Omapatrilat versus lisinopril - Efficacy and neurohormonal profile in salt-sensitive hypertensive patients

被引:55
作者
Campese, VM
Lasseter, KC
Ferrario, CM
Smith, WB
Ruddy, MC
Grim, CE
Smith, RD
Vargas, R
Habashy, MF
Vesterqvist, O
Delaney, CL
Liao, WC
机构
[1] Univ So Calif, Med Ctr, Keck Sch Med, Div Nephrol, Los Angeles, CA 90033 USA
[2] Clin Pharmacol Associates, Miami, FL USA
[3] Bowman Gray Sch Med, Winston Salem, NC USA
[4] New Orleans Ctr Clin Res, New Orleans, LA USA
[5] Univ Med & Dent New Jersey, Robert Wood Johnson Med Sch, New Brunswick, NJ USA
[6] Med Coll Wisconsin, Milwaukee, WI 53226 USA
[7] Wake Forest Univ, Winston Salem, NC 27109 USA
[8] Bristol Myers Squibb Pharmaceut Res Inst, Princeton, NJ USA
[9] Covance Inc, Princeton, NJ USA
关键词
omapatrilat; lisinopril; vasopeptidase inhibitor; salt sensitivity;
D O I
10.1161/hy1201.096569
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Omapatrilat, a vasopeptidase inhibitor, simultaneously inhibits neutral endopeptidase and ACE. The efficacy and hormonal profile of omapatrilat and lisinopril were compared in salt-sensitive hypertensive patients. On enrollment, antihypertensive medications were withdrawn, and patients received a single-blind placebo. On day 15, salt-sensitivity determinations were made. Salt-sensitive hypertensive patients returned within 5 to 10 days for baseline evaluations of ambulatory diastolic blood pressure, ambulatory systolic blood pressure, and atrial natriuretic peptide. Salt-sensitive hypertensive patients were randomized to receive double-blind omapatrilat (n=28) or lisinopril (n=33) at initial doses of 10 mg for 1 week, increasing to 40 and 20 mg, respectively, for an additional 3 weeks. Ambulatory blood pressure and urinary atrial natriuretic peptide were assessed at study termination. Both omapatrilat and lisinopril significantly reduced mean 24-hour ambulatory diastolic and systolic blood pressures, however, omapatrilat produced significantly greater reductions in mean 24-hour ambulatory diastolic blood pressure (P=0.008), ambulatory systolic blood pressure (P=0.004), and ambulatory mean arterial pressure (P=0.005) compared with values from lisinopril. Both drugs potently inhibited ACE over 24 hours. Omapatrilat significantly (P<0.001) increased urinary excretion of atrial natriuretic peptide over 0- to 24-hour (3.8-fold) and 12- to 24-hour (2-fold) intervals; lisinopril produced no change. Omapatrilat significantly (P<0.001) increased urinary excretion of cGMP over the 0- to 24- and 4- to 8-hour intervals compared with that from lisinopril. Neither drug had a diuretic, natriuretic, or kaliuretic effect. In conclusion, in salt-sensitive hypertensive patients, omapatrilat demonstrated the hormonal profile of a vasopeptidase inhibitor and lowered ambulatory diastolic and systolic blood pressures more than lisinopril.
引用
收藏
页码:1342 / 1348
页数:7
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