Baik Minyoul, Nam Hyo Suk, Heo Ji Hoe, Lee Hye Sun, Kim Young Dae
Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea; Department of Neurology, Yongin Severance Hospital, Yonsei University College of Medicine, Yongin-si, Gyeonggi-do, South Korea.
Department of Neurology, Yonsei University College of Medicine, Seoul, South Korea; Integrative Research Center for Cerebrovascular and Cardiovascular Diseases, Seoul, South Korea.
Atherosclerosis. 2023 Apr;371:14-20. doi: 10.1016/j.atherosclerosis.2023.03.014. Epub 2023 Mar 20.
To reduce cardiovascular risk, low-density lipoprotein cholesterol (LDL-C) is the primary target of statin treatment, while apolipoprotein B (ApoB) is secondary. We investigated the association between atherosclerotic stenosis and LDL-C or ApoB levels and whether a difference in association exists according to pre-admission statin use in ischemic stroke patients.
This retrospective cross-sectional study included consecutive patients with acute ischemic stroke or transient ischemic attack who underwent lipid profile and angiographic testing. Patients were categorized into four groups according to stenosis location: normal, extracranial atherosclerotic stenosis (ECAS), intracranial atherosclerotic stenosis (ICAS), or ECAS + ICAS. Subgroup analyses were performed by pre-admission statin use.
Of the 6338 patients included, 1980 (31.2%) were in the normal group, 718 (11.3%) in the ECAS group, 1845 (29.1%) in the ICAS group, and 1795 (28.3%) in the ECAS + ICAS group. Both LDL-C and ApoB levels were associated with every location of stenosis. A significant interaction was found between pre-admission statin use and LDL-C level (p for interaction <0.05). LDL-C was associated with stenosis only in statin-naïve patients, whereas ApoB was associated with ICAS, with or without ECAS, in both statin-naïve and statin-treated patients. ApoB also showed a consistent association with symptomatic ICAS in both statin-treated and statin-naïve patients, whereas LDL-C did not.
ApoB was consistently associated with ICAS, particularly symptomatic stenosis, in both statin-naïve and statin-treated patients. The close association between ApoB levels and residual risk in statin-treated patients could be partially explained by these results.
为降低心血管风险,低密度脂蛋白胆固醇(LDL-C)是他汀类药物治疗的主要靶点,而载脂蛋白B(ApoB)是次要靶点。我们研究了缺血性脑卒中患者动脉粥样硬化狭窄与LDL-C或ApoB水平之间的关联,以及根据入院前他汀类药物使用情况,这种关联是否存在差异。
这项回顾性横断面研究纳入了连续的急性缺血性脑卒中或短暂性脑缺血发作患者,这些患者接受了血脂检测和血管造影检查。根据狭窄部位,患者被分为四组:正常组、颅外动脉粥样硬化狭窄(ECAS)组、颅内动脉粥样硬化狭窄(ICAS)组或ECAS + ICAS组。根据入院前他汀类药物使用情况进行亚组分析。
纳入的6338例患者中,正常组1980例(31.2%),ECAS组718例(11.3%),ICAS组1845例(29.1%),ECAS + ICAS组1795例(28.3%)。LDL-C和ApoB水平与各狭窄部位均相关。发现入院前他汀类药物使用与LDL-C水平之间存在显著交互作用(交互作用p<0.05)。LDL-C仅与未使用他汀类药物的患者的狭窄相关,而ApoB在未使用他汀类药物和使用他汀类药物的患者中均与ICAS相关,无论是否合并ECAS。ApoB在使用他汀类药物和未使用他汀类药物的患者中也均与有症状的ICAS存在一致的关联,而LDL-C则不然。
在未使用他汀类药物和使用他汀类药物的患者中,ApoB均与ICAS,尤其是有症状的狭窄持续相关。这些结果可以部分解释ApoB水平与使用他汀类药物患者的残余风险之间的密切关联。