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中等强度他汀类药物对冠心病患者颈动脉斑块内新生血管的影响:一项回顾性队列研究

Effect of moderate-intensity statin on carotid intraplaque neovascularization of coronary artery disease: a retrospective cohort study.

作者信息

Han Yanyan, Ren Ling, Fei Xiang, Wang Jingjing, Chen Tao, Guo Jun, Wang Qi

机构信息

Department of Cardiology, Sixth Medical Center of Chinese PLA General Hospital, Beijing, China.

Department of Ultrasound, First Medical Center of Chinese PLA General Hospital, Beijing, China.

出版信息

Quant Imaging Med Surg. 2024 Feb 1;14(2):1660-1672. doi: 10.21037/qims-23-1104. Epub 2024 Jan 23.

Abstract

BACKGROUND

Statin treatment can reduce atherosclerotic plaque as detected via invasive intracoronary methods. However, few studies have evaluated the effect of moderate-intensity statin therapy on carotid intraplaque neovascularization (IPN) using semiquantitative indices. This study thus aimed to assess the effect of statin on the carotid IPN of coronary artery disease with contrast-enhanced ultrasound (CEUS).

METHODS

In this noncontrol, retrospective, cohort study, 35 inpatients who underwent coronary angiography, serial CEUS, and laboratory evaluations were consecutively enrolled from June 2020 to December 2022 at the Department of Cardiology, Chinese PLA General Hospital. All patients were administered moderate-intensity statin during serial CEUS, and continuous and categorical assessment of IPN and maximum plaque height (MPH) of carotid plaque was performed. Patients with a target low-density lipoprotein cholesterol (LDL-C) <1.8 mmol/L at 12-month follow-up were compared with those who did not reach the LDL-C 1.8 mmol/L target.

RESULTS

From baseline to 12-month follow-up, there were significant differences in the LDL-C levels between patients (2.71±1.29 1.35±0.83 mmol/L), those with 12-month follow-up LDL-C <1.8 mmol/L (2.58±1.24 1.08±0.52 mmol/L), and those with 12-month follow-up LDL-C ≥1.8 mmol/L (3.24±1.44 2.56±0.85 mmol/L) all P values <0.05, with decreases of 41%, 49%, and 11% from baseline, respectively. The mean MPH (12 months to baseline) decreased from 2.47±0.63 to 2.22±0.60 mm (P<0.05), and the IPN also decreased from 1.15±0.62 to 0.58±0.56, representing a reduction of 0.57±0.59 from baseline (P<0.001). In the LDL-C <1.8 mmol/L patients, there were significant differences between baseline and 12 months in MPH (2.37±0.56 2.03±0.52 mm; P<0.05) and IPN (1.32±0.77 0.54±0.63; P<0.05) compared with those with a follow-up LDL-C ≥1.8 mmol/L. Patients with a follow-up LDL-C <1.8 mmol/L, compared with those with a follow-up LDL-C ≥1.8 mmol/L, showed a significantly greater reduction in MPH (-0.34±0.46 -0.13±0.39; P<0.05) and IPN (-0.79±0.63 -0.57±0.79; P<0.05). Additionally, patients with carotid IPN regression showed a higher percent change in LDL-C compared with those without carotid IPN regression (-53.31±23.20 -29.55±19.47; P<0.05).

CONCLUSIONS

Controlling the LDL-C to <1.8 mmol/L under moderate-intensity statin can stabilize and reduce carotid IPN as detected by the semiquantitative noninvasive CEUS.

摘要

背景

他汀类药物治疗可通过侵入性冠状动脉方法检测到动脉粥样硬化斑块减少。然而,很少有研究使用半定量指标评估中等强度他汀类药物治疗对颈动脉斑块内新生血管形成(IPN)的影响。因此,本研究旨在通过对比增强超声(CEUS)评估他汀类药物对冠心病患者颈动脉IPN的影响。

方法

在这项非对照、回顾性队列研究中,2020年6月至2022年12月在中国人民解放军总医院心内科连续纳入35例接受冠状动脉造影、系列CEUS和实验室评估的住院患者。所有患者在系列CEUS期间接受中等强度他汀类药物治疗,并对颈动脉斑块的IPN和最大斑块高度(MPH)进行连续和分类评估。将12个月随访时目标低密度脂蛋白胆固醇(LDL-C)<1.8 mmol/L的患者与未达到LDL-C 1.8 mmol/L目标的患者进行比较。

结果

从基线到12个月随访,患者的LDL-C水平存在显著差异(2.71±1.29对1.35±0.83 mmol/L),12个月随访时LDL-C<1.8 mmol/L的患者(2.58±1.24对1.08±0.52 mmol/L)和LDL-C≥1.8 mmol/L的患者(3.24±1.44对2.56±0.85 mmol/L),所有P值<0.05,分别较基线下降4l%、49%和11%。平均MPH(12个月与基线相比)从2.47±0.63降至2.22±0.60 mm(P<0.05),IPN也从1.15±0.62降至0.58±0.56,较基线减少0.57±0.59(P<0.001)。在LDL-C<1.8 mmol/L的患者中,与随访LDL-C≥1.8 mmol/L的患者相比,基线和12个月时MPH(2.37±0.56对2.03±0.52 mm;P<0.05)和IPN(1.32±0.77对0.54±0.63;P<0.05)存在显著差异。随访LDL-C<1.8 mmol/L的患者与随访LDL-C≥1.8 mmol/L的患者相比,MPH(-0.34±0.46对-0.13±0.39;P<0.05)和IPN(-0.79±0.63对-0.57±0.79;P<0.05)的降低幅度显著更大。此外,与无颈动脉IPN消退的患者相比,有颈动脉IPN消退的患者LDL-C的百分比变化更高(-53.31±23.20对-29.55±19.47;P<0.05)。

结论

在中等强度他汀类药物治疗下将LDL-C控制在<1.8 mmol/L可稳定并减少通过半定量无创CEUS检测到的颈动脉IPN。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0828/10895147/9d64cc5c6eeb/qims-14-02-1660-f1.jpg

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