Maher G M, Dalman C, O'Keeffe G W, Kearney P M, McCarthy F P, Kenny L C, Khashan A S
INFANT Research Centre, Cork, Ireland.
School of Public Health, University College Cork, Cork, Ireland.
Acta Psychiatr Scand. 2020 Oct;142(4):275-283. doi: 10.1111/acps.13162. Epub 2020 Feb 29.
To examine the association between preeclampsia and attention-deficit hyperactivity disorder (ADHD), using a large Swedish-based registry cohort.
This study comprised 2 047 619 children, with 114 934 (5.6%) cases of ADHD. Preeclampsia was based on two alternate definitions: (i) preeclampsia (using ICD-9/ICD-10) and (ii) preeclampsia and small for gestational age (SGA) combined. ADHD was determined in one of two ways: (i) if a diagnosis of ADHD was present in the National Patient Register or (ii) if an individual was in receipt of ADHD medication in the Prescribed Drug Register. Multivariate Cox proportional hazards regression analysis allowed adjustment for several perinatal/sociodemographic factors. Sibling-matched analysis further controlled for shared genetic and familial confounding.
In the adjusted Cox model, preeclampsia was associated with an increase in likelihood of ADHD (HR: 1.15, 95% CI: 1.12, 1.19). The HR for preeclampsia and those born SGA was 1.43 (95% CI: 1.31, 1.55) in the adjusted model, compared to those unexposed to preeclampsia/SGA. The sibling-matched analysis did not materially change these associations (HR: 1.13, 95% CI: 1.05, 1.22) and 1.55 (95% CI: 1.28, 1.88).
Exposure to preeclampsia or preeclampsia/SGA was associated with ADHD, independent of genetic/familial factors shared by siblings. However, it is important to note that sibling-matched analysis can only adjust for factors that are constant between pregnancies; therefore, residual confounding cannot be ruled out. Further research is needed to explore modifiable risk factors and identify those most-at-risk babies following delivery.
利用一个基于瑞典的大型登记队列,研究子痫前期与注意力缺陷多动障碍(ADHD)之间的关联。
本研究纳入了2047619名儿童,其中114934例(5.6%)患有ADHD。子痫前期基于两种不同定义:(i)子痫前期(使用ICD - 9/ICD - 10)和(ii)子痫前期合并小于胎龄儿(SGA)。ADHD通过两种方式之一确定:(i)国家患者登记册中是否存在ADHD诊断,或(ii)个体是否在处方药登记册中接受ADHD药物治疗。多变量Cox比例风险回归分析对多个围产期/社会人口统计学因素进行了调整。同胞匹配分析进一步控制了共同的遗传和家族混杂因素。
在调整后的Cox模型中,子痫前期与ADHD发生可能性增加相关(风险比:1.15,95%置信区间:1.12,1.19)。与未暴露于子痫前期/SGA的人群相比,调整模型中,子痫前期合并SGA出生者的风险比为1.43(95%置信区间:1.31,1.55)。同胞匹配分析并未实质性改变这些关联(风险比:1.13,95%置信区间:1.05,1.22)和1.55(95%置信区间:1.28,1.88)。
暴露于子痫前期或子痫前期/SGA与ADHD相关,独立于同胞共享的遗传/家族因素。然而,需要注意的是,同胞匹配分析只能调整妊娠之间恒定的因素;因此,不能排除残余混杂因素。需要进一步研究以探索可改变的风险因素,并识别出生后风险最高的婴儿。