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Record W4205544024 · doi:10.1093/brain/awab432

Gene-mapping study of extremes of cerebral small vessel disease reveals TRIM47 as a strong candidate

2021· article· en· W4205544024 on OpenAlexafffund
Aniket Mishra, Cécile Duplàa, Dina Vojinović, Hideaki Suzuki, Nuno R. Zilhäo, Shuo Li, Traci M. Bartz, Xueqiu Jian, Wei Zhao, Edith Hofer, Katharina Wittfeld, Sarah E. Harris, Sandra Van der Auwera, Michelle Luciano, Hieab H.H. Adams, Claudia L. Satizábal, Rebecca F. Gottesman, Piyush Gampawar, Robin Bülow, Stefan Weiß, Miao Yu, Mark E. Bastin, Oscar L. Lopez, Meike W. Vernooij, Alexa Beiser, Uwe Völker, Tim Kacprowski, Aïcha Soumaré, Jennifer A. Smith, David S. Knopman, Zoë Morris, Yi‐Cheng Zhu, Jerome I. Rotter, Carole Dufouil, María Valdés Hernández, Susana Muñoz Maniega, Mark Lathrop, Erik Boerwinkle, Reinhold Schmidt, Masafumi Ihara, Bernard Mazoyer, Qiong Yang, Anne Joutel, Elisabeth Tournier‐Lasserve, Lenore J. Launer, Ian J. Deary, Thomas H. Mosley, Philippe Amouyel, Charles DeCarli, Bruce M. Psaty, Christophe Tzourio, Sharon L. R. Kardia, Hans J. Grabe, Alexander Teumer, Cornelia M. van Duijn, Helena Schmidt, Joanna M. Wardlaw, M. Arfan Ikram, Myriam Fornage, Vilmundur Guðnason, Sudha Seshadri, Paul M. Matthews, W.T. Longstreth, Thierry Couffinhal, Stéphanie Debette

Bibliographic record

VenueBrain · 2021
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicCancer-related molecular mechanisms research
Canadian institutionsMcGill Genome Centre
FundersCilagNational Institute of Neurological Disorders and StrokeNational Heart, Lung, and Blood InstituteNational Institute on AgingCanadian Institutes of Health ResearchIpsenMedical Research CouncilNeuraxpharmMedical Research Council CanadaUniversité de BordeauxBundesministerium für Wissenschaft, Forschung und WirtschaftBundesministerium für Bildung und ForschungBiotechnology and Biological Sciences Research CouncilJohns Hopkins UniversityZonMwUK Research and InnovationServierEU Joint Programme – Neurodegenerative Disease ResearchAgence Nationale de la RechercheNational Health and Medical Research CouncilFresenius Medical Care North AmericaCelgeneBiogenGlaxoSmithKlineEuropean CommissionNational Institutes of HealthU.S. Department of Health and Human Services
KeywordsMendelian randomizationExomeGenome-wide association studyExome sequencingCandidate geneGenetic associationDiseaseDementiaPopulationMedicineGeneticsPathologyBiologySingle-nucleotide polymorphismPhenotypeGenotypeGene

Abstract

fetched live from OpenAlex

Cerebral small vessel disease is a leading cause of stroke and a major contributor to cognitive decline and dementia, but our understanding of specific genes underlying the cause of sporadic cerebral small vessel disease is limited. We report a genome-wide association study and a whole-exome association study on a composite extreme phenotype of cerebral small vessel disease derived from its most common MRI features: white matter hyperintensities and lacunes. Seventeen population-based cohorts of older persons with MRI measurements and genome-wide genotyping (n = 41 326), whole-exome sequencing (n = 15 965), or exome chip (n = 5249) data contributed 13 776 and 7079 extreme small vessel disease samples for the genome-wide association study and whole-exome association study, respectively. The genome-wide association study identified significant association of common variants in 11 loci with extreme small vessel disease, of which the chr12q24.11 locus was not previously reported to be associated with any MRI marker of cerebral small vessel disease. The whole-exome association study identified significant associations of extreme small vessel disease with common variants in the 5' UTR region of EFEMP1 (chr2p16.1) and one probably damaging common missense variant in TRIM47 (chr17q25.1). Mendelian randomization supports the causal association of extensive small vessel disease severity with increased risk of stroke and Alzheimer's disease. Combined evidence from summary-based Mendelian randomization studies and profiling of human loss-of-function allele carriers showed an inverse relation between TRIM47 expression in the brain and blood vessels and extensive small vessel disease severity. We observed significant enrichment of Trim47 in isolated brain vessel preparations compared to total brain fraction in mice, in line with the literature showing Trim47 enrichment in brain endothelial cells at single cell level. Functional evaluation of TRIM47 by small interfering RNAs-mediated knockdown in human brain endothelial cells showed increased endothelial permeability, an important hallmark of cerebral small vessel disease pathology. Overall, our comprehensive gene-mapping study and preliminary functional evaluation suggests a putative role of TRIM47 in the pathophysiology of cerebral small vessel disease, making it an important candidate for extensive in vivo explorations and future translational work.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Bench or experimental · Consensus signal: Bench or experimental
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.008
Threshold uncertainty score0.653

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0000.000
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0000.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.024
GPT teacher head0.291
Teacher spread0.267 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one teacher head, not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designBench or experimental
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations33
Published2021
Admission routes2
Has abstractyes

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