Evidence map›Paper›PMID 42302269›Full record

ArticleJMIR research protocols2026

Prevalence of and Risk Factors for Metabolic Syndrome, Vascular Damage, and Accelerated Aging (MetVasA) After Pediatric Hematopoietic Stem Cell Transplantation for Hematological Malignancy: Protocol for a Cross-Sectional Cohort Study.

Lisa J Asbroek, Helena Jh van der Pal, Marta Fiocco, Elizabeth Am Feijen, Lucienne H Grundeken, Maria Mw Koopman, Raphaële Rl van Litsenburg, Patrick van der Torre, Jan Westerink, Leontien Cm Kremer and 2 more

Abstract read
In one paragraph

Article in JMIR research protocols, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Lisa J AsbroekPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0009-0008-1295-2945
Helena Jh van der PalPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0003-2253-2115
Marta FioccoPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0001-5588-0277
Elizabeth Am FeijenPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0001-8930-3160
Lucienne H GrundekenTrial and Data Center, Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0009-0009-8935-3585
Maria Mw KoopmanPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0009-0002-9451-4098
Raphaële Rl van LitsenburgPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0003-1779-6159
Patrick van der TorrePrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0001-9697-2418
Jan WesterinkDepartment of Internal Medicine, Isala Hospital, Zwolle, The Netherlands.ORCID 0000-0001-5021-5227
Leontien Cm KremerPrincess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0001-7422-3248
Saskia Mf Pluijm *Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0002-4459-7799
Dorine Bresters *Princess Máxima Center for Pediatric Oncology, Utrecht, The Netherlands.ORCID 0000-0002-5417-4159

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSurvivors of hematopoietic stem cell transplantation (HSCT) in childhood face a high risk of metabolic and cardiovascular disease as well as accelerated aging. Estimates of the prevalence of these severe late effects have varied widely because they have been based on small cohorts or mixed populations of patients that received transplantations for both malignant and nonmalignant diseases, and the co-occurrence of these late effects was not assessed. Therefore, the true burden of these complications in survivors of hematological malignancies remains unclear. Moreover, the role of potentially modifiable risk factors such as health behaviors and inflammation has not yet been determined.

objectiveThis study aims to determine the prevalence of metabolic syndrome (MetS), endothelial dysfunction (ED), and accelerated aging and their risk factors, including treatment-related factors, inflammation, and health behaviors, in a large representative cohort of Dutch survivors of HSCT in childhood. Additionally, the study will examine the co-occurrence of these late effects.

methodsThis cross-sectional cohort study will combine 2 cohorts of survivors of HSCT in childhood for a hematological malignancy. The first cohort (cohort 1; n=102) consists of survivors who received transplantations before 2002 and were participants of the Dutch Childhood Cancer Survivor Study LATER 2 cohort, a nationwide cohort study focusing on late effects among long-term childhood cancer survivors. The second cohort will include survivors who received transplantations between 2002 and 2021 (cohort 2; projected n=120) and visited the late effects (LATER) outpatient clinic of the Princess Máxima Center between 2024 and 2026. Key outcomes will be the prevalence of MetS (≥3 of 5 clinical criteria), accelerated aging (3 of 5 biological and clinical criteria), and ED (assessed by endothelial peripheral arterial tonometry) and their co-occurrence. A broad range of potential and modifiable risk factors will be investigated, including treatment-related factors; transplant complications (eg, graft-versus-host disease); and health behaviors, including physical activity, dietary intake and status assessed with nutritional biomarkers, substance use, sun exposure, and relaxation.

resultsPatient recruitment started in January 2024 and is estimated to last until June 2026. As of September 2025, a total of 77 participants have been included in the study.

conclusionsThis study will provide insight into the prevalence of MetS, ED, and accelerated aging, as well as potentially modifiable risk factors, including those that have not been previously examined, among survivors of HSCT for hematological malignancies in childhood. The findings will inform surveillance guidelines and support the development of health behavioral and anti-inflammatory interventions to mitigate the risk of these severe late effects. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/77429.

Indexed as

Hematologic NeoplasmsHematopoietic Stem Cell TransplantationMetabolic SyndromeVascular DiseasesAdolescentAgingCancer SurvivorsChildChild, PreschoolCohort StudiesCross-Sectional StudiesFemaleHumansMaleNetherlandsPrevalenceaccelerated agingendothelial dysfunctionhealth behaviorshematopoietic (stem) cell transplantationlate effectsmetabolic syndromepediatric oncologysurvivors of childhood cancervascular damage

Identifiers

PMID42302269
PMCPMC13320015

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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.