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低至中等剂量的他汀类药物与传统药物治疗相结合可改善急性缺血性中风的功能预后。

Low-to-moderate dose statins improve the functional outcome of acute ischemic stroke with conventional medication treatment.

作者信息

Bao Jiajia, Zhang Yang, Li Yanbo, Guo Jian, He Li

机构信息

Department of Neurology, West China Hospital, Sichuan University, Chengdu, China.

出版信息

Cardiovasc Diagn Ther. 2023 Aug 31;13(4):686-699. doi: 10.21037/cdt-23-77. Epub 2023 Jul 13.

Abstract

BACKGROUND

Low-to-moderate dose statins (LMDSs) are more commonly used among Asian acute ischemic stroke (AIS) patients in clinical practice. However, the correlation between the LMDS use and prognosis has not been evaluated in AIS patients with conventional medication treatment alone. This study aimed to investigate the influence of LMDS on the prognosis of AIS patients and how prognosis and potential prognostic factors interact with different statin doses.

METHODS

This retrospective cohort study included AIS patients who were admitted within 7 days after symptom onset and received conventional medication treatment alone from November 2019 to November 2020 in the Neurology, Department of West China Hospital, Sichuan University. From a total of 782 initial patients, a final cohort of 327 patients was included in the study. These patients were divided into three groups based on statin doses: non-statin (48 patients), LMDS (152 patients), and high-dose statin (HDS) (127 patients). The follow-up period was 3 months after the onset of stroke and the primary outcome was defined as a modified Rankin scale (mRS) score of 0 to 2 at 3 months, secondary outcomes were hemorrhagic transformation (HT) and death within 3 months. Stratified analysis was also conducted to test the robustness of the relationship between the use of different statin doses and functional outcomes in various subgroups.

RESULTS

Compared with non-statin therapy, both LMDS therapy and HDS therapy were associated with good functional outcomes [odds ratio (OR) =3.68, 95% confidence interval (CI): 1.13-12.01, P=0.0309; OR =3.45, 95% CI: 1.06-11.26, P=0.0402, respectively] and a lower risk of HT (OR =0.30, 95% CI: 0.11-0.86, P=0.0253; OR =0.36, 95% CI: 0.13-0.99, P=0.0488, respectively). However, there was no significant difference in all-cause death within 3 months among the three groups (OR =0.84, 95% CI: 0.29-2.46, P=0.7468; OR =0.76, 95% CI: 0.26-2.22, P=0.6104). Additionally, no significant differences were observed between LMDS therapy and HDS therapy regarding good functional outcomes at 3 months (OR =0.94, 95% CI: 0.50-1.77, P=0.8411) and the occurrence of HT (OR =1.19, 95% CI: 0.47-3.02, P=0.7093). The results of the relationship between different statin doses and 3-month good functional outcome were consistent after interaction tests.

CONCLUSIONS

Our findings provide evidence for the benefit and safety of LMDS therapy in AIS patients with medication treatment alone. LMDS therapy is associated with favorable impacts on 3-month functional outcomes and a reduced risk of HT compared to non-statin therapy. There were no significant differences in achieving 3-month good functional outcome, the risk of HT or death within 3 months were observed between LMDS and HDS therapy in our study. Further studies with prospective design and larger sample sizes are necessary to validate our results.

摘要

背景

在临床实践中,低至中等剂量他汀类药物(LMDSs)在亚洲急性缺血性卒中(AIS)患者中使用更为普遍。然而,仅接受常规药物治疗的AIS患者中,LMDS使用与预后之间的相关性尚未得到评估。本研究旨在探讨LMDS对AIS患者预后的影响,以及预后和潜在预后因素如何与不同他汀类药物剂量相互作用。

方法

这项回顾性队列研究纳入了2019年11月至2020年11月在四川大学华西医院神经内科症状发作后7天内入院且仅接受常规药物治疗的AIS患者。在总共782例初始患者中,最终有327例患者纳入研究。这些患者根据他汀类药物剂量分为三组:非他汀组(48例患者)、LMDS组(152例患者)和高剂量他汀组(HDS组,127例患者)。随访期为卒中发作后3个月,主要结局定义为3个月时改良Rankin量表(mRS)评分为0至2分,次要结局为3个月内出血转化(HT)和死亡。还进行了分层分析,以检验不同他汀类药物剂量使用与各亚组功能结局之间关系的稳健性。

结果

与非他汀治疗相比,LMDS治疗和HDS治疗均与良好的功能结局相关[优势比(OR)=3.68,95%置信区间(CI):1.13 - 12.01,P = 0.0309;OR = 3.45,95% CI:1.06 - 11.26,P = 0.0402],且HT风险较低(OR = 0.30,95% CI:0.11 - 0.86,P = 0.0253;OR = 0.36,95% CI:0.13 - 0.99,P = 0.0488)。然而,三组3个月内全因死亡无显著差异(OR = 0.84,95% CI:0.29 - 2.46,P = 0.7468;OR = 0.76,95% CI:0.26 - 2.22,P = 0.6104)。此外,在3个月时良好功能结局方面(OR = 0.94,95% CI:0.50 - 1.77,P = 0.8411)以及HT发生方面(OR = 1.19,95% CI:0.47 - 3.02,P = 0.7093),LMDS治疗与HDS治疗之间未观察到显著差异。交互检验后,不同他汀类药物剂量与3个月良好功能结局之间关系的结果一致。

结论

我们的研究结果为仅接受药物治疗的AIS患者中LMDS治疗的益处和安全性提供了证据。与非他汀治疗相比,LMDS治疗对3个月功能结局有有利影响,且HT风险降低。在我们的研究中,LMDS治疗与HDS治疗在实现3个月良好功能结局、HT风险或3个月内死亡方面未观察到显著差异。需要进一步进行前瞻性设计和更大样本量的研究来验证我们的结果。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c493/10478016/ebef00db02c1/cdt-13-04-686-f1.jpg

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