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Record W4385443568 · doi:10.1093/jnen/nlad059

LATE-NC risk alleles (in <i>TMEM106B, GRN</i>, and <i>ABCC9</i> genes) among persons with African ancestry

2023· article· en· W4385443568 on OpenAlexfundno aff
Yuriko Katsumata, David W. Fardo, Lincoln M. P. Shade, James D. Bowen, Paul K. Crane, Gail P. Jarvik, C. Dirk Keene, Eric B. Larson, Wayne C. McCormick, Susan M. McCurry, Shubhabrata Mukherjee, Neil W. Kowall, Ann C. McKee, Robert A Honig, Sandra Lawrence, Jean Paul Vonsattel, Jennifer Williamson, Scott A. Small, James R. Burke, Christine M. Hulette, Kathleen A. Welsh‐Bohmer, Marla Gearing, James J. Lah, Allan I. Levey, Thomas S. Wingo, Liana G. Apostolova, Martin R. Farlow, Bernardino Ghetti, Andrew J. Saykin, Salvatore Spina, Marilyn S. Albert, Constantine G. Lyketsos, Juan C. Troncoso, Matthew P. Frosch, Robert C. Green, John H. Growdon, Bradley T. Hyman, Rudolph E. Tanzi, Huntington Potter, Dennis W. Dickson, Nilüfer Ertekin‐Taner, Neill R. Graff‐Radford, Joseph E. Parisi, Ronald Petersen, Ranjan Duara, Joseph D. Buxbaum, Alison Goate, Mary Sano, Arjun V. Masurkar, Thomas Wısnıewskı, Eileen H. Bigio, Marsel Mesulam, Sandra Weıntraub, Robert Vassar, Jeffrey Kaye, Joseph F. Quinn, Randall L. Woltjer, Lisa L. Barnes, David A. Bennett, Julie A. Schneider, Lei Yu, Victor W. Henderson, Kenneth B. Fallon, Lindy E. Harrell, Daniel Marson, Erik D. Roberson, Charles DeCarli, Lee‐Way Jin, John Olichney, Ronald Kim, Frank M. LaFerla, Edwin S. Monuki, Elizabeth Head, David L. Sultzer, Daniel H. Geschwind, Harry V. Vinters, Marie‐Françoise Chesselet, Douglas Galasko, James B. Brewer, Adam Boxer, Anna Karydas, Joel H. Kramer, Bruce L. Miller, Howard J. Rosen, William W. Seeley, Jeffrey M. Burns, Russell H. Swerdlow, Erin L. Abner, Linda J. Van Eldik, Roger L. Albin, Andrew P. Lieberman, Henry L. Paulson, Steven E. Arnold, John Q. Trojanowski, Vivianna M. Van Deerlin, Ronald L. Hamilton, M. Ilyas Kamboh, Oscar L. López, James T. Becker, Chuanhai Cao, Ashok Raj, Amanda Smith, Helena C. Chui, Carol A. Miller, John M. Ringman, Lon S. Schneider, Thomas D. Bird, Joshua A. Sonnen, Chang‐En Yu, Thomas J. Grabowski, Elaine R. Peskind, Murray A. Raskind, Ge Li, Debby W. Tsuang, Sanjay Asthana, Craig Atwood, Cynthia M. Carlsson, Mark A. Sager, Nathaniel A. Chin, Suzanne Craft, Nigel J. Cairns, John C. Morris, Carlos Cruchaga, Stephen M. Strittmatter, Eric M. Reiman, Thomas G. Beach, Matthew J. Huentelman, John Hardy, Amanda Myers, John Kauwe, Håkon Håkonarson, Deborah Blacker, Thomas J. Montine, Clinton T. Baldwin, Lindsay A. Farrer, Gyungah Jun, Kathryn L. Lunetta, William S. Bush, Jonathan L. Haines, Alan J. Lerner, Xiongwei Zhou, Sandra Barral, Christiane Reitz, Badri N. Vardarajan, Richard Mayeux, Gary W. Beecham, Regina M. Carney, Michael L. Cuccaro, John R. Gilbert, Kara L. Hamilton‐Nelson, Brian W. Kunkle, Eden R. Martin, Margaret A Pericak‐Vance, Jeffery M. Vance, Laura B. Cantwell, Amanda P Kuzma, John Malamon, Adam C. Naj, Liming Qu, Gerard D. Schellenberg, Otto Valladares, Li‐San Wang, Yi Zhao, James B. Leverenz, Philip L. De Jager, Denis A. Evans, Mindy J. Katz, Richard B. Lipton, Bradley F. Boeve, Mariet Allen, Minerva M. Carrasquillo, Steven G. Younkin, Walter A. Kukull, Kelley Faber, Tatiana M. Foroud, Valory Pavlik, Paul J. Massman, Eveleen Darby, Monica Rodriguear, Aisha Khaleeq, Donald R. Royall, Alan Stevens, Marcia G. Ory, John C. DeToledo, Henrick Wilms, Kim G. Johnson, Victòria Aurora Ferrer Pérez, Michelle L. Hernandez, Kirk C. Wilhelmsen, Jeffrey L. Tilson, Scott Chasse, Robert C. Barber, Thomas Fairchild, Sid E. O’Bryant, Janice Knebl, James Hall, Leigh Johnson, Douglas Mains, Lisa Alvarez, Adriana C. Gamboa, David Paydarfar, John Bertelson, Martin Woon, Gayle Ayres, Alyssa Aguirre, Raymond F. Palmer, Marsha J. Polk, Perrie M. Adams, Ryan Huebinger, Joan Reisch, Roger N. Rosenberg, C. Munro Cullum, Benjamin J. Williams, Mary Quiceno, Linda S. Hynan, Janet L. Smith, Barb Davis, Trung Dung Nguyen, Ekaterina Rogaeva, Peter St George‐Hyslop, Peter T. Nelson

Bibliographic record

VenueJournal of Neuropathology & Experimental Neurology · 2023
Typearticle
Languageen
FieldMedicine
TopicAlzheimer's disease research and treatments
Canadian institutionsnot available
FundersNational Institute of Biomedical Imaging and BioengineeringNational Human Genome Research InstituteNational Institute of Mental HealthNational Institute on AgingStichting MS ResearchCanadian Institutes of Health ResearchJohns Hopkins UniversityUniversity of California, San DiegoNational Institutes of HealthNational Institute of Neurological Disorders and StrokeIXICOH. Lundbeck A/SUniversitat de BarcelonaNational Cancer InstituteMedical Research CouncilBoston UniversityServierNewcastle UniversityNational Institute on Minority Health and Health DisparitiesGenentechNational Alzheimer's Coordinating CenterPfizerBiogenBioClinicaNational Center for Research ResourcesF. Hoffmann-La RocheEmory UniversityUniversity of PennsylvaniaWellcome TrustDuke UniversityFoundation for the National Institutes of HealthUniversity of Southern CaliforniaEisaiHoward Hughes Medical InstituteNorthern California Institute for Research and EducationColumbia UniversityMassachusetts General HospitalNorth Bristol NHS TrustBristol-Myers SquibbAlzheimer's Research TrustU.S. Department of DefenseHersenstichtingEli Lilly and CompanyBrightFocus FoundationNovartis Pharmaceuticals CorporationAlzheimer's AssociationIndiana UniversityMeso Scale Diagnostics
KeywordsAlleleHippocampal sclerosisDiseaseSingle-nucleotide polymorphismBiologyGeneticsMedicineGeneGenotypePathologyNeuroscience

Abstract

fetched live from OpenAlex

Limbic-predominant age-related TDP-43 encephalopathy (LATE) affects approximately one-third of older individuals and is associated with cognitive impairment. However, there is a highly incomplete understanding of the genetic determinants of LATE neuropathologic changes (LATE-NC) in diverse populations. The defining neuropathologic feature of LATE-NC is TDP-43 proteinopathy, often with comorbid hippocampal sclerosis (HS). In terms of genetic risk factors, LATE-NC and/or HS are associated with single nucleotide variants (SNVs) in 3 genes-TMEM106B (rs1990622), GRN (rs5848), and ABCC9 (rs1914361 and rs701478). We evaluated these 3 genes in convenience samples of individuals of African ancestry. The allele frequencies of the LATE-associated alleles were significantly different between persons of primarily African (versus European) ancestry: In persons of African ancestry, the risk-associated alleles for TMEM106B and ABCC9 were less frequent, whereas the risk allele in GRN was more frequent. We performed an exploratory analysis of data from African-American subjects processed by the Alzheimer's Disease Genomics Consortium, with a subset of African-American participants (n = 166) having corroborating neuropathologic data through the National Alzheimer's Coordinating Center (NACC). In this limited-size sample, the ABCC9/rs1914361 SNV was associated with HS pathology. More work is required concerning the genetic factors influencing non-Alzheimer disease pathology such as LATE-NC in diverse cohorts.

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 machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.001
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.006
Threshold uncertainty score0.011

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0000.001
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0020.000

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 head0.025
GPT teacher head0.301
Teacher spread0.276 · 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 source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
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".

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Citations17
Published2023
Admission routes1
Has abstractyes

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