利用高分辨率血管壁成像技术研究颅内动脉粥样硬化斑块重塑与糖尿病之间的关系。

IF 4.2 3区 医学 Q1 ENDOCRINOLOGY & METABOLISM World Journal of Diabetes Pub Date : 2024-01-15 DOI:10.4239/wjd.v15.i1.72
Yong-Qian Mo, Hai-Yu Luo, Han-Wen Zhang, Yu-Feng Liu, Kan Deng, Xiao-Lei Liu, Biao Huang, Fan Lin
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引用次数: 0

摘要

背景:颅内动脉粥样硬化是导致中风的主要原因之一,涉及动脉斑块的形成。目的:使用高分辨率血管壁成像(HR-VWI)研究颅内动脉粥样硬化重塑模式的因素以及颅内动脉粥样硬化重塑与糖尿病之间的关系:方法: 选取了94名确诊为大脑中动脉或基底动脉粥样硬化的患者。收集了他们的基本临床数据,并进行了 HR-VWI 分析。使用图像后处理软件划定并测量斑块处血管面积(VAMLN)和正常参考血管面积(VAreference),并计算重塑指数(RI)。根据 RI 值,将患者分为阳性重塑(PR)组、中间重塑(IR)组、阴性重塑(NR)组、PR 组和非 PR(N-PR)组:PR组的糖尿病发病率和血清胆固醇水平高于IR组和NR组[分别为45.2%,4.54 (4.16, 5.93) vs 25%,4.80 ± 1.22和16.4%,4.14 (3.53, 4.75),P < 0.05]。PR 组的糖尿病发病率也明显高于 N-PR 组(45.2% vs 17.5%,P < 0.05)。此外,与 N-PR 组相比,PR 组的血清甘油三酯和胆固醇水平升高 [1.64 (1.23, 2.33) 和 4.54 (4.16, 5.93) vs 4.54 (4.16, 5.93) 和 4.24 (3.53, 4.89),P < 0.05]。逻辑回归分析显示,糖尿病是斑块-PR 的独立影响因素[几率比(95% 置信区间):3.718(1.207-11.454),P <0.05]:HR-VWI可清晰显示颅内血管壁和斑块的形态和信号特征。糖尿病患者的颅内动脉粥样硬化斑块更容易出现 PR,这表明斑块的稳定性较差,发生脑卒中的风险更大。
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Investigating the relationship between intracranial atherosclerotic plaque remodelling and diabetes using high-resolution vessel wall imaging.

Background: Intracranial atherosclerosis, a leading cause of stroke, involves arterial plaque formation. This study explores the link between plaque remodelling patterns and diabetes using high-resolution vessel wall imaging (HR-VWI).

Aim: To investigate the factors of intracranial atherosclerotic remodelling patterns and the relationship between intracranial atherosclerotic remodelling and diabetes mellitus using HR-VWI.

Methods: Ninety-four patients diagnosed with middle cerebral artery or basilar artery atherosclerosis were enrolled. Their basic clinical data were collected, and HR-VWI was performed. The vascular area at the plaque (VAMLN) and normal reference vessel (VAreference) were delineated and measured using image postprocessing software, and the Remodelling index (RI) was calculated. According to the value of the RI, the patients were divided into a positive remodelling (PR) group, intermediate remodelling (IR) group, negative remodelling (NR) group, PR group and non-PR (N-PR) group.

Results: The PR group exhibited a higher prevalence of diabetes and serum cholesterol levels than the IR and NR groups [45.2%, 4.54 (4.16, 5.93) vs 25%, 4.80 ± 1.22 and 16.4%, 4.14 (3.53, 4.75), respectively, P < 0.05]. The diabetes incidence was also significantly greater in the PR group than in the N-PR group (45.2% vs 17.5%, P < 0.05). Furthermore, the PR group displayed elevated serum triglyceride and cholesterol levels compared to the N-PR group [1.64 (1.23, 2.33) and 4.54 (4.16, 5.93) vs 4.54 (4.16, 5.93) and 4.24 (3.53, 4.89), P < 0.05]. Logistic regression analysis revealed diabetes mellitus as an independent influencing factor in plaque-PR [odds ratio (95% confidence interval): 3.718 (1.207-11.454), P < 0.05].

Conclusion: HR-VWI can clearly show the morphology and signal characteristics of intracranial vascular walls and plaques. Intracranial atherosclerotic plaques in diabetic patients are more likely to show PR, suggesting poor plaque stability and a greater risk of stroke.

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来源期刊
World Journal of Diabetes
World Journal of Diabetes ENDOCRINOLOGY & METABOLISM-
自引率
2.40%
发文量
909
期刊介绍: The WJD is a high-quality, peer reviewed, open-access journal. The primary task of WJD is to rapidly publish high-quality original articles, reviews, editorials, and case reports in the field of diabetes. In order to promote productive academic communication, the peer review process for the WJD is transparent; to this end, all published manuscripts are accompanied by the anonymized reviewers’ comments as well as the authors’ responses. The primary aims of the WJD are to improve diagnostic, therapeutic and preventive modalities and the skills of clinicians and to guide clinical practice in diabetes. Scope: Diabetes Complications, Experimental Diabetes Mellitus, Type 1 Diabetes Mellitus, Type 2 Diabetes Mellitus, Diabetes, Gestational, Diabetic Angiopathies, Diabetic Cardiomyopathies, Diabetic Coma, Diabetic Ketoacidosis, Diabetic Nephropathies, Diabetic Neuropathies, Donohue Syndrome, Fetal Macrosomia, and Prediabetic State.
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