Papadakis J A, Ganotakis E S, Jagroop I A, Mikhailidis D P, Winder A F
Department of Chemical Pathology and Human Metabolism, Royal Free Hospital & School of Medicine, University of London, England.
Am J Hypertens. 1999 Jul;12(7):673-81. doi: 10.1016/s0895-7061(99)00049-7.
We measured the serum lipid profile, together with plasma fibrinogen and serum lipoprotein(a) (Lp[a]), glucose, bilirubin, and albumin levels in 491 patients (310 men) who were referred for the management of primary dyslipidemia. All these variables have been shown to predict vascular events. The patients were not taking lipid-lowering drugs; hypertension was present in 156 (31.7%) of them. Of the hypertensive patients, 52 (33%) were not receiving any treatment to control their blood pressure. This omission was not due to a lower prevalence of established vascular disease. The treated hypertensives were divided into three groups according to their treatment: 62 were taking lipid-hostile antihypertensives (beta-blockers, thiazides), 37 were taking lipid-neutral antihypertensives (angiotensin converting enzyme inhibitors, Ca-channel blockers, angiotensin II receptor blockers, indapamide sustained release), and five were taking lipid-friendly antihypertensives (doxazosin). Lipid-hostile antihypertensive drugs were associated with a significantly higher fibrinogen concentration when compared with untreated hypertensives or those taking lipid-neutral/lipid-friendly drugs (median values: 383, 353, and 336 mg/dL, respectively; P < .01). Lipid-neutral/lipid-friendly antihypertensive drugs were associated with lower Lp(a) levels when compared with untreated hypertensives (median values: 22 and 45 mg/dL, respectively; P < .05). The serum bilirubin level was significantly lower in the untreated hypertensives when compared with normotensives or the treated hypertensives. There were no significant differences in lipids, glucose, or albumin among the groups of hypertensives or normotensives. The influence of antihypertensive drugs on additional cardiovascular risk factors should be considered when selecting medication to reduce blood pressure.
我们测量了491例因原发性血脂异常前来就诊的患者(310名男性)的血清脂质谱、血浆纤维蛋白原和血清脂蛋白(a) [Lp(a)]、血糖、胆红素及白蛋白水平。所有这些变量均已被证明可预测血管事件。这些患者未服用降脂药物;其中156例(31.7%)患有高血压。在高血压患者中,52例(33%)未接受任何控制血压的治疗。这种遗漏并非由于已确诊血管疾病的患病率较低。接受治疗的高血压患者根据其治疗情况分为三组:62例服用对脂质有不良影响的降压药(β受体阻滞剂、噻嗪类),37例服用对脂质无影响的降压药(血管紧张素转换酶抑制剂、钙通道阻滞剂、血管紧张素II受体阻滞剂、吲达帕胺缓释剂),5例服用对脂质有益的降压药(多沙唑嗪)。与未治疗的高血压患者或服用对脂质无影响/有益药物的患者相比,对脂质有不良影响的降压药与纤维蛋白原浓度显著升高相关(中位数分别为:383、353和336 mg/dL;P <.01)。与未治疗的高血压患者相比,对脂质无影响/有益的降压药与较低的Lp(a)水平相关(中位数分别为:22和45 mg/dL;P <.05)。与血压正常者或接受治疗的高血压患者相比,未治疗的高血压患者血清胆红素水平显著较低。高血压组和血压正常组之间在血脂、血糖或白蛋白方面无显著差异。在选择降压药物时,应考虑降压药物对其他心血管危险因素的影响。