Potential of Activin B as a Clinical Biomarker in Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS), 2021, Gravelsina et al

Sly Saint

Senior Member (Voting Rights)
Abstract
Reliable serum biomarkers are of immense need for diagnostic purposes of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS)—a disabling and complex disease for which diagnosis is mainly based on clinical symptoms.

The aim of this study was to evaluate a possible diagnostic potential of activin B by directly comparing 134 cases of ME/CFS with 54 healthy controls. Analyses of human activin B level in plasma samples were performed using a validated human activin B ELISA assay. The results of the study show that activin B levels did not differ statistically significantly between ME/CFS patients and healthy controls (p = 0.6511). No gender or age-related differences in activin B levels were observed in the ME/CFS group and healthy controls. The level of activin B tended to decrease with increasing visual analogue scale score (r = −0.2004; p = 0.5085) nevertheless

the results obtained so far does not support the clinical utility of activin B as a biomarker for ME/CFS.

https://www.mdpi.com/2218-273X/11/8/1189
 
This study uses Fukuda, the previous studies, linked below, on Activin used CCC, which may explain the differing findings.
Not sure if this would explain the difference between studies.

The authors discuss this point as follows:
Although different ME/CFS diagnostic criteria were used (Canadian consensus criteria in the study mentioned below [26] and Fukuda criteria in our study), comparing the clinical symptoms in the activin B positive group to the ones reported in the cross sectional study regarding activin B [26], the respondents apart from post‐exertional fatigue present with difficulty concentrating and sleep disturbances in both cohorts, although respond‐ ents in our study were more prone to have myalgia, arthralgia and headache (compared to less than 10% in the study mentioned [26]). There were no patients presenting with new allergies or arrhythmias in our study, compared to approximately 50% of study participants having these symptoms in the other cohort. As stated above, activin B has the potential role to induce muscle wasting and pain [25]. Nevertheless, one of the core symptoms in the activin B positive group was myalgia, reported by 92%. The fact that 96% reported having it in the activin B negative group may imply that activin B does not in‐ fluence the clinical presentation of muscle pain in ME/CFS patients. This finding is also substantiated by the fact that the VAS score did not show any statistically significant differences in both groups and even tends to decrease in the activin B positive group. Although we did not find any significant differences in clinical presentation of symptoms in both activin B positive and negative groups, more reports comparing the symptoms in both groups would be needed.

Here's the main data. Seems like there are lots of participants that are close to the quantification limit.
upload_2021-8-15_21-16-32.png
 
the respondents apart from post‐exertional fatigue present with difficulty concentrating and sleep disturbances in both cohorts,

So are they claiming there that both cohorts had 'post-exertional fatigue', which I also assume they believe is equivalent to PEM? Unless there is more detail on their assumptions I remain unconvinced that they are necessarily looking at comparable cohorts.
 
So are they claiming there that both cohorts had 'post-exertional fatigue', which I also assume they believe is equivalent to PEM? Unless there is more detail on their assumptions I remain unconvinced that they are necessarily looking at comparable cohorts.
The original study also speaks of "post-exertional fatigue" rather than PEM. Activin B is a novel biomarker for chronic fatigue syndrome/myalgic encephalomyelitis (CFS/ME) diagnosis: a cross sectional study (biomedcentral.com)

I think it is sometimes underestimated how few studies correctly assessed PEM (as PEM is understood in the online patient community).
 
In the 80s it was recommended that all studies be done on patients who were standing or at least fatigued. I remember one where they did a QEEG (?) where they found a problem in Me patients who were standing against the usual way where they were lying down.
 
Back
Top Bottom