Evidence map›Paper›PMID 35437568›Full record

ArticleCancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology2022

Metabolically Defined Body Size Phenotypes and Risk of Endometrial Cancer in the European Prospective Investigation into Cancer and Nutrition (EPIC).

Nathalie Kliemann, Romain Ould Ammar, Carine Biessy, Audrey Gicquiau, Verena Katzke, Rudolf Kaaks, Anne Tjønneland, Anja Olsen, Maria-Jose Sánchez, Marta Crous-Bou and 21 more

Registry-linked trialAbstract read
In one paragraph

Article in Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07262593 (Family-Based Meal Timing for Cancer Prevention Among Native Hawaiian and Other Pacific Islanders), which is not on this map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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.

NCT07262593 naterminatednot on this mapstarted 2024, after this paper: background citation

Family-Based Meal Timing for Cancer Prevention Among Native Hawaiian and Other Pacific Islanders: FAMTIME

TypeinterventionalSponsorUniversity of UtahRan2024 to 2024Enrolled2ConditionsCancer PreventionArmsTime Restricted Eating (TRE), Medically Tailored Meals (MTM)
3 · Its place in the literature

Who cites it

7 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
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

31 authors.

Nathalie KliemannInternational Agency for Research on Cancer, Lyon, France.ORCID 0000-0002-1778-9998
Romain Ould AmmarInternational Agency for Research on Cancer, Lyon, France.ORCID 0000-0003-4801-3401
Carine BiessyInternational Agency for Research on Cancer, Lyon, France.ORCID 0000-0003-3950-0929
Audrey GicquiauInternational Agency for Research on Cancer, Lyon, France.
Verena KatzkeDivision of Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID 0000-0002-6509-6555
Rudolf KaaksDivision of Cancer Epidemiology, German Cancer Research Center (DKFZ), Heidelberg, Germany.ORCID 0000-0003-3751-3929
Anne TjønnelandDanish Cancer Society Research Center, Copenhagen, Denmark.
Anja OlsenDepartment of Public Health, University of Copenhagen, Copenhagen, Denmark.ORCID 0000-0003-4788-503X
Maria-Jose SánchezEscuela Andaluza de Salud Pública (EASP), Granada, Spain.ORCID 0000-0003-4817-0757
Marta Crous-BouUnit of Nutrition and Cancer, Cancer Epidemiology Research Program, Catalan Institute of Oncology (ICO)-Bellvitge Biomedical Research Institute (IDIBELL), L'Hospitalet de Llobregat, Barcelona, Spain.
Fabrizio PasanisiDipartimento di Medicina Clinica e Chirurgia, Federico II University, Naples, Italy.
Sandar Tin TinNuffield Department of Population Health, Cancer Epidemiology Unit, University of Oxford, Oxford, England.
Aurora Perez-CornagoNuffield Department of Population Health, Cancer Epidemiology Unit, University of Oxford, Oxford, England.ORCID 0000-0002-5652-356X
Dagfinn AuneDepartment of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, United Kingdom.ORCID 0000-0002-4533-1722
Sofia ChristakoudiDepartment of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, United Kingdom.
Alicia K HeathDepartment of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, United Kingdom.ORCID 0000-0001-6517-1300
Sandra M Colorado-YoharCentro de Investigación Biomédica en Red de Epidemiología y Salud Pública (CIBERESP), Madrid, Spain.
Sara GrioniEpidemiology and Prevention Unit, Fondazione IRCCS Istituto Nazionale dei Tumori di Milano, Milano, Italy.ORCID 0000-0002-5891-8426
Guri SkeieDepartment of Community Medicine, UIT-The Arctic University of Norway, Tromsø, Norway.ORCID 0000-0003-2476-4251
Hanna SartorDiagnostic Radiology, Lund University, Lund, Sweden.ORCID 0000-0002-1116-5199
Annika IdahlDepartment of Clinical Sciences, Obstetrics and Gynecology, Umeå University, Umeå, Sweden.ORCID 0000-0002-7865-4560
Charlotta RylanderDepartment of Community Medicine, UIT-The Arctic University of Norway, Tromsø, Norway.
Anne M MayJulius Center for Health Sciences and Primary care, University Medical Center Utrecht, Utrecht, the Netherlands.
Elisabete WeiderpassInternational Agency for Research on Cancer, Lyon, France.ORCID 0000-0003-2237-0128
Heinz FreislingInternational Agency for Research on Cancer, Lyon, France.ORCID 0000-0001-8648-4998
Mary C PlaydonDepartment of Nutrition and Integrative Physiology, University of Utah, Salt Lake City, Utah.ORCID 0000-0001-6082-0447
Sabina RinaldiInternational Agency for Research on Cancer, Lyon, France.
Neil MurphyInternational Agency for Research on Cancer, Lyon, France.
Inge HuybrechtsInternational Agency for Research on Cancer, Lyon, France.ORCID 0000-0003-3838-855X
Laure DossusInternational Agency for Research on Cancer, Lyon, France.ORCID 0000-0003-2716-5748
Marc J GunterInternational Agency for Research on Cancer, Lyon, France.ORCID 0000-0001-5472-6761

Funding

Cancer Research UK 14136Cancer Research UK C19335/A21351Cancer Research UK C8221/A29017Department of HealthMedical Research Council 1000143Medical Research Council G0401527Medical Research Council G1000143Medical Research Council MR/M012190/1Medical Research Council MR/N003284/1World Health Organization 001
6 · The paper itself

Abstract

backgroundObesity is a risk factor for endometrial cancer but whether metabolic dysfunction is associated with endometrial cancer independent of body size is not known.

methodsThe association of metabolically defined body size phenotypes with endometrial cancer risk was investigated in a nested case-control study (817 cases/ 817 controls) within the European Prospective Investigation into Cancer and Nutrition (EPIC). Concentrations of C-peptide were used to define metabolically healthy (MH; <1st tertile) and metabolically unhealthy (MU; ≥1st tertile) status among the control participants. These metabolic health definitions were combined with normal weight (NW); body mass index (BMI)<25 kg/m2 or waist circumference (WC)<80 cm or waist-to-hip ratio (WHR)<0.8) and overweight (OW; BMI≥25 kg/m2 or WC≥80 cm or WHR≥0.8) status, generating four phenotype groups for each anthropometric measure: (i) MH/NW, (ii) MH/OW, (iii) MU/NW, and (iv) MU/OW.

resultsIn a multivariable-adjusted conditional logistic regression model, compared with MH/NW individuals, endometrial cancer risk was higher among those classified as MU/NW [ORWC, 1.48; 95% confidence interval (CI), 1.05-2.10 and ORWHR, 1.68; 95% CI, 1.21-2.35] and MU/OW (ORBMI, 2.38; 95% CI, 1.73-3.27; ORWC, 2.69; 95% CI, 1.92-3.77 and ORWHR, 1.83; 95% CI, 1.32-2.54). MH/OW individuals were also at increased endometrial cancer risk compared with MH/NW individuals (ORWC, 1.94; 95% CI, 1.24-3.04).

conclusionsWomen with metabolic dysfunction appear to have higher risk of endometrial cancer regardless of their body size. However, OW status raises endometrial cancer risk even among women with lower insulin levels, suggesting that obesity-related pathways are relevant for the development of this cancer beyond insulin. IMPACT: Classifying women by metabolic health may be of greater utility in identifying those at higher risk for endometrial cancer than anthropometry per se.

Indexed as

Endometrial NeoplasmsObesityBody Mass IndexBody SizeCase-Control StudiesC-PeptideFemaleHumansPhenotypeProspective StudiesRisk FactorsC-Peptide

Identifiers

PMID35437568
PMCPMC9355542

What OpenQuestion holds

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LicenceCC BY-NC-ND
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Registered trials

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.