473 results match your criteria: "Institut du Cerveau (Paris Brain Institute) ICM[Affiliation]"

Objective: Monoallelic variants in the transient receptor potential melastatin-related type 3 gene (TRPM3) have been associated with neurodevelopmental manifestations, but knowledge on the clinical manifestations and treatment options is limited. We characterized the clinical spectrum, highlighting particularly the epilepsy phenotype, and the effect of treatments.

Methods: We analyzed retrospectively the phenotypes and genotypes of 43 individuals with TRPM3 variants, acquired from GeneMatcher and collaborations (n = 21), and through a systematic literature search (n = 22).

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E4F1 coordinates pyruvate metabolism and the activity of the elongator complex to ensure translation fidelity during brain development.

Nat Commun

January 2025

Institut de Recherche en Cancérologie de Montpellier (IRCM), INSERM U1194, Univ. Montpellier, Institut régional du Cancer de Montpellier (ICM), Montpellier, France.

Pyruvate metabolism defects lead to severe neuropathies such as the Leigh syndrome (LS) but the molecular mechanisms underlying neuronal cell death remain poorly understood. Here, we unravel a connection between pyruvate metabolism and the regulation of the epitranscriptome that plays an essential role during brain development. Using genetically engineered mouse model and primary neuronal cells, we identify the transcription factor E4F1 as a key coordinator of AcetylCoenzyme A (AcCoA) production by the pyruvate dehydrogenase complex (PDC) and its utilization as an essential co-factor by the Elongator complex to acetylate tRNAs at the wobble position uridine 34 (U).

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Backtracking Cell Phylogenies in the Human Brain with Somatic Mosaic Variants.

Methods Mol Biol

January 2025

Sorbonne Université, Institut du Cerveau (Paris Brain Institute) ICM, Inserm, CNRS, Hôpital de la Pitié Salpêtrière, Paris, France.

Somatic mosaic variants, and especially somatic single nucleotide variants (sSNVs), occur in progenitor cells in the developing human brain frequently enough to provide permanent, unique, and cumulative markers of cell divisions and clones. Here, we describe an experimental workflow to perform lineage studies in the human brain using somatic variants. The workflow consists in two major steps: (1) sSNV calling through whole-genome sequencing (WGS) of bulk (non-single-cell) DNA extracted from human fresh-frozen tissue biopsies, and (2) sSNV validation and cell phylogeny deciphering through single nuclei whole-genome amplification (WGA) followed by targeted sequencing of sSNV loci.

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Different whole-brain computational models have been recently developed to investigate hypotheses related to brain mechanisms. Among these, the Dynamic Mean Field (DMF) model is particularly attractive, combining a biophysically realistic model that is scaled up via a mean-field approach and multimodal imaging data. However, an important barrier to the widespread usage of the DMF model is that current implementations are computationally expensive, supporting only simulations on brain parcellations that consider less than 100 brain regions.

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Polygenic risk score to the rescue of monogenic diseases? The case of epilepsy.

EBioMedicine

December 2024

Sorbonne Université, AP-HP Sorbonne Université, Department of Medical Genetics, Paris, France; Sorbonne Université, Paris, France; Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, Inserm, CNRS, Paris, France. Electronic address:

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Schizophrenia (SCZ), bipolar (BD) and major depression disorder (MDD) are severe psychiatric disorders that are challenging to treat, often leading to treatment resistance (TR). It is crucial to develop effective methods to identify and treat patients at risk of TR at an early stage in a personalized manner, considering their biological basis, their clinical and psychosocial characteristics. Effective translation of theoretical knowledge into clinical practice is essential for achieving this goal.

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Challenges in Describing Tremor and Dystonia.

Neurology

January 2025

Departments of Neurology, Human Genetics and Pediatrics, Emory University, Atlanta, GA.

Tremor is defined as an oscillatory and rhythmical movement. By contrast, dystonia is defined by sustained or intermittent abnormal postures, repetitive movements, or both. Tremor and dystonia often coexist in the same individual.

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Recent human intracerebral recordings reveal that frontoparietal circuits linked by the superior longitudinal fasciculus (SLF) have critical, hemisphere-asymmetric contributions to conscious perception. Right-hemisphere networks are crucial for attention-based prioritization of information; left-hemisphere regions contribute to perceptual decisions and model building. These asymmetries confirm and specify clinical evidence from neglect patients.

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A Machine Learning Model to Harmonize Volumetric Brain MRI Data for Quantitative Neuroradiological Assessment of Alzheimer Disease.

Radiol Artif Intell

December 2024

From the Laboratory of Neuroinformatics, IRCCS Istituto Centro San Giovanni di Dio Fatebenefratelli, Via Pilastroni 4, Brescia 25125, Italy (D.A., A.R.); Department of Neurology, Alzheimer Center Amsterdam, Vrije Universiteit, Amsterdam UMC, location VUmc, Amsterdam, the Netherlands (V.V., W.M.v.d.F., B.M.T.); Department of Neurodegeneration, Amsterdam Neuroscience, Amsterdam, the Netherlands (V.V., W.M.v.d.F., B.M.T.); Brain Imaging Centre, Research Centre for Natural Sciences, Budapest, Hungary (B.W., T.A., Z.V.); Biomatics and Applied Artificial Intelligence Institute, John von Neumann Faculty of Informatics, Óbuda University, Budapest, Hungary (B.W.); Department of CSIRO Health and Biosecurity, The Australian e-Health Research Centre, Brisbane, Australia (P.B.); School of Psychology, University of Surrey, Guildford, United Kingdom (T.A.); Sorbonne Université, Institut du Cerveau- Paris Brain Institute-ICM, CNRS, Inria, Inserm, AP-HP, Hôpital Pitié-Salpêtrière, Paris, France (S.D.); Department of Epidemiology and Data Science, Vrije Universiteit, Amsterdam UMC, location VUmc, Amsterdam, the Netherlands (W.M.v.d.F.); Department of Radiology & Nuclear Medicine, Amsterdam UMC, Vrije Universiteit, Amsterdam the Netherlands (F.B.); Queen Square Institute of Neurology, University College London, United Kingdom (F.B.); and UCL Centre for Medical Image Computing, Department of Medical Physics and Biomedical Engineering and Department of Computer Science, University College London, London, United Kingdom (F.B., D.C.A., A.A., N.P.O.).

Purpose To extend a previously developed machine learning algorithm for harmonizing brain volumetric data of individuals undergoing neuroradiological assessment of Alzheimer disease not encountered during model training. Materials and Methods Neuroharmony is a recently developed method that uses image quality metrics (IQM) as predictors to remove scanner-related effects in brain-volumetric data using random forest regression. To account for the interactions between Alzheimer disease pathology and IQM during harmonization, the authors developed a multiclass extension of Neuroharmony for individuals with and without cognitive impairment.

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Determining Clinical Disease Progression in Symptomatic Patients With CADASIL.

Neurology

January 2025

From the ARAMIS (S.K., S.T.D.M.), Sorbonne Université, Institut du Cerveau - Paris Brain Institute - ICM, CNRS, Inria, Inserm, AP-HP, Groupe Hospitalier Sorbonne Université; Centre de référence pour les maladies vasculaires rares du cerveau et de l'œil (CERVCO) and Centre Neurovascular Translationnel (CNVT) (D.H., A.J., S.R., C.M., S.G., A.T., F.F., H.C.), AP-HP, Paris; and INSERM U1141 - FHU NeuroVasc (D.H., S.G., H.C.), Université Paris Cité, France.

Background And Objectives: Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) is the most frequent small artery brain disease caused by pathogenic variants of the NOTCH3 gene. During the disease, we still do not know how the various deficits progress and develop with each other at different stages of the disease. We aim to model disease progression and identify possible progressive subgroups and the effects of different covariates on clinical worsening.

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Recognition memory decline is associated with the progression to prodromal Alzheimer's disease in asymptomatic at-risk individuals.

J Neurol

December 2024

Sorbonne Université, Institut du Cerveau-Paris Brain Institute-ICM, INSERM, U 1127, CNRS, UMR 7225, AP-HP, CENIR, Centre MEG-EEG, Hôpital de La Pitié-Salpêtrière, 47 Boulevard de L'Hôpital, 75013, Paris, France.

Episodic memory (EM) alterations are a hallmark of Alzheimer's disease (AD). We assessed EM longitudinally in cognitively normal elders at-risk for AD (with subjective memory complaints), as a function of amyloid-β (Aβ) burden, neurodegeneration (N), and progression to prodromal AD. We stratified 264 INSIGHT-preAD study subjects in controls (Aβ-/N-), stable/N- or N + (Aβ +), and progressors/N- or N + (Aβ +) groups (progressors were included only until AD-diagnosis).

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Predicting attentional focus: Heartbeat-evoked responses and brain dynamics during interoceptive and exteroceptive processing.

PNAS Nexus

December 2024

Institut du Cerveau-Paris Brain Institute-ICM, Inserm, Sorbonne Université, CNRS, APHP,Hôpital de la Pitié Salpêtrière, 75013 Paris, France.

Attention shapes our consciousness content and perception by increasing the probability of becoming aware and/or better encoding a selection of the incoming inner or outer sensory world. Engaging interoceptive and exteroceptive attention should elicit distinctive neural responses to visceral and external stimuli and could be useful in detecting covert command-following in unresponsive patients. We designed a task to engage healthy participants' attention toward their heartbeats or auditory stimuli and investigated whether brain dynamics and the heartbeat-evoked potential (HEP) distinguished covert interoceptive-exteroceptive attention.

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Background: Disorders of consciousness (DoC) refers to a group of clinical conditions of altered consciousness. To improve their diagnosis and prognosis, multimodal assessment can be of great importance. Informal caregivers of people with DoC who are confronted with new technologies as such can benefit from interventions to expand their health literacy, i.

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IAPRD new consensus classification of myoclonus.

Parkinsonism Relat Disord

December 2024

Department of Neurology, Mayo Clinic, 13400 East Shea Blvd, Scottsdale, AZ, 85259, USA. Electronic address:

Introduction: Recent new advances in myoclonus characterization and etiology justify an update of the 40-year-old respected classification of myoclonus proposed by Marsden, Hallett, and Fahn. New advances include genetic studies and clinical neurophysiology characterization.

Methods: The IAPRD appointed an expert panel to develop a new myoclonus classification.

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Lesional focal epilepsy (LFE) is a common and severe seizure disorder caused by epileptogenic lesions, including malformations of cortical development (MCD) and low-grade epilepsy-associated tumors (LEAT). Understanding the genetic etiology of these lesions can inform medical and surgical treatment. We conducted a somatic variant enrichment mega-analysis in brain tissue from 1386 individuals who underwent epilepsy surgery, including 599 previously unpublished individuals with ultra-deep ( > 1600x) targeted panel sequencing.

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Background: Persons with schizophrenia are excluded from psychedelic-assisted therapy due to concerns about the risk of triggering or worsening psychosis. However, there is limited meta-analytic data on the risk of psychedelic-induced psychosis in individuals with pre-existing psychotic disorders.

Methods: We conducted a systematic review, meta-analysis, and overview of reviews to assess the incidence of psychedelic-induced psychosis and symptom exacerbation in schizophrenia.

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Article Synopsis
  • - Genetic generalized epilepsy (GGE) includes types like childhood absence epilepsy and juvenile myoclonic epilepsy, showing a higher risk of occurrence in first-degree relatives of affected individuals, suggesting a strong genetic component.
  • - Research, including whole exome sequencing from families in Sudan, has identified specific genetic variants linked to GGE, indicating it is genetically diverse and likely influenced by multiple genes rather than a single cause.
  • - The study emphasizes the importance of examining familial cases, as well as using populations with unique genetic backgrounds, to better understand the complex genetics of GGE, reinforcing the idea that it may have oligogenic inheritance patterns.
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Article Synopsis
  • The study aimed to explore patient interactions during disorders of arousal (DoA), despite current diagnoses focusing on absent responsiveness.
  • It involved three studies: a questionnaire on verbal responsiveness in 61 patients, auditory stimulation during sleep in 14 patients, and analysis of 364 home videos from 19 patients.
  • Findings revealed that many patients reported occasional conversations during episodes, indicating varying levels of consciousness and responsiveness, which challenge existing diagnostic criteria for DoA.
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WONOEP appraisal: Targeted therapy development for early onset epilepsies.

Epilepsia

November 2024

Saul R. Korey Department of Neurology, Isabelle Rapin Division of Child Neurology, Laboratory of Developmental Epilepsy, Dominick P. Purpura Department of Neuroscience, Albert Einstein College of Medicine, Bronx, New York, USA.

The early onset epilepsies encompass a heterogeneous group of disorders, some of which result in drug-resistant seizures, developmental delay, psychiatric comorbidities, and sudden death. Advancement in the widespread use of targeted gene panels as well as genome and exome sequencing has facilitated the identification of different causative genes in a subset of these patients. The ability to recognize the genetic basis of early onset epilepsies continues to improve, with de novo coding variants accounting for most of the genetic etiologies identified.

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Hippocampal neuroinflammation induced by lipopolysaccharide causes sex-specific disruptions in action selection, food approach memories, and neuronal activation.

Brain Behav Immun

November 2024

School of Life Sciences, Faculty of Science, University of Technology Sydney, Sydney, New South Wales 2007, Australia; Centre for Neuroscience and Regenerative Medicine, St. Vincent's Centre for Applied Medical Research, St. Vincent's Health Network, Sydney, New South Wales 2010, Australia. Electronic address:

Hippocampal neuroinflammation is present in multiple diseases and disorders that impact motivated behaviour in a sex-specific manner, but whether neuroinflammation alone is sufficient to disrupt this behaviour is unknown. We investigated this question here using mice. First, the application of an endotoxin to primary cultures containing only hippocampal neurons did not affect their activation.

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Gliomas are the most common primary malignant brain tumours in adults. Despite decades of research into novel therapeutic approaches, the prognosis remains poor. PARP1-2 are critical for DNA repair, cell survival and genomic stability and PARP inhibition (PARPi) may be a promising therapeutic approach for gliomas.

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Obsessive-compulsive disorder (OCD) is a frequent and disabling condition, with many patients being treatment-resistant. Improved understanding of its neurobiology is vital for better therapies. Evidence is still conflicting regarding specific serotonergic-related dysfunctions in OCD.

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Article Synopsis
  • - The study focused on how parieto-motor paired stimulation affects brain plasticity in patients with writer's cramp (WC) and cervical dystonia (CD) compared to healthy volunteers.
  • - Using paired transcranial magnetic stimulation, researchers found that the stimulation increased motor cortex excitability in WC patients but not in CD patients or healthy individuals.
  • - The results indicate that while the stimulation enhances brain function in WC, it doesn't seem to relate to changes in the connectivity between the posterior parietal cortex and the motor cortex.
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