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Aldosterone--Mark

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Mark,

Thanks for your thoughts on hyperpigmentation. Maybe it just isn't an

extreme enough situation for that to show up.

Concerning aldosterone, I haven't done much studying on that, because

I had been under the impression that it was found at normal levels in

PWCs. But maybe not. Here are a couple of abstracts you might find

interesting:

Clin Auton Res 1997 Aug;7(4):185-90

Pathogenesis and management of delayed orthostatic hypotension in

patients with chronic fatigue syndrome.

De Lorenzo F, Hargreaves J, Kakkar VV.

Thrombosis Research Institute, London, UK.

The relationship between orthostatic hypotension and chronic fatigue

syndrome (CFS) has been reported previously. To study the pathogenesis

and management of delayed orthostatic hypotension in patients with

CFS, a case comparison study with follow-up of 8 weeks has been

designed. A group of 78 patients with CFS (mean age 40 years; 49% men

and 51% women), who fulfilled the Centre for Disease Control and

Prevention criteria were studied. There were 38 healthy controls (mean

age 43 years; 47% men and 53% women). At entry to the study each

subject underwent an upright tilt-table test, and clinical and

laboratory evaluation. Patients with orthostatic hypotension were

offered therapy with sodium chloride (1200 mg) in a sustained-release

formulation for 3 weeks, prior to resubmission to the tilt-table

testing, and clinical and laboratory evaluation. An abnormal response

to upright tilt was observed in 22 of 78 patients with CFS. After

sodium chloride therapy for 8 weeks, tilt-table testing was repeated

on the 22 patients with an abnormal response at baseline. Of these 22

patients, 10 redeveloped orthostatic hypotension, while

11 did not show an abnormal response to the test and reported an

improvement of CFS symptoms. However, those CFS patients who again

developed an abnormal response to tilt-test had a significantly

reduced plasma renin activity (0.79 pmol/ml per h) compared

both with healthy controls (1.29 pmol/ml per h) and with those 11

chronic fatigue patients (1.0 pmol/ml per h) who improved after sodium

chloride therapy (p = 0.04). In conclusion, in our study CFS patients

who did not respond to sodium chloride therapy were found to

have low plasma renin activity. In these patients an abnormal

renin-angiotensin-aldosterone system could explain the pathogenesis of

orthostatic hypotension and the abnormal response to treatment.

[Chronic fatigue syndrome, a case of high anti-HHV-6 antibody titer

and one associated with primary hyperaldosteronism.]

[Article in Japanese]

Kato Y, Kamijima S, Kashiwagi A, Oguri T.

Second Department of Internal Medicine, Aichi Medical College.

Two cases of chronic fatigue syndrome (CFS) were reported which were

suggestive for the study of the etiology and a cure for CFS. Case 1: A

31-year-old woman was admitted for chronic fatigue syndrome.

Examination revealed a high titer of anti HHV-6 antigen of x2560

and an increased percentage of suppressor T lymphocytes in the

peripheral blood. HHV-6 was speculated to be reactivated and

stimulating the immune system in CFS. Case 2: A 46-year-old woman

suffering from CFS had been in remission for 6 years. She was

admitted for hypertension associated with right adrenal adenoma and

hyperaldosteronism. After right adrenalectomy, there was a recurrence

of high fever and other CFS symptoms. It was suggested that CFS

symptoms may be ameliorated by aldosterone.

Rich

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Rich,

Thanks for doing the leg work on those studies. How exactly the

remission could be related to aldosterone I don't know in that

Japanese study. Very curious. Hmmm.

Mark

> Mark,

>

> Thanks for your thoughts on hyperpigmentation. Maybe it just isn't

an

> extreme enough situation for that to show up.

>

> Concerning aldosterone, I haven't done much studying on that,

because

> I had been under the impression that it was found at normal levels

in

> PWCs. But maybe not. Here are a couple of abstracts you might

find

> interesting:

>

> Clin Auton Res 1997 Aug;7(4):185-90

>

> Pathogenesis and management of delayed orthostatic hypotension in

> patients with chronic fatigue syndrome.

>

> De Lorenzo F, Hargreaves J, Kakkar VV.

>

> Thrombosis Research Institute, London, UK.

>

> The relationship between orthostatic hypotension and chronic

fatigue

> syndrome (CFS) has been reported previously. To study the

pathogenesis

> and management of delayed orthostatic hypotension in patients with

> CFS, a case comparison study with follow-up of 8 weeks has been

> designed. A group of 78 patients with CFS (mean age 40 years; 49%

men

> and 51% women), who fulfilled the Centre for Disease Control and

> Prevention criteria were studied. There were 38 healthy controls

(mean

> age 43 years; 47% men and 53% women). At entry to the study each

> subject underwent an upright tilt-table test, and clinical and

> laboratory evaluation. Patients with orthostatic hypotension were

> offered therapy with sodium chloride (1200 mg) in a sustained-

release

> formulation for 3 weeks, prior to resubmission to the tilt-table

> testing, and clinical and laboratory evaluation. An abnormal

response

> to upright tilt was observed in 22 of 78 patients with CFS. After

> sodium chloride therapy for 8 weeks, tilt-table testing was

repeated

> on the 22 patients with an abnormal response at baseline. Of these

22

> patients, 10 redeveloped orthostatic hypotension, while

> 11 did not show an abnormal response to the test and reported an

> improvement of CFS symptoms. However, those CFS patients who again

> developed an abnormal response to tilt-test had a significantly

> reduced plasma renin activity (0.79 pmol/ml per h) compared

> both with healthy controls (1.29 pmol/ml per h) and with those 11

> chronic fatigue patients (1.0 pmol/ml per h) who improved after

sodium

> chloride therapy (p = 0.04). In conclusion, in our study CFS

patients

> who did not respond to sodium chloride therapy were found to

> have low plasma renin activity. In these patients an abnormal

> renin-angiotensin-aldosterone system could explain the pathogenesis

of

> orthostatic hypotension and the abnormal response to treatment.

>

>

> [Chronic fatigue syndrome, a case of high anti-HHV-6 antibody titer

> and one associated with primary hyperaldosteronism.]

>

> [Article in Japanese]

>

> Kato Y, Kamijima S, Kashiwagi A, Oguri T.

>

> Second Department of Internal Medicine, Aichi Medical College.

>

> Two cases of chronic fatigue syndrome (CFS) were reported which

were

> suggestive for the study of the etiology and a cure for CFS. Case

1: A

> 31-year-old woman was admitted for chronic fatigue syndrome.

> Examination revealed a high titer of anti HHV-6 antigen of x2560

> and an increased percentage of suppressor T lymphocytes in the

> peripheral blood. HHV-6 was speculated to be reactivated and

> stimulating the immune system in CFS. Case 2: A 46-year-old woman

> suffering from CFS had been in remission for 6 years. She was

> admitted for hypertension associated with right adrenal adenoma and

> hyperaldosteronism. After right adrenalectomy, there was a

recurrence

> of high fever and other CFS symptoms. It was suggested that CFS

> symptoms may be ameliorated by aldosterone.

>

> Rich

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