医学
分子成像
正电子发射断层摄影术
磁共振成像
骨关节炎
生物标志物
疾病
生物信息学
病理
放射科
生物
生物化学
生物技术
替代医学
体内
作者
Maria I. Menendez Montes,Christine T. N. Pham,Yongjian Liu,Farshid Guilak
标识
DOI:10.1080/03008207.2025.2535425
摘要
F]-NaF) can assess synovial inflammation and subchondral bone remodeling, their lack of specificity hinders further advances. We also review the recent development of radiotracers targeting specific immune and mesenchymal cell populations, such as translocator protein (TSPO) and fibroblast activation protein inhibitor (FAPI) that have demonstrated potential for characterizing the inflammatory endotype in OA and monitoring treatment response. Given the lack of validated cell-specific tracers, limited studies in early-stage or asymptomatic OA, and few longitudinal data sets, future research should prioritize development and validation of pathophysiology-specific tracers and incorporation of PET into longitudinal and interventional studies. This evolving field holds promise not only for advancing OA preclinical research but also for informing precision diagnostics and early therapeutic strategies in clinical practice.
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