Cornelissen Anne, Gadhoke Neel V, Ryan Kathleen, Hodonsky Chani J, Mitchell Rebecca, Bihlmeyer Nathan, Duong ThuyVy, Chen Zhifen, Dikongue Armelle, Sakamoto Atsushi, Sato Yu, Kawakami Rika, Mori Masayuki, Kawai Kenji, Fernandez Raquel, Ghosh Saikat Kumar B, Braumann Ryan, Abebe Biniyam, Kutys Robert, Kutyna Matthew, Romero Maria E, Kolodgie Frank D, Miller Clint L, Hong Charles C, Grove Megan L, Brody Jennifer A, Sotoodehnia Nona, Arking Dan E, Schunkert Heribert, Mitchell Braxton D, Guo Liang, Virmani Renu, Finn Aloke V
bioRxiv. 2023 Jul 7:2023.07.05.547891. doi: 10.1101/2023.07.05.547891.
Polygenic risk scores (PRS) for coronary artery disease (CAD) potentially improve cardiovascular risk prediction. However, their relationship with histopathologic features of CAD has never been examined systematically.
From 4,327 subjects referred to CVPath by the State of Maryland Office Chief Medical Examiner (OCME) for sudden death between 1994 and 2015, 2,455 cases were randomly selected for genotyping. We generated PRS from 291 known CAD risk loci. Detailed histopathologic examination of the coronary arteries was performed in all subjects. The primary study outcome measurements were histopathologic plaque features determining severity of atherosclerosis, including %stenosis, calcification, thin-cap fibroatheromas (TCFA), and thrombotic CAD.
After exclusion of cases with insufficient DNA sample quality or with missing data, 954 cases (mean age 48.8±14.7; 75.7% men) remained in the final study cohort. Subjects in the highest PRS quintile exhibited more severe atherosclerosis compared to subjects in the lowest quintile, with greater %stenosis (80.3%±27.0% vs. 50.4%±38.7%; adjusted p<0.001) and a higher frequency of calcification (69.6% vs. 35.8%; adjusted p=0.004) and TCFAs (26.7% vs. 9.5%; adjusted p=0.007). Even after adjustment for traditional CAD risk factors subjects within the highest PRS quintile had higher odds of severe atherosclerosis (i.e., ≥75% stenosis; adjusted OR 3.77; 95%CI 2.10-6.78; p<0.001) and plaque rupture (adjusted OR 4.05; 95%CI 2.26-7.24; p<0.001). Moreover, subjects within the highest quintile had higher odds of CAD-associated cause of death, especially among those aged 50 years and younger (adjusted OR 4.08; 95%CI 2.01-8.30; p<0.001). No associations were observed with plaque erosion.
This is the first autopsy study investigating associations between PRS and atherosclerosis severity at the histopathologic level in subjects with sudden death. Our pathological analysis suggests PRS correlates with plaque burden and features of advanced atherosclerosis and may be useful as a method for CAD risk stratification, especially in younger subjects.
In this autopsy study including 954 subjects within the CVPath Sudden Death Registry, high PRS correlated with plaque burden and atherosclerosis severity.The PRS showed differential associations with plaque rupture and plaque erosion, suggesting different etiologies to these two causes of thrombotic CAD.PRS may be useful for risk stratification, particularly in the young. Further examination of individual risk loci and their association with plaque morphology may help understand molecular mechanisms of atherosclerosis, potentially revealing new therapy targets of CAD.
A polygenic risk score, generated from 291 known CAD risk loci, was assessed in 954 subjects within the CVPath Sudden Death Registry. Histopathologic examination of the coronary arteries was performed in all subjects. Subjects in the highest PRS quintile exhibited more severe atherosclerosis as compared to subjects in the lowest quintile, with a greater plaque burden, more calcification, and a higher frequency of plaque rupture.
冠状动脉疾病(CAD)的多基因风险评分(PRS)可能会改善心血管疾病风险预测。然而,其与CAD组织病理学特征之间的关系从未被系统研究过。
从1994年至2015年间因猝死被马里兰州首席法医办公室(OCME)转介至CVPath的4327名受试者中,随机选取2455例进行基因分型。我们从291个已知的CAD风险位点生成PRS。对所有受试者的冠状动脉进行详细的组织病理学检查。主要研究结局指标是确定动脉粥样硬化严重程度的组织病理学斑块特征,包括狭窄百分比、钙化、薄帽纤维粥样斑块(TCFA)和血栓性CAD。
在排除DNA样本质量不足或数据缺失的病例后,最终研究队列中剩下954例(平均年龄48.8±14.7岁;75.7%为男性)。与PRS最低五分位数的受试者相比,最高五分位数的受试者表现出更严重的动脉粥样硬化,狭窄百分比更高(80.3%±27.0%对50.4%±38.7%;校正p<0.001),钙化频率更高(69.6%对35.8%;校正p=0.004)和TCFA频率更高(26.7%对9.5%;校正p=0.007)。即使在调整了传统CAD危险因素后,PRS最高五分位数内的受试者发生严重动脉粥样硬化(即狭窄≥75%;校正OR 3.77;95%CI 2.10 - 6.78;p<0.001)和斑块破裂(校正OR 4.05;95%CI 2.26 - 7.24;p<0.001)的几率更高。此外,最高五分位数内的受试者CAD相关死因的几率更高,尤其是在50岁及以下的人群中(校正OR 4.08;95%CI 2.01 - 8.30;p<0.001)。未观察到与斑块侵蚀的关联。
这是第一项在猝死受试者中研究PRS与组织病理学水平上动脉粥样硬化严重程度之间关联的尸检研究。我们的病理分析表明,PRS与斑块负荷及晚期动脉粥样硬化特征相关,可能作为CAD风险分层的一种方法,特别是在年轻受试者中。
在这项纳入CVPath猝死登记处954名受试者的尸检研究中,高PRS与斑块负荷和动脉粥样硬化严重程度相关。PRS与斑块破裂和斑块侵蚀表现出不同的关联,提示这两种血栓性CAD病因的不同发病机制。PRS可能有助于风险分层,特别是在年轻人中。进一步研究单个风险位点及其与斑块形态的关联可能有助于理解动脉粥样硬化的分子机制,潜在地揭示CAD的新治疗靶点。
从291个已知的CAD风险位点生成的多基因风险评分,在CVPath猝死登记处的954名受试者中进行评估。对所有受试者的冠状动脉进行组织病理学检查。与PRS最低五分位数的受试者相比,最高五分位数的受试者表现出更严重的动脉粥样硬化,斑块负荷更大、钙化更多且斑块破裂频率更高。