Department of Cardiovascular Medicine, Shiga University of Medical Science, Seta tsukinowa-cho, Otsu, Shiga, 520-2192, Japan.
Department of Cardiovascular Medicine, Koto Memorial Hospital, Higashiomi, Japan.
Heart Vessels. 2022 Nov;37(11):1817-1828. doi: 10.1007/s00380-022-02104-0. Epub 2022 Jun 20.
Clinical evidence demonstrating the impact of statins for preventing late target lesion revascularization (TLR) after newer-generation drug-eluting stent implantation and differences in the effect of statins on late TLR according to pre-interventional vessel remodeling and vessel size is limited. We retrospectively evaluated 1193 de novo lesions in 720 patients who underwent everolimus-eluting stent implantation using intravascular ultrasound from January 2010 to December 2012. The primary endpoint was late TLR. Lesions were divided into the statin group (n = 825) and non-statin group (n = 368). The incidence of late TLR was significantly lower in the statin than non-statin group (1.7% vs. 5.2%, respectively; p = 0.001), and within the statin group, it was significantly lower in the follow-up low-density lipoprotein cholesterol (LDL-C) < 100 than ≥ 100 mg/dL level subgroup (1.0% vs. 3.6%, respectively; p = 0.006). Furthermore, in positive remodeling lesions and non-small vessel size lesions, the incidence of late TLR was significantly lower in the statin than non-statin group (1.6% vs. 8.5% and 1.3% vs. 5.3%, respectively; p = 0.001 and p = 0.004). Lowering the LDL-C level using statins was more effective for preventing late TLR after everolimus-eluting stent implantation. Evaluating pre-interventional vessel remodeling patterns and vessel size might be helpful to stratify lesions at high risk of late TLR.
临床证据表明,他汀类药物可预防新一代药物洗脱支架植入后晚期靶病变血运重建(TLR),并且他汀类药物对晚期 TLR 的影响因预介入血管重构和血管大小的不同而不同。我们回顾性分析了 2010 年 1 月至 2012 年 12 月期间 720 例患者接受依维莫司洗脱支架植入术的 1193 例初发病变患者的血管内超声资料。主要终点为晚期 TLR。将病变分为他汀组(n=825)和非他汀组(n=368)。他汀组的晚期 TLR 发生率明显低于非他汀组(分别为 1.7%和 5.2%;p=0.001),且在他汀组中,随访时 LDL-C<100mg/dL 水平亚组的晚期 TLR 发生率明显低于 LDL-C≥100mg/dL 水平亚组(分别为 1.0%和 3.6%;p=0.006)。此外,在正性重构病变和非小血管病变中,他汀组的晚期 TLR 发生率明显低于非他汀组(分别为 1.6%和 8.5%和 1.3%和 5.3%;p=0.001 和 p=0.004)。使用他汀类药物降低 LDL-C 水平对预防依维莫司洗脱支架植入后晚期 TLR 更为有效。评估预介入血管重构模式和血管大小可能有助于对晚期 TLR 高危病变进行分层。