Antonini-Canterin Francesco, Popescu Bogdan A, Huang Guoqian, Korcova-Miertusova Renata, Rivaben Dante, Faggiano Pompilio, Pavan Daniela, Piazza Rita, Bolis Angiola, Ciavattone Antonio, Ruggiero Alberto, Nicolosi Gian Luigi
S Maria degli Angeli Hospital, Pordenone, Italy.
Ital Heart J. 2005 Feb;6(2):119-24.
It has recently been suggested that statins could slow the progression of aortic stenosis, but this hypothesis has not been validated in large series. Moreover, there is little information about the role of statin treatment in patients with aortic valve sclerosis.
From our database 1988--2002, we retrospectively identified 1136 consecutive patients with aortic valve sclerosis (peak aortic velocity [Vmax] > 1.5 and < 2 m/s), or mild to moderate aortic stenosis (Vmax 2.0-3.9 m/s) and with > or = 2 echocardiographic studies > or = 6 months apart; 121 (11 %) were treated with statins. As a control group we randomly selected 121 age-gender-matched patients not treated with statins, with similar initial Vmax.
The mean follow-up duration was 54+/-34 months in the statin group, and 50+/-33 months in controls (p = 0.35). There were no differences between statin-treated patients and controls with respect to age, gender, and prevalence of hypertension. More patients in the statin group had documented hypercholesterolemia, diabetes, or had proven coronary artery disease. Overall, the rate of change of Vmax was not different between statin-treated patients and controls (0.13+/-0.24 vs 0.14+/-0.19 m/s/year, p = 0.72). However, in the subgroup of patients with aortic valve sclerosis (n = 52, 26 statin-treated, 26 controls), the rate of change of Vmax was significantly lower in statin-treated patients (0.04+/-0.04 vs 0.08+/-0.06 m/s/year, p = 0.007).
The results of our retrospective study show that statins could be beneficial in retarding the progression of valvular aortic sclerosis to aortic stenosis. This suggests that statins retard the progression of aortic valve lesion in its early stage, a finding that may have important implications in the management of this very common disease.
最近有人提出他汀类药物可能减缓主动脉瓣狭窄的进展,但这一假说尚未在大量病例中得到验证。此外,关于他汀类药物治疗在主动脉瓣硬化患者中的作用,几乎没有相关信息。
从我们1988年至2002年的数据库中,我们回顾性地确定了1136例连续的主动脉瓣硬化患者(主动脉峰值流速[Vmax]>1.5且<2m/s)或轻度至中度主动脉瓣狭窄患者(Vmax 2.0 - 3.9m/s),且有≥2次间隔≥6个月的超声心动图检查;其中121例(11%)接受了他汀类药物治疗。作为对照组,我们随机选择了121例年龄和性别匹配且未接受他汀类药物治疗、初始Vmax相似的患者。
他汀类药物治疗组的平均随访时间为54±34个月,对照组为50±33个月(p = 0.35)。在年龄、性别和高血压患病率方面,接受他汀类药物治疗的患者与对照组之间没有差异。他汀类药物治疗组中有更多患者记录有高胆固醇血症、糖尿病或已证实患有冠状动脉疾病。总体而言,接受他汀类药物治疗的患者与对照组之间Vmax的变化率没有差异(0.13±0.24对0.14±0.19m/s/年,p = 0.72)。然而,在主动脉瓣硬化患者亚组(n = 52,26例接受他汀类药物治疗,26例为对照)中,接受他汀类药物治疗的患者Vmax的变化率显著更低(0.04±0.04对0.08±0.06m/s/年,p = 0.007)。
我们的回顾性研究结果表明,他汀类药物可能有助于延缓瓣膜性主动脉硬化进展为主动脉瓣狭窄。这表明他汀类药物在主动脉瓣病变的早期阶段可延缓其进展,这一发现可能对这种非常常见疾病的管理具有重要意义。