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急性髓系白血病患者 IDH1/2 突变与冠状动脉疾病和心功能障碍风险:回顾性倾向评分分析。

IDH1/2 mutations in acute myeloid leukemia patients and risk of coronary artery disease and cardiac dysfunction-a retrospective propensity score analysis.

机构信息

Department of Cardiology and Angiology, Hannover Medical School, Carl-Neuberg Strasse 1, 30625, Hannover, Germany.

Department of Cardiovascular Physiology, European Center for Angioscience (ECAS), Medical Faculty Mannheim of Heidelberg University, Ludolf-Krehl-Strasse 7-11, 68167, Mannheim, Germany.

出版信息

Leukemia. 2021 May;35(5):1301-1316. doi: 10.1038/s41375-020-01043-x. Epub 2020 Sep 18.

DOI:10.1038/s41375-020-01043-x
PMID:32948843
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8102189/
Abstract

Clonal hematopoiesis of indeterminate potential (CHIP) is linked to leukemia gene mutations and associates with an increased risk for coronary artery disease and poor prognosis in ischemic cardiomyopathy. Two recurrently mutated genes in CHIP and adult acute myeloid leukemia (AML) encode for isocitrate dehydrogenases 1 and 2 (IDH1 and IDH2). Global expression of mutant IDH2 in transgenic mice-induced dilated cardiomyopathy and muscular dystrophy. In this retrospective observational study, we investigated whether mutant IDH1/2 predisposes to cardiovascular disease in AML patients. Among 363 AML patients, IDH1 and IDH2 mutations were detected in 26 (7.2%) and 39 patients (10.7%), respectively. Mutant IDH1 patients exhibited a significantly higher prevalence of coronary artery disease (26.1% vs. 6.4%, p = 0.002). Applying inverse probability-weighting analysis, patients with IDH1/2 mutations had a higher risk for a declining cardiac function during AML treatment compared to IDH1/2 wild type patients [left ventricular ejection fraction pretreatment compared to 10 months after diagnosis: 59.2% to 41.9% (p < 0.001) vs 58.5% to 55.4% (p = 0.27), respectively]. Mechanistically, RNA sequencing and immunostaining in hiPS-derived cardiomyocytes indicated that the oncometabolite R-2HG exacerbated doxorubicin mediated cardiotoxicity. Evaluation of IDH1/2 mutation status may therefore help identifying AML patients at risk for cardiovascular complications during cytotoxic treatment.

摘要

不确定潜能的克隆性造血 (CHIP) 与白血病基因突变相关,并与冠状动脉疾病风险增加和缺血性心肌病预后不良相关。CHIP 和成人急性髓系白血病 (AML) 中两种经常发生突变的基因编码异柠檬酸脱氢酶 1 和 2 (IDH1 和 IDH2)。突变 IDH2 的全局表达在转基因小鼠诱导的扩张型心肌病和肌肉萎缩症中。在这项回顾性观察研究中,我们研究了突变 IDH1/2 是否会使 AML 患者易患心血管疾病。在 363 名 AML 患者中,分别检测到 IDH1 和 IDH2 突变 26 例 (7.2%) 和 39 例 (10.7%)。突变 IDH1 患者的冠心病患病率明显更高 (26.1%比 6.4%,p = 0.002)。应用逆概率加权分析,与 IDH1/2 野生型患者相比,IDH1/2 突变患者在 AML 治疗期间心脏功能下降的风险更高[左心室射血分数预处理与诊断后 10 个月:59.2%比 41.9%(p < 0.001)比 58.5%比 55.4%(p = 0.27)]。从机制上讲,hiPS 衍生的心肌细胞中的 RNA 测序和免疫染色表明致癌代谢物 R-2HG 加剧了多柔比星介导的心脏毒性。因此,评估 IDH1/2 突变状态可能有助于识别在细胞毒性治疗期间易发生心血管并发症的 AML 患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/abdc/8102189/222b0682d7c5/41375_2020_1043_Fig5_HTML.jpg
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