Ferrier C, Ferrari P, Weidmann P, Keller U, Beretta-Piccoli C, Riesen W F
Medizinische Poliklinik, University of Berne, Switzerland.
Drugs. 1992;44 Suppl 1:74-84. doi: 10.2165/00003495-199200441-00014.
The purpose of the present study was to assess the efficacy and tolerability of diuretic-free antihypertensive therapy with a calcium antagonist and/or an angiotensin converting enzyme (ACE) inhibitor in patients with diabetes mellitus. 54 hypertensive [blood pressure (BP) above 140/90mm Hg] patients with diabetes mellitus type 1 (n = 7) or 2 (n = 47) and normal serum creatinine levels (mean 82 +/- 6 mumol/L) received either verapamil or enalapril after a 2-week washout and a 4-week placebo phase. If BP remained elevated, both agents were combined. Verapamil or enalapril alone normalised diastolic BP (to less than 90mm Hg) in 36 patients; verapamil decreased BP from 159/98 to 147/87mm Hg (n = 19, p < 0.001) and enalapril decreased BP from 166/99 to 146/88mm Hg (n = 17, p < 0.001). In 18 patients who remained hypertensive after 10 weeks of monotherapy, a combination of both drugs decreased BP from 169/104 to 151/90mm Hg (p < 0.001). Overall, 87% of patients achieved a target BP response at 30 weeks. Urinary albumin as related to creatinine excretion (UAE; micrograms albumin:mg creatinine) was on average not significantly changed after verapamil or enalapril treatment, alone or combined. Nevertheless, in patients with initial microalbuminuria, UAE decreased (p < 0.05) during enalapril treatment. Serum potassium, total lipids, high density lipoprotein cholesterol, low density lipoprotein cholesterol, glycosylated haemoglobin, serum C peptide and fructosamine levels were not significantly modified by treatment. Subjective tolerability of the drugs was also generally good. Thus, in hypertensive patients with diabetes, a diuretic-free therapy based on the calcium antagonist verapamil or the ACE inhibitor enalapril, alone or combined, can effectively decrease BP without adversely affecting carbohydrate and lipid metabolism.
本研究的目的是评估在糖尿病患者中使用钙拮抗剂和/或血管紧张素转换酶(ACE)抑制剂进行无利尿剂降压治疗的疗效和耐受性。54例高血压[血压(BP)高于140/90mmHg]的1型糖尿病患者(n = 7)或2型糖尿病患者(n = 47),血清肌酐水平正常(平均82±6μmol/L),在经过2周的洗脱期和4周的安慰剂阶段后,接受维拉帕米或依那普利治疗。如果血压仍升高,则将两种药物联合使用。单独使用维拉帕米或依那普利使36例患者的舒张压恢复正常(降至90mmHg以下);维拉帕米使血压从159/98降至147/87mmHg(n = 19,p < 0.001),依那普利使血压从166/99降至146/88mmHg(n = 17,p < 0.001)。在单药治疗10周后仍为高血压的18例患者中,两种药物联合使用使血压从169/104降至151/90mmHg(p < 0.001)。总体而言,87%的患者在30周时达到了目标血压反应。单独或联合使用维拉帕米或依那普利治疗后,尿白蛋白与肌酐排泄量的比值(UAE;微克白蛋白:毫克肌酐)平均无显著变化。然而,在初始有微量白蛋白尿的患者中,依那普利治疗期间UAE降低(p < 0.05)。治疗后血清钾、总脂质、高密度脂蛋白胆固醇、低密度脂蛋白胆固醇、糖化血红蛋白、血清C肽和果糖胺水平无显著改变。药物的主观耐受性总体也良好。因此,在糖尿病高血压患者中,基于钙拮抗剂维拉帕米或ACE抑制剂依那普利的无利尿剂治疗,单独或联合使用,可有效降低血压,而不会对碳水化合物和脂质代谢产生不利影响。