Department of Cardiology, Geisinger Medical Center, 100 North Academy Avenue, Danville, PA 17822-2160, USA.
Curr Cardiol Rep. 2009 Mar;11(2):148-54. doi: 10.1007/s11886-009-0022-z.
Left ventricular (LV) remodeling is a major determinant of the clinical course and outcome of systolic heart failure (HF). Activation of neurohormonal and inflammatory cytokine pathways and their effects on intracellular signal transduction cascades through stimulation of membrane-bound receptors mediate LV remodeling. Although major advances have been made in clinical management of HF through large randomized trials, its prognosis remains poor. Interindividual differences, often genetically based, are increasingly recognized as important determinants of LV remodeling. Identification of the influence of these individual factors on the clinical course of HF has stimulated a search for specific pathophysiologic mechanisms that operate at the individual level and can be targeted directly. This article summarizes the current application of molecular imaging techniques to the understanding of the cellular and molecular mechanisms involved in LV remodeling in an attempt to provide the tools necessary for personalized, truly "evidence-based" assessment, serial evaluation, and monitoring of HF.
左心室(LV)重构是收缩性心力衰竭(HF)临床过程和结局的主要决定因素。神经激素和炎症细胞因子途径的激活及其通过刺激膜结合受体对细胞内信号转导级联的影响介导 LV 重构。尽管通过大型随机试验在 HF 的临床管理方面取得了重大进展,但预后仍然很差。个体差异,通常基于遗传,被认为是 LV 重构的重要决定因素。确定这些个体因素对 HF 临床过程的影响,刺激了对在个体水平上起作用并可直接靶向的特定病理生理机制的寻找。本文总结了分子成像技术在理解 LV 重构中涉及的细胞和分子机制方面的当前应用,试图为个性化、真正的“循证”评估、HF 的连续评估和监测提供必要的工具。