Evidence map›Paper›PMID 31134308›Full record

ArticleDiabetologia2019

Cellular circadian period length inversely correlates with HbA

Flore Sinturel, Anne-Marie Makhlouf, Patrick Meyer, Christel Tran, Zoltan Pataky, Alain Golay, Guillaume Rey, Cédric Howald, Emmanouil T Dermitzakis, Claude Pichard and 3 more

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In one paragraph

Article in Diabetologia, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.1field-weighted citation impact, top 26% 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

9 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Overview of growth differentiation factor 15 in metabolic syndrome.Journal of cellular and molecular medicine · 2023
    Review
  5. Review
  6. Review
  7. Regulation of diurnal energy balance by mitokines.Cellular and molecular life sciences : CMLS · 2021
    Review
  8. Circadian Clocks, Sleep, and Metabolism.Advances in experimental medicine and biology · 2021
    Article
  9. Article
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 3 institutions in 1 country.

Flore SinturelDepartment of Medicine, Division of Endocrinology, Diabetes, Hypertension and Nutrition, Faculty of Medicine, University of Geneva, Rue Michel-Servet, 1, CH-1211, 14, Geneva, Switzerland.
Anne-Marie MakhloufDepartment of Medicine, Division of Endocrinology, Diabetes, Hypertension and Nutrition, Faculty of Medicine, University of Geneva, Rue Michel-Servet, 1, CH-1211, 14, Geneva, Switzerland.
Patrick MeyerDepartment of Medicine, Division of Endocrinology, Diabetes, Hypertension and Nutrition, Faculty of Medicine, University of Geneva, Rue Michel-Servet, 1, CH-1211, 14, Geneva, Switzerland.
Christel TranDepartment of Medicine, Division of Endocrinology, Diabetes, Hypertension and Nutrition, Faculty of Medicine, University of Geneva, Rue Michel-Servet, 1, CH-1211, 14, Geneva, Switzerland.
Zoltan PatakyDivision for Therapeutic Patient Education for Chronic Diseases, University Hospital of Geneva, Geneva, Switzerland.
Alain GolayDivision for Therapeutic Patient Education for Chronic Diseases, University Hospital of Geneva, Geneva, Switzerland.
Guillaume ReyDiabetes Center, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Cédric HowaldInstitute of Genetics and Genomics of Geneva (iGE3), University of Geneva, Geneva, Switzerland.
Emmanouil T DermitzakisDiabetes Center, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
Claude PichardDepartment of Medicine, Division of Endocrinology, Diabetes, Hypertension and Nutrition, Faculty of Medicine, University of Geneva, Rue Michel-Servet, 1, CH-1211, 14, Geneva, Switzerland.
Jacques PhilippeDepartment of Medicine, Division of Endocrinology, Diabetes, Hypertension and Nutrition, Faculty of Medicine, University of Geneva, Rue Michel-Servet, 1, CH-1211, 14, Geneva, Switzerland.
Steven A BrownInstitute of Pharmacology and Toxicology, University of Zurich, Zurich, Switzerland.
Charna DibnerDepartment of Medicine, Division of Endocrinology, Diabetes, Hypertension and Nutrition, Faculty of Medicine, University of Geneva, Rue Michel-Servet, 1, CH-1211, 14, Geneva, Switzerland. Charna.Dibner@hcuge.ch.
University of Geneva · CHUniversity Hospital of Geneva · CHUniversity of Zurich · CH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aims/hypothesisThe circadian system plays an essential role in regulating the timing of human metabolism. Indeed, circadian misalignment is strongly associated with high rates of metabolic disorders. The properties of the circadian oscillator can be measured in cells cultured in vitro and these cellular rhythms are highly informative of the physiological circadian rhythm in vivo. We aimed to discover whether molecular properties of the circadian oscillator are altered as a result of type 2 diabetes.

methodsWe assessed molecular clock properties in dermal fibroblasts established from skin biopsies taken from nine obese and eight non-obese individuals with type 2 diabetes and 11 non-diabetic control individuals. Following in vitro synchronisation, primary fibroblast cultures were subjected to continuous assessment of circadian bioluminescence profiles based on lentiviral luciferase reporters.

resultsWe observed a significant inverse correlation (ρ = -0.592; p < 0.05) between HbA CONCLUSIONS/

interpretationWe provide for the first time a potential molecular link between glycaemic control in individuals with type 2 diabetes and circadian clock machinery. This paves the way for further mechanistic understanding of circadian oscillator changes upon type 2 diabetes development in humans. DATA AVAILABILITY: RNA sequencing data and clinical phenotypic data have been deposited at the European Genome-phenome Archive (EGA), which is hosted by the European Bioinformatics Institute (EBI) and the Centre for Genomic Regulation (CRG), ega-box-1210, under accession no. EGAS00001003622.

Indexed as

Circadian RhythmAdultAgedBiopsyBlood GlucoseCircadian ClocksCLOCK ProteinsDiabetes Mellitus, Type 2FemaleFibroblastsGlycated HemoglobinHumansIntercellular Adhesion Molecule-1LentivirusMaleMiddle AgedBlood GlucoseCLOCK protein, humanCLOCK ProteinsGlycated Hemoglobinhemoglobin A1c protein, humanICAM1 protein, humanIntercellular Adhesion Molecule-1Circadian bioluminescence recordingCircadian clockHbA1cHumansICAM1Type 2 diabetes

Identifiers

PMID31134308
OpenAlexW2947884562

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.