颈动脉斑块在磁共振血管造影和血管壁成像上有无易损特征的蛋白质组学分析:一项初步研究

Q3 Medicine
Benjamin J. Madden BSc , Camilo Polania-Sandoval MD , Ganesh P. Pujari MD , Kiran K. Mangalaparthi PhD , M. Cristine Charlesworth PhD, MS , Mercedes Prudencio PhD , Tania Gendron PhD , Sukhwinder J.S. Sandhu MD , Aziza Nassar MD, MPH , Leonard Petrucelli PhD , James F. Meschia MD , Akhilesh Pandey MD, PhD , Young Erben MD
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引用次数: 0

摘要

目的颅内外颈动脉病变占缺血性脑卒中的15% ~ 20%。磁共振血管造影(MRA)与血管壁成像(VWI)的进步使易损斑块的识别成为可能,有助于神经血管事件的风险分层。本初步研究旨在鉴定斑块中有无VWI MRA易损特征的蛋白质。方法将连续行颈动脉内膜切除术的患者纳入术前MRA和VWI的研究队列。回顾性图表分析提取相关临床资料,包括心血管危险因素和药物。蛋白质组学分析包括肽的串联质量标签(TMTpro)标记,碱性pH高效液相色谱分离和nanolc串联质谱分析。结果蛋白质组学分析显示,易损斑块中有23个蛋白显著升高,包括蛋白酶3 (PRTN3)、磷脂转移蛋白(PLTP)和S100钙结合蛋白A12 (S100A12),丰度增加超过2倍或以上(P <;措施)。相反,三种蛋白在易损斑块中表现出丰度降低,包括动力蛋白-3 (DNM3)、跨膜蛋白181 (TMEM181)和内收蛋白-3 (ADD3) (P <;. 05)。结论本研究有助于了解与颈动脉斑块易感性相关的蛋白质生物标志物,为疾病进展和卒中预防提供见解。易损斑块分泌的蛋白质不仅可能提供早期疾病识别的潜力;但也可以成为未来药物治疗的目标在一个毁灭性的神经事件之前。需要进一步的验证研究和多中心试验来确认这些潜在生物标志物的价值。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Proteomic analysis of carotid artery plaques with and without vulnerable features on magnetic resonance angiography with vessel wall imaging: a pilot study

Objective

Extracranial carotid artery pathology accounts for 15% to 20% of ischemic strokes. Advancements in magnetic resonance angiography (MRA) with vessel wall imaging (VWI) have enabled the identification of vulnerable plaques, aiding in risk stratification for neurovascular events. This pilot study aimed to identify proteins in plaques with and without vulnerable features on MRA with VWI.

Methods

Consecutive patients undergoing carotid endarterectomy were included in the study cohort with preoperative MRA with VWI. A retrospective chart review was conducted to extract pertinent clinical data including cardiovascular risk factors and medications. Proteomic analysis involved Tandem Mass Tag (TMTpro) labeling of peptides, basic pH high-performance liquid chromatography fractionation, and NanoLC-tandem mass spectrometry.

Results

Proteomic analysis revealed 23 proteins significantly elevated in vulnerable plaques, including Proteinase 3 (PRTN3), Phospholipid Transfer Protein (PLTP), and S100 Calcium-Binding Protein A12 (S100A12), with increased abundance exceeding two-fold changes or above (P < .001). Conversely, three proteins exhibited reduced abundance in vulnerable plaques including Dynamin-3 (DNM3), Transmembrane Protein 181 (TMEM181), and Adducin-3 (ADD3) (P < .05).

Conclusions

This study contributes to the understanding of protein biomarkers associated with carotid plaque vulnerability, offering insights into disease progression and stroke prevention. Proteins secreted by vulnerable plaques may offer not only the potential for early disease recognition; but can also become a target for future pharmacologic therapy prior to a devastating neurologic event. Further validation studies and multi-center trials will be needed to confirm the value of these potential biomarkers.
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CiteScore
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