume and distribution is presented. Some preliminary findings on microstructural brain organization such as neuropil space and cellular distribution in key neurotransmitters and neuropeptides involved in social behaviour and cognition is presented. Though these studies are in their infancy, the findings point to potentially important differences in brain organization that may underlie bonobo and chimpanzees’ differences in social behaviour, communication and cognition. Les bonobos et les chimpanzés sont deux espèces du genus Pan prochement liées, néanmoins ils montrent des différences anatomiques, comportementales et cognitives marquées. Pour cette raison, les études comparatives sur le comportement social, la cognition et l’organisation corticale entre ces deux espèces fournissent des idées sur les modèles évolutionnaires des origines humaines. Dans ce chapitre, nous résumons des études sur les compétences socio-communicatives et la cognition sociale chez les chimpanzés et les bonobos de notre laboratoire en comparaison avec des rapports précédents. En plus, nous présentons des données récentes sur les différences et similarités d’organisation corticale du volume et distribution de la matière grise entre espèces. Nous présentons plus de résultats préliminaires sur l’organisation corticale microstructurale comme l’espace neuropile et la division cellulaire dans des neurotransmetteurs clés et les neuropeptides impliqués dans le comportement social et la cognition. Bien que ces études sont dans leur enfance, les résultats montrent des différences d’organisation corticale importantes qui sont à la base des différences de comportement social, la communication et la cognition entre les bonobos et les chimpanzés.

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Modelling the cascade of biomarker changes in GRN-related frontotemporal dementia

Journal of Neurology Neurosurgery & Psychiatry ◽

10.1136/jnnp-2020-323541 ◽

2021 ◽

pp. jnnp-2020-323541

Author(s):

Jessica L Panman ◽

Vikram Venkatraghavan ◽

Emma L van der Ende ◽

Rebecca M E Steketee ◽

Lize C Jiskoot ◽

...

Keyword(s):

White Matter ◽

Frontotemporal Dementia ◽

Disease Severity ◽

Grey Matter ◽

Clinical Stage ◽

Data Driven ◽

Grey Matter Volume ◽

Matter Volume ◽

Mutation Carriers ◽

Individual Disease

ObjectiveProgranulin-related frontotemporal dementia (FTD-GRN) is a fast progressive disease. Modelling the cascade of multimodal biomarker changes aids in understanding the aetiology of this disease and enables monitoring of individual mutation carriers. In this cross-sectional study, we estimated the temporal cascade of biomarker changes for FTD-GRN, in a data-driven way.MethodsWe included 56 presymptomatic and 35 symptomatic GRN mutation carriers, and 35 healthy non-carriers. Selected biomarkers were neurofilament light chain (NfL), grey matter volume, white matter microstructure and cognitive domains. We used discriminative event-based modelling to infer the cascade of biomarker changes in FTD-GRN and estimated individual disease severity through cross-validation. We derived the biomarker cascades in non-fluent variant primary progressive aphasia (nfvPPA) and behavioural variant FTD (bvFTD) to understand the differences between these phenotypes.ResultsLanguage functioning and NfL were the earliest abnormal biomarkers in FTD-GRN. White matter tracts were affected before grey matter volume, and the left hemisphere degenerated before the right. Based on individual disease severities, presymptomatic carriers could be delineated from symptomatic carriers with a sensitivity of 100% and specificity of 96.1%. The estimated disease severity strongly correlated with functional severity in nfvPPA, but not in bvFTD. In addition, the biomarker cascade in bvFTD showed more uncertainty than nfvPPA.ConclusionDegeneration of axons and language deficits are indicated to be the earliest biomarkers in FTD-GRN, with bvFTD being more heterogeneous in disease progression than nfvPPA. Our data-driven model could help identify presymptomatic GRN mutation carriers at risk of conversion to the clinical stage.

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Clinical and anatomical heterogeneity in autistic spectrum disorder: a structural MRI study

Psychological Medicine ◽

10.1017/s0033291709991541 ◽

2009 ◽

Vol 40 (7) ◽

pp. 1171-1181 ◽

Cited By ~ 70

Author(s):

F. Toal ◽

E. M. Daly ◽

L. Page ◽

Q. Deeley ◽

B. Hallahan ◽

...

Keyword(s):

Asperger Syndrome ◽

Autistic Spectrum Disorder ◽

Grey Matter ◽

Clinical Phenotype ◽

Brain Regions ◽

Spectrum Disorder ◽

Grey Matter Volume ◽

Brain Anatomy ◽

Autistic Spectrum ◽

Adults With Asd

BackgroundAutistic spectrum disorder (ASD) is characterized by stereotyped/obsessional behaviours and social and communicative deficits. However, there is significant variability in the clinical phenotype; for example, people with autism exhibit language delay whereas those with Asperger syndrome do not. It remains unclear whether localized differences in brain anatomy are associated with variation in the clinical phenotype.MethodWe used voxel-based morphometry (VBM) to investigate brain anatomy in adults with ASD. We included 65 adults diagnosed with ASD (39 with Asperger syndrome and 26 with autism) and 33 controls who did not differ significantly in age or gender.ResultsVBM revealed that subjects with ASD had a significant reduction in grey-matter volume of medial temporal, fusiform and cerebellar regions, and in white matter of the brainstem and cerebellar regions. Furthermore, within the subjects with ASD, brain anatomy varied with clinical phenotype. Those with autism demonstrated an increase in grey matter in frontal and temporal lobe regions that was not present in those with Asperger syndrome.ConclusionsAdults with ASD have significant differences from controls in the anatomy of brain regions implicated in behaviours characterizing the disorder, and this differs according to clinical subtype.

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Sex differences in neural correlates of common psychopathological symptoms in early adolescence

Psychological Medicine ◽

10.1017/s0033291720005140 ◽

2021 ◽

pp. 1-11

Author(s):

Francesca Biondo ◽

Charlotte Nymberg Thunell ◽

Bing Xu ◽

Congying Chu ◽

Tianye Jia ◽

...

Keyword(s):

Internalizing Symptoms ◽

Grey Matter ◽

Neural Correlates ◽

Brain Regions ◽

Female Adolescents ◽

Grey Matter Volume ◽

Community Based ◽

Psychopathological Symptom ◽

Strengths And Difficulties ◽

The Brain

Abstract Background Sex-related differences in psychopathology are known phenomena, with externalizing and internalizing symptoms typically more common in boys and girls, respectively. However, the neural correlates of these sex-by-psychopathology interactions are underinvestigated, particularly in adolescence. Methods Participants were 14 years of age and part of the IMAGEN study, a large (N = 1526) community-based sample. To test for sex-by-psychopathology interactions in structural grey matter volume (GMV), we used whole-brain, voxel-wise neuroimaging analyses based on robust non-parametric methods. Psychopathological symptom data were derived from the Strengths and Difficulties Questionnaire (SDQ). Results We found a sex-by-hyperactivity/inattention interaction in four brain clusters: right temporoparietal-opercular region (p < 0.01, Cohen's d = −0.24), bilateral anterior and mid-cingulum (p < 0.05, Cohen's d = −0.18), right cerebellum and fusiform (p < 0.05, Cohen's d = −0.20) and left frontal superior and middle gyri (p < 0.05, Cohen's d = −0.26). Higher symptoms of hyperactivity/inattention were associated with lower GMV in all four brain clusters in boys, and with higher GMV in the temporoparietal-opercular and cerebellar-fusiform clusters in girls. Conclusions Using a large, sex-balanced and community-based sample, our study lends support to the idea that externalizing symptoms of hyperactivity/inattention may be associated with different neural structures in male and female adolescents. The brain regions we report have been associated with a myriad of important cognitive functions, in particular, attention, cognitive and motor control, and timing, that are potentially relevant to understand the behavioural manifestations of hyperactive and inattentive symptoms. This study highlights the importance of considering sex in our efforts to uncover mechanisms underlying psychopathology during adolescence.

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