Childhood Developmental Milestones and Risk of Adult Cerebrovascular Disease: The Northern Finland Birth Cohort 1966.

IF 2.2 3区 医学 Q3 CLINICAL NEUROLOGY
Milja Kivelä, Ina Rissanen, Eero Kajantie, Marja Ojaniemi, Harri Rusanen, Jouko Miettunen, Markus Paananen
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引用次数: 0

Abstract

Introduction: 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.

Methods: 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.

Results: 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.

Conclusions: 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.

儿童发育里程碑与成人颅脑疾病风险--1966 年北芬兰出生队列。
引言 据我们所知,以前没有研究探讨过儿童发育里程碑与成年后患脑血管疾病(CeVD)风险之间的关系。我们研究了成年后患脑血管疾病的风险是否与运动和语言发育里程碑的延迟有关。方法 在 1966 年北芬兰出生队列(Northern Finland Birth Cohort 1966)中,共对 11,688 人进行了从出生到死亡、移居国外或 54 岁的跟踪调查。CeVD诊断,即缺血性和出血性脑卒中以及短暂性脑缺血发作,是从国家登记册中提取的,并根据世界卫生组织的建议进行了诊断编码。采用按性别分层的 Cox 比例危险模型来估计 0 至 4 岁期间运动发育和语言里程碑与成年 CeVD 的相关性,并针对每个发育里程碑估计女性与男性的相对危险比 (RHR)。分析根据家庭社会经济状况和胎龄体重进行了调整。结果 随访期间共记录了 498 例(4.3%)心血管疾病。在男女儿童中,每延迟一个月从背部转向腹部与成年后缺血性心血管疾病相关,男性的调整后危险比(aHR)为1.25,95%置信区间(CI)为1.06-1.46,女性的调整后危险比为1.20(CI为1.02-1.42)。以运动里程碑主成分得分为模型的整体运动发育延迟与男性缺血性心血管疾病的风险增加有关(aHR 1.50;CI 1.03-2.19)。在男性中,较晚实现发音与任何心血管疾病(aHR 2.74;CI 1.39-5.40),尤其是缺血性心血管疾病(aHR 3.41;CI 1.65-7.06)相关,在任何心血管疾病中,女性对男性的 RHR 为 0.17(95% CI 0.04-0.81),在缺血性中风中,女性对男性的 RHR 为 0.18(95% CI 0.04-0.89),表明女性的风险低于男性。结论 这些研究结果表明,儿童期里程碑的后期成就可能是心血管疾病风险发展的预测因素。这些结果表明了一种共同的神经发育背景,可以部分解释终生累积的心血管疾病风险。
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来源期刊
Cerebrovascular Diseases
Cerebrovascular Diseases 医学-临床神经学
CiteScore
4.50
自引率
0.00%
发文量
90
审稿时长
1 months
期刊介绍: A rapidly-growing field, stroke and cerebrovascular research is unique in that it involves a variety of specialties such as neurology, internal medicine, surgery, radiology, epidemiology, cardiology, hematology, psychology and rehabilitation. ''Cerebrovascular Diseases'' is an international forum which meets the growing need for sophisticated, up-to-date scientific information on clinical data, diagnostic testing, and therapeutic issues, dealing with all aspects of stroke and cerebrovascular diseases. It contains original contributions, reviews of selected topics and clinical investigative studies, recent meeting reports and work-in-progress as well as discussions on controversial issues. All aspects related to clinical advances are considered, while purely experimental work appears if directly relevant to clinical issues.
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