Evidence map›Paper›PMID 32750002›Full record

ArticleJMIR research protocols2021

Metabolic Syndrome Parameters, Determinants, and Biomarkers in Adult Survivors of Childhood Cancer: Protocol for the Dutch Childhood Cancer Survivor Study on Metabolic Syndrome (Dutch LATER METS).

Vincent Pluimakers, Marta Fiocco, Jenneke van Atteveld, Monique Hobbelink, Dorine Bresters, Eline Van Dulmen-den Broeder, Margriet Van der Heiden-van der Loo, Geert O Janssens, Leontien Kremer, Jacqueline Loonen and 8 more

Abstract read
In one paragraph

Article in JMIR research protocols, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–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.

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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

18 authors.

Vincent Pluimakers *Princess Maxima Center for Pediatric Oncology, Utrecht, Netherlands.ORCID https://orcid.org/0000-0002-3066-3951
Marta FioccoPrincess Maxima Center for Pediatric Oncology, Utrecht, Netherlands.ORCID https://orcid.org/0000-0001-5588-0277
Jenneke van AtteveldPrincess Maxima Center for Pediatric Oncology, Utrecht, Netherlands.ORCID https://orcid.org/0000-0002-4436-0089
Monique HobbelinkDepartment of Radiation Oncology, University Medical Center Utrecht, Utrecht, Netherlands.ORCID https://orcid.org/0000-0003-3435-917X
Dorine BrestersPrincess Maxima Center for Pediatric Oncology, Utrecht, Netherlands.ORCID https://orcid.org/0000-0002-5417-4159
Eline Van Dulmen-den BroederPrincess Maxima Center for Pediatric Oncology, Utrecht, Netherlands.ORCID https://orcid.org/0000-0002-8870-6539
Margriet Van der Heiden-van der LooDutch Childhood Oncology Group, Utrecht, Netherlands.ORCID https://orcid.org/0000-0001-5767-854X
Geert O JanssensPrincess Maxima Center for Pediatric Oncology, Utrecht, Netherlands.ORCID https://orcid.org/0000-0002-0331-713X
Leontien KremerPrincess Maxima Center for Pediatric Oncology, Utrecht, Netherlands.ORCID https://orcid.org/0000-0002-7619-7845
Jacqueline LoonenDepartment of Hematology, Radboud University Medical Center, Nijmegen, Netherlands.ORCID https://orcid.org/0000-0002-9963-8367
Marloes LouwerensDepartment of Internal Medicine, Leiden University Medical Center, Leiden, Netherlands.ORCID https://orcid.org/0000-0002-6748-3540
Helena Van der PalPrincess Maxima Center for Pediatric Oncology, Utrecht, Netherlands.ORCID https://orcid.org/0000-0003-2253-2115
Cécile RonckersPrincess Maxima Center for Pediatric Oncology, Utrecht, Netherlands.ORCID https://orcid.org/0000-0003-3524-4657
Hanneke Van SantenPrincess Maxima Center for Pediatric Oncology, Utrecht, Netherlands.ORCID https://orcid.org/0000-0002-6773-6931
Birgitta VersluysPrincess Maxima Center for Pediatric Oncology, Utrecht, Netherlands.ORCID https://orcid.org/0000-0002-4283-5503
Andrica De VriesPrincess Maxima Center for Pediatric Oncology, Utrecht, Netherlands.ORCID https://orcid.org/0000-0003-0964-0007
Marry Van den Heuvel-EibrinkPrincess Maxima Center for Pediatric Oncology, Utrecht, Netherlands.ORCID https://orcid.org/0000-0002-7760-879X
Sebastian NeggersPrincess Maxima Center for Pediatric Oncology, Utrecht, Netherlands.ORCID https://orcid.org/0000-0002-7698-0282

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPotential late effects of treatment for childhood cancer include adiposity, insulin resistance, dyslipidemia, and hypertension. These risk factors cluster together as metabolic syndrome and increase the risk for development of diabetes mellitus and cardio- and cerebrovascular disease. Knowledge on risk factors, timely diagnosis, and preventive strategies is of importance to prevent cardio- and cerebrovascular complications and improve quality of life. Currently, no national cohort studies on the prevalence and determinants of metabolic syndrome in childhood cancer survivors, including biomarkers and genetic predisposition, are available.

objectiveThe objectives of the Dutch LATER METS study are to assess 1) the prevalence and risk factors of metabolic syndrome and its separate components, and 2) the potential diagnostic and predictive value of additional biomarkers for surveillance of metabolic syndrome in the national cohort of adult long-term survivors of childhood cancer.

methodsThis is a cross-sectional study based on recruitment of all survivors treated in the Netherlands between 1963 and 2002. Metabolic syndrome will be classified according to the definitions of the third Adult Treatment Panel Report of the National Cholesterol Education Program as well as the Joint Interim Statement and compared to reference data. Dual-energy x-ray absorptiometry scans were performed to assess body composition in more detail. The effect of patient characteristics, previous treatment, and genetic variation on the risk of metabolic syndrome will be assessed. The diagnostic and predictive value of novel biomarkers will be tested.

resultsPatient accrual started in 2016 and lasted until April 2020. A total of 2380 survivors from 7 pediatric oncology hospitals have participated. From July 2020, biomarker testing, single nucleotide polymorphism analysis, and data analysis will be performed.

conclusionsThe Dutch LATER METS study will provide knowledge on clinical and genetic determinants of metabolic syndrome and the diagnostic value of biomarkers in childhood cancer survivors. The results of this study will be used to optimize surveillance guidelines for metabolic syndrome in survivors based on enhanced risk stratification and screening strategies. This will improve diagnosis of metabolic syndrome and prevent complications. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/21256.

Indexed as

childhood cancer survivorDutch Childhood Cancer Survivor StudyDutch LATER METSmetabolic syndromemethodology

Identifiers

PMID32750002
PMCPMC7875697

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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.