Evidence map›Paper›PMID 27491833›Full record

ArticleDiabetologia2016

ANGPTL2 is associated with an increased risk of cardiovascular events and death in diabetic patients.

Barnabas Gellen, Nathalie Thorin-Trescases, Philippe Sosner, Elise Gand, Pierre-Jean Saulnier, Stéphanie Ragot, Mathilde Fraty, Stéphanie Laugier, Grégory Ducrocq, David Montaigne and 7 more

Open access · bronzeAbstract read
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In one paragraph

Article in Diabetologia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.1field-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

22 citing papers in PubMed, 35 citations in OpenAlex.

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  12. Vitreous levels of vascular endothelial growth factor, stromal cell-derived factor-1α, and angiopoietin-like protein 2 in patients with active proliferative diabetic retinopathy.Graefe's archive for clinical and experimental ophthalmology = Albrecht von Graefes Archiv fur klinische und experimentelle Ophthalmologie · 2021
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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

17 authors at 9 institutions in 2 countries.

Barnabas GellenELSAN, Polyclinique de Poitiers, 1 Rue de la Providence, F-8600, Poitiers, France. barnabas.gellen.cardio@gmail.com.ORCID 0000-0002-1128-2985
Nathalie Thorin-TrescasesDepartment of Surgery, Faculty of Medicine, Université de Montréal, Montreal Heart Institute, Montreal, QC, Canada.
Philippe SosnerCHU de Poitiers Centre d'Investigation Clinique, Poitiers, France.
Elise GandCHU de Poitiers, Pôle Dune, Poitiers, France.
Pierre-Jean SaulnierCHU de Poitiers Centre d'Investigation Clinique, Poitiers, France.
Stéphanie RagotCHU de Poitiers Centre d'Investigation Clinique, Poitiers, France.
Mathilde FratyCHU de Poitiers, Pôle Dune, Poitiers, France.
Stéphanie LaugierUFR Médecine Pharmacie, Université de Poitiers, Poitiers, France.
Grégory DucrocqDépartement Hospitalo-Universitaire FIRE, APHP, Hôpital Bichat, Paris, France.
David MontaigneCHU Lille, Service d'Explorations Fonctionnelles Cardiovasculaires, Hôpital Cardiologique, Lille, France.
Pierre LlatyCHU de Poitiers Centre d'Investigation Clinique, Poitiers, France.
Vincent RigalleauCHU Bordeaux, Haut-Lévêque Hospital, Nutrition-Diabetology Department, Pessac, France.
Philippe ZaouiCHU de Grenoble, Service Néphrologie, Dialyse et Transplantation, Grenoble, France.
Jean-Michel HalimiCHU de Tours, Service Néphrologie, Dialyse et Transplantation, Tours, France.
Ronan RousselDépartement Hospitalo-Universitaire FIRE, APHP, Hôpital Bichat, Paris, France.
Eric ThorinDepartment of Surgery, Faculty of Medicine, Université de Montréal, Montreal Heart Institute, Montreal, QC, Canada.
Samy HadjadjCHU de Poitiers Centre d'Investigation Clinique, Poitiers, France.
Centre Hospitalier Universitaire de Poitiers · FRInserm · FRMontreal Heart Institute · CAUniversité de Poitiers · FRCentre Hospitalier Universitaire de Tours · FRCentre Hospitalier Universitaire Henri-Mondor · FRDélégation Paris 7 · FRHôpital Cardiologique du Haut-Lévêque · FRUniversité Joseph Fourier · FR

Funding

CIHR 13364CIHR 14496
6 · The paper itself

Abstract

aims/hypothesisA high serum angiopoietin-like 2 (ANGPTL2) concentration is an independent risk factor for developing diabetes and is associated with insulin resistance and atherosclerosis. In this work, we have examined the impact of serum ANGPTL2 on improving cardiovascular (CV) risk stratification in patients with type 2 diabetes.

methodsA prospective, monocentric cohort of consecutive type 2 diabetes patients (the SURDIAGENE cohort; total of 1353 type 2 diabetes patients; 58% men, mean ± SD age 64 ± 11 years) was followed for a median of 6.0 years for death as primary endpoint and major adverse CV events (MACE; i.e. CV death, myocardial infarction or stroke) as a secondary endpoint. Patients with end-stage renal disease, defined as a requirement for dialysis or a history of kidney transplantation, were excluded. Patients were grouped into quartiles according to ANGPTL2 concentrations at inclusion: <11.2 (Q1), 11.2-14.7 (Q2), 14.8-19.5 (Q3) or >19.5 (Q4) ng/ml.

resultsDuring follow up, 367 patients (representing 4.5% of the total person-years) died and 290 patients (representing 3.7% of the total person-years) presented with MACE. Both the survival and MACE-free survival rates were significantly different between ANGPTL2 quartiles (logrank 82.12, p < 0.0001 for death; and logrank 65.14, p < 0.0001 for MACE). Patients with ANGPTL2 concentrations higher than 19.5 ng/ml (Q4) had a significantly higher risk of death and MACE than those with ANGPTL2 levels of 19.5 ng/ml or less (Q1-3) (HR for death 2.44 [95% CI 1.98, 3.00], p < 0.0001; HR for MACE 2.43 [95% CI 1.92, 3.06], p < 0.0001) after adjustment for sex, age and established CV risk factors. Using ANGPTL2 concentrations, prediction of the risk of mortality, as assessed by integrated discrimination improvement (IDI), was significantly improved (IDI 0.006 ± 0.002, p = 0.0002). CONCLUSIONS/

interpretationIn patients with type 2 diabetes, serum ANGPTL2 concentrations were independently associated with death and MACE. Therefore, ANGPTL2 is a promising candidate biomarker for improving risk stratification in type 2 diabetes patients, and may prove to be a valuable therapeutic target.

Indexed as

AgedAngiopoietin-Like Protein 2Angiopoietin-like ProteinsAngiopoietinsBiomarkersCardiovascular DiseasesDiabetes Mellitus, Type 2FemaleHumansMaleMiddle AgedMyocardial InfarctionProspective StudiesRisk FactorsStrokeAngiopoietin-Like Protein 2Angiopoietin-like ProteinsAngiopoietinsANGPTL2 protein, humanBiomarkersAngiopoietin-like 2ANGPTL2BiomarkerDeathMACEType 2 diabetes

Identifiers

PMID27491833
OpenAlexW2506225517

What OpenQuestion holds

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Registered trials

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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.