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Record W2036632755 · doi:10.1371/journal.pgen.1002921

New Susceptibility Loci Associated with Kidney Disease in Type 1 Diabetes

2012· review· en· W2036632755 on OpenAlexafffund
Niina Sandholm, Rany M. Salem, Amy Jayne McKnight, Eoin Brennan, Carol Forsblom, Tamara Isakova, Gareth J. McKay, Winfred W. Williams, Denise M. Sadlier, Ville‐Petteri Mäkinen, Elizabeth Swan, Andrew P. Boright, Emma Ahlqvist, Harshal Deshmukh, Benjamin J. Keller, Huateng Huang, Aila J. Ahola, Emma Fagerholm, Daniel Gordin, Valma Harjutsalo, Bing He, Outi Heikkilä, Kustaa Hietala, Janne Kytö, Päivi Lahermo, Markku Lehto, Raija Lithovius, Anne‐May Österholm, Maija Parkkonen, Janne Pitkäniemi, Milla Rosengård‐Bärlund, Markku Saraheimo, Cinzia Sarti, Jenny Söderlund, Aino Soro‐Paavonen, Anna Syreeni, Lena M. Thorn, Heikki Tikkanen, Nina Tolonen, Karl Tryggvason, Jaakko Tuomilehto, Johan Wadén, Geoffrey Gill, Sarah Prior, Candace Guiducci, Daniel B. Mirel, Andrew M. Taylor, S. Mohsen Hosseini, Hans‐Henrik Parving, Peter Rossing, Lise Tarnow, Claes Ladenvall, François Alhenc‐Gelas, Pierre Lefèbvre, Vincent Rigalleau, Ronan Roussel, David‐Alexandre Trégouët, Anna Maestroni, Silvia Maestroni, Henrik Falhammar, Tianwei Gu, Anna Möllsten, Dănuţ Cimponeriu, Mihai Ioana, Maria Moța, Eugen Moța, Cristian Serafinceanu, Monica Stavarachi, Robert L. Hanson, Robert G. Nelson, Matthias Kretzler, Helen M. Colhoun, Nicolae Mircea Panduru, Harvest F. Gu, Kerstin Brismar, Gianpaolo Zerbini, Samy Hadjadj, Michel Marre, Leif Groop, Maria Lajer, Shelley B. Bull, Daryl Waggott, Andrew D. Paterson, David A. Savage, Stephen C. Bain, Finian Martin, Joel N. Hirschhorn, Catherine Godson, José C. Florez, Per‐Henrik Groop, Alexander P. Maxwell

Bibliographic record

VenuePLoS Genetics · 2012
Typereview
Languageen
FieldMedicine
TopicChronic Kidney Disease and Diabetes
Canadian institutionsLunenfeld-Tanenbaum Research InstituteHospital for Sick ChildrenPublic Health OntarioUniversity of Toronto
FundersNational Center for Research ResourcesMedical Research CouncilDiabetes UKCanadian Institutes of Health ResearchEli Lilly and CompanyGenome CanadaU.S. Public Health ServiceDiabetesforeningenPublic Health AgencyNovo NordiskNational Institute of Diabetes and Digestive and Kidney DiseasesTekesLunds UniversitetKarolinska InstitutetInstitut National de la Santé et de la Recherche MédicaleWilhelm och Else Stockmanns StiftelseNational Institutes of HealthOrionin TutkimussäätiöOntario GenomicsMcKnight FoundationOntario Genomics InstituteScience Foundation IrelandHealth Research BoardEuropean CommissionPfizerHelsingin ja Uudenmaan Sairaanhoitopiiri
KeywordsSingle-nucleotide polymorphismBiologyGenome-wide association studyDiabetic nephropathyGeneticsHaplotypeSNPEnd stage renal diseaseInternal medicineDiseaseGenotypeGeneKidneyMedicine

Abstract

fetched live from OpenAlex

Diabetic kidney disease, or diabetic nephropathy (DN), is a major complication of diabetes and the leading cause of end-stage renal disease (ESRD) that requires dialysis treatment or kidney transplantation. In addition to the decrease in the quality of life, DN accounts for a large proportion of the excess mortality associated with type 1 diabetes (T1D). Whereas the degree of glycemia plays a pivotal role in DN, a subset of individuals with poorly controlled T1D do not develop DN. Furthermore, strong familial aggregation supports genetic susceptibility to DN. However, the genes and the molecular mechanisms behind the disease remain poorly understood, and current therapeutic strategies rarely result in reversal of DN. In the GEnetics of Nephropathy: an International Effort (GENIE) consortium, we have undertaken a meta-analysis of genome-wide association studies (GWAS) of T1D DN comprising ~2.4 million single nucleotide polymorphisms (SNPs) imputed in 6,691 individuals. After additional genotyping of 41 top ranked SNPs representing 24 independent signals in 5,873 individuals, combined meta-analysis revealed association of two SNPs with ESRD: rs7583877 in the AFF3 gene (P = 1.2 × 10(-8)) and an intergenic SNP on chromosome 15q26 between the genes RGMA and MCTP2, rs12437854 (P = 2.0 × 10(-9)). Functional data suggest that AFF3 influences renal tubule fibrosis via the transforming growth factor-beta (TGF-β1) pathway. The strongest association with DN as a primary phenotype was seen for an intronic SNP in the ERBB4 gene (rs7588550, P = 2.1 × 10(-7)), a gene with type 2 diabetes DN differential expression and in the same intron as a variant with cis-eQTL expression of ERBB4. All these detected associations represent new signals in the pathogenesis of DN.

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)0.002
metaresearch head score (Gemma)0.004
Version: metacan-v3-hybrid-931329e0061cValidation 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: none
Teacher disagreement score0.005
Threshold uncertainty score0.018

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0020.004
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.004
Bibliometrics0.0020.004
Science and technology studies0.0010.000
Scholarly communication0.0020.000
Open science0.0010.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0050.000

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 head0.051
GPT teacher head0.301
Teacher spread0.250 · 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 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".

Quick stats

Citations281
Published2012
Admission routes2
Has abstractyes

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