首页> 外文期刊>Pediatric cardiology >Cranial irradiation as an additional risk factor for anthracycline cardiotoxicity in childhood cancer survivors: an analysis from the cardiac risk factors in childhood cancer survivors study.
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Cranial irradiation as an additional risk factor for anthracycline cardiotoxicity in childhood cancer survivors: an analysis from the cardiac risk factors in childhood cancer survivors study.

机译:颅骨照射是儿童癌症幸存者中蒽环类药物心脏毒性的另一个危险因素:一项对儿童癌症幸存者中心脏危险因素的分析。

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Anthracycline-treated childhood cancer survivors experience cardiac damage that results in decreased left ventricular (LV) mass, leading to increased LV wall stress, which underlies their greater risk of cardiomyopathy. Many of these survivors also are at risk of growth hormone (GH) abnormalities from cranial irradiation exposure, although it is unknown whether such exposure is associated with cardiotoxicity. Echocardiograms and insulin-like growth factor-1 (IGF-1), a marker of GH, were measured in 130 anthracycline-treated childhood cancer survivors, 59 of whom had been exposed to cranial irradiation, a mean 10 years after their cancer diagnosis. Echocardiographic parameters and IGF-1 were standardized relative to age or body surface area using data from sibling control subjects and expressed as the percentage difference from normal values. The results showed that after adjustment for other risk factors, survivors exposed to cranial irradiation had an additional 12 % decrease in LV mass compared with unexposed survivors (P < 0.01) and an additional 3.6 % decrease in LV dimension (P = 0.03). Survivors exposed to cranial irradiation also had a 30.8 % decrease in IGF-1 relative to normal values, which was greater than the 10.5 % decrease in unexposed survivors (P < 0.01). The above findings led us to conclude that in anthracycline-treated childhood cancer survivors a mean 10 years after their diagnosis, those with cranial irradiation exposure had significantly greater decreases in LV mass and dimension. Because cranial irradiation also was associated with decreased IGF-1, it is possible that GH deficiencies mediated this effect, suggesting that GH replacement therapy may help to prevent the development of cardiotoxicity.
机译:接受蒽环类药物治疗的儿童期癌症幸存者会遭受心脏损伤,从而导致左心室(LV)质量下降,导致LV壁应力增加,这使他们患心肌病的风险更高。尽管尚不清楚此类暴露是否与心脏毒性有关,但许多幸存者也有因颅骨暴露而导致生长激素(GH)异常的风险。在130名接受蒽环类药物治疗的儿童期癌症幸存者中测量了超声心动图和GH标记的胰岛素样生长因子-1(IGF-1),其中59名曾接受颅骨照射,即癌症确诊后的10年。使用来自同级对照受试者的数据,相对于年龄或体表面积将超声心动图参数和IGF-1标准化,并表示为与正常值的百分比差异。结果表明,在调整了其他风险因素后,与未暴露的幸存者相比,接受颅骨照射的幸存者的左心室质量降低了12%(P <0.01),而左心室尺寸又降低了3.6%(P = 0.03)。相对于正常值,暴露于颅骨照射的幸存者的IGF-1降低了30.8%,大于未暴露幸存者的IGF-1降低了10.5%(P <0.01)。上述发现使我们得出结论,在接受蒽环类药物治疗的儿童癌症幸存者确诊后平均10年,其颅骨照射暴露者的LV质量和尺寸明显降低。由于颅骨照射也与IGF-1降低有关,因此GH缺乏可能介导了这种作用,这表明GH替代疗法可能有助于预防心脏毒性的发生。

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