Evidence map›Paper›PMID 36221106›Full record

ArticleCardiovascular diabetology2022

Leukocyte telomere length, allelic variations in related genes and risk of coronary heart disease in people with long-standing type 1 diabetes.

Manuel Sanchez, Caroline Kannengiesser, Sophie Hoang, Louis Potier, Frédéric Fumeron, Nicolas Venteclef, André Scheen, Jean-François Gautier, Samy Hadjadj, Michel Marre and 3 more

Open access · goldAbstract readMulticenter Study
In one paragraph

Article in Cardiovascular diabetology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

7 citing papers in PubMed, 9 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

13 authors at 10 institutions in 2 countries.

Manuel SanchezINSERM UMR-S1151, CNRS UMR-S8253, Institut Necker-Enfants Malades, Université Paris Cité, Paris, France. manuel.sanchez@aphp.fr.
Caroline KannengiesserUFR de Médecine, Université Paris Cité, Paris, France.
Sophie HoangDepartment of Geriatrics, Charles-Foix University Hospital, Vitry sur Seine, France.
Louis PotierINSERM UMR-S1151, CNRS UMR-S8253, Institut Necker-Enfants Malades, Université Paris Cité, Paris, France.
Frédéric FumeronINSERM UMR-S1151, CNRS UMR-S8253, Institut Necker-Enfants Malades, Université Paris Cité, Paris, France.
Nicolas VenteclefINSERM UMR-S1151, CNRS UMR-S8253, Institut Necker-Enfants Malades, Université Paris Cité, Paris, France.
André ScheenDepartment of Diabetology, Endocrinology and Nutrition, Sart Tilman University Hospital, Liège, Belgium.
Jean-François GautierINSERM UMR-S1151, CNRS UMR-S8253, Institut Necker-Enfants Malades, Université Paris Cité, Paris, France.
Samy HadjadjInstitut du Thorax, INSERM, CNRS, CHU Nantes, Université de Nantes, Nantes, France.
Michel MarreClinique Ambroise Paré, Neuilly-sur-Seine, France.
Ronan RousselINSERM UMR-S1151, CNRS UMR-S8253, Institut Necker-Enfants Malades, Université Paris Cité, Paris, France.
Kamel MohammediINSERM U1034, Bordeaux University and Hospital, Bordeaux, France.
Gilberto VelhoINSERM UMR-S1151, CNRS UMR-S8253, Institut Necker-Enfants Malades, Université Paris Cité, Paris, France.
Institut Necker Enfants Malades · FRInserm · FRAssistance Publique – Hôpitaux de Paris · FRBordeaux Population Health · FRCentre National de la Recherche Scientifique · FRClinique Ambroise Paré · FRHôpital Charles-Foix · FRHôpital Lariboisière · FRUniversité Paris Cité · FRUniversity of Liège · BE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundType 1 diabetes is associated with accelerated vascular aging and advanced atherosclerosis resulting in increased rates of cardiovascular disease and premature death. We evaluated associations between Leukocyte telomere length (LTL), allelic variations (SNPs) in LTL-related genes and the incidence of coronary heart disease (CHD) in adults with long-standing type 1 diabetes.

methodsWe assessed associations of LTL, measured at baseline by RT-PCR, and of SNPs in 11 LTL-related genes with the risk of coronary heart disease (CHD: myocardial infarction or coronary revascularization) and all-cause death during follow-up in two multicenter French-Belgian prospective cohorts of people with long-standing type 1 diabetes.

resultsIn logistic and Cox analyses, the lowest tertile of LTL distribution (short telomeres) at baseline was associated with the prevalence of myocardial infarction at baseline and with increased risk of CHD (Hazard ratio 3.14 (1.39-7.70), p = 0.005, for shorter vs longer tertile of LTL) and all-cause death (Hazard ratio 1.63 (95% CI 1.04-2.55), p = 0.03, for shorter vs combined intermediate and longer tertiles of LTL) during follow-up. Allelic variations in six genes related to telomere biology (TERC, NAF1, TERT, TNKS, MEN1 and BICD1) were also associated with the incidence of CHD during follow-up. The associations were independent of sex, age, duration of diabetes, and a range of relevant confounding factors at baseline.

conclusionsOur results suggest that short LTL is an independent risk factor for CHD in people with type 1 diabetes.

Indexed as

Coronary DiseaseDiabetes Mellitus, Type 1Myocardial InfarctionAdaptor Proteins, Signal TransducingAdultCytoskeletal ProteinsHumansLeukocytesProspective StudiesTelomereAdaptor Proteins, Signal TransducingBICD1 protein, humanCytoskeletal ProteinsCohort studyCoronary heart diseaseLeukocyte telomere lengthTelomereType 1 diabetes

Identifiers

PMID36221106
PMCPMC9554968
OpenAlexW4304203419

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.