Evidence map›Paper›PMID 28302133›Full record

Observational studyJournal of translational medicine2017

Activin B is a novel biomarker for chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) diagnosis: a cross sectional study.

Brett A Lidbury, Badia Kita, Donald P Lewis, Susan Hayward, Helen Ludlow, Mark P Hedger, David M de Kretser

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in Journal of translational medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06233890 (The Analysis of Fatigue on Tyrosine Kinase Inhibitor Therapy in Chronic Myeloid Leukaemia), which is not on this map. Cited by 22 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 2 pooled it
–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.

NCT06233890 unknown statusnot on this mapstarted 2023, after this paper: background citation

The Analysis of Fatigue on Tyrosine Kinase Inhibitor Therapy in Chronic Myeloid Leukaemia

TypeobservationalSponsorImperial College Healthcare NHS TrustRan2023 to 2026Enrolled50ConditionsChronic Myeloid Leukemia, Chronic Myeloid Leukemia, Chronic Phase, Fatigue, Sleep DisturbanceArmsMotion watch
3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 2 syntheses or guidelines pooled it.

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  18. The clinical value of cytokines in chronic fatigue syndrome.Journal of translational medicine · 2019
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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

7 authors.

Brett A LidburyPattern Recognition and Pathology, Department of Genome Sciences, The John Curtin School of Medical Research, The Australian National University, Canberra, ACT, 2601, Australia. brett.lidbury@anu.edu.au.ORCID 0000-0003-2211-989X
Badia KitaParanta Biosciences Limited, Caulfield North, VIC, 3161, Australia.
Donald P LewisCFS Discovery, Donvale Medical Specialist Centre, Donvale, VIC, 3111, Australia.
Susan HaywardThe Hudson Medical Research Institute, Monash University, Clayton, VIC, 3168, Australia.
Helen LudlowCentre for Proteins and Peptides, School of Life Sciences, Oxford Brookes University, Headington, Oxford, OX3 0BP, UK.
Mark P HedgerThe Hudson Medical Research Institute, Monash University, Clayton, VIC, 3168, Australia.
David M de KretserThe Hudson Medical Research Institute, Monash University, Clayton, VIC, 3168, Australia.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInvestigations of activin family proteins as serum biomarkers for chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME). CFS/ME is a disease with complex, wide-ranging symptoms, featuring persistent fatigue of 6 months or longer, particularly post exertion. No definitive biomarkers are available.

methodsA cross-sectional, observational study of CFS/ME patients fulfilling the 2003 Canadian Consensus Criteria, in parallel with healthy non-fatigued controls, was conducted. Comparisons with a previously defined activin reference population were also performed. For the total study cohort the age range was 18-65 years with a female: male participant ratio of greater than 3:1. All participants were assessed via a primary care community clinic. Blood samples were collected for pathology testing after physical examination and orthostatic intolerance assessment. Cytokines, activin A, activin B and follistatin were also measured in sera from these samples. All data were compared between the CFS/ME and control cohorts, with the activins and follistatin also compared with previously defined reference intervals.

resultsSerum activin B levels for CFS/ME participants were significantly elevated when compared to the study controls, as well as the established reference interval. Serum activin A and follistatin were within their normal ranges. All routine and special pathology markers were within the normal laboratory reference intervals for the total study cohort, with no significant differences detected between CFS/ME and control groups. Also, no significant differences were detected for IL-2, IL-4, IL-6, IL-10, IL-17A, TNF or IFN-gamma.

conclusionElevated activin B levels together with normal activin A levels identified patients with the diagnostic symptoms of CFS/ME, thus providing a novel serum based test. The activins have multiple physiological roles and capture the diverse array of symptoms experienced by CFS/ME patients.

Indexed as

ActivinsAdultAgedBiomarkersCase-Control StudiesCohort StudiesCross-Sectional StudiesFatigue Syndrome, ChronicFemaleFollistatinHumansMaleMiddle AgedROC CurveYoung Adultactivin Aactivin BActivinsBiomarkersFollistatinActivinsBiomarkerChronic fatigue syndrome (CFS)DiagnosisMyalgic encephalomyelitis (ME)

Identifiers

PMID28302133
PMCPMC5353946

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Registered trials

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.