{"title":"冠状动脉CT血管造影评估血清尿酸与高危斑块的关系。","authors":"Xinguang Long, Yao Jing, Zhou Haitao","doi":"10.1136/openhrt-2025-003579","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>To investigate the association between serum uric acid (UA) and high-risk plaques (HRPs) assessed by coronary CT angiography (CCTA).</p><p><strong>Methods: </strong>In this retrospective study, we included outpatients who underwent CCTA. HRP was defined as ≥any 2 of the following features: positive remodelling, low-attenuation plaque (LAP), napkin ring sign and spotty calcification. Plaque volume, Agatston score, vessel stenosis, segment stenosis score (SSS) and segment involvement score (SIS) were also determined by CCTA. Logistic regression analysis was used to assess the relationship between serum UA and the risk of HRP. Receiver operating characteristic (ROC) curve analysis was performed to assess model's accuracy and discrimination. Subgroup analysis based on sex (male/female), diabetes mellitus (yes/no), smoking status (yes/no), alcohol use (yes/no), obstructive coronary artery disease (CAD) (yes/no), Agatston score (<300 or ≥300) was performed.</p><p><strong>Results: </strong>1411 subjects were included in the final analysis, with a mean age of 64.26±9.92 years and a median serum UA value of 425 µmol/L (IQR 296-622). A total of 344 cases of HRPs were identified. Multivariable logistic regression showed that serum UA (OR 2.96 per SD increment, 95% CI 1.85~4.76, p<0.001) was associated with higher risk of HRP after adjustment of sex, diabetes mellitus, smoking, obstructive CAD, age, Agatston score, total plaque volume, LAP volume, SSS and SIS. ROC analysis showed that area under curve of the model was 0.86 (95% CI 0.83 to 0.88, p<0.001). In subgroup analysis, no effect modification was found (all p>0.05).</p><p><strong>Conclusion: </strong>Serum UA is an independent risk factor for high-risk coronary artery plaques on CCTA. Measuring serum UA might provide improvement of discrimination and reclassification for CAD when added to clinical characteristics.</p>","PeriodicalId":19505,"journal":{"name":"Open Heart","volume":"12 2","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2025-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12458807/pdf/","citationCount":"0","resultStr":"{\"title\":\"Association between serum uric acid and high-risk plaques assessed by coronary CT angiography.\",\"authors\":\"Xinguang Long, Yao Jing, Zhou Haitao\",\"doi\":\"10.1136/openhrt-2025-003579\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Objectives: </strong>To investigate the association between serum uric acid (UA) and high-risk plaques (HRPs) assessed by coronary CT angiography (CCTA).</p><p><strong>Methods: </strong>In this retrospective study, we included outpatients who underwent CCTA. HRP was defined as ≥any 2 of the following features: positive remodelling, low-attenuation plaque (LAP), napkin ring sign and spotty calcification. Plaque volume, Agatston score, vessel stenosis, segment stenosis score (SSS) and segment involvement score (SIS) were also determined by CCTA. Logistic regression analysis was used to assess the relationship between serum UA and the risk of HRP. Receiver operating characteristic (ROC) curve analysis was performed to assess model's accuracy and discrimination. Subgroup analysis based on sex (male/female), diabetes mellitus (yes/no), smoking status (yes/no), alcohol use (yes/no), obstructive coronary artery disease (CAD) (yes/no), Agatston score (<300 or ≥300) was performed.</p><p><strong>Results: </strong>1411 subjects were included in the final analysis, with a mean age of 64.26±9.92 years and a median serum UA value of 425 µmol/L (IQR 296-622). A total of 344 cases of HRPs were identified. Multivariable logistic regression showed that serum UA (OR 2.96 per SD increment, 95% CI 1.85~4.76, p<0.001) was associated with higher risk of HRP after adjustment of sex, diabetes mellitus, smoking, obstructive CAD, age, Agatston score, total plaque volume, LAP volume, SSS and SIS. ROC analysis showed that area under curve of the model was 0.86 (95% CI 0.83 to 0.88, p<0.001). In subgroup analysis, no effect modification was found (all p>0.05).</p><p><strong>Conclusion: </strong>Serum UA is an independent risk factor for high-risk coronary artery plaques on CCTA. Measuring serum UA might provide improvement of discrimination and reclassification for CAD when added to clinical characteristics.</p>\",\"PeriodicalId\":19505,\"journal\":{\"name\":\"Open Heart\",\"volume\":\"12 2\",\"pages\":\"\"},\"PeriodicalIF\":2.8000,\"publicationDate\":\"2025-09-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12458807/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Open Heart\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1136/openhrt-2025-003579\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CARDIAC & CARDIOVASCULAR SYSTEMS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Open Heart","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1136/openhrt-2025-003579","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0
摘要
目的:探讨血清尿酸(UA)与冠状动脉CT血管造影(CCTA)评估的高危斑块(HRPs)之间的关系。方法:在这项回顾性研究中,我们纳入了接受CCTA的门诊患者。HRP定义为≥以下任意2项特征:阳性重构、低衰减斑块(LAP)、餐巾环征和点状钙化。CCTA测定斑块体积、Agatston评分、血管狭窄、节段狭窄评分(SSS)和节段累及评分(SIS)。采用Logistic回归分析评估血清UA与HRP风险之间的关系。采用受试者工作特征(ROC)曲线分析评价模型的准确性和判别性。基于性别(男/女)、糖尿病(是/否)、吸烟(是/否)、饮酒(是/否)、阻塞性冠状动脉疾病(CAD)(是/否)、Agatston评分进行亚组分析(结果:最终分析纳入1411名受试者,平均年龄64.26±9.92岁,血清UA中位数为425µmol/L (IQR 296-622)。共发现344例hrp。多变量logistic回归结果显示血清UA (OR 2.96 / SD增量,95% CI 1.85~4.76, p0.05)。结论:血清尿酸是CCTA显示的高危冠状动脉斑块的独立危险因素。若将血清尿酸测定与临床特征相结合,可改善CAD的鉴别和再分类。
Association between serum uric acid and high-risk plaques assessed by coronary CT angiography.
Objectives: To investigate the association between serum uric acid (UA) and high-risk plaques (HRPs) assessed by coronary CT angiography (CCTA).
Methods: In this retrospective study, we included outpatients who underwent CCTA. HRP was defined as ≥any 2 of the following features: positive remodelling, low-attenuation plaque (LAP), napkin ring sign and spotty calcification. Plaque volume, Agatston score, vessel stenosis, segment stenosis score (SSS) and segment involvement score (SIS) were also determined by CCTA. Logistic regression analysis was used to assess the relationship between serum UA and the risk of HRP. Receiver operating characteristic (ROC) curve analysis was performed to assess model's accuracy and discrimination. Subgroup analysis based on sex (male/female), diabetes mellitus (yes/no), smoking status (yes/no), alcohol use (yes/no), obstructive coronary artery disease (CAD) (yes/no), Agatston score (<300 or ≥300) was performed.
Results: 1411 subjects were included in the final analysis, with a mean age of 64.26±9.92 years and a median serum UA value of 425 µmol/L (IQR 296-622). A total of 344 cases of HRPs were identified. Multivariable logistic regression showed that serum UA (OR 2.96 per SD increment, 95% CI 1.85~4.76, p<0.001) was associated with higher risk of HRP after adjustment of sex, diabetes mellitus, smoking, obstructive CAD, age, Agatston score, total plaque volume, LAP volume, SSS and SIS. ROC analysis showed that area under curve of the model was 0.86 (95% CI 0.83 to 0.88, p<0.001). In subgroup analysis, no effect modification was found (all p>0.05).
Conclusion: Serum UA is an independent risk factor for high-risk coronary artery plaques on CCTA. Measuring serum UA might provide improvement of discrimination and reclassification for CAD when added to clinical characteristics.
期刊介绍:
Open Heart is an online-only, open access cardiology journal that aims to be “open” in many ways: open access (free access for all readers), open peer review (unblinded peer review) and open data (data sharing is encouraged). The goal is to ensure maximum transparency and maximum impact on research progress and patient care. The journal is dedicated to publishing high quality, peer reviewed medical research in all disciplines and therapeutic areas of cardiovascular medicine. Research is published across all study phases and designs, from study protocols to phase I trials to meta-analyses, including small or specialist studies. Opinionated discussions on controversial topics are welcomed. Open Heart aims to operate a fast submission and review process with continuous publication online, to ensure timely, up-to-date research is available worldwide. The journal adheres to a rigorous and transparent peer review process, and all articles go through a statistical assessment to ensure robustness of the analyses. Open Heart is an official journal of the British Cardiovascular Society.