Gazzaruso C, Buscaglia P, Garzaniti A, Falcone C, Mariotti S, Savino S, Bonetti G, Finardi G, Geroldi D
Department of Internal Medicine and Medical Therapeutics, IRCCS Policlinico San Matteo, University of Pavia, Italy.
J Hypertens. 1997 Mar;15(3):227-35. doi: 10.1097/00004872-199715030-00003.
Besides hypertension, several cardiovascular risk factors can play a role in the development of coronary heart disease (CHD) in hypertensive patients. Lipoprotein(a) [Lp(a)] is an important and independent cardiovascular risk factor, but its role in the development of CHD in hypertensives has not been studied.
To investigate whether or not Lp(a) levels and isoforms of apolipoprotein(a) [apo(a)] are predictors of CHD in patients with essential hypertension.
Lp(a) levels and apo(a) polymorphism were evaluated in 249 patients with essential hypertension, in 142 non-hypertensive patients with CHD and in 264 healthy controls.
Hypertensives with CHD (n = 61) had Lp(a) levels [19 (range 0.5-73.5) versus 7 mg/dl (range 0-83.5), P < 0.001] and a percentage of apo(a) isoforms of low (< 655 kDa) relative molecular mass (RMM, 59.2 versus 25.9%, P < 0.001) higher than did those without CHD (n = 188). Moreover, there were more subjects with at least one apo(a) isoform of low RMM in the subgroup of patients with CHD than there were in that of those without CHD (80.3 versus 30.8%, P< 0.001). Lp(a) levels and apo(a) polymorphism did not differ significantly between hypertensive and non-hypertensive patients with CHD. Stepwise regression analysis indicated that high Lp(a) levels (P= 0.002073) and particularly the presence of at least one apo(a) isoform of low RMM (P < 0.000001) are strong predictors of CHD in hypertensive patients.
Our data show that high Lp(a) levels and the presence of at least one apo(a) isoform of low RMM are strong and independent genetic risk factors for CHD in hypertensive patients. These findings suggest that Lp(a) and apo(a) isoforms should be assessed together with other cardiovascular risk factors to establish the overall CHD risk status of each hypertensive patient
除高血压外,多种心血管危险因素可在高血压患者冠心病(CHD)的发生中起作用。脂蛋白(a)[Lp(a)]是一种重要的独立心血管危险因素,但其在高血压患者冠心病发生中的作用尚未得到研究。
研究Lp(a)水平和载脂蛋白(a)[apo(a)]异构体是否为原发性高血压患者冠心病的预测指标。
对249例原发性高血压患者、142例非高血压冠心病患者和264例健康对照者进行Lp(a)水平和apo(a)多态性评估。
患有冠心病的高血压患者(n = 61)的Lp(a)水平[19(范围0.5 - 73.5)对7mg/dl(范围0 - 83.5),P < 0.001]以及相对分子质量(RMM)低(< 655kDa)的apo(a)异构体百分比(59.2对25.9%,P < 0.001)高于未患冠心病的患者(n = 188)。此外,冠心病患者亚组中至少有一种低RMM的apo(a)异构体的受试者比未患冠心病的患者亚组更多(80.3对30.8%,P < 0.001)。高血压和非高血压冠心病患者之间的Lp(a)水平和apo(a)多态性无显著差异。逐步回归分析表明,高Lp(a)水平(P = 0.002073),尤其是至少有一种低RMM的apo(a)异构体的存在(P < 0.000001)是高血压患者冠心病的强预测指标。
我们的数据表明,高Lp(a)水平和至少一种低RMM的apo(a)异构体的存在是高血压患者冠心病的强且独立的遗传危险因素。这些发现表明,应将Lp(a)和apo(a)异构体与其他心血管危险因素一起评估,以确定每位高血压患者的整体冠心病风险状况。