Evidence map›Paper›PMID 32040670›Full record

ArticleDiabetologia2020

Serum tenascin-C is independently associated with increased major adverse cardiovascular events and death in individuals with type 2 diabetes: a French prospective cohort.

Barnabas Gellen, Nathalie Thorin-Trescases, Eric Thorin, Elise Gand, Philippe Sosner, Sonia Brishoual, Vincent Rigalleau, David Montaigne, Vincent Javaugue, Yann Pucheu and 5 more

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Diabetologia, 2020. 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
2.4field-weighted citation impact, top 12% 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, 22 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Association ofGenetic testing and molecular biomarkers · 2024
    Article
  7. Article
  8. Article
  9. Article
  10. Tenascin-C in fibrosis in multiple organs: Translational implications.Seminars in cell & developmental biology · 2022
    Review
  11. Review
  12. The Role of Matrix Proteins in Cardiac Pathology.International journal of molecular sciences · 2022
    Review
  13. Article
  14. Tenascin-C in Heart Diseases-The Role of Inflammation.International journal of molecular sciences · 2021
    Review
  15. Tenascin-C: an emerging prognostic biomarker in diabetes.Annals of translational medicine · 2020
    Article
  16. Article
  17. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors at 4 institutions in 2 countries.

Barnabas GellenELSAN, Polyclinique de Poitiers, 1 Rue de la Providence, F-86000, Poitiers, France. barnabas.gellen.cardio@gmail.com.ORCID 0000-0002-1128-2985
Nathalie Thorin-TrescasesResearch Center, Montreal Heart Institute, Montreal, QC, Canada.
Eric ThorinResearch Center, Montreal Heart Institute, Montreal, QC, Canada.
Elise GandINSERM, Centre d'Investigation Clinique CIC1402, Université de Poitiers, CHU de Poitiers, Poitiers, France.
Philippe SosnerINSERM, Centre d'Investigation Clinique CIC1402, Université de Poitiers, CHU de Poitiers, Poitiers, France.
Sonia BrishoualINSERM, Centre d'Investigation Clinique CIC1402, Université de Poitiers, CHU de Poitiers, Poitiers, France.
Vincent RigalleauEndocrinology - Diabetology - Nutrition, CHU de Bordeaux, Hôpital Haut-Lévêque, Pessac, France.
David MontaigneDepartment of Clinical Physiology - Echocardiography, CHU Lille, Lille, France.
Vincent JavaugueINSERM, Centre d'Investigation Clinique CIC1402, Université de Poitiers, CHU de Poitiers, Poitiers, France.
Yann PucheuCardiology, CHU de Bordeaux, Pessac, France.
Philippe GataultTransplantation, Immunology and Inflammation (T2I) - EA4245, CHRU de Tours, Nephrology-Hypertension, Dialysis and Renal Transplantation, FHU SUPORT, Université de Tours, Tours, France.
Xavier PiguelEndocrinology-Diabetology, CHU de Poitiers, Poitiers, France.
Samy HadjadjTransplantation, Immunology and Inflammation (T2I) - EA4245, CHRU de Tours, Nephrology-Hypertension, Dialysis and Renal Transplantation, FHU SUPORT, Université de Tours, Tours, France.
Pierre-Jean SaulnierINSERM, Centre d'Investigation Clinique CIC1402, Université de Poitiers, CHU de Poitiers, Poitiers, France.
SURDIAGENE Study group
Inserm · FRUniversité de Tours · FRMontreal Heart Institute · CACentre Hospitalier Universitaire de Bordeaux · FR

Funding

Association Française des Diabétiques Research grant 2003ELSAN clinics Research grant 2016French Ministry of Health PHRC-Poitiers 2004; PHRC-IR 2008
6 · The paper itself

Abstract

aims/hypothesisTenascin-C (TN-C) is an extracellular matrix glycoprotein highly expressed in inflammatory and cardiovascular (CV) diseases. Serum TN-C has not yet been specifically studied in individuals with type 2 diabetes, a condition associated with chronic low-grade inflammation and increased CV disease risk. In this study, we hypothesised that elevated serum TN-C at enrolment in participants with type 2 diabetes would be associated with increased risk of death and major adverse CV events (MACE) during follow-up.

methodsWe used a prospective, monocentric cohort of consecutive type 2 diabetes participants (the SURDIAGENE [SUivi Rénal, DIAbète de type 2 et GENEtique] cohort) with all-cause death as a primary endpoint and MACE (CV death, non-fatal myocardial infarction or stroke) as a secondary endpoint. We used a proportional hazard model after adjustment for traditional risk factors and the relative integrated discrimination improvement (rIDI) to assess the incremental predictive value of TN-C for these risk factors.

resultsWe monitored 1321 individuals (58% men, mean age 64 ± 11 years) for a median of 89 months. During follow-up, 442 individuals died and 497 had MACE. Multivariate Cox analysis showed that serum TN-C concentrations were associated with an increased risk of death (HR per 1 SD: 1.27 [95% CI 1.17, 1.38]; p < 0.0001) and MACE (HR per 1 SD: 1.23 [95% CI 1.13, 1.34]; p < 0.0001). Using TN-C concentrations on top of traditional risk factors, prediction of the risk of all-cause death (rIDI: 8.2%; p = 0.0006) and MACE (rIDI: 6.7%; p = 0.0014) improved significantly, but modestly. CONCLUSIONS/

interpretationIn individuals with type 2 diabetes, increased serum TN-C concentrations were independently associated with death and MACE. Therefore, including TN-C as a prognostic biomarker could improve risk stratification in these individuals.

Indexed as

AgedBiomarkersCardiovascular DiseasesDiabetes Mellitus, Type 2FemaleHumansMaleMiddle AgedPrognosisProspective StudiesRisk FactorsTenascinBiomarkersTenascinCardiovascular riskMACETenascin-CType 2 diabetes

Identifiers

PMID32040670
OpenAlexW3005529771

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.