Kessous Roy, Sheiner Eyal, Rosen Guy Beck, Kapelushnik Joseph, Wainstock Tamar
Department of Obstetrics and Gynecology, Soroka University Medical Center, Ben-Gurion University of the Negev, 84101, Beer-Sheva, Israel.
Pediatric Hemato-Oncology Department, Saban Pediatric Medical Center, Soroka University Medical Center, Beer-Sheva, Israel.
Arch Gynecol Obstet. 2022 Nov;306(5):1485-1494. doi: 10.1007/s00404-022-06410-w. Epub 2022 Feb 8.
The aim of this study was to evaluate whether children that were born small for gestational age (SGA) have an increased risk for childhood neoplasm.
A population-based cohort analysis comparing the risk for long-term childhood neoplasms (benign and malignant) in children that were born SGA vs. those that were appropriate for gestational age (AGA), between the years1991-2014. Childhood neoplasms were predefined based on ICD-9 codes, as recorded in the hospital medical files. Kaplan-Meier survival curves were constructed to compare cumulative oncological morbidity in both groups over time. Cox proportional hazards model was used to control for confounders.
During the study period 231,973 infants met the inclusion criteria; out of those 10,998 were born with a diagnosis of SGA. Children that were SGA at birth had higher incidence of lymphoma (OR 2.50, 95% CI 1.06-5.82; p value = 0.036). In addition, cumulative incidence over time of total childhood lymphoma was significantly higher in SGA children (Log Rank = 0.030). In a Cox regression model controlling for other perinatal confounders; SGA at birth remained independently associated with an increased risk for childhood lymphoma (adjusted HR 2.41, 95% CI 1.03-5.56, p value = 0.043).
Being delivered SGA is associated with an increased long-term risk for childhood malignancy and specifically lymphoma.
本研究旨在评估小于胎龄儿(SGA)患儿童肿瘤的风险是否增加。
一项基于人群的队列分析,比较1991年至2014年间出生的SGA儿童与适于胎龄儿(AGA)患儿童期长期肿瘤(良性和恶性)的风险。儿童肿瘤根据医院医疗档案中记录的ICD-9编码预先定义。构建Kaplan-Meier生存曲线以比较两组随时间的累积肿瘤发病率。使用Cox比例风险模型控制混杂因素。
在研究期间,231,973名婴儿符合纳入标准;其中10,998名出生时被诊断为SGA。出生时为SGA的儿童患淋巴瘤的发病率更高(OR 2.50,95%CI 1.06-5.82;p值=0.036)。此外,SGA儿童中儿童期淋巴瘤的累积发病率随时间显著更高(对数秩检验=0.030)。在控制其他围产期混杂因素的Cox回归模型中,出生时为SGA仍然与儿童淋巴瘤风险增加独立相关(调整后HR 2.41,95%CI 1.03-5.56,p值=0.043)。
出生时为SGA与儿童期恶性肿瘤尤其是淋巴瘤的长期风险增加相关。