Neurological Disorders Research Center, Qatar Biomedical Research Institute (QBRI), Hamad Bin Khalifa University, Doha, Qatar.
Center for Pediatric Neurosciences, Cleveland Clinic, Cleveland, OH, USA.
J Child Psychol Psychiatry. 2019 Dec;60(12):1254-1268. doi: 10.1111/jcpp.13066. Epub 2019 May 8.
Few epidemiological data on autism spectrum disorders (ASD) exist for Arabic countries. We conducted the first survey of ASD in Qatar, a population with high consanguinity level.
This cross-sectional survey was conducted from 2015 to 2018 in Qatar school-age children (N = 176,960) from national and immigrant families. Children diagnosed with ASD were identified through medical centers and special needs schools. Records were abstracted and supplemented by parental interviews. Additionally, children attending 93 schools were screened; ASD case status was confirmed in random samples of screen-positive and screen-negative children. Prevalence was estimated after taking into account different sampling fractions and participation rates at each survey phase.
One thousand three hundred and ninety-three children already diagnosed with ASD were identified. Among 9,074 school survey participants, 760 screen-negative children and 163 screen-positive children were evaluated; 17 were confirmed to have ASD including five children newly diagnosed. Prevalence was 1.14% (95% CI: 0.89-1.46) among 6- to 11-year-olds. ASD was reported in full siblings/extended relatives in 5.9% (95% CI: 0.042-0.080)/11.8% (95% CI: 0.095-0.146) families. First-degree consanguinity in Qatari cases (45%) was comparable to known population levels. Among 844 ASD cases (mean age: 7.2 years; 81% male), most children experienced language delay (words: 75.1%; phrase speech: 91.4%), and 19.4% reported developmental regression. At the time of the survey, persisting deficits in expressive language (19.4%) and peer interactions (14.0%) were reported in conjunction with behavioral problems (ADHD: 30.2%; anxiety: 11.0%). In multivariate logistic regression, ASD severity was associated with parental consanguinity, gestational diabetes, delay in walking, and developmental regression.
ASD prevalence in Qatar is consistent with recent international studies. The methods employed in this study should help designing comparable surveys in the region. We estimated that 187,000 youths under age 20 have ASD in Gulf countries. This figure should assist in planning health and educational services for a young, fast-growing population.
阿拉伯国家的自闭症谱系障碍(ASD)的流行病学数据很少。我们在卡塔尔进行了首次 ASD 调查,这是一个近亲结婚率很高的国家。
这项横断面调查于 2015 年至 2018 年在卡塔尔全国和移民家庭的学龄儿童(N=176960 人)中进行。通过医疗中心和特殊需要学校确定患有 ASD 的儿童。记录通过父母访谈进行了摘录和补充。此外,对 93 所学校的 933 名儿童进行了筛查;在筛查阳性和筛查阴性儿童的随机样本中确认了 ASD 病例的状态。在考虑到每个调查阶段的不同抽样分数和参与率后,对患病率进行了估计。
发现 1393 名已确诊患有 ASD 的儿童。在 9074 名学校调查参与者中,评估了 760 名筛查阴性儿童和 163 名筛查阳性儿童;其中 17 名被确诊为 ASD,包括 5 名新诊断的儿童。6 至 11 岁儿童的患病率为 1.14%(95%CI:0.89-1.46)。在同胞/远房亲属中报告了 ASD,比例为 5.9%(95%CI:0.042-0.080)/11.8%(95%CI:0.095-0.146)。卡塔尔病例的一级近亲结婚率(45%)与已知的人口水平相当。在 844 例 ASD 病例(平均年龄:7.2 岁;81%为男性)中,大多数儿童经历了语言延迟(单词:75.1%;短语语言:91.4%),19.4%报告了发育性倒退。在调查时,19.4%的儿童表达性语言和 14.0%的同伴互动存在持续缺陷,同时还伴有行为问题(ADHD:30.2%;焦虑:11.0%)。在多变量逻辑回归中,ASD 严重程度与父母近亲结婚、妊娠糖尿病、行走延迟和发育性倒退有关。
卡塔尔的 ASD 患病率与最近的国际研究一致。本研究采用的方法应有助于在该地区设计可比调查。我们估计,海湾国家有 187000 名 20 岁以下的年轻人患有 ASD。这个数字应该有助于为快速增长的年轻人口规划卫生和教育服务。