Developmental and Behavioral Pediatric & Child Primary Care Department, Ministry of Education-Shanghai Key Laboratory of Children's Environmental Health, Xinhua Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, 200092, China.
Shanghai Children's Medical Center, Shanghai Jiao Tong University School of Medicine, Shanghai, 200127, China.
Neurosci Bull. 2018 Dec;34(6):981-991. doi: 10.1007/s12264-018-0238-2. Epub 2018 Jun 9.
Chromosome microarray analysis (CMA) is a cost-effective molecular cytogenetic technique that has been used as a first-line diagnostic test in neurodevelopmental disorders in the USA since 2011. The impact of CMA results on clinical practice in China is not yet well studied, so we aimed to better evaluate this phenomenon. We analyzed the CMA results from 434 patients in our clinic, and characterized their molecular diagnoses, clinical features, and follow-up clinical actions based on these results. The overall diagnostic yield for our patients was 13.6% (59 out of 434). This gave a detection rate of 14.7% for developmental delay/intellectual disability (DD/ID, 38/259) and 12% for autism spectrum disorders (ASDs, 21/175). Thirty-three recurrent (n ≥ 2) variants were found, distributed at six chromosomal loci involving known chromosome syndromes (such as DiGeorge, Williams Beuren, and Angelman/Prader-Willi syndromes). The spectrum of positive copy number variants in our study was comparable to that reported in Caucasian populations, but with specific characteristics. Parental origin tests indicated an effect involving a significant maternal transmission bias to sons. The majority of patients with positive results (94.9%) had benefits, allowing earlier diagnosis (36/59), prioritized full clinical management (28/59), medication changes (7/59), a changed prognosis (30/59), and prenatal genetic counseling (15/59). Our results provide information on de novo mutations in Chinese children with DD/ID and/or ASDs. Our data showed that microarray testing provides immediate clinical utility for patients. It is expected that the personalized medical care of children with developmental disabilities will lead to improved outcomes in long-term developmental potential. We advocate using the diagnostic yield of clinically actionable results to evaluate CMA as it provides information of both clinical validity and clinical utility.
染色体微阵列分析(CMA)是一种具有成本效益的分子细胞遗传学技术,自 2011 年以来,已被美国用于神经发育障碍的一线诊断测试。CMA 结果对中国临床实践的影响尚未得到很好的研究,因此我们旨在更好地评估这种现象。我们分析了我们诊所 434 例患者的 CMA 结果,并根据这些结果对其分子诊断、临床特征和随访临床措施进行了描述。我们患者的总体诊断率为 13.6%(59/434)。这使得发育迟缓/智力障碍(DD/ID,38/259)的检出率为 14.7%,自闭症谱系障碍(ASD,21/175)的检出率为 12%。发现了 33 个反复出现的(n≥2)变体,分布在涉及已知染色体综合征的六个染色体位点(如 DiGeorge、Williams Beuren 和 Angelman/Prader-Willi 综合征)。我们研究中阳性拷贝数变异的谱与在白种人群中报道的谱相当,但具有特定的特征。父母来源测试表明存在涉及显著母亲向儿子传递偏倚的影响。大多数阳性结果患者(94.9%)受益,可更早诊断(36/59)、优先进行全面临床管理(28/59)、改变药物治疗(7/59)、改变预后(30/59)和进行产前遗传咨询(15/59)。我们的结果提供了中国患有 DD/ID 和/或 ASD 的儿童中新发生突变的信息。我们的数据表明,微阵列检测为患者提供了直接的临床应用。预计对发育障碍儿童进行个性化医疗将导致其长期发育潜力的改善结果。我们提倡使用具有临床可操作性的结果的诊断率来评估 CMA,因为它提供了临床有效性和临床实用性的信息。