Evidence map›Paper›PMID 24947790›Full record

ArticleDiabetes care2014

Metabolite traits and genetic risk provide complementary information for the prediction of future type 2 diabetes.

Geoffrey A Walford, Bianca C Porneala, Marco Dauriz, Jason L Vassy, Susan Cheng, Eugene P Rhee, Thomas J Wang, James B Meigs, Robert E Gerszten, Jose C Florez

Open access · bronzeAbstract read
In one paragraph

Article in Diabetes care, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed
9.8field-weighted citation impact, top 2% 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

54 citing papers in PubMed, 101 citations in OpenAlex.

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  11. An epidemiological introduction to human metabolomic investigations.Trends in endocrinology and metabolism: TEM · 2023
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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

10 authors at 6 institutions in 2 countries.

Geoffrey A WalfordCenter for Human Genetic Research, Massachusetts General Hospital, Boston, MA Diabetes Unit, Massachusetts General Hospital, Boston, MA Department of Medicine, Harvard Medical School, Boston, MA gwalford@partners.org jcflorez@partners.org.
Bianca C PornealaGeneral Medicine Division, Massachusetts General Hospital, Boston, MA.
Marco DaurizDepartment of Medicine, Harvard Medical School, Boston, MA General Medicine Division, Massachusetts General Hospital, Boston, MA Division of Endocrinology and Metabolic Diseases, Department of Medicine, University of Verona Medical School and Hospital Trust of Verona, Verona, Italy.
Jason L VassyDepartment of Medicine, Harvard Medical School, Boston, MA Section of General Internal Medicine, VA Boston Healthcare System, Boston, MA Division of General Medicine and Primary Care, Brigham and Women's Hospital, Boston, MA.
Susan ChengDepartment of Medicine, Harvard Medical School, Boston, MA Cardiovascular Division, Brigham and Women's Hospital, Boston, MA.
Eugene P RheeDepartment of Medicine, Harvard Medical School, Boston, MA Renal Division, Massachusetts General Hospital, Boston, MA.
Thomas J WangDivision of Cardiology, Vanderbilt University Medical Center, Nashville, TN.
James B MeigsDepartment of Medicine, Harvard Medical School, Boston, MA General Medicine Division, Massachusetts General Hospital, Boston, MA Framingham Heart Study of the National Heart, Lung, and Blood Institute, Framingham, MA.
Robert E GersztenDepartment of Medicine, Harvard Medical School, Boston, MA Cardiovascular Research Center, Massachusetts General Hospital, Boston, MA Cardiology Division, Massachusetts General Hospital, Boston, MA.
Jose C FlorezCenter for Human Genetic Research, Massachusetts General Hospital, Boston, MA Diabetes Unit, Massachusetts General Hospital, Boston, MA Department of Medicine, Harvard Medical School, Boston, MA Program in Medical and Population Genetics, Broad Institute, Cambridge, MA gwalford@partners.org jcflorez@partners.org.
Massachusetts General Hospital · USHarvard University · USBrigham and Women's Hospital · USBroad Institute · USVA Boston Healthcare System · USVanderbilt University Medical Center · US

Funding

Integration of Whole Genome Sequencing into Clinical MedicineU01HG006500 · NHGRI · BRIGHAM AND WOMEN'S HOSPITAL · PI GREEN, ROBERT C. · 2012 to 2016
$11.5M
Metabolomic predictors of insulin resistance and diabetesR01DK081572 · NIDDK · VANDERBILT UNIVERSITY · PI CLISH, CLARY B, GERSZTEN, ROBERT E · 2008 to 2025
$9.3M
Common Genetic Variation and Quantitative Diabetes TraitsR01DK078616 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MEIGS, JAMES B · 2008 to 2014
$5.0M
Rare Sequence Variation and Diabetes Quantitative TraitsU01DK078616 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MEIGS, JAMES B · 2015 to 2019
$3.6M
Epidemiology of Precursors to Type 2 DiabetesK24DK080140 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MEIGS, JAMES B · 2007 to 2016
$1.9M
Trace Elements and CVD Risks Factors Among Young AdultsR01HL081572 · NHLBI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI KAHE, KA · 2006 to 2008
$1.2M
Myocardial and Arterial Aging: Spectrum, Correlates, and PrognosisK99HL107642 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI CHENG, SUSAN · 2012 to 2013
$276k
THE FRAMINGHAM HEART STUDY-N01HC25195-268025195-268025195N01HC025195 · HC · TRUSTEES OF BOSTON UNIVERSITY · PI WOLF, PHILIP A · 2002 to 2006
–
NHGRI NIH HHS U01 HG006500NHGRI NIH HHS U01-HG006500NHLBI NIH HHS K99 HL107642NHLBI NIH HHS K99-HL-107642NHLBI NIH HHS N01 HC025195NHLBI NIH HHS N01-HC-25195NHLBI NIH HHS R01 HL081572NIDDK NIH HHS K24 DK080140NIDDK NIH HHS K24-DK-080140NIDDK NIH HHS L30 DK089597NIDDK NIH HHS L30-DK-089597NIDDK NIH HHS R01 DK078616NIDDK NIH HHS R01-DK-078616NIDDK NIH HHS R01-DK-HL081572NIDDK NIH HHS U01 DK078616
6 · The paper itself

Abstract

objectiveA genetic risk score (GRS) comprised of single nucleotide polymorphisms (SNPs) and metabolite biomarkers have each been shown, separately, to predict incident type 2 diabetes. We tested whether genetic and metabolite markers provide complementary information for type 2 diabetes prediction and, together, improve the accuracy of prediction models containing clinical traits. RESEARCH DESIGN AND

methodsDiabetes risk was modeled with a 62-SNP GRS, nine metabolites, and clinical traits. We fit age- and sex-adjusted logistic regression models to test the association of these sources of information, separately and jointly, with incident type 2 diabetes among 1,622 initially nondiabetic participants from the Framingham Offspring Study. The predictive capacity of each model was assessed by area under the curve (AUC).

resultsTwo hundred and six new diabetes cases were observed during 13.5 years of follow-up. The AUC was greater for the model containing the GRS and metabolite measurements together versus GRS or metabolites alone (0.820 vs. 0.641, P < 0.0001, or 0.820 vs. 0.803, P = 0.01, respectively). Odds ratios for association of GRS or metabolites with type 2 diabetes were not attenuated in the combined model. The AUC was greater for the model containing the GRS, metabolites, and clinical traits versus clinical traits only (0.880 vs. 0.856, P = 0.002).

conclusionsMetabolite and genetic traits provide complementary information to each other for the prediction of future type 2 diabetes. These novel markers of diabetes risk modestly improve the predictive accuracy of incident type 2 diabetes based only on traditional clinical risk factors.

Indexed as

Genetic Predisposition to DiseaseArea Under CurveDiabetes Mellitus, Type 2FemaleHumansLogistic ModelsMaleMetabolomeMiddle AgedOdds RatioPhenotypePolymorphism, Single NucleotideRisk Factors

Identifiers

PMID24947790
PMCPMC4140156
OpenAlexW2161287598

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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.