Thomopoulos Thomas P, Skalkidou Alkistis, Dessypris Nick, Chrousos George, Karalexi Maria A, Karavasilis Theodoros G, Baka Margarita, Hatzipantelis Emmanuel, Kourti Maria, Polychronopoulou Sophia, Sidi Vasiliki, Stiakaki Eftichia, Moschovi Maria, Loutradis Dimitrios, Petridou Eleni Th
aDepartment of Hygiene, Epidemiology and Medical Statistics, School of Medicine bFirst Department of Pediatrics, 'Aghia Sophia' Children's Hospital, School of Medicine, University of Athens cDepartment of Pediatric Hematology-Oncology, 'Pan. & Agl. Kyriakou' Children's Hospital dDepartment of Pediatric Haematology-Oncology, 'Aghia Sophia' Children's Hospital eHaematology-Oncology Unit, First Department of Pediatrics, Athens University Medical School, 'Aghia Sophia' Children's Hospital fFirst Department of Obstetrics and Gynecology, 'Alexandra' Hospital, School of Medicine, University of Athens, Athens gSecond Department of Pediatrics, AHEPA General Hospital, Aristotelion University of Thessaloniki hDepartment of Pediatric Hematology and Oncology, Hippokration Hospital, Thessaloniki iDepartment of Pediatric Hematology-Oncology, University Hospital of Heraklion, Heraklion, Greece jDepartment of Women's and Children's Health, Uppsala University, Uppsala, Sweden.
Eur J Cancer Prev. 2016 Mar;25(2):155-61. doi: 10.1097/CEJ.0000000000000151.
The long-term impact of cesarean delivery (CD) on the health of the offspring is being explored methodically. We sought to investigate the effect of birth by (a) prelabor and (b) during-labor CD on the risk of early-onset (≤3 years) acute lymphoblastic leukemia (ALL), specifically of its prevailing precursor B (B-ALL) subtype. A total of 1099 incident cases of ALL (957 B-ALL), 131 of acute myeloid leukemia (AML), and their 1 : 1 age-matched and sex-matched controls, derived from the Nationwide Registry for Childhood Hematological Malignancies (1996-2013), were analyzed using multivariate regression models. A null association was found between prelabor and/or during labor CD and either ALL (B-ALL) or AML in the 0-14 age range. By contrast, birth by CD increased significantly the risk of early-onset ALL [odds ratioCD (ORCD)=1.57, 95% confidence interval (CI): 1.10-2.24] mainly on account of prelabor CD (ORprelaborCD=1.66, 95% CI: 1.13-2.43). The respective figures were even higher for the early-onset precursor B-ALL (ORCD=1.66, 95% CI: 1.15-2.40 and ORprelaborCD=1.79, 95% CI: 1.21-2.66), whereas no association emerged for early-onset AML. Prelabor CD, which deprives exposure of the fetus/infant to the presumably beneficial effect of stress hormones released in both vaginal labor and during labor CD, was associated exclusively with an increased risk of early-onset ALL, particularly the precursor B-ALL subtype. If confirmed, these adverse long-term outcomes of CD may point to re-evaluation of prelabor CD practices and prompt scientific discussion on the best ways to simulate the effects of vaginal delivery, such as a precesarean induction of labor.
剖宫产(CD)对后代健康的长期影响正在被系统地探究。我们试图研究(a)临产前和(b)产时剖宫产分娩对早发型(≤3岁)急性淋巴细胞白血病(ALL)风险的影响,特别是其主要的前体B(B-ALL)亚型。使用多变量回归模型分析了来自全国儿童血液系统恶性肿瘤登记处(1996 - 2013年)的总共1099例ALL(957例B-ALL)、131例急性髓系白血病(AML)病例及其年龄和性别匹配的1:1对照。在0 - 14岁年龄范围内,未发现临产前和/或产时剖宫产与ALL(B-ALL)或AML之间存在关联。相比之下,剖宫产分娩显著增加了早发型ALL的风险[剖宫产优势比(ORCD)=1.57,95%置信区间(CI):1.10 - 2.24],主要是由于临产前剖宫产(ORprelaborCD = 1.66,95% CI:1.13 - 2.43)。早发型前体B-ALL的相应数值甚至更高(ORCD = 1.66,95% CI:1.15 - 2.40和ORprelaborCD = 1.79,95% CI:1.21 - 2.66),而早发型AML未发现关联。临产前剖宫产使胎儿/婴儿无法接触到阴道分娩和产时剖宫产时释放的可能有益的应激激素,这仅与早发型ALL风险增加有关,特别是前体B-ALL亚型。如果得到证实,剖宫产这些不良的长期后果可能指向对临产前剖宫产做法的重新评估,并促使就模拟阴道分娩效果的最佳方法展开科学讨论,例如剖宫产术前引产。