Evidence map›Paper›PMID 39916355›Full record

ArticleThe Journal of clinical endocrinology and metabolism2025

Prevalence and Determinants of Diabetes Mellitus in 2338 Long-Term Dutch Childhood Cancer Survivors (DCCS-LATER2 Study).

Melissa Bolier, Demi T C de Winter, Marta Fiocco, Sjoerd A A van den Berg, Dorine Bresters, Eline van Dulmen-den Broeder, Margriet van der Heiden-van der Loo, Imo Hoefer, Geert O Janssens, Leontien C M Kremer and 10 more

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Article in The Journal of clinical endocrinology and metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

20 authors.

Melissa BolierDepartment of Internal Medicine, Section Endocrinology, Erasmus Medical Center, 3015 GD Rotterdam, the Netherlands.ORCID 0000-0002-6334-0593
Demi T C de WinterDepartment of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, the Netherlands.
Marta FioccoDepartment of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, the Netherlands.
Sjoerd A A van den BergDepartment of Internal Medicine, Section Endocrinology, Erasmus Medical Center, 3015 GD Rotterdam, the Netherlands.
Dorine BrestersDepartment of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, the Netherlands.
Eline van Dulmen-den BroederPediatric Oncology, Cancer Center Amsterdam, Emma Children's Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, 1081 HV Amsterdam, the Netherlands.
Margriet van der Heiden-van der LooDepartment of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, the Netherlands.
Imo HoeferCentral Diagnostic Laboratory, University Medical Center Utrecht, 3584 CX Utrecht, the Netherlands.
Geert O JanssensDepartment of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, the Netherlands.
Leontien C M KremerDepartment of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, the Netherlands.
Jacqueline J LoonenDepartment of Hematology, Radboud University Medical Center, 6525 GA Nijmegen, the Netherlands.
Marloes LouwerensDepartment of Internal Medicine, Leiden University Medical Center, 2333 ZA Leiden, the Netherlands.
Heleen J van der PalDepartment of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, the Netherlands.
Saskia M F PluijmDepartment of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, the Netherlands.
Wim J E TissingDepartment of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, the Netherlands.
Hanneke M van SantenDepartment of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, the Netherlands.
Andrica C H de VriesDepartment of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, the Netherlands.
Aart-Jan van der LelyDepartment of Internal Medicine, Section Endocrinology, Erasmus Medical Center, 3015 GD Rotterdam, the Netherlands.
Marry M van den Heuvel-EibrinkDepartment of Pediatric Oncology, Princess Máxima Center for Pediatric Oncology, 3584 CS Utrecht, the Netherlands.ORCID 0000-0002-7760-879X
Sebastian J C M M NeggersDepartment of Internal Medicine, Section Endocrinology, Erasmus Medical Center, 3015 GD Rotterdam, the Netherlands.ORCID 0000-0002-7698-0282

Funding

Children Cancer-free FoundationDutch Ministry of Economic AffairsDutch Ministry of Health, Welfare and SportGroningen UniversityKiKaRoWODAS foundationProvinces in the North of the NetherlandsUniversity Medical Center Groningen
6 · The paper itself

Abstract

contextDiabetes mellitus (DM), a possible adverse effect of childhood cancer treatment, is strongly associated with cardiovascular disease and early mortality in adult childhood cancer survivors (CCS).

objectiveHere, we assess the prevalence and determinants of DM in our nationwide CCS cohort.

methodsIn this cross-sectional study, the prevalence of DM was assessed in 2338 CCS, using the Lifelines cohort (n = 132 226 adults with no history of cancer) as a reference. DM was defined through serum glucose measurement (fasting glucose ≥7.0 mmol/L or nonfasting ≥11.1 mmol/L) and/or self-report (previous diagnosis and/or medication use). Multivariable logistic regression models, adjusted for age, sex, and body mass index (BMI), were used to assess the cohort effect on the presence of DM. Multivariable logistic regression analysis was used to identify determinants of DM in CCS.

resultsSurvivors (median age 34.7 years, median follow-up time 27.1 years) showed increased odds for hyperglycemia (aOR = 2.72; 95% CI, 2.06-3.59), previous DM diagnosis (aOR = 3.03; 95% CI, 2.33-3.95), and antidiabetic medication use (aOR = 2.94; 95% CI, 2.17-3.99), compared to the reference cohort. Age (OR = 4.32; 95% CI, 1.84-10.15, >35 vs 18-35 years), BMI (OR = 1.12; 95% CI, 1.08-1.16, per point), family history of DM (OR = 2.38; 95% CI, 1.51-3.76), prior abdominal/pelvic radiotherapy (OR = 4.19; 95% CI, 2.32-7.55), total body irradiation (OR = 14.31; 95% CI, 6.98-29.34), hypogonadism (OR = 2.40; 95% CI, 1.15-4.99), hypertension (OR = 1.71; 95% CI, 1.06-2.76), and dyslipidemia (OR = 3.81; 95% CI, 2.15-6.75) were associated with DM in CCS. A statistically significant interaction between age and sex on the development of DM in survivors was identified.

conclusionThe identified 3-fold increased risk of DM in CCS, along with the clinically relevant and some modifiable determinants, underscores the importance of early risk-based screening and the exploration of lifestyle interventions in this population.

Indexed as

Cancer SurvivorsDiabetes MellitusNeoplasmsAdolescentAdultBlood GlucoseChildCross-Sectional StudiesFemaleFollow-Up StudiesHumansMaleMiddle AgedNetherlandsPrevalenceRisk FactorsBlood Glucosechildhood cancer survivordiabetes mellituslate effectrisk factor

Identifiers

PMID39916355
PMCPMC12448592

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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.