de Paula Silva Neimar, de Souza Reis Rejane, Garcia Cunha Rafael, Pinto Oliveira Júlio Fernando, Santos Marceli de Oliveira, Pombo-de-Oliveira Maria S, de Camargo Beatriz
Pediatric Hematology and Oncology Program, Research Center, Instituto Nacional de Câncer, Rio de Janeiro-RJ, Brazil.
Divisão de Vigilância e Análise de Situação Coordenação de Prevenção e Vigilância, Instituto Nacional do Câncer, Rio de Janeiro-RJ, Brazil.
PLoS One. 2016 Oct 21;11(10):e0164398. doi: 10.1371/journal.pone.0164398. eCollection 2016.
Several maternal and birth characteristics have been reported to be associated with an increased risk of many childhood cancers. Our goal was to evaluate the risk of childhood embryonal solid tumors in relation to pre- and perinatal characteristics.
A case-cohort study was performed using two population-based datasets, which were linked through R software. Tumors were classified as central nervous system (CNS) or non-CNS-embryonal (retinoblastoma, neuroblastoma, renal tumors, germ cell tumors, hepatoblastoma and soft tissue sarcoma). Children aged <6 years were selected. Adjustments were made for potential confounders. Odds ratios (OR) with 95% confidence intervals (CI) were computed by unconditional logistic regression analysis using SPSS.
Males, high maternal education level, and birth anomalies were independent risk factors. Among children diagnosed older than 24 months of age, cesarean section (CS) was a significant risk factor. Five-minute Apgar ≤8 was an independent risk factor for renal tumors. A decreasing risk with increasing birth order was observed for all tumor types except for retinoblastoma. Among children with neuroblastoma, the risk decreased with increasing birth order (OR = 0.82 (95% CI 0.67-1.01)). Children delivered by CS had a marginally significantly increased OR for all tumors except retinoblastoma. High maternal education level showed a significant increase in the odds for all tumors together, CNS tumors, and neuroblastoma.
This evidence suggests that male gender, high maternal education level, and birth anomalies are risk factors for childhood tumors irrespective of the age at diagnosis. Cesarean section, birth order, and 5-minute Apgar score were risk factors for some tumor subtypes.
据报道,多种母亲和出生特征与儿童期多种癌症风险增加有关。我们的目标是评估与产前和围产期特征相关的儿童胚胎性实体瘤风险。
使用两个基于人群的数据集进行病例队列研究,通过R软件将其关联起来。肿瘤分为中枢神经系统(CNS)或非CNS胚胎性肿瘤(视网膜母细胞瘤、神经母细胞瘤、肾肿瘤、生殖细胞肿瘤、肝母细胞瘤和软组织肉瘤)。选取年龄小于6岁的儿童。对潜在混杂因素进行了调整。使用SPSS通过无条件逻辑回归分析计算比值比(OR)及其95%置信区间(CI)。
男性、母亲教育水平高和出生异常是独立危险因素。在诊断年龄超过24个月的儿童中,剖宫产(CS)是一个显著危险因素。5分钟阿氏评分≤8是肾肿瘤的独立危险因素。除视网膜母细胞瘤外,所有肿瘤类型均观察到出生顺序增加风险降低。在神经母细胞瘤患儿中,风险随出生顺序增加而降低(OR = 0.82(95%CI 0.67 - 1.01))。除视网膜母细胞瘤外,剖宫产分娩的儿童患所有肿瘤的OR略有显著增加。母亲教育水平高显示所有肿瘤、CNS肿瘤和神经母细胞瘤的患病几率显著增加。
该证据表明,无论诊断年龄如何,男性、母亲教育水平高和出生异常都是儿童肿瘤的危险因素。剖宫产、出生顺序和5分钟阿氏评分是某些肿瘤亚型的危险因素。