Gao Jiang-Ping, Zhang Hong-Peng, Xiong Jiang, Jia Xin, Ma Xiao-Hui, Guo Wei
Department of Vascular Surgery, Chinese PLA General Hospital, Medical School of Chinese PLA, Beijing, China.
Department of Vascular Surgery, Chinese PLA General Hospital, Beijing, China.
J Endovasc Ther. 2025 Aug;32(4):893-901. doi: 10.1177/15266028231204807. Epub 2023 Oct 18.
To investigate the association between the imaging biomarker (volumetric perivascular characterization index [VPCI]) which indicates the aortic wall inflammation by mapping the spatial changes of perivascular fat attenuation on computed tomography angiography (CTA) and the reintervention risk for abdominal aortic aneurysm (AAA) patients after endovascular aortic repair (EVAR).
This case-control study included AAA patients undergoing EVAR from a single center (n=260). Cases were AAA patients undergoing reintervention after EVAR and a 1:1 frequency-matched control group of AAA patients post-EVAR with a shrunken or ≥3-year stable sac and free of reintervention signs during the follow-up. The predictive variable (VPCI trajectory) was converted to binary variables according to the changing trend of VPCI with follow-up time. As a quasi-complete separation data pattern, least absolute shrinkage and selection operator (lasso) regression was used to screen and prove the VPCI trajectory as the best predictor, and the performance was evaluated by calculating the accuracy, sensitivity, and specificity.
Between 2010 and 2021, 15 AAA patients after EVAR with type I/III endoleak, aneurysm rupture, or impending rupture were included. Compared with the 1:1 frequency-matched controls with a shrunken or ≥3-year stable sac and free of reintervention signs during the follow-up, VPCI trajectories of the case group were all upward trends, whereas the controls showed 86.7% downward trends (p<0.001). The best predictive model of lasso regressions included 4 variables, and VPCI trajectory was the most outstanding, followed by the proximal landing zone, the distal landing zone, and the infrarenal β angle. The accuracy, sensitivity, and specificity of predicting the risk of reintervention were as follows, respectively: 93.3%, 100%, and 86.7%.
The wall inflammation detected by imaging perivascular adipose tissue based on the CTAs was strongly associated with the reintervention risk for AAA patients after EVAR, which might hold major promise as a new imaging biomarker for the mechanism and treatment study of human AAAs before and after EVAR.Clinical ImpactThe study introduces a novel imaging biomarker which indicates the aortic wall inflammation by mapping spatial changes of perivascular fat attenuation on CTA. This biomarker demonstrates a strong association with the reintervention risk in AAA patients after EVAR. Incorporation of VPCI into clinical practice has the potential to enhance the traditional surveillance methods (CT/CTAs) by providing clinicians with a non-invasive method to assess aortic wall inflammation and predict the risk of reintervention. Additionally, this study might offer a valuable tool for mechanism and treatment research in humans with AAAs both pre- and post-EVAR, ultimately improving patient outcomes and refining therapeutic strategies.
通过在计算机断层血管造影(CTA)上描绘血管周围脂肪衰减的空间变化来研究指示主动脉壁炎症的成像生物标志物(体积血管周围特征指数 [VPCI])与腹主动脉瘤(AAA)患者接受血管腔内主动脉修复(EVAR)后再次干预风险之间的关联。
本病例对照研究纳入了来自单一中心的接受 EVAR 的 AAA 患者(n = 260)。病例为 EVAR 后接受再次干预的 AAA 患者,以及 1:1 频率匹配的 EVAR 后 AAA 患者对照组,其瘤腔缩小或稳定≥3 年且在随访期间无再次干预迹象。根据 VPCI 随随访时间的变化趋势将预测变量(VPCI 轨迹)转换为二元变量。作为一种准完全分离数据模式,使用最小绝对收缩和选择算子(lasso)回归来筛选并证明 VPCI 轨迹是最佳预测因子,并通过计算准确性、敏感性和特异性来评估其性能。
2010 年至 2021 年期间,纳入了 15 例 EVAR 后出现 I/III 型内漏、动脉瘤破裂或即将破裂的 AAA 患者。与随访期间瘤腔缩小或稳定≥3 年且无再次干预迹象的 1:1 频率匹配对照组相比,病例组的 VPCI 轨迹均呈上升趋势,而对照组有 86.7%呈下降趋势(p<0.001)。lasso 回归的最佳预测模型包括 4 个变量,VPCI 轨迹最为突出,其次是近端锚定区、远端锚定区和肾下β角。预测再次干预风险的准确性、敏感性和特异性分别如下:93.3%、100%和 86.7%。
基于 CTA 通过成像血管周围脂肪组织检测到的壁炎症与 EVAR 后 AAA 患者的再次干预风险密切相关,这可能有望成为一种用于人类 AAA 在 EVAR 前后机制和治疗研究的新成像生物标志物。临床影响本研究引入了一种新型成像生物标志物,通过在 CTA 上描绘血管周围脂肪衰减的空间变化来指示主动脉壁炎症。这种生物标志物显示出与 EVAR 后 AAA 患者的再次干预风险密切相关。将 VPCI 纳入临床实践有可能通过为临床医生提供一种评估主动脉壁炎症和预测再次干预风险的非侵入性方法来增强传统监测方法(CT/CTA)。此外,本研究可能为人类 AAA 在 EVAR 前后的机制和治疗研究提供有价值的工具,最终改善患者预后并优化治疗策略。