Bieleninik Łucja, Posserud Maj-Britt, Geretsegger Monika, Thompson Grace, Elefant Cochavit, Gold Christian
GAMUT-The Grieg Academy Music Therapy Research Centre, Uni Research Health, Bergen, Norway.
Department of Child and Adolescent Psychiatry, Division of Psychiatry, Haukeland University Hospital, Bergen, Norway.
PLoS One. 2017 Sep 21;12(9):e0183160. doi: 10.1371/journal.pone.0183160. eCollection 2017.
Exploring ways to improve the trajectory and symptoms of autism spectrum disorder is prevalent in research, but less is known about the natural prognosis of autism spectrum disorder and course of symptoms. The objective of this study was to examine the temporal stability of autism spectrum disorder and autism diagnosis, and the longitudinal trajectories of autism core symptom severity. We furthermore sought to identify possible predictors for change.
We searched PubMed, PsycInfo, EMBASE, Web of Science, Cochrane Library up to October 2015 for prospective cohort studies addressing the autism spectrum disorder/autism diagnostic stability, and prospective studies of intervention effects. We included people of all ages with autism spectrum disorder/autism or at risk of having autism spectrum disorder, who were diagnosed and followed up for at least 12 months using the Autism Diagnostic Observation Schedule (ADOS). Both continuous ADOS scores and dichotomous diagnostic categories were pooled in random-effects meta-analysis and meta-regression.
Of 1443 abstracts screened, 44 were eligible of which 40 studies contained appropriate data for meta-analysis. A total of 5771 participants from 7 months of age to 16.5 years were included. Our analyses showed no change in ADOS scores across time as measured by Calibrated Severity Scores (mean difference [MD] = 0.05, 95% CI -0.26 to 0.36). We observed a minor but statistically significant change in ADOS total raw scores (MD = -1.51, 95% CI -2.70 to -0.32). There was no improvement in restricted and repetitive behaviours (standardised MD [SMD] = -0.04, 95% CI -0.19 to 0.11), but a minor improvement in social affect over time (SMD = -0.31, 95% CI -0.50 to -0.12). No changes were observed for meeting the autism spectrum disorder criteria over time (risk difference [RD] = -0.01, 95% CI -0.03 to 0.01), but a significant change for meeting autism criteria over time (RD = -0.18, 95% CI -0.29 to -0.07). On average, there was a high heterogeneity between studies (I2 range: 65.3% to 93.1%).
While 18% of participants shifted from autism to autism spectrum disorder diagnosis, the overall autism spectrum disorder prevalence was unchanged. Overall autism core symptoms were remarkably stable over time across childhood indicating that intervention studies should focus on other areas, such as quality of life and adaptive functioning. However, due to high heterogeneity between studies and a number of limitations in the studies, the results need to be interpreted with caution.
探索改善自闭症谱系障碍病程及症状的方法在研究中很普遍,但对于自闭症谱系障碍的自然预后及症状发展过程了解较少。本研究的目的是检验自闭症谱系障碍及自闭症诊断的时间稳定性,以及自闭症核心症状严重程度的纵向发展轨迹。我们还试图确定可能的变化预测因素。
我们检索了截至2015年10月的PubMed、PsycInfo、EMBASE、科学引文索引、考克兰图书馆,以查找关于自闭症谱系障碍/自闭症诊断稳定性的前瞻性队列研究以及干预效果的前瞻性研究。我们纳入了所有年龄段患有自闭症谱系障碍/自闭症或有患自闭症谱系障碍风险的人,他们使用自闭症诊断观察量表(ADOS)进行诊断并随访至少12个月。连续的ADOS分数和二分诊断类别都纳入随机效应荟萃分析和荟萃回归。
在筛选的1443篇摘要中,44篇符合条件,其中40项研究包含适合荟萃分析的数据。共纳入了5771名年龄从7个月至16.5岁的参与者。我们的分析显示,根据校准严重程度评分,ADOS分数随时间没有变化(平均差异[MD]=0.05,95%置信区间-0.26至0.36)。我们观察到ADOS总原始分数有轻微但具有统计学意义的变化(MD=-1.51,95%置信区间-2.70至-0.32)。受限和重复行为没有改善(标准化平均差异[SMD]=-0.04,95%置信区间-0.19至0.11),但随着时间推移社交情感有轻微改善(SMD=-0.31,95%置信区间-0.50至-0.12)。随着时间推移,符合自闭症谱系障碍标准没有变化(风险差异[RD]=-0.01,95%置信区间-0.03至0.01),但符合自闭症标准有显著变化(RD=-0.18,95%置信区间-0.29至-0.07)。平均而言,各研究之间存在高度异质性(I平方范围:65.3%至93.1%)。
虽然18%的参与者从自闭症诊断转变为自闭症谱系障碍诊断,但总体自闭症谱系障碍患病率没有变化。在整个儿童期,总体自闭症核心症状随时间相当稳定,这表明干预研究应关注其他领域,如生活质量和适应功能。然而,由于研究之间存在高度异质性以及研究中的一些局限性,结果需要谨慎解释。