Sleep–wake rhythm disruption is associated with cancer-related fatigue in pediatric acute lymphoblastic leukemia

Author:

Steur Lindsay M H1ORCID,Kaspers Gertjan J L123,Van Someren Eus J W456ORCID,Van Eijkelenburg Natasha K A2,Van der Sluis Inge M27,Dors Natasja28,Van den Bos Cor29,Tissing Wim J E210,Grootenhuis Martha A2,Van Litsenburg Raphaële R L12ORCID

Affiliation:

1. Emma Children’s Hospital, Amsterdam UMC, Vrije Universiteit Amsterdam, Pediatric Oncology, Cancer Center Amsterdam, Amsterdam, The Netherlands

2. Princess Máxima Center for Pediatric Oncology, Utrecht, the Netherlands

3. Dutch Childhood Oncology Group, Utrecht, the Netherlands

4. Department of Sleep and Cognition, Netherlands Institute for Neuroscience (An Institute of the Royal Netherlands Academy of Arts and Sciences), Amsterdam, The Netherlands

5. Department of Integrative Neurophysiology, Amsterdam Neuroscience, Center for Neurogenomics and Cognitive Research (CNCR), VU University Amsterdam, Amsterdam, The Netherlands

6. Amsterdam UMC, Vrije Universiteit Amsterdam, Psychiatry, Amsterdam Neuroscience, Amsterdam, The Netherlands

7. Department of Pediatric Oncology, Sophia Children’s Hospital, Erasmus Medical Center, Rotterdam, the Netherlands

8. Department of Pediatric Oncology, Amalia Children’s Hospital, Radboud University Medical Center, Nijmegen, the Netherlands

9. Department of Pediatric Oncology, Emma Children’s Hospital, Amsterdam UMC, Academic Medical Center, Amsterdam, the Netherlands

10. Department of Pediatric Oncology, University of Groningen, University Medical Center Groningen, Groningen, the Netherlands

Abstract

Abstract Study Objectives To compare sleep–wake rhythms, melatonin, and cancer-related fatigue in pediatric patients with acute lymphoblastic leukemia (ALL) to healthy children and to assess the association between sleep–wake outcomes and cancer-related fatigue. Methods A national cohort of ALL patients (2–18 years) was included. Sleep–wake rhythms were measured using actigraphy and generated the following variables: Interdaily stability (IS): higher IS reflects higher stability; intradaily variability (IV): lower IV indicates less fragmentation; L5 and M10 counts: activity counts during the five least and 10 most active hours, respectively; and relative amplitude (RA): the ratio of L5 and M10 counts (higher RA reflects a more robust rhythm). The melatonin metabolite, 6-sulfatoxymelatonin (aMT6s), was assessed in urine. Cancer-related fatigue was assessed with the PedsQL Multidimensional Fatigue Scale. Using regression models sleep–wake rhythms, aMT6s, and cancer-related fatigue were compared to healthy children and associations between sleep–wake outcomes and cancer-related fatigue were assessed in ALL patients. Results In total, 126 patients participated (response rate: 67%). IS, RA, and M10 counts were lower in patients compared to healthy children (p < 0.001). aMT6s levels were comparable to healthy children (p = 0.425). Patients with ALL were more fatigued compared to healthy children (p < 0.001). Lower IS, RA and M10 counts and higher IV were significantly associated with more parent-reported cancer-related fatigue. Associations between sleep–wake rhythms and self-reported cancer-related fatigue were not statistically significant. Conclusions Sleep–wake rhythm impairment is associated with more cancer-related fatigue in pediatric ALL patients. Interventions aimed to improve sleep hygiene and encourage physical activity may reduce cancer-related fatigue.

Funder

Dutch Cancer Society

Publisher

Oxford University Press (OUP)

Subject

Physiology (medical),Neurology (clinical)

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