Evidence map›Paper›PMID 28573393›Full record

ArticleDiabetologia2017

Genetic risk scores in the prediction of plasma glucose, impaired insulin secretion, insulin resistance and incident type 2 diabetes in the METSIM study.

Alena Stančáková, Teemu Kuulasmaa, Johanna Kuusisto, Karen L Mohlke, Francis S Collins, Michael Boehnke, Markku Laakso

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Diabetologia, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 26 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
26citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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

26 citing papers in PubMed, 1 synthesis or guideline pooled it, 36 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

7 authors at 5 institutions in 2 countries.

Alena StančákováInstitute of Clinical Medicine, Internal Medicine, University of Eastern Finland, Yliopistonranta 1 B, 70210, Kuopio, Finland.
Teemu KuulasmaaInstitute of Clinical Medicine, Internal Medicine, University of Eastern Finland, Yliopistonranta 1 B, 70210, Kuopio, Finland.
Johanna KuusistoInstitute of Clinical Medicine, Internal Medicine, University of Eastern Finland, Yliopistonranta 1 B, 70210, Kuopio, Finland.
Karen L MohlkeDepartment of Genetics, University of North Carolina, Chapel Hill, NC, USA.
Francis S CollinsNational Human Genome Research Institute, National Institutes for Health (NIH), Bethesda, MD, USA.
Michael BoehnkeDepartment of Biostatistics and Center for Statistical Genetics, University of Michigan, Ann Arbor, MI, USA.
Markku LaaksoInstitute of Clinical Medicine, Internal Medicine, University of Eastern Finland, Yliopistonranta 1 B, 70210, Kuopio, Finland. markku.laakso@uef.fi.
University of Eastern Finland · FIKuopio University Hospital · FINational Human Genome Research Institute · USUniversity of Michigan–Ann Arbor · USUniversity of North Carolina at Chapel Hill · US

Funding

Identifying Genes for Type 2 Diabetes: FUSIONU01DK062370 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI BOEHNKE, MICHAEL L, SCOTT, LAURA J. · 2009 to 2021
$11.6M
GF DK062370, DK072193, DK093757NIDDK NIH HHS U01 DK062370
6 · The paper itself

Abstract

aims/hypothesisMany SNPs have been associated with glycaemic traits and type 2 diabetes, but their joint effects on glycaemic traits and the underlying mechanisms leading to hyperglycaemia over time are largely unknown. We aimed to investigate the association of six genetic risk scores (GRSs) with changes in plasma glucose, insulin sensitivity, insulin secretion and incident type 2 diabetes in the prospective METabolic Syndrome In Men (METSIM) study.

methodsWe generated weighted GRSs for fasting plasma glucose ([FPG] GRS

resultsGRS CONCLUSIONS/

interpretationIn the METSIM follow-up study, GRS

Indexed as

AdultBlood GlucoseDiabetes Mellitus, Type 2FemaleGlucose Tolerance TestHumansHyperglycemiaInsulin ResistanceMaleMiddle AgedPolymorphism, Single NucleotideProspective StudiesRisk FactorsBlood GlucoseGenetic risk scoreGenetic variantInsulin resistanceInsulin secretionType 2 diabetes

Identifiers

PMID28573393
OpenAlexW2621290111

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.