Circadian rhythm abnormalities and autonomic dysfunction in patients with Chronic Fatigue Syndrome/Myalgic Encephalomyelitis, 2018, Cambras et al

Andy

Retired committee member
Abstract
Chronic Fatigue Syndrome/Myalgic Encephalomyelitis (CFS/ME) patients frequently show autonomic symptoms which may be associated with a hypothalamic dysfunction. This study aimed to explore circadian rhythm patterns in rest and activity and distal skin temperature (DST) and their association with self-reported outcome measures, in CFS/ME patients and healthy controls at two different times of year.

Ten women who met both the 1994 CDC/Fukuda definition and 2003 Canadian criteria for CFS/ME were included in the study, along with ten healthy controls matched for age, sex and body mass index. Self-reported measures were used to assess fatigue, sleep quality, anxiety and depression, autonomic function and health-related quality of life. The ActTrust actigraph was used to record activity, DST and light intensity, with data intervals of one minute over seven consecutive days. Sleep variables were obtained through actigraphic analysis and from subjective sleep diary. The circadian variables and the spectral analysis of the rhythms were calculated. Linear regression analysis was used to evaluate the relationship between the rhythmic variables and clinical features. Recordings were taken in the same subjects in winter and summer.

Results showed no differences in rhythm stability, sleep latency or number of awakenings between groups as measured with the actigraph. However, daily activity, the relative amplitude and the stability of the activity rhythm were lower in CFS/ME patients than in controls. DST was sensitive to environmental temperature and showed lower nocturnal values in CFS/ME patients than controls only in winter. A spectral analysis showed no differences in phase or amplitude of the 24h rhythm, but the power of the second harmonic (12h), revealed differences between groups (controls showed a post-lunch dip in activity and peak in DST, while CFS/ME patients did not) and correlated with clinical features. These findings suggest that circadian regulation and skin vasodilator responses may play a role in CFS/ME.
Open access at http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0198106
 
These seem like well-meaning researchers.

Since it has been reported that graded exercise markedly improves symptoms and activities of daily living in CFS/ME patients [41], we suggest that determining the time of day when actigraphic activity shows the highest values might help to indicate the best time for these patients to schedule their activities.

Can someone invite them to a conference so that they can update their knowledge on GET? And/or send them some information about the PACE trial?
 
These seem like well-meaning researchers.



Can someone invite them to a conference so that they can update their knowledge on GET? And/or send them some information about the PACE trial?
Actually their evidence for their statement isn't the PACE trial. Their reference is "Patient education to encourage graded exercise in chronic fatigue syndrome. 2-year follow-up of randomised controlled trial.", https://www.ncbi.nlm.nih.gov/pubmed/14754826, this response to the study, https://www.bmj.com/content/322/7301/1545, seems to indicate many of the usual problems with it.
 
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