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Prevalence and determinants of dyslipidemia in 2338 Dutch childhood cancer survivors: a DCCS-LATER 2 study

  • Melissa Bolier*
  • , Vincent G. Pluimakers
  • , Demi T. C. de Winter
  • , Marta Fiocco
  • , Sjoerd A. A. van den Berg
  • , Dorine Bresters
  • , Eline van Dulmen-den Broeder
  • , Margriet M. van der Heiden-van der Loo
  • , Imo Höfer
  • , Geert O. Janssens
  • , Leontien C. M. Kremer
  • , Jacqueline J. Loonen
  • , Marloes Louwerens
  • , Helena J. van der Pal
  • , Saskia M. F. Pluijm
  • , Wim J. E. Tissing
  • , Hanneke M. van Santen
  • , Andrica C. H. de Vries
  • , Aart-Jan van der Lely
  • , Marry M. van den Heuvel-Eibrink
  • Sebastian J. C. M. M. Neggers
*Corresponding author for this work
  • Erasmus University Rotterdam
  • Princess Máxima Center for Pediatric Oncology
  • Leiden University
  • Vrije Universiteit Amsterdam
  • Utrecht University
  • University of Amsterdam
  • Radboud University Nijmegen
  • University of Groningen

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Objective: Childhood cancer survivors (CCS) face an increased risk of early cardiovascular disease (CVD). In our nationwide CCS cohort, we assessed the prevalence and determinants of dyslipidemia, a well-established risk factor for accelerated atherosclerosis and CVD. Methods: Prevalence of dyslipidemia was cross-sectionally assessed in 2338 adult CCS and compared to adults with no cancer history (Lifelines, n = 132 226). Dyslipidemia was defined by multiple classifications as well as lipid abnormalities to investigate the impact on prevalence and determinants. Logistic regression models, adjusted for age, sex, and BMI, were used to assess the cohort effect on presence of dyslipidemia. Determinants of dyslipidemia were identified through multivariable logistic regression. Results: CCS (median age 34.7 year, median follow-up 27.1 year) had significantly increased odds of dyslipidemia compared to the reference cohort according to all classifications (NCEP-ATP-III, WHO, EGIR, CTCAEv.4.03). In survivors without lipid-lowering agents (n = 2007), lipid abnormalities were present in 20.6% (triglycerides > 1.7 mmol/L), 30.3% (HDL-c < 1.0/1.3 mmol/L (male/female)), 29.9% (total cholesterol > 5.2 mmol/L), 7.3% (LDL-c > 4.1 mmol/L), and 7.7% (apolipoprotein-B > 130 mg/dL). Compared to references without lipid-lowering agents (n = 126 631), survivors had increased odds of high triglycerides (aOR = 1.89, 95% CI = 1.68-2.13), low HDL-c (aOR = 2.73, 95% CI = 2.46-3.03), and high apolipoprotein-B (aOR = 1.84, 95% CI = 1.53-2.20). Sex, age, BMI, physical activity, abdominal/pelvic, cranial, and total body irradiation, alkylating agents, smoking, growth hormone deficiency, and diabetes mellitus were associated with (≥1 definition of) dyslipidemia in CCS. Conclusions: CCS is at increased risk of dyslipidemia, with various modifiable and non-modifiable determinants identified, underscoring the importance of survivor-specific risk assessment tools to control cardiovascular morbidity and mortality in this high-risk population.
Original languageEnglish
Pages (from-to)588-603
JournalEuropean Journal of Endocrinology
Volume191
Issue number6
DOIs
Publication statusPublished - 1 Dec 2024

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

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