Evidence map›Paper›PMID 23343465›Full record

ArticleBMC medical genetics2013

Assessment of the 9p21.3 locus in severity of coronary artery disease in the presence and absence of type 2 diabetes.

Natalia V Rivera, Robert Carreras-Torres, Roberta Roncarati, Chiara Viviani-Anselmi, Francesca De Micco, Alessandra Mezzelani, Werner Koch, Petra Hoppmann, Adnan Kastrati, Alexandre F R Stewart and 15 more

Open access · goldAbstract read
In one paragraph

Article in BMC medical genetics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
3.2field-weighted citation impact, top 8% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Trial
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  3. Journal of clinical medicine · 2023
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  15. The genetics of diabetic complications.Nature reviews. Nephrology · 2015
    Review
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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

25 authors at 10 institutions in 7 countries.

Natalia V RiveraIRCCS Multimedica, Via Fantoli 16/15, 20138, Milan, Italy. natalia.rivera@guest.unimi.it
Robert Carreras-Torres
Roberta Roncarati
Chiara Viviani-Anselmi
Francesca De Micco
Alessandra Mezzelani
Werner Koch
Petra Hoppmann
Adnan Kastrati
Alexandre F R Stewart
Li Chen
Robert Roberts
Lennart C Karssen
Najaf Amin
Valentina Trimarco
Raffaele Izzo
Guido Iaccarino
Gerolama Condorelli
Annibale A Puca
Paolo Pagnotta
Flavio Airoldi
Bruno Trimarco
Cornelia M van Duijn
Gianluigi Condorelli
Carlo Briguori
MultiMedica · ITDeutsches Herzzentrum der Charité · DEErasmus MC · NLFederico II University Hospital · ITHumanitas University · ITUniversity of Ottawa · CAUniversity of Salerno · ITClinica Mediterranea · ITInstitute of Biomedical Technologies · ITUniversitat de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe 9p21.3 locus is strongly associated with the risk of coronary artery disease (CAD) and with type 2 diabetes (T2D). We investigated the association of 9p21.3 variants with severity of CAD (defined by the number of vessel diseased [VD]) in the presence and absence of T2D.

methodsWe tested 11 9p21.3-variants for association in a white Italian study (N = 2,908), and carried out replication in 2 independent white populations, a German study (N = 2,028) and a Canadian Study (N=950). SNP association and permutation analyses were conducted.

resultsWe identified two 9p21.3-variants, rs4977574 (P < 4×10(-4)) and rs2383207 (P < 1.5×10(-3)) that were associated with severity of CAD in subjects without T2D. Association of rs4977574 with severity of CAD was confirmed in the Canadian Study. Results from subgroup analysis among patients with T2D showed an interaction between rs10738610 and T2D with P = 4.82×10(-2). Further investigation showed that rs10738610 (P < 1.99×10(-2)) was found to be significantly associated with severity of CAD in subjects with T2D.

conclusionsThe 9p21.3 locus is significantly associated with severity of CAD. The number of associations of 9p21.3 variants with severity of CAD is variable to the presence and absence of T2D. In a CAD-susceptible region of 115 kb, there is only one variant associated with the severity of coronary vessel disease in the presence of type 2 diabetes.

Indexed as

Chromosomes, Human, Pair 9ChildCoronary Artery DiseaseDiabetes Mellitus, Type 2HumansSeverity of Illness Index

Identifiers

PMID23343465
PMCPMC3556499
OpenAlexW2129073176

What OpenQuestion holds

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LicenceCC BY
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.