Evidence map›Paper›PMID 36054767›Full record

ArticleInternational journal of cancer2023

Longitudinal associations of plasma metabolites with persistent fatigue among colorectal cancer survivors up to 2 years after treatment.

Eline H van Roekel, Martijn J L Bours, Stéphanie O Breukink, Michèl Aquarius, Eric T P Keulen, Audrey Gicquiau, Sabina Rinaldi, Paolo Vineis, Ilja C W Arts, Marc J Gunter and 3 more

Open access · greenAbstract read
In one paragraph

Article in International journal of cancer, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 14% of its field
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

8 citing papers in PubMed, 13 citations in OpenAlex.

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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

13 authors at 7 institutions in 5 countries.

Eline H van RoekelDepartment of Epidemiology, GROW School for Oncology and Developmental Biology, Maastricht University, Maastricht, The Netherlands.ORCID 0000-0002-9402-2029
Martijn J L BoursDepartment of Epidemiology, GROW School for Oncology and Developmental Biology, Maastricht University, Maastricht, The Netherlands.
Stéphanie O BreukinkDepartment of Surgery, GROW School for Oncology and Developmental Biology, School of Nutrition and Translational Research in Metabolism, Maastricht University Medical Center+, Maastricht, The Netherlands.
Michèl AquariusDepartment of Gastroenterology, VieCuri Medical Center, Venlo, The Netherlands.
Eric T P KeulenDepartment of Internal Medicine and Gastroenterology, Zuyderland Medical Centre, Sittard-Geleen, The Netherlands.
Audrey GicquiauNutrition and Metabolism Branch, International Agency for Research on Cancer (IARC-WHO), Lyon, France.
Sabina RinaldiNutrition and Metabolism Branch, International Agency for Research on Cancer (IARC-WHO), Lyon, France.ORCID 0000-0002-6846-1204
Paolo VineisMRC Centre for Environment and Health, School of Public Health, Imperial College, London, UK.
Ilja C W ArtsMaastricht Centre for Systems Biology (MaCSBio), Maastricht University, Maastricht, The Netherlands.
Marc J GunterNutrition and Metabolism Branch, International Agency for Research on Cancer (IARC-WHO), Lyon, France.
Michael F LeitzmannDepartment of Epidemiology and Preventive Medicine, University of Regensburg, Regensburg, Germany.
Augustin ScalbertNutrition and Metabolism Branch, International Agency for Research on Cancer (IARC-WHO), Lyon, France.
Matty P WeijenbergDepartment of Epidemiology, GROW School for Oncology and Developmental Biology, Maastricht University, Maastricht, The Netherlands.
Centre international de recherche sur le cancer · FRMaastricht University · NLMaastricht University Medical Centre · NLItalian Institute of Technology · ITUniversity of Regensburg · DEVieCuri Medisch Centrum · NLZuyderland Medisch Centrum · NL

Funding

Medical Research Council MR/S019669/1World Health Organization 001
6 · The paper itself

Abstract

The underlying biological mechanisms causing persistent fatigue complaints after colorectal cancer treatment need further investigation. We investigated longitudinal associations of circulating concentrations of 138 metabolites with total fatigue and subdomains of fatigue between 6 weeks and 2 years after colorectal cancer treatment. Among stage I-III colorectal cancer survivors (n = 252), blood samples were obtained at 6 weeks, and 6, 12 and 24 months posttreatment. Total fatigue and fatigue subdomains were measured using a validated questionnaire. Tandem mass spectrometry was applied to measure metabolite concentrations (BIOCRATES AbsoluteIDQp180 kit). Confounder-adjusted longitudinal associations were analyzed using linear mixed models, with false discovery rate (FDR) correction. We assessed interindividual (between-participant differences) and intraindividual longitudinal associations (within-participant changes over time). In the overall longitudinal analysis, statistically significant associations were observed for 12, 32, 17 and three metabolites with total fatigue and the subscales "fatigue severity," "reduced motivation" and "reduced activity," respectively. Specifically, higher concentrations of several amino acids, lysophosphatidylcholines, diacylphosphatidylcholines, acyl-alkylphosphatidylcholines and sphingomyelins were associated with less fatigue, while higher concentrations of acylcarnitines were associated with more fatigue. For "fatigue severity," associations appeared mainly driven by intraindividual associations, while for "reduced motivation" stronger interindividual associations were found. We observed longitudinal associations of several metabolites with total fatigue and fatigue subscales, and that intraindividual changes in metabolites over time were associated with fatigue severity. These findings point toward inflammation and an impaired energy metabolism due to mitochondrial dysfunction as underlying mechanisms. Mechanistic studies are necessary to determine whether these metabolites could be targets for intervention.

Indexed as

Cancer SurvivorsColorectal NeoplasmsFatigueHumansPlasmaSurvivorsamino acidscancer-related fatiguecolorectal cancerphospholipidstargeted metabolomics

Identifiers

PMID36054767
PMCPMC9825888
OpenAlexW4293775622

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.