Crump Casey, Sundquist Jan, Sieh Weiva, Winkleby Marilyn A, Sundquist Kristina
Department of Medicine, Stanford University, Stanford, California.
Cancer. 2015 Apr 1;121(7):1040-7. doi: 10.1002/cncr.29172. Epub 2014 Nov 21.
Perinatal factors including high birth weight have been found to be associated with acute lymphoblastic leukemia (ALL) in case-control studies. However, to the best of our knowledge, these findings have seldom been examined in large population-based cohort studies, and the specific contributions of gestational age and fetal growth remain unknown.
The authors conducted a national cohort study of 3,569,333 individuals without Down syndrome who were born in Sweden between 1973 and 2008 and followed for the incidence of ALL through 2010 (maximum age, 38 years) to examine perinatal and familial risk factors.
There were 1960 ALL cases with 69.7 million person-years of follow-up. After adjusting for potential confounders, risk factors for ALL included high fetal growth (incidence rate ratio [IRR] per additional 1 standard deviation, 1.07; 95% confidence interval [95% CI], 1.02-1.11 [P =.002]; and IRR for large vs appropriate for gestational age, 1.22; 95% CI, 1.06-1.40 [P =.005]), first-degree family history of ALL (IRR, 7.41; 95% CI, 4.60-11.95 [P<.001]), male sex (IRR, 1.20; 95% CI, 1.10-1.31 [P<.001]), and parental country of birth (IRR for both parents born in Sweden vs other countries, 1.13; 95% CI, 1.00-1.27 [P =.045]). These risk factors did not appear to vary by patient age at the time of diagnosis of ALL. Gestational age at birth, season of birth, birth order, multiple birth, parental age, and parental education level were not found to be associated with ALL.
In this large cohort study, high fetal growth was found to be associated with an increased risk of ALL in childhood through young adulthood, independent of gestational age at birth, suggesting that growth factor pathways may play an important long-term role in the etiology of ALL.
在病例对照研究中,已发现包括高出生体重在内的围产期因素与急性淋巴细胞白血病(ALL)有关。然而,据我们所知,这些发现很少在基于人群的大型队列研究中得到检验,而且胎龄和胎儿生长的具体作用仍不清楚。
作者对1973年至2008年在瑞典出生且无唐氏综合征的3569333人进行了一项全国性队列研究,并随访至2010年ALL的发病率(最大年龄38岁),以检验围产期和家族性危险因素。
共有1960例ALL病例,随访人年数达6970万。在对潜在混杂因素进行调整后,ALL的危险因素包括胎儿生长过快(每增加1个标准差的发病率比[IRR]为1.07;95%置信区间[95%CI]为1.02 - 1.11[P = 0.002];与适于胎龄儿相比,大于胎龄儿的IRR为1.22;95%CI为1.06 - 1.40[P = 0.005])、ALL一级家族史(IRR为7.41;95%CI为4.60 - 11.95[P<0.001])、男性(IRR为1.20;95%CI为1.10 - 1.31[P<0.001])以及父母的出生国家(父母均出生于瑞典与其他国家相比的IRR为1.13;95%CI为1.00 - 1.27[P = 0.045])。这些危险因素在ALL诊断时的患者年龄方面似乎没有差异。未发现出生时的胎龄、出生季节、出生顺序、多胎妊娠、父母年龄和父母教育水平与ALL有关。
在这项大型队列研究中,发现胎儿生长过快与儿童期至青年期ALL风险增加有关,且独立于出生时的胎龄,这表明生长因子途径可能在ALL的病因学中发挥重要的长期作用。