Changes in the prevalence of intellectual disability among 10-year-old children in Sweden during 2011 through 2021: a total population study.

IF 4.1 2区 医学 Q1 CLINICAL NEUROLOGY Journal of Neurodevelopmental Disorders Pub Date : 2024-10-23 DOI:10.1186/s11689-024-09576-3
Maki Morinaga, Viktor H Ahlqvist, Michael Lundberg, Anna-Clara Hollander, Dheeraj Rai, Cecilia Magnusson
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Abstract

Background: Recent studies have suggested an increasing prevalence of intellectual disability diagnoses in some countries. Our aim was to describe the trend in the prevalence of intellectual disability diagnoses in Sweden and explore whether associated sociodemographic and perinatal factors can explain changes in the prevalence.

Methods: We used a register-based nationwide cohort of residents in Sweden born between 2001 and 2011. We calculated the prevalence of intellectual disability diagnoses by age 10 for each birth cohort and the prevalence ratios in relation to the baseline year 2011, overall and by severity of intellectual disability, and comorbidity of autism and attention-deficit/hyperactivity disorder. The prevalence ratios were stratified and adjusted for associated sociodemographic and perinatal factors.

Results: Among 1,096,800 individuals, 8,577 were diagnosed with intellectual disability by age 10. Among these, 3,949 (46%) and 2,768 (32%) were also diagnosed with autism and attention-deficit/hyperactivity disorder, respectively, and 4% were diagnosed with profound, 8% severe, 20% moderate, 52% mild, and 16% other/unspecific intellectual disability. The recorded age-10 prevalence of intellectual disability diagnoses increased from 0.64% (95% confidence interval 0.59-0.69%) in 2011 to 1.00% (0.94-1.06%) in 2021, corresponding to an annual prevalence ratio of 1.04 (1.04-1.05). The increase was, however, restricted to mild, moderate, and other/unspecific intellectual disability diagnoses, while the trends for profound and severe intellectual disability diagnoses were stable. The increasing trend was perhaps less pronounced among females and children with diagnosed attention-deficit/hyperactivity disorder, but independent of the co-occurrence of autism. The prevalence ratios did not change with stratification or adjustment for other associated demographic and perinatal factors.

Conclusion: The recorded prevalence of diagnosed mild and moderate intellectual disability among 10-year-olds in Sweden has increased over the recent decade. This increase could not be explained by changes in associated sociodemographic or perinatal factors, including birth weight, gestational age, and parental age, migration status, and education at the child's birth. The increase instead may be due to changes in diagnostic practices in Sweden over time.

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2011 年至 2021 年期间瑞典 10 岁儿童智力残疾患病率的变化:总人口研究。
背景:最近的研究表明,在一些国家,智力残疾诊断的流行率在不断上升。我们的目的是描述瑞典智障诊断患病率的趋势,并探讨相关的社会人口和围产期因素能否解释患病率的变化:我们使用了一个基于登记的全国性队列,对象是 2001 年至 2011 年间出生的瑞典居民。我们计算了每个出生队列中 10 岁以下智力残疾诊断的患病率,以及与 2011 年基线年相比的患病率比率,包括总体患病率、智力残疾严重程度以及自闭症和注意力缺陷/多动症的合并症。患病率比率根据相关的社会人口和围产期因素进行了分层和调整:在 1,096,800 人中,有 8,577 人在 10 岁前被诊断为智力障碍。其中,3949 人(46%)和 2768 人(32%)还分别被诊断患有自闭症和注意力缺陷/多动障碍,4% 的人被诊断患有深度智力障碍,8% 的人患有重度智力障碍,20% 的人患有中度智力障碍,52% 的人患有轻度智力障碍,16% 的人患有其他/非特异性智力障碍。有记录的 10 岁智障诊断流行率从 2011 年的 0.64%(95% 置信区间为 0.59-0.69%)增至 2021 年的 1.00%(0.94-1.06%),相当于每年 1.04(1.04-1.05)的流行率。不过,这一增长仅限于轻度、中度和其他/非特异性智力残疾诊断,而深度和重度智力残疾诊断的趋势则保持稳定。女性和被诊断患有注意力缺陷/多动障碍的儿童的患病率上升趋势可能不那么明显,但与同时患有自闭症无关。患病率比率没有随着分层或其他相关人口和围产期因素的调整而发生变化:结论:近十年来,瑞典 10 岁儿童中确诊的轻度和中度智障患病率有所上升。这一增长无法用相关社会人口或围产期因素的变化来解释,这些因素包括出生体重、胎龄、父母年龄、移民身份以及儿童出生时的教育程度。增加的原因可能是瑞典的诊断方法随着时间的推移发生了变化。
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来源期刊
CiteScore
7.60
自引率
4.10%
发文量
58
审稿时长
>12 weeks
期刊介绍: Journal of Neurodevelopmental Disorders is an open access journal that integrates current, cutting-edge research across a number of disciplines, including neurobiology, genetics, cognitive neuroscience, psychiatry and psychology. The journal’s primary focus is on the pathogenesis of neurodevelopmental disorders including autism, fragile X syndrome, tuberous sclerosis, Turner Syndrome, 22q Deletion Syndrome, Prader-Willi and Angelman Syndrome, Williams syndrome, lysosomal storage diseases, dyslexia, specific language impairment and fetal alcohol syndrome. With the discovery of specific genes underlying neurodevelopmental syndromes, the emergence of powerful tools for studying neural circuitry, and the development of new approaches for exploring molecular mechanisms, interdisciplinary research on the pathogenesis of neurodevelopmental disorders is now increasingly common. Journal of Neurodevelopmental Disorders provides a unique venue for researchers interested in comparing and contrasting mechanisms and characteristics related to the pathogenesis of the full range of neurodevelopmental disorders, sharpening our understanding of the etiology and relevant phenotypes of each condition.
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