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Record W2795107814 · doi:10.1093/schbul/sby017.532

F1. GENOME-WIDE ASSOCIATION STUDIES SUGGESTED ASSOCIATION BETWEEN DGKB AND ANTIPSYCHOTIC INDUCED WEIGHT GAIN IN EUROPEANS AND AFRICAN AMERICANS

2018· article· en· W2795107814 on OpenAlexaff
Małgorzata Maciukiewicz, Arun K. Tiwari, Vanessa F. Gonçalves, Clement C. Zai, Eva J. Brandl, Natalie Freeman, Jeffrey A. Lieberman, Herbert Y. Meltzer, Christopher Laughlin, Erika L. Nurmi, James L. Kennedy, Daniel J. Müller

Bibliographic record

VenueSchizophrenia Bulletin · 2018
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicGenetic Associations and Epidemiology
Canadian institutionsUniversity of TorontoCentre for Addiction and Mental Health
Fundersnot available
KeywordsGenome-wide association studySchizoaffective disorderClozapineAntipsychoticSchizophrenia (object-oriented programming)Genetic associationSingle-nucleotide polymorphismWeight gainInternal medicineSNPAlleleMedicineGeneticsBiologyOncologyPsychiatryGenePsychosisBody weightGenotype

Abstract

fetched live from OpenAlex

Schizophrenia (SCZ) is a severe, devastating disorder with a life-time prevalence of 1% irrespective of gender or ethnic group, treated primarily with antipsychotic (AP) medications. Despite clinical efficacy of APs, they are associated with severe side effects including antipsychotic-induced weight gain (AIWG). We investigated n=201 schizophrenia or schizoaffective disorder patients of European and African American ancestry who were treated mostly with clozapine or olanzapine. Individuals were genotyped on the Infinium Omni2.5 BeadChip. We conducted genome-wide association analysis for AIWG defined primarily as the percentage of weight change from baseline. Additionally, we ran pathway, enrichment, network, and polygenic risk score analyses to investigate top genes using in silico methods. In the mixed sample, we observed genome-wide significant association between the diacylglycerol kinase beta (DGKB) variant (β=0.411; p=3.15 × 10–9) and percentage of weight change. The association remained nominally significant in both Europeans (β=0.271; p=0.002) and African Americans (β=0.579; p=5.73 × 10–5) for the same risk allele. In Europeans, the top variant (β=0.406; p=1.26 × 10–6) was located upstream of the Stanniocalcin 2 (STC2) gene. Bayesian fine mapping suggested the variant nearby SNP upstream of STC2 (p=0.034; PHRED=3.691, posterior prob.=0.496) to be the most significant. We noticed no significant enrichment in metabolic pathways for SNPs, but our top genes (p<5 × 10–5) were enriched in the GWAS catalog for risk of obesity (pmixed=0.018; pEuropeans=0.015) and schizophrenia (pmixed=0.006). Top genes also interacted with known risk factors for obesity (Glucose-6-Phosphate Dehydrogenase (G6PD)) and schizophrenia (NudE Neurodevelopment Protein 1 Like 1 (NDEL1)), and are targeted by microRNAs related to schizophrenia (mir-34a) and obesity (mir-19b). Polygenic risk score analyses did not provide support for major genetic overlap between obesity-related and lipid-associated SNPs and the risk of AIWG. Our findings suggested that a variant in DGKB is associated with the percentage of weight gain in both African Americans and Europeans.

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)0.001
metaresearch head score (Gemma)0.003
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 score0.054
Threshold uncertainty score0.180

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.003
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0000.001
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0010.000
Insufficient payload (model declined to judge)0.0540.002

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 head0.019
GPT teacher head0.271
Teacher spread0.252 · 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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Citations0
Published2018
Admission routes1
Has abstractyes

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