daisybell
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Have there been studies looking at this in healthy controls?
I can't count the number of times in the past I've seen questionnaire responses interpreted in a most convenient way. Each time from my own experience I found that there were potentially other very sound and valid reasons for a very different interpretation.
That's a bit of a red rag to this bull: as a self-confessed science-geek I'm always deeply suspicious of simply rejecting a study without reading it. It also implies 'others are right' without appropriate scrutiny. I think a bg reason there has been so little progress in mecfs research during the tweny years I've been ill is that the standard of research has been so poor, and that sadly applies to biomedical research too (lack of funds is a major issue of course, but poor studies are still poor studies). I don't believe in giving anyone an easy ride: mediocre research won't find the answers to our illness, whatever the motivations of the researchers. Though I am much more optimistic now than I've ever been, with large rigorous studies breaking out all over the place.I believe many of these psych endeavors are not about pure Science and genuine scientific inquiry...
Plus, they are flat out wrong.
Well, it certainly wasn't convincing in this study! What kind of investigations of the HPA axis do you think are needed?Differences in the wakening cortisol levels can be caused by simple differences, like different sleeping rhythms. Far deeper biological investigations are needed if the hypothesis (of disrupted HPA axis) is to be investigated.
Measuring coritsol levels is just a pretend way of linking bio to psycho, but it never does it in a convincing way.
At least the discussion should include other factors besides trauma that could plausibly account for HPA dysfunction (infections, head injury, autoimmunity, etc).Well, it certainly wasn't convincing in this study! What kind of investigations of the HPA axis do you think are needed?
Another thing with this type of studies is that reduced HPA axis function might make people more prone to a gloomy anxious mood. Cortisol is known to improve mood. This could easily affect how they respond to questionnaires. "emotional abuse" and "emotional neglect" are much more open to interpretation than the other scores.
I don't know about this test specifically, but there are indeed studies where psychs were told the case files were psych cases and asked to diagnose them. They were actually healthy controls. They found reasons to find psych disorders in most of them. Diagnosis is often highly problematic. I cited such a study a few weeks back, back in the 60s I think.Have there been studies looking at this in healthy controls?
Yeah, hypocortisolemia is actually associated with the symptom known as interpersonal rejection sensitivity (a common finding in atypical depression and other states where the HPA axis is blunted) so I wouldn't take as gospel self-reported emotional neglect from such patients.
I'm not sure why you feel that way.
HPA axis has long been implicated with CFS.
A study to investigate the HPA axis in patients is something I'd even donate to support.
The HPA axis is located in the midbrain and compromises of three glands which affect and regulate the body in vast number of ways.
You really think studies linking dysfunction of the midbrain with CFS/ME are redundant?
Well, it certainly wasn't convincing in this study! What kind of investigations of the HPA axis do you think are needed?
Measurements of the other related hormones either directly/indirectly (within reason), within the same group of patients. Eg Vasopressin levels have never really been measured.
Acta Neurol Scand. 1993 Mar;87(3):234-8.
Abnormal arginine-vasopressin secretion and water metabolism in patients with postviral fatigue syndrome.
Bakheit AM1, Behan PO, Watson WS, Morton JJ.
Author information
Abstract
Water metabolism and the responses of the neurohypophysis to changes in plasma osmolality during the water loading and water deprivation tests were studied in nine patients with postviral fatigue syndrome (PVFS) and eight age and six-matched healthy control subjects. Secretion of arginine-vasopressin (AVP) was erratic in these patients as shown by lack of correlation between serum and urine osmolality and the corresponding plasma AVP levels. Patients with PVFS had significantly low baseline arginine-vasopressin levels when compared with healthy subjects. Patients with PVFS as a group also showed evidence of increased total body water content. These results may be indicative of hypothalamic dysfunction in patients with PVFS.
It's the attempt to make it into a psychosocial cause that is objectionable. There are other biomedical reasons for HPA axis problems. This "study" is just another waste of money, paid out to the psychobabblers.
Just think of all the groups whose members have been "abused" in one way or another, and who do not get ME/CFS: children abused by priests, children abused in war zones, the "lost boys" of Africa, etc.
Stress has long been related with CFS. There's been many cases of CFS onset after a traumatic event. In some people, stress is handled fine by the different pathways. However, in a select few, the high stress triggers an abnormal reaction by the body which results in CFS.
Stress has long been related with CFS. There's been many cases of CFS onset after a traumatic event. In some people, stress is handled fine by the different pathways. However, in a select few, the high stress triggers an abnormal reaction by the body which results in CFS.
What do you mean by "stress". I mean disease by definition involves stress at a cellular level, resulting in lesions, but I'm guessing this is not what you meant.
If you mean a specific type of psychological stress, then you need to say that, rather than use the non-specific 'stress'.
As for psychological stress, it is potentially a risk factor for many diseases. But studies have shown that it is not a specific nor sensitive predictor for ME/CFS, nor has such pathology been indicated through medical studies, hence it cannot (at this time) be considered a cause for ME/CFS.
Stress HAS been linked with CFS/ME for decades. To deny that is ridiculous. Whether you agree with it or not is another point.
Just because some psychobabblers keep saying that CFS is caused by psychological stress doesn't make it so. It's an unfalsifiable claim. A correlation between psychological stress and onset of symptoms doesn't mean much - correlation doesn't imply causation. It could easily be that the underlying disease impairs patients ability to handle stress or responsibilities of daily living so that they do indeed experience more psychological stress. In fact hypocortisolism does just that.
But the link is there nevertheless.