Evidence map›Paper›PMID 26644205›Full record

ArticleThe pharmacogenomics journal2017

CRTC2 polymorphism as a risk factor for the incidence of metabolic syndrome in patients with solid organ transplantation.

L Quteineh, P-Y Bochud, D Golshayan, S Crettol, J-P Venetz, O Manuel, Z Kutalik, A Treyer, R Lehmann, N J Mueller and 9 more

Open access · greenAbstract read
PubMed Publisher
In one paragraph

Article in The pharmacogenomics journal, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 1 pooled it
1.6field-weighted citation impact, top 18% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors at 8 institutions in 1 country.

L QuteinehDepartment of Psychiatry, Unit of Pharmacogenetics and Clinical Psychopharmacology, Lausanne University Hospital, Prilly, Switzerland.
P-Y BochudService of Infectious Diseases, Lausanne University Hospital, Lausanne, Switzerland.
D GolshayanTransplant Center, Lausanne University Hospital, Lausanne, Switzerland.
S CrettolDepartment of Psychiatry, Unit of Pharmacogenetics and Clinical Psychopharmacology, Lausanne University Hospital, Prilly, Switzerland.
J-P VenetzTransplant Center, Lausanne University Hospital, Lausanne, Switzerland.
O ManuelService of Infectious Diseases, Lausanne University Hospital, Lausanne, Switzerland.
Z KutalikInstitute of Social and Preventive Medicine, Lausanne University Hospital, Lausanne, Switzerland.ORCID 0000-0001-8285-7523
A TreyerDepartment of Psychiatry, Unit of Pharmacogenetics and Clinical Psychopharmacology, Lausanne University Hospital, Prilly, Switzerland.ORCID 0000-0002-4533-7761
R LehmannService of Endocrinology and Diabetes, University Hospital, Zurich, Switzerland.
N J MuellerDivision of Infectious Diseases and Hospital Epidemiology, University Hospital, Zurich, Switzerland.
I BinetService of Nephrology and Transplantation Medicine, Kantonsspital, St Gallen, Switzerland.
C van DeldenService of Infectious Diseases, University Hospital, Geneva, Switzerland.
J SteigerService of Nephrology, University Hospital, Basel, Switzerland.
P MohacsiDepartments of Cardiology Swiss Cardiovascular Centre, University Hospital, Bern, Switzerland.
J-F DufourDepartment of Clinical Pharmacology, University Hospital, Bern, Switzerland.
P M SoccalService of Pulmonary Medicine, University Hospital, Geneva, Switzerland.
M PascualTransplant Center, Lausanne University Hospital, Lausanne, Switzerland.
C B EapDepartment of Psychiatry, Unit of Pharmacogenetics and Clinical Psychopharmacology, Lausanne University Hospital, Prilly, Switzerland.
The Swiss Transplant Cohort Study
University of Lausanne · CHUniversity Hospital of Geneva · CHKantonsspital St. Gallen · CHUniversity Hospital of Basel · CHUniversity Hospital of Zurich · CHSIB Swiss Institute of Bioinformatics · CHUniversity Hospital of Bern · CHUniversity of Geneva · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolic syndrome after transplantation is a major concern following solid organ transplantation (SOT). The CREB-regulated transcription co-activator 2 (CRTC2) regulates glucose metabolism. The effect of CRTC2 polymorphisms on new-onset diabetes after transplantation (NODAT) was investigated in a discovery sample of SOT recipients (n

Indexed as

Polymorphism, Single NucleotideDiabetes MellitusDyslipidemiasGene FrequencyGenetic Predisposition to DiseaseHeterozygoteHomozygoteHumansIncidenceLinear ModelsLogistic ModelsMetabolic SyndromeMultivariate AnalysisObesityOdds RatioOrgan TransplantationCRTC2 protein, humanTranscription Factors

Identifiers

PMID26644205
OpenAlexW2189671188

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.