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首页> 外文期刊>Chinese journal of cancer >The association between early-onset cardiac events caused by neoadjuvant or adjuvant chemotherapy in triple-negative breast cancer patients and some novel autophagy-related polymorphisms in their genomic DNA: a real-world study
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The association between early-onset cardiac events caused by neoadjuvant or adjuvant chemotherapy in triple-negative breast cancer patients and some novel autophagy-related polymorphisms in their genomic DNA: a real-world study

机译:三阴性乳腺癌患者新辅助化疗或辅助化疗引起的早发性心脏事件与基因组DNA中某些新型自噬相关多态性之间的关联:一项现实世界研究

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Background An increasing number of cancer patients die of cardiovascular diseases. The cardiotoxicity of chemotherapy is particularly important in triple-negative breast cancer (TNBC) with limited therapeutic options. Cardiac autophagy is an important mechanism of cardiotoxicity. This research was aimed to investigate the cardiotoxicity of chemotherapy in TNBC, screen the susceptible population, and determine the relationship between cardiotoxicity and autophagy-related polymorphisms. Methods From a total of 2450 stage I-III TNBC patients, 147 met the inclusion criteria and finally recruited. Electrocardiography (ECG) was performed before most chemotherapy cycles, and echocardiography (UCG) was performed according to clinical needs. All ECG and UCG records were re-interpreted by cardiologists at the National Center for Cardiovascular Disease, Fuwai Hospital. According to the National Center for Biotechnology Information and the Catalog of Somatic Mutations in Cancer database, we selected 25 single nucleotide polymorphisms (SNPs) related to autophagy and genotyped the 147 TNBC patients. Paired-sample T tests, Chi squared tests, and logistic regression models were employed for the analysis. Results Only 46 (31.3%) patients had normal ECG records after every chemotherapy cycle. Among the 16 patients who underwent UCG, 2 (12.5%) had a reversible decrease of left ventricular ejection fraction. The use of anthracyclines and excessive alcohol consumption were risk factors of ECG abnormalities. With the continuation of chemotherapy, heart rate gradually increased. Anthracyclines were associated with QRS duration abnormalities ( P =?0.043). After genotyping for 25 autophagy-related SNPs, we found that the G allele of autophagy-related 13 ( ATG13 ) rs10838611 was significantly associated with ECG abnormalities (odds ratio?=?2.258, 95% confidence interval?=?1.318–3.869; P =?0.003). Conclusion ECG abnormalities caused by chemotherapy are common in the real world. Autophagy-related SNPs are associated with chemotherapy-induced cardiotoxicity, thereby providing new evidence for autophagy as a cause of chemotherapy-induced cardiac damage.
机译:背景技术越来越多的癌症患者死于心血管疾病。在三阴性乳腺癌(TNBC)中,化学疗法的心脏毒性在治疗选择有限的情况下尤其重要。心脏自噬是心脏毒性的重要机制。这项研究旨在调查TNBC化疗的心脏毒性,筛选易感人群,并确定心脏毒性与自噬相关多态性之间的关系。方法对2450例I-III期TNBC患者中的147例符合入组标准并最终入组。在大多数化疗周期之前进行心电图(ECG),并根据临床需要进行超声心动图(UCG)。富威医院国家心血管疾病中心的心脏病专家对所有ECG和UCG记录进行了重新解释。根据国家生物技术信息中心和癌症数据库中的体细胞突变目录,我们选择了25种与自噬相关的单核苷酸多态性(SNP),并对147例TNBC患者进行了基因分型。分析采用配对样本T检验,卡方检验和逻辑回归模型。结果在每个化疗周期后,只有46(31.3%)位患者的ECG记录正常。在接受UCG的16例患者中,有2例(12.5%)的左心室射血分数可逆下降。使用蒽环类药物和过量饮酒是心电图异常的危险因素。随着化学疗法的继续,心率逐渐升高。蒽环类药物与QRS持续时间异常有关(P =?0.043)。对25个自噬相关SNPs进行基因分型后,我们发现自噬相关13个(ATG13)rs10838611的G等位基因与ECG异常显着相关(几率=?2.258,95%置信区间== 1.318-3.869; P =?0.003)。结论化疗引起的心电图异常在现实世界中很普遍。自噬相关的SNP与化疗引起的心脏毒性相关,从而为自噬作为化疗引起的心脏损害的原因提供了新的证据。

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