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  • Parallel-group 8-week study on chlorthalidone effects in hypertensives with low kidney function.

Parallel-group 8-week study on chlorthalidone effects in hypertensives with low kidney function.

Hypertension (Dallas, Tex. : 1979) (2014-01-08)
Massimo Cirillo, Fabiana Marcarelli, Alessandra A Mele, Massimo Romano, Cinzia Lombardi, Giancarlo Bilancio
ABSTRACT

Short-term effects of chlorthalidone are unknown in low kidney function. The effects of 8-week treatment with 25-mg chlorthalidone on the top of ongoing treatment were compared between control hypertensives and low kidney function hypertensives as assessed by estimated glomerular filtration rate <60 mL/min×1.73 m(2). Screening period consisted of 2 visits for patient selection and pretreatment laboratory evaluations (baseline). Inclusion criteria were uncontrolled hypertension on nondiuretic antihypertensive treatment. Exclusion criteria were chlorthalidone contraindications, refused consent, treatment with >3 antihypertensive drugs, severe hypertension, severe comorbidities, unreliable estimated glomerular filtration rate. Treatment period consisted of 5 visits (weeks 1, 2, 4, 6, and 8). Post-treatment laboratory evaluations were performed 3 to 4 days before week-8 visit. The 2 groups differed for baseline estimated glomerular filtration rate (low kidney function and control: n=60 and 60; mean, 39 and 76; range, 15-59 and 60-104) but not for sex, age, and baseline blood pressure. Week-8 blood pressure changes were a decrease in both groups (low kidney function and control: systolic pressure, -20 and -23; 95% confidence interval, -22/-18 and -26/-19; diastolic pressure, -9 and -10, -11/-7, and -13/-8) without significant between-group differences. Incidence of adverse events was similar in the 2 groups (15.0% and 16.7%). Baseline estimated glomerular filtration rate did not predict blood pressure changes and adverse events in either groups (P>0.6). In both groups, post-treatment changes were a decrease for estimated glomerular filtration rate and serum potassium, an increase for serum uric acid (P<0.01). Data show that short-term chlorthalidone effects were not reduced in hypertensives with low kidney function.

MATERIALS
Product Number
Brand
Product Description

USP
Chlorthalidone, United States Pharmacopeia (USP) Reference Standard
Chlorthalidone, European Pharmacopoeia (EP) Reference Standard
Sigma-Aldrich
Chlorthalidone, ≥98% (HPLC)
Sigma-Aldrich
Uric acid, ≥99%, crystalline