Schafer Andrew I, Mann Douglas L
Richard T. Silver MPN Center, Department of Medicine, Weill Cornell Medical College, New York-Presbyterian Hospital/Weill Cornell, New York, NY 10021, USA.
The Center for Cardiovascular Research, Washington University, St. Louis, MO 63110, USA.
J Clin Med. 2024 Oct 12;13(20):6084. doi: 10.3390/jcm13206084.
The most common causes of morbidity and mortality in the myeloproliferative neoplasms (MPNs), with the exception of myelofibrosis, are venous and arterial thrombosis, as well as more recently discovered cardiovascular disease (CVD). Clonal hematopoiesis of indeterminate potential (CHIP) is the subclinical finding in an individual of somatic mutations that are also found in clinically overt MPNs and other myeloid malignancies. The prevalence of "silent" CHIP increases with age. CHIP can transform into a clinically overt MPN at an estimated rate of 0.5 to 1% per year. It is likely, therefore, but not proven, that many, if not all, MPN patients had antecedent CHIP, possibly for many years. Moreover, both individuals with asymptomatic CHIP, as well as clinically diagnosed patients with MPN, can develop thrombotic complications. An unexpected and remarkable discovery during the last few years is that even CHIP (as well as MPNs) are significant, independent risk factors for CVD. This review discusses up-to-date information on the types of thrombotic and cardiovascular complications that are found in CHIP and MPN patients. A systemic inflammatory state (that is often subclinical) is most likely to be a major mediator of adverse reciprocal bone marrow-cardiovascular interplay that may fuel the development of progression of MPNs, including its thrombotic and vascular complications, as well as the worsening of cardiovascular disease, possibly in a "vicious cycle". Translating this to clinical practice for hematologists and oncologists who treat MPN patients, attention should now be paid to ensuring that cardiovascular risk factors are controlled and minimized, either by the patient's cardiologist or primary care physician or by the hematologist/oncologist herself or himself. This review is intended to cover the clinical aspects of thrombosis and cardiovascular complications in the MPN, accompanied by pathobiological comments.
除骨髓纤维化外,骨髓增殖性肿瘤(MPN)发病和死亡的最常见原因是静脉和动脉血栓形成,以及最近发现的心血管疾病(CVD)。不确定潜能克隆造血(CHIP)是个体中出现的亚临床现象,其体细胞突变也见于临床明显的MPN和其他髓系恶性肿瘤。“沉默”CHIP的患病率随年龄增长而增加。CHIP每年转化为临床明显MPN的估计发生率为0.5%至1%。因此,很可能但未经证实的是,许多(如果不是所有)MPN患者之前存在CHIP,可能已经存在多年。此外,无症状CHIP个体以及临床诊断为MPN的患者都可能发生血栓并发症。过去几年一个意外而显著的发现是,即使是CHIP(以及MPN)也是CVD的重要独立危险因素。本综述讨论了CHIP和MPN患者中发现的血栓形成和心血管并发症类型的最新信息。全身炎症状态(通常是亚临床的)很可能是不良骨髓-心血管相互作用的主要介导因素,这可能促使MPN进展,包括其血栓形成和血管并发症,以及心血管疾病恶化,可能形成“恶性循环”。对于治疗MPN患者的血液科医生和肿瘤内科医生而言,将此转化为临床实践时,现在应注意确保心血管危险因素得到控制并降至最低,这可由患者的心脏病专家或初级保健医生或血液科医生/肿瘤内科医生自己来完成。本综述旨在涵盖MPN中血栓形成和心血管并发症的临床方面,并伴有病理生物学评论。