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3.
Clin Exp Hypertens A ; 4(7): 1151-76, 1982.
Article in English | MEDLINE | ID: mdl-7116662

ABSTRACT

1. Although systolic blood pressure elevation is responsible for increased incidence of cardiovascular accidents in old people, the preventive benefit of lowering systolic hypertension in elderly has not been confirmed. 2. A double blind study comparing the effects of a placebo and of an active regimen (hydrochlorothiazide-triamterene with or without methyldopa) in people over 60 years with isolated systolic hypertension has been undertaken by the European Working Party on High blood pressure in the Elderly (EWPHE). 3. The actively treated group shows a lowered sitting blood pressure (-15/6 mm Hg), a mild increase of serum creatine, serum uric acid and blood glucose and a mild decrease of serum potassium after two years of treatment when compared to the spontaneous changes observed in the placebo treated group. 4. The study is continuing to evaluate if the blood pressure reduction prevents or reduces the incidence of cardiovascular accidents, although some biochemical changes were provoked by the treatment.


Subject(s)
Hydrochlorothiazide/therapeutic use , Hypertension/drug therapy , Methyldopa/therapeutic use , Triamterene/therapeutic use , Aged , Blood Glucose/metabolism , Blood Pressure/drug effects , Creatinine/blood , Drug Therapy, Combination , Electrolytes/blood , Female , Humans , Hypertension, Renal/drug therapy , Hypertension, Renovascular/drug therapy , Male , Systole/drug effects , Uric Acid/blood
4.
Acta Cardiol ; 37(4): 235-44, 1982.
Article in English | MEDLINE | ID: mdl-6751003

ABSTRACT

In the European Working Party trial on High blood pressure in the Elderly, patients over 60 are randomly allocated either to receive diuretic capsules containing 25 mg hydrochlorothiazide and 50 mg triamterene or matching placebos. If the blood pressure remains high those receiving active diuretic treatment also receive methyldopa. Those receiving a placebo diuretic area given placebo methyldopa tablets. The study is double blind, started in 1974 and is still in progress. Three hundred and thirty-one patients have now been followed for 1 year and of these 190 have been followed for 2 and 90 for 3 years. After 1 year the serum cholesterol in the placebo group fell by an average of 10.4 mg/100 ml; over 2 years the fall was 16.0 mg/100 ml and over 3 years 20.8 mg/100 ml (6.7%). The corresponding results for the actively treated group were falls of 3.1 mg/100 ml; 20.3 mg/100 ml and 17.3 mg/100 ml (6.6%). Over a period of up to 3 years the average fall in cholesterol was 5.9 mg/100 ml/year in the placebo group and 5.0 mg/100 ml/year in the actively treated group. Thus the changes in serum cholesterol were similar whether the patients received active or placebo medication. In particular there was no evidence for an increase in cholesterol nor for a smaller decrease during diuretic therapy. In the actively treated group the fall in blood pressure in the more hypertensive patients was accompanied by a fall both in haematocrit and serum cholesterol. In patients with less severe hypertension, active treatment was not accompanied by a fall in either hematocrit or cholesterol. These different responses of serum cholesterol in the more and less severe hypertensives in the present study could explain some of the previous conflicting reports on the influence of diuretic treatment on serum cholesterol.


Subject(s)
Aging , Cholesterol/blood , Hypertension/drug therapy , Aged , Blood Pressure/drug effects , Clinical Trials as Topic , Europe , Female , Follow-Up Studies , Hematocrit , Humans , Hydrochlorothiazide/therapeutic use , Hypertension/blood , Hypertension/physiopathology , International Cooperation , Male , Middle Aged , Triamterene/therapeutic use
7.
Lancet ; 1(8066): 681-3, 1978 Apr 01.
Article in English | MEDLINE | ID: mdl-76223

ABSTRACT

119 elderly, hypertensive patients were followed-up for 1 year and 48 for 2 years in a double-blind, randomised, controlled trial in which they received either placebo or 25-50 mg hydrochlorothiazide and 50-100 mg of triamterene daily. Half of the active treatment group also received 250 mg to 2 g methyldopa daily. After 2 years the active treatment group had an average increase in fasting blood-sugar of 9.6 mg/dl compared with an average fall of 3.1 mg in the placebo group (p less than 0.001). Blood-glucose rose by an average of 26.6 mg/dl in the active group when determined 1 hour after 50 g oral glucose and decreased by an average of 5.3 mg/dl in patients who had been on placebo for two years (p less than 0.05). The hyperglycaemic effect of diuretics appeared to be related to potassium loss since, in both groups, impairment of glucose tolerance was most marked in those in whom the serum-potassium decreased over the 2 years.


Subject(s)
Hydrochlorothiazide/adverse effects , Hyperglycemia/chemically induced , Hypertension/drug therapy , Triamterene/adverse effects , Aged , Blood Glucose/analysis , Clinical Trials as Topic , Female , Follow-Up Studies , Glucose Tolerance Test , Humans , Hydrochlorothiazide/therapeutic use , Hypokalemia/complications , Male , Methyldopa/therapeutic use , Middle Aged , Placebos , Research Design , Triamterene/therapeutic use
8.
Acta Cardiol ; 33(2): 113-34, 1978.
Article in English | MEDLINE | ID: mdl-356497

ABSTRACT

Three hundred forty nine hypertensive patients above the age of 60 have entered the double-blind multicentre trial of the European Working Party on High blood pressure in the Elderly (EWPHE). After stratification and randomisation half were treated with one or two capsules containing 25 mg hydrochlorothiazide and 50 mg triamterene and if blood pressure control was insufficient methyldopa was added up to 2 g daily; the other half received matching placebo. No significant differences between the groups were present prior to randomisation. A significant blood pressure difference of 25/10 mm Hg was obtained between the groups and maintained during two years of follow-up. No major disturbances in serum potassium or serum sodium were noted with the present drug combination. However, during the initial phase an increase in serum creatinine and serum uric acid was noted in the actively treated group, which was maintained for two years. Also glucose tolerance was impaired after 2 years in the actively treated group. A favourable influence on prognosis by active treatment can be expected on the basis of the blood pressure reduction and in the absence of major electrolytes disturbances. But this benefit must be proven by observed statistical differences in terminating events between the groups. Therefore the patients are being followed for a longer period of time and more patients are admitted into the trial.


Subject(s)
Hydrochlorothiazide/therapeutic use , Hypertension/drug therapy , Triamterene/therapeutic use , Aged , Blood Pressure/drug effects , Body Weight , Clinical Trials as Topic , Creatinine/blood , Double-Blind Method , Europe , Female , Humans , Male , Methyldopa/therapeutic use , Middle Aged , Potassium/blood , Random Allocation , Sodium/blood , Uric Acid/blood
11.
Obstet Gynecol ; 36(1): 93-100, 1970 Jul.
Article in English | MEDLINE | ID: mdl-5422095

ABSTRACT

PIP: The suppressive action of norethisterone enanthate and acetate on follicle-stimulating hormone (FSH) and luteinizing hormone (LH) levels was studied by radioimmunoassay in postmenopausal and normally menstruating women. Postmenopausal women, injected with 200 mg of norethisterone acetate, intramuscularly, showed a marked, rapid, and prolonged decrease in serum LH levels. FSH also declined but the decrease was less rapid, less pronounced, and briefer. 1 month after injection, FSH values had returned to pretreatment levels. Oral norethisterone acetate, administered in .3 mg/day doses for 16 days to postmenopausal subjects, did not produce a statistically significant change in serum FSH levels, although serum LH concentrations gradually declined until the end of the treatment period. An oral dose of .3 mg./day of norethisterone acetate suppressed FSH and LH peaks in normally menstruating women who had displayed the peaks prior to treatment. Baseline levels of FSH and LH, however, were not lowered.^ieng


Subject(s)
Follicle Stimulating Hormone/metabolism , Luteinizing Hormone/metabolism , Norethindrone/pharmacology , Radioimmunoassay , Acetates/pharmacology , Female , Follicle Stimulating Hormone/blood , Humans , Luteinizing Hormone/blood , Menopause
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