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1.
Blood Press ; 1(4): 212-8, 1992 Dec.
Article in English | MEDLINE | ID: mdl-1345218

ABSTRACT

In a randomized double blind study 100 men (mean age 46 (22-64) years) with mild to moderate hypertension were followed every 3rd month for one year. Fifty were randomized to atenolol 50 mg and 50 to hydrochlorothiazide 25 mg+amiloride 5 mg (co-amiloride) once daily. The doses were doubled at 3 or 6 months if diastolic blood pressure (DBP) remained > or = 95 mmHg. If DBP was > or = 95 mmHg even at 6 or 9 months, patients were classified as non-responders, and nifedipine 20 mg b.i.d. was added. After one year 31/50 randomized to atenolol and 17/50 randomized to co-amiloride had responded to monotherapy (p < 0.05). Neither clinical findings nor haemodynamic measurements by Doppler at baseline could distinguish between co-amiloride responders and non-responders. Conversely, non-responders to atenolol as compared with atenolol responders had higher body weight (p = 0.02), higher systolic BP (p = 0.03), higher DBP (p = 0.009), stroke volume (p = 0.04), and cardiac output (p = 0.0002) combined with lower total systemic vascular resistance (p = 0.02). This suggests that some were apparent non-responders due to too low dosing of atenolol rather than true non-responders. Measurements of haemodynamics may be of importance in the assessment of optimal antihypertensive therapy according to baseline and follow-up haemodynamic aberrations.


Subject(s)
Amiloride/therapeutic use , Atenolol/therapeutic use , Hemodynamics/drug effects , Hydrochlorothiazide/therapeutic use , Hypertension/drug therapy , Hypertension/physiopathology , Adult , Blood Pressure/drug effects , Cardiac Output/drug effects , Drug Combinations , Heart Rate/drug effects , Hemodynamics/physiology , Humans , Hypertension/diagnostic imaging , Male , Middle Aged , Ultrasonography , Vascular Resistance/drug effects
2.
J Intern Med ; 231(5): 493-501, 1992 May.
Article in English | MEDLINE | ID: mdl-1534831

ABSTRACT

In a randomized double-blind study to compare the effect of atenolol vs. hydrochlorothiazide and amiloride (Moduretic) on left ventricular dimensions and systolic function, 100 hypertensive men were followed up during 1 year of treatment, 50 subjects being randomized to each drug. Echocardiography was performed at baseline, and after 3 and 12 months of treatment. A significant reduction in left ventricular mass with atenolol was paralleled by a decrease in left ventricular wall thickness and an increase in stroke volume. A similar reduction of left ventricular mass with Moduretic without a change in relative wall thickness and a decrease in stroke volume was observed. Cardiac output decreased in both groups.


Subject(s)
Atenolol/therapeutic use , Cardiomegaly/diagnosis , Hydrochlorothiazide/therapeutic use , Hypertension/drug therapy , Systole/drug effects , Adult , Aged , Atenolol/adverse effects , Atenolol/pharmacology , Double-Blind Method , Echocardiography , Humans , Hydrochlorothiazide/adverse effects , Hydrochlorothiazide/pharmacology , Male , Middle Aged , Nifedipine/therapeutic use , Time Factors
3.
Scand J Clin Lab Invest ; 52(2): 83-93, 1992 Apr.
Article in English | MEDLINE | ID: mdl-1589701

ABSTRACT

A double-blind randomized study comparing the effects of 1 year's treatment with atenolol (A) 50 mg or hydrochlorothiazide 25 mg plus amiloride 5 mg (Moduretic (M)) on the lipid profile was performed in 100 hypertensive men (mean age 47, range 22-64 years). After 4 weeks' wash-out and 4 weeks on placebo therapy subjects were randomized to either A or M therapy and followed up every third month for 1 year. If the diastolic blood pressure (DBP) was greater than or equal to 95 mmHg at a subsequent visit, the doses were doubled (n = 17 for A and n = 12 for M) and, if DBP was still greater than or equal to 95 mmHg on double dose, nifedipine 20 mg b.d. was added (n = 15 for A and n = 27 for M, p less than 0.05). The lowering of heart rate (p = 0.0001) and DBP (p = 0.005) was more pronounced with A after 1 year. During that time no significant treatment differences were noted for total cholesterol, low-density lipoprotein (LDL) cholesterol or apoproteins A and B. High-density lipoprotein (HDL) cholesterol decreased from a mean of 1.19 (+/- 0.36) mmol l-1 to 1.13 (+/- 0.35) with A, and increased from 1.14 (+/- 0.30) mmol l-1 to 1.22 (+/- 0.28) with M, and this treatment difference was significant (p = 0.0002). The triglycerides increased from 2.0 (+/- 1.2) mmol l-1 to 2.3 (+/- 1.6) in the A group and did not change with M treatment (p = 0.02) for treatment difference). In view of similar effects on cholesterol, LDL cholesterol and apoproteins, the prognostic importance of the observed treatment differences on HDL cholesterol and triglycerides remains to be established.


Subject(s)
Amiloride/administration & dosage , Atenolol/therapeutic use , Hydrochlorothiazide/administration & dosage , Hypertension/drug therapy , Lipids/blood , Adult , Apoproteins/blood , Drug Therapy, Combination , Humans , Hypertension/blood , Infant, Newborn , Lipoproteins/blood , Male , Middle Aged
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