Kivelä Milja, Rissanen Ina, Kajantie Eero, Ojaniemi Marja, Rusanen Harri, Miettunen Jouko, Paananen Markus
Research Unit of Population Health, University of Oulu, Oulu, Finland.
Medical Research Center, Oulu University Hospital and University of Oulu, Oulu, Finland.
Cerebrovasc Dis. 2025;54(4):585-595. doi: 10.1159/000541702. Epub 2024 Oct 3.
To the best of our knowledge, no previous studies have examined the relationship between childhood developmental milestones and risk of adulthood cerebrovascular disease (CeVD). We studied whether the risk of adult CeVD is associated with delayed attainment of motor and language milestones.
Within the Northern Finland Birth Cohort 1966, a total of 11,688 persons were followed from birth to either death, moving abroad or 54 years of age. CeVD diagnoses, i.e., ischemic and hemorrhagic strokes and transient ischemic attacks, were extracted from national registers with diagnostic coding based on recommendations of the World Health Organization. Cox proportional hazard models stratified by sex were used to estimate associations of motor development and language milestones between ages 0 and 4 years and adult CeVD women-to-men relative hazard ratios (RHRs) were estimated for each developmental milestone. Analyses were adjusted for family socioeconomic status and birth weight for gestational age.
Altogether 498 (4.3%) CeVDs were recorded during follow-up. Among both sexes, later turning from back to tummy was associated with ischemic CeVD in adulthood with an adjusted hazard ratio (aHR) of 1.25 and 95% confidence interval (CI) 1.06-1.46 for men and an aHR: 1.20 (CI: 1.02-1.42) for women per 1 month delay in achievement. Delayed overall motor development, modeled by motor milestone principal component score, was related to increased risk of ischemic CeVD (aHR: 1.50; CI: 1.03-2.19) among men. Later achievement of making sounds was associated with any CeVD (aHR: 2.74; CI: 1.39-5.40) and especially ischemic CeVD (aHR: 3.41; CI: 1.65-7.06) among men with women-to-men RHR's of 0.17 (95% CI: 0.04-0.81) for any CeVD and RHR 0.18 (95% CI: 0.04-0.89) for ischemic stroke indicating risk to be lower in women compared to men.
These findings suggest that later achievement of childhood milestones could be a predictor for development of CeVD risk. The results point toward a common neurodevelopmental background and could in part explain lifetime CeVD risk accumulation.
据我们所知,此前尚无研究探讨儿童发育里程碑与成年期脑血管疾病(CeVD)风险之间的关系。我们研究了成年期CeVD风险是否与运动和语言里程碑的延迟达成有关。
在1966年芬兰北部出生队列中,共有11688人从出生开始被随访至死亡、移民国外或54岁。CeVD诊断,即缺血性和出血性中风以及短暂性脑缺血发作,从国家登记处提取,并根据世界卫生组织的建议进行诊断编码。使用按性别分层的Cox比例风险模型来估计0至4岁之间运动发育和语言里程碑与成年期CeVD的关联,并针对每个发育里程碑估计成年女性与男性的相对风险比(RHR)。分析对家庭社会经济地位和出生时的孕周体重进行了调整。
随访期间共记录了498例(4.3%)CeVD。在两性中,从仰卧翻身到俯卧的时间较晚与成年期缺血性CeVD相关,男性每延迟1个月达成,调整后的风险比(aHR)为1.25,95%置信区间(CI)为1.06 - 1.46;女性的aHR为1.20(CI:1.02 - 1.42)。以运动里程碑主成分得分建模的总体运动发育延迟与男性缺血性CeVD风险增加有关(aHR:1.50;CI:1.03 - 2.19)。发声较晚与男性的任何CeVD(aHR:2.74;CI:1.39 - 5.40),尤其是缺血性CeVD(aHR:3.41;CI:1.65 - 7.06)相关,女性与男性的RHR,任何CeVD为0.17(95% CI:0.04 - 0.81),缺血性中风为0.18(95% CI:0.04 - 0.89),表明女性的风险低于男性。
这些发现表明,儿童里程碑达成较晚可能是CeVD风险发展的一个预测因素。结果指向一个共同的神经发育背景,并且可以部分解释CeVD风险在一生中的积累。