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Record W4282973468 · doi:10.1016/j.kint.2022.05.021

Genetic loci and prioritization of genes for kidney function decline derived from a meta-analysis of 62 longitudinal genome-wide association studies

2022· review· en· W4282973468 on OpenAlexaff
Mathias Gorski, Humaira Rasheed, Alexander Teumer, Laurent F. Thomas, Sarah E. Graham, Garðar Sveinbjörnsson, Thomas W. Winkler, Felix Günther, Klaus Stark, Jin Fang Chai, Bamidele O. Tayo, Matthias Wuttke, Yong Li, Adrienne Tin, Tarunveer S. Ahluwalia, Johan Ärnlöv, Bjørn Olav Åsvold, Stephan J. L. Bakker, Bernhard Banas, Nisha Bansal, Mary L. Biggs, Ginevra Biino, Michael Böhnke, Eric Boerwinkle, Erwin P. Böttinger, Hermann Brenner, Ben Brumpton, Robert J. Carroll, Layal Chaker, John Chalmers, Miao-Li Chee, Miao-Ling Chee, Ching‐Yu Cheng, Audrey Y. Chu, Marina Ciullo, Massimiliano Cocca, James P. Cook, Josef Coresh, Daniele Cusi, Martin H. de Borst, Frauke Degenhardt, Kai‐Uwe Eckardt, Karlhans Endlich, Michele K. Evans, Mary F. Feitosa, André Franke, Sandra Freitag‐Wolf, Christian Fuchsberger, Piyush Gampawar, Ron T. Gansevoort, Mohsen Ghanbari, Sahar Ghasemi, Vilmantas Giedraitis, Christian Gieger, Daníel F. Guðbjartsson, Stein Hallan, Pavel Hamet, Asahi Hishida, Kevin Ho, Edith Hofer, Bernd Holleczek, Hilma Hólm, Anselm Hoppmann, Katrin Horn, Nina Hutri‐Kähönen, Kristian Hveem, Shih‐Jen Hwang, M. Arfan Ikram, Navya Shilpa Josyula, Bettina Jung, Mika Kähönen, Irma Karabegović, Chiea Chuen Khor, Wolfgang Köenig, Holly Kramer, Bernhard K. Krämer, Brigitte Kühnel, Johanna Kuusisto, Markku Laakso, Leslie A. Lange, Terho Lehtimäki, Man Li, Wolfgang Lieb, Lars Lind, Cecilia M. Lindgren, Ruth J. F. Loos, Mary Ann Lukas, Leo‐Pekka Lyytikäinen, Anubha Mahajan, Pamela R. Matías‐García, Christa Meisinger, Thomas Meitinger, Olle Melander, Yuri Milaneschi, Pashupati P. Mishra, Nina Mononen, Andrew P. Morris, Josyf C. Mychaleckyj, Girish N. Nadkarni, Mariko Naito, Masahiro Nakatochi, Mike A. Nalls, Matthias Nauck, Kjell Nikus, Boting Ning, Ilja M. Nolte, Teresa Nutile, Michelle L. O’Donoghue, Jeffrey R. O’Connell, Ísleifur Ólafsson, Marju Orho‐Melander, Afshin Parsa, Sarah A. Pendergrass, Brenda W.J.H. Penninx, Mario Pirastu, Michael Preuß, Bruce M. Psaty, Laura M. Raffield, Olli Raitakari, Myriam Rheinberger, Kenneth Rice, Federica Rizzi, Alexander R. Rosenkranz, Peter Rossing, Jerome I. Rotter, Daniela Ruggiero, Kathleen A. Ryan, Charumathi Sabanayagam, Erika Salvi, Helena Schmidt, Reinhold Schmidt, Markus Scholz, Ben Schöttker, Christina‐Alexandra Schulz, Sanaz Sedaghat, Christian M. Shaffer, Karsten B. Sieber, Xueling Sim, Mario Sims, Harold Snieder, Kira J. Stanzick, Unnur Þorsteinsdóttir, Hannah Stocker, Konstantin Strauch, Heather M. Stringham, Patrick Sulem, Silke Szymczak, Kent D. Taylor, Chris H. L. Thio, Johanne Tremblay, Simona Vaccargiu, Pim van der Harst, Peter J. van der Most, Niek Verweij, Uwe Völker, Kenji Wakai, Mélanie Waldenberger, Lars Wallentin, Stefan Wallner, Judy Wang, Dawn Waterworth, Harvey D. White, Cristen J. Willer, Tien Yin Wong, Mark Woodward, Qiong Yang, Laura M. Yerges-Armstrong, Martina E. Zimmermann, Alan B. Zonderman, Tobias Bergler, Kāri Stefánsson, Carsten A. Böger, Cristian Pattaro, Anna Köttgen, Florian Kronenberg, Iris M. Heid

Bibliographic record

VenueKidney International · 2022
Typereview
Languageen
FieldMedicine
TopicBirth, Development, and Health
Canadian institutionsMedpharmgene (Canada)
FundersH2020 European Research CouncilNational Center for Advancing Translational SciencesNational Institute of Neurological Disorders and StrokeNational Center for Research ResourcesNational Institute of General Medical SciencesNational Cancer InstituteNational Institute of Mental HealthNational Institute on AgingMünchner Zentrum für Gesundheitswissenschaften, Ludwig-Maximilians-Universität MünchenBiomedical Research CouncilNational Medical Research CouncilMedical Research CouncilNational Institutes of HealthSirtex MedicalNational Heart, Lung, and Blood InstituteMinisterium für Soziales, Gesundheit, Frauen und Familie, SaarlandNational Human Genome Research InstituteSkånes universitetssjukhusInnovative Medicines InitiativeRegion SkåneNovo Nordisk FondenSvenska DiabetesstiftelsenAmerican RegentKfH-Stiftung PräventivmedizinUniversitätsklinikum RegensburgSigrid Juséliuksen SäätiöEunice Kennedy Shriver National Institute of Child Health and Human DevelopmentGlaxoSmithKlineSigne ja Ane Gyllenbergin SäätiöPaavo Nurmen SäätiöSanofi GenzymeNovo NordiskHelse Midt-NorgeOesterreichische NationalbankHORIZON EUROPE Framework ProgrammeJuho Vainion SäätiöDeutsche ForschungsgemeinschaftNederlandse Organisatie voor Wetenschappelijk OnderzoekElse Kröner-Fresenius-StiftungDirektör Albert Påhlssons StiftelseAcademy of FinlandErasmus Universiteit RotterdamErasmus Medisch CentrumBundesministerium für Forschung und TechnologieStiftelsen för Strategisk ForskningTampereen TuberkuloosisäätiöRijksuniversiteit GroningenVetenskapsrådetEisaiFresenius Medical Care North AmericaU.S. National Library of MedicineEuropean Federation of Pharmaceutical Industries and AssociationsWellcome TrustJapan Agency for Medical Research and DevelopmentMinisterie van Economische Zaken en KlimaatSanofiNorges Teknisk-Naturvitenskapelige UniversitetEli Lilly and CompanyEmil Aaltosen SäätiöAstraZenecaCSL BehringYrjö Jahnssonin SäätiöJuvenile Diabetes Research Foundation United States of AmericaNational Institute of Diabetes and Digestive and Kidney DiseasesGilead SciencesKnut och Alice Wallenbergs StiftelseJapan Society for the Promotion of ScienceBayerYale UniversityUniversitair Medisch Centrum GroningenKowa CompanyCERNSuomen KulttuurirahastoZonMwPfizerBill and Melinda Gates FoundationAmgenMinisterium für Wissenschaft, Forschung und Kunst Baden-Württemberg
KeywordsGenome-wide association studyPrioritizationGenetic associationMeta-analysisBiologyGeneComputational biologyGenomeGeneticsFunction (biology)Evolutionary biologyBioinformaticsMedicineSingle-nucleotide polymorphismInternal medicineGenotype

Abstract

fetched live from OpenAlex

Estimated glomerular filtration rate (eGFR) reflects kidney function. Progressive eGFR-decline can lead to kidney failure, necessitating dialysis or transplantation. Hundreds of loci from genome-wide association studies (GWAS) for eGFR help explain population cross section variability. Since the contribution of these or other loci to eGFR-decline remains largely unknown, we derived GWAS for annual eGFR-decline and meta-analyzed 62 longitudinal studies with eGFR assessed twice over time in all 343,339 individuals and in high-risk groups. We also explored different covariate adjustment. Twelve genome-wide significant independent variants for eGFR-decline unadjusted or adjusted for eGFR-baseline (11 novel, one known for this phenotype), including nine variants robustly associated across models were identified. All loci for eGFR-decline were known for cross-sectional eGFR and thus distinguished a subgroup of eGFR loci. Seven of the nine variants showed variant-by-age interaction on eGFR cross section (further about 350,000 individuals), which linked genetic associations for eGFR-decline with age-dependency of genetic cross-section associations. Clinically important were two to four-fold greater genetic effects on eGFR-decline in high-risk subgroups. Five variants associated also with chronic kidney disease progression mapped to genes with functional in-silico evidence (UMOD, SPATA7, GALNTL5, TPPP). An unfavorable versus favorable nine-variant genetic profile showed increased risk odds ratios of 1.35 for kidney failure (95% confidence intervals 1.03-1.77) and 1.27 for acute kidney injury (95% confidence intervals 1.08-1.50) in over 2000 cases each, with matched controls). Thus, we provide a large data resource, genetic loci, and prioritized genes for kidney function decline, which help inform drug development pipelines revealing important insights into the age-dependency of kidney function genetics.

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)0.001
metaresearch head score (Gemma)0.003
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesMeta-epidemiology (narrow), Insufficient payload (model declined to judge)
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Meta-analysis · Consensus signal: none
GenreCandidate signal: Review · Consensus signal: Review
Teacher disagreement score0.626
Threshold uncertainty score1.000

Codex and Gemma teacher scores by category

CategoryCodexGemma
Metaresearch0.0010.003
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0030.001
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0010.000

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 head0.153
GPT teacher head0.387
Teacher spread0.234 · 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.

Study designMeta-analysis
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".

Quick stats

Citations54
Published2022
Admission routes1
Has abstractyes

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