Peyster Eliot, Yuan Cai, Arabyarmohammadi Sara, Lal Priti, Feldman Michael, Fu Pingfu, Margulies Kenneth, Madabhushi Anant
University of Pennsylvania.
Emory University.
Res Sq. 2024 May 15:rs.3.rs-4364681. doi: 10.21203/rs.3.rs-4364681/v1.
Both overt and indolent inflammatory insults in heart transplantation can accelerate pathologic cardiac remodeling, but there are few tools for monitoring the speed and severity of remodeling over time. To address this need, we developed an automated computational pathology system to measure pathologic remodeling in transplant biopsy samples in a large, retrospective cohort of n=2167 digitized heart transplant biopsy slides. Biopsy images were analyzed to identify the pathologic stromal changes associated with future allograft loss or advanced allograft vasculopathy. Biopsy images were then analyzed to assess which historical allo-inflammatory events drive progression of these pathologic stromal changes over time in serial biopsy samples. The top-5 features of pathologic stromal remodeling most strongly associated with adverse outcomes were also strongly associated with histories of both overt and indolent inflammatory events. Our findings identify previously unappreciated subgroups of higher- and lower-risk transplant patients, and highlight the translational potential of digital pathology analysis.
心脏移植中明显的和隐匿的炎症损伤均可加速病理性心脏重塑,但用于长期监测重塑速度和严重程度的工具很少。为满足这一需求,我们开发了一种自动化计算病理学系统,以测量来自n = 2167例数字化心脏移植活检切片的大型回顾性队列中移植活检样本的病理性重塑。分析活检图像以识别与未来移植物丢失或晚期移植物血管病变相关的病理性基质变化。然后分析活检图像,以评估哪些既往的同种异体炎症事件在系列活检样本中随时间推移推动这些病理性基质变化的进展。与不良结局最密切相关的病理性基质重塑的前5个特征也与明显的和隐匿的炎症事件史密切相关。我们的研究结果识别出了之前未被认识到的高风险和低风险移植患者亚组,并突出了数字病理学分析的转化潜力。