Li Sihui, Cai Siyu, Huang Cheng, Chai Xi, Wang Xindi, Wang Xisi, Zhao Wen, Nie Xiaolu, Peng Xiaoxia, Ma Xiaoli
Beijing Key Laboratory of Pediatric Hematology Oncology National Discipline of Pediatrics Ministry of Education MOE Key Laboratory of Major Diseases in Children Hematology Oncology Center Beijing Children's Hospital Capital Medical University National Center for Children's Health Beijing China.
National Center for Clinical Epidemiology and Evidence-based Medicine Beijing Children's Hospital Capital Medical University National Center for Children's Health Beijing China.
Pediatr Investig. 2018 Jul 16;2(2):107-113. doi: 10.1002/ped4.12039. eCollection 2018 Jun.
Childhood solid tumors account for the highest proportion of childhood cancers and are one of the leading causes of death in childhood. However, their pathogenesis is unclear.
To explore prenatal and perinatal risk factors for solid malignancies in children.
We enrolled 71 consecutive pediatric patients (44 boys and 27 girls; median age, 30 months) with solid tumors who were diagnosed and treated at our center from January 2013 to December 2016 as the case group. We also enrolled 211 age- and residence-matched healthy children (ratio of approximately 3:1 with the case group) as the control group. We conducted a questionnaire-based survey with the parents of these 282 children. Univariate and multivariate conditional logistic regression analyses of the collected data were performed.
Confirmed solid malignancies included neuroblastoma (=32), rhabdomyosarcoma (=18), retinoblastoma (=7), renal tumors (=3), and other tumors (=11). Risk factors for solid childhood tumors in the univariate analysis were the parents' age, gravidity, parity, abortion history, vaginal bleeding, family history of malignancy, and prenatal use of folic acid or hematinics/iron supplements (<0.05), and those in the multivariate analysis were higher parity (odds ratio [OR], 2.482; 95% confidence interval [CI], 1.521-4.048), family history of malignancy (OR, 3.667; 95% CI, 1.679-8.009), and prenatal use of hematinics/iron supplements (OR, 2.882; 95% CI, 1.440-5.767). In contrast, use of prenatal folic acid was protective (OR, 0.334; 95% CI, 0.160-0.694).
A family history of malignancy, use of prenatal hematinics/iron supplements, and higher parity are risk factors for solid childhood tumors, whereas use of prenatal folic acid is a protective factor.
儿童实体瘤在儿童癌症中占比最高,是儿童死亡的主要原因之一。然而,其发病机制尚不清楚。
探讨儿童实体恶性肿瘤的产前和围产期危险因素。
我们纳入了2013年1月至2016年12月在本中心诊断和治疗的71例连续的患有实体瘤的儿科患者(44名男孩和27名女孩;中位年龄30个月)作为病例组。我们还纳入了211名年龄和居住地匹配的健康儿童(与病例组比例约为3:1)作为对照组。我们对这282名儿童的父母进行了问卷调查。对收集到的数据进行单因素和多因素条件逻辑回归分析。
确诊的实体恶性肿瘤包括神经母细胞瘤(=32)、横纹肌肉瘤(=18)、视网膜母细胞瘤(=7)、肾肿瘤(=3)和其他肿瘤(=11)。单因素分析中儿童实体瘤的危险因素包括父母年龄、妊娠次数、产次、流产史、阴道出血、恶性肿瘤家族史以及产前使用叶酸或补血剂/铁补充剂(<0.05),多因素分析中的危险因素包括较高产次(比值比[OR],2.482;95%置信区间[CI],1.521 - 4.048)、恶性肿瘤家族史(OR,3.667;95% CI,1.679 - 8.009)和产前使用补血剂/铁补充剂(OR,2.882;95% CI,1.440 - 5.767)。相比之下,产前使用叶酸具有保护作用(OR,0.334;95% CI,0.160 - 0.694)。
恶性肿瘤家族史、产前使用补血剂/铁补充剂和较高产次是儿童实体瘤的危险因素,而产前使用叶酸是保护因素。