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Record W3034100708 · doi:10.1161/strokeaha.119.027544

Common Genetic Variation Indicates Separate Causes for Periventricular and Deep White Matter Hyperintensities

2020· review· en· W3034100708 on OpenAlexafffund
Nicola J. Armstrong, Karen A. Mather, Muralidharan Sargurupremraj, Maria J. Knol, Rainer Malik, Claudia L. Satizábal, Lisa R. Yanek, Wei Wen, Vilmundur Guðnason, Nicole Dueker, Lloyd T. Elliott, Edith Hofer, Joshua C. Bis, Neda Jahanshad, Shuo Li, Mark Logue, Michelle Luciano, Markus Scholz, Albert V. Smith, Stella Trompet, Dina Vojinović, Rui Xia, Fidel Alfaro‐Almagro, David Ames, Najaf Amin, Philippe Amouyel, Alexa S. Beiser, Henry Brodaty, Ian J. Deary, Christine Fennema‐Notestine, Piyush Gampawar, Rebecca Gottesman, Ludovica Griffanti, Clifford R. Jack, Mark Jenkinson, Jiyang Jiang, Brian G. Kral, John B. Kwok, Leonie Lampe, David C. Liewald, Pauline Maillard, Jonathan Marchini, Mark E. Bastin, Bernard Mazoyer, Lukas Pirpamer, José R. Romero, Gennady V. Roshchupkin, Peter R. Schofield, Matthias L. Schroeter, David J. Stott, Anbupalam Thalamuthu, Julian N. Trollor, Christophe Tzourio, Jeroen van der Grond, Meike W. Vernooij, A. Veronica Witte, Margaret J. Wright, Qiong Yang, Zoë Morris, Siggi Siggurdsson, Bruce M. Psaty, Arno Villringer, Helena Schmidt, Asta K. Håberg, Cornelia M. van Duijn, J. Wouter Jukema, Martin Dichgans, Ralph L. Sacco, Clinton B. Wright, William S. Kremen, Lewis C. Becker, Paul M. Thompson, Thomas H. Mosley, Joanna M. Wardlaw, M. Arfan Ikram, Hieab H.H. Adams, Sudha Seshadri, Perminder S. Sachdev, Stephen M. Smith, L. J. Launer, W.T. Longstreth, Charles DeCarli, Reinhold Schmidt, Myriam Fornage, Stéphanie Debette, Paul Nyquist

Bibliographic record

VenueStroke · 2020
Typereview
Languageen
FieldMedicine
TopicDementia and Cognitive Impairment Research
Canadian institutionsSimon Fraser University
FundersNational Institute of Biomedical Imaging and BioengineeringDementia Centre for Research CollaborationHjartaverndKarl-Franzens-Universität GrazNational Institute on AgingCentre for Cognitive Ageing and Cognitive EpidemiologyLudwig-Maximilians-Universität MünchenHáskóli ÍslandsSimon Fraser UniversityMurdoch UniversityInstitut National de la Santé et de la Recherche MédicaleNeuroscience Research AustraliaUniversity of OxfordParkinson's UKNational Institute of Neurological Disorders and StrokeMcGovern Medical SchoolAgence Nationale de la RechercheBiotechnology and Biological Sciences Research CouncilNational Center for PTSD, U.S. Department of Veterans AffairsUniversity of SydneyDr. John T. MacDonald FoundationUniversity of Southern CaliforniaWellcome TrustMcKnight FoundationUniversity of MiamiJohns Hopkins UniversityUniversity of WashingtonLeonard M. Miller School of MedicineUniversity of California, San DiegoUniversity of New South WalesSchool of Medicine, Boston UniversityMedical Research CouncilLeids Universitair Medisch CentrumUniversiteit LeidenMedizinische Universität GrazUniversity of Texas Health Science Center at Houston
KeywordsLocus (genetics)Genome-wide association studyDementiaMedicineGenetic associationGeneticsGenetic architectureHyperintensityGenetic epidemiologyDiseaseBiologyEvolutionary biologyBioinformaticsQuantitative trait locusGeneSingle-nucleotide polymorphismPathologyGenotypeMagnetic resonance imaging

Abstract

fetched live from OpenAlex

Background and Purpose: Periventricular white matter hyperintensities (WMH; PVWMH) and deep WMH (DWMH) are regional classifications of WMH and reflect proposed differences in cause. In the first study, to date, we undertook genome-wide association analyses of DWMH and PVWMH to show that these phenotypes have different genetic underpinnings. Methods: Participants were aged 45 years and older, free of stroke and dementia. We conducted genome-wide association analyses of PVWMH and DWMH in 26,654 participants from CHARGE (Cohorts for Heart and Aging Research in Genomic Epidemiology), ENIGMA (Enhancing Neuro-Imaging Genetics Through Meta-Analysis), and the UKB (UK Biobank). Regional correlations were investigated using the genome-wide association analyses -pairwise method. Cross-trait genetic correlations between PVWMH, DWMH, stroke, and dementia were estimated using LDSC. Results: In the discovery and replication analysis, for PVWMH only, we found associations on chromosomes 2 ( NBEAL ), 10q23.1 ( TSPAN14/FAM231A ), and 10q24.33 ( SH3PXD2A). In the much larger combined meta-analysis of all cohorts, we identified ten significant regions for PVWMH: chromosomes 2 (3 regions), 6, 7, 10 (2 regions), 13, 16, and 17q23.1. New loci of interest include 7q36.1 ( NOS3 ) and 16q24.2. In both the discovery/replication and combined analysis, we found genome-wide significant associations for the 17q25.1 locus for both DWMH and PVWMH. Using gene-based association analysis, 19 genes across all regions were identified for PVWMH only, including the new genes: CALCRL (2q32.1), KLHL24 (3q27.1), VCAN (5q27.1), and POLR2F (22q13.1). Thirteen genes in the 17q25.1 locus were significant for both phenotypes. More extensive genetic correlations were observed for PVWMH with small vessel ischemic stroke. There were no associations with dementia for either phenotype. Conclusions: Our study confirms these phenotypes have distinct and also shared genetic architectures. Genetic analyses indicated PVWMH was more associated with ischemic stroke whilst DWMH loci were implicated in vascular, astrocyte, and neuronal function. Our study confirms these phenotypes are distinct neuroimaging classifications and identifies new candidate genes associated with PVWMH only.

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: Not applicable · Consensus signal: none
GenreCandidate signal: Review · Consensus signal: Review
Teacher disagreement score0.948
Threshold uncertainty score0.852

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0000.000
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
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 head0.027
GPT teacher head0.332
Teacher spread0.305 · 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 designNot applicable
Domainnot available
GenreReview

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".

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Citations119
Published2020
Admission routes2
Has abstractyes

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