Sapkota Yadav, Liu Qi, Li Nan, Bhatt Neel S, Ehrhardt Matthew J, Wilson Carmen L, Wang Zhaoming, Jefferies John L, Zhang Jinghui, Armstrong Gregory T, Hudson Melissa M, Robison Leslie L, Mulrooney Daniel A, Yasui Yutaka
Department of Epidemiology and Cancer Control, St. Jude Children's Research Hospital, Memphis, Tennessee, USA.
School of Public Health, University of Alberta, Edmonton, Alberta, Canada.
JACC CardioOncol. 2022 Jun 21;4(2):258-267. doi: 10.1016/j.jaccao.2022.04.003. eCollection 2022 Jun.
Adverse cardiovascular outcomes such as coronary artery disease (CAD) are the leading noncancer causes of morbidity and mortality among childhood cancer survivors.
The aim of this study was to assess the role of a genome-wide polygenic score (GPS) for CAD, well validated in the general population, and its interplay with cancer-related risk factors among childhood cancer survivors.
In a cohort study of 2,472 5-year childhood cancer survivors from the St. Jude Lifetime Cohort, the association between the GPS and the risk of CAD was performed using Cox regression models adjusted for age at cancer diagnosis, sex, cumulative dose of anthracyclines, and mean heart radiation dose.
Among survivors of European ancestry, the GPS was significantly associated with the risk of CAD (HR per 1 SD of the GPS: 1.25; 95% CI: 1.04-1.49; 0.014). Compared with the first tertile, survivors in the upper tertile had a greater risk of CAD (1.51-fold higher HR of CAD [95% CI: 0.96-2.37; 0.074]), although the difference was not statistically significant. The GPS-CAD association was stronger among survivors diagnosed with cancer at age <10 years exposed to >25 Gy heart radiation (HR top vs. bottom tertile of GPS: 15.49; 95% CI: 5.24-45.52; = 0.005) but not among those diagnosed at age ≥10 years ( ≥ 0.77) and not among those diagnosed at age <10 years exposed to ≤25 Gy heart radiation ( = 0.23). Among high-risk survivors, defined by an estimated relative hazard ≥3.0 from fitted Cox models including clinical risk factors alone, the cumulative incidence of CAD at 40 years from diagnosis was 29% (95% CI: 13%-45%). After incorporating the GPS into the model, the cumulative incidence increased to 48% (95% CI: 26%-69%).
Childhood cancer survivors are at risk for premature CAD. A GPS may help identify those who may benefit from targeted screening and personalized preventive interventions.
诸如冠状动脉疾病(CAD)等不良心血管结局是儿童癌症幸存者中发病和死亡的主要非癌症原因。
本研究的目的是评估在一般人群中得到充分验证的CAD全基因组多基因评分(GPS)的作用,以及它与儿童癌症幸存者中癌症相关危险因素的相互作用。
在一项对来自圣裘德终身队列的2472名5岁儿童癌症幸存者的队列研究中,使用Cox回归模型对癌症诊断时的年龄、性别、蒽环类药物累积剂量和平均心脏辐射剂量进行调整,分析GPS与CAD风险之间的关联。
在欧洲血统的幸存者中,GPS与CAD风险显著相关(GPS每增加1个标准差的风险比:1.25;95%置信区间:1.04 - 1.49;P = 0.014)。与第一三分位数相比,处于最高三分位数的幸存者患CAD的风险更高(CAD的风险比高1.51倍[95%置信区间:0.96 - 2.37;P = 0.074]),尽管差异无统计学意义。在10岁前被诊断为癌症且接受超过25 Gy心脏辐射的幸存者中,GPS与CAD的关联更强(GPS最高与最低三分位数的风险比:15.49;95%置信区间:5.24 - 45.52;P = 0.005),但在10岁及以上被诊断的幸存者中(P≥0.77)以及在10岁前被诊断且接受≤25 Gy心脏辐射的幸存者中(P = 0.23)并非如此。在由仅包含临床危险因素的拟合Cox模型估计相对风险≥3.0定义的高危幸存者中,从诊断起40年时CAD的累积发病率为29%(95%置信区间:13% - 45%)。将GPS纳入模型后,累积发病率增至48%(95%置信区间:26% - 69%)。
儿童癌症幸存者有过早患CAD的风险。GPS可能有助于识别那些可能从靶向筛查和个性化预防干预中获益的人。