Division of Hematology, Department of Medicine, Mayo Clinic, Rochester, Minnesota, USA.
Am J Hematol. 2023 Jun;98(6):951-964. doi: 10.1002/ajh.26915. Epub 2023 Mar 30.
Clonal hematopoiesis (CH) refers to age-associated expansion of somatic variants in hematopoietic stem and progenitor cells (HSPC).
CH of indeterminate potential (CHIP) is operationally defined as pathogenic variants in HSPCs at a variant allele frequency ≥2%.
CH is associated with increased occurrence of several hematological conditions such as cytopenias (also called clonal cytopenia of undetermined significance), hematological (predominantly myeloid but also lymphoid) neoplasms, cytosis (including monocytosis), and non-hematological conditions such as atherosclerotic cardiovascular and cerebrovascular disease, ischemic congestive heart failure, venous thromboembolism, type 2 diabetes mellitus, chronic obstructive pulmonary disease, osteoporosis, gout, with a potential protective effect in Alzheimer's disease (AD).
As of now, there is limited prospective data for CH testing; however, CH detection is becoming increasingly prevalent due to ubiquitous use of somatic and germline NGS testing. This in addition to data suggesting that therapy related myeloid neoplasm (tMN) in many cases is preceded by the detection of CH clones, has led to the establishment of CH clinics at several institutions. At our institution, on a research basis, we currently recommend testing for CH for individuals with persistent (≥4 months) unexplained cytopenias, in patients with malignancies prior to adjuvant cytotoxic chemotherapy and/or radiation or radionuclide therapy, screening prior to autologous hematopoietic stem cell transplantation and chimeric antigen receptor T cell (CAR-T) therapy and to assess as to whether or not, potential germline mosaic variants actually represent CH.
克隆性造血(CH)是指造血干细胞和祖细胞(HSPC)中与年龄相关的体细胞变异的扩增。
未确定的潜在克隆性造血(CHIP)被定义为 HSPC 中变异等位基因频率≥2%的致病性变异。
CH 与多种血液疾病的发生率增加有关,如血细胞减少症(也称为意义未明的克隆性血细胞减少症)、血液系统(主要是骨髓性,但也包括淋巴性)肿瘤、细胞增多症(包括单核细胞增多症)和非血液系统疾病,如动脉粥样硬化性心血管和脑血管疾病、缺血性充血性心力衰竭、静脉血栓栓塞、2 型糖尿病、慢性阻塞性肺疾病、骨质疏松症、痛风,在阿尔茨海默病(AD)中具有潜在的保护作用。
目前,CH 检测的前瞻性数据有限;然而,由于体细胞和种系 NGS 检测的广泛应用,CH 检测变得越来越普遍。此外,数据表明,在许多情况下,治疗相关的髓性肿瘤(tMN)之前都检测到了 CH 克隆,这导致了几个机构建立了 CH 诊所。在我们的机构,基于研究,我们目前建议对持续(≥4 个月)不明原因血细胞减少症的个体进行 CH 检测,对恶性肿瘤患者在辅助细胞毒性化疗和/或放疗或放射性核素治疗之前进行检测,在自体造血干细胞移植和嵌合抗原受体 T 细胞(CAR-T)治疗之前进行筛查,并评估潜在的种系镶嵌变体是否实际上代表 CH。