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巴西 5778 例神经发育障碍和先天性畸形患者的染色体微阵列分析。

Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil.

机构信息

The Human Genome and Stem Cell Research Center, Department of Genetics and Evolutionary Biology, Institute of Biosciences, University of São Paulo, Rua do Matão 277, São Paulo, ZIP Code 05508-090, Brazil.

Diagnósticos da América S.A., DASA, São Paulo, Brazil.

出版信息

Sci Rep. 2022 Sep 7;12(1):15184. doi: 10.1038/s41598-022-19274-6.

Abstract

Chromosomal microarray analysis (CMA) has been recommended and practiced routinely since 2010 both in the USA and Europe as the first-tier cytogenetic test for patients with unexplained neurodevelopmental delay/intellectual disability, autism spectrum disorders, and/or multiple congenital anomalies. However, in Brazil, the use of CMA is still limited, due to its high cost and complexity in integrating the results from both the private and public health systems. Although Brazil has one of the world's largest single-payer public healthcare systems, nearly all patients referred for CMA come from the private sector, resulting in only a small number of CMA studies in Brazilian cohorts. To date, this study is by far the largest Brazilian cohort (n = 5788) studied by CMA and is derived from a joint collaboration formed by the University of São Paulo and three private genetic diagnostic centers to investigate the genetic bases of neurodevelopmental disorders and congenital abnormalities. We identified 2,279 clinically relevant CNVs in 1886 patients, not including the 26 cases of UPD found. Among detected CNVs, the corresponding frequency of each category was 55.6% Pathogenic, 4.4% Likely Pathogenic and 40% VUS. The diagnostic yield, by taking into account Pathogenic, Likely Pathogenic and UPDs, was 19.7%. Since the rational for the classification is mostly based on Mendelian or highly penetrant variants, it was not surprising that a second event was detected in 26% of those cases of predisposition syndromes. Although it is common practice to investigate the inheritance of VUS in most laboratories around the world to determine the inheritance of the variant, our results indicate an extremely low cost-benefit of this approach, and strongly suggest that in cases of a limited budget, investigation of the parents of VUS carriers using CMA should not be prioritized.

摘要

自 2010 年以来,染色体微阵列分析(CMA)已被推荐并常规用于美国和欧洲,作为不明原因的神经发育迟缓/智力障碍、自闭症谱系障碍和/或多发先天性异常患者的一线细胞遗传学检测。然而,在巴西,由于其成本高且难以整合公私医疗系统的结果,CMA 的使用仍然有限。尽管巴西拥有世界上最大的单一支付者公共医疗保健系统之一,但几乎所有转介进行 CMA 的患者都来自私营部门,导致巴西队列中的 CMA 研究数量很少。迄今为止,这项研究是迄今为止巴西最大的队列(n=5788)的 CMA 研究,源自圣保罗大学与三个私人基因诊断中心的联合合作,旨在研究神经发育障碍和先天性异常的遗传基础。我们在 1886 名患者中发现了 2279 个临床相关的 CNV,不包括发现的 26 例 UPD。在所检测到的 CNV 中,每个类别的相应频率分别为 55.6%致病性、4.4%可能致病性和 40% VUS。考虑到致病性、可能致病性和 UPDs,诊断率为 19.7%。由于分类的合理依据主要基于孟德尔或高外显率变异,因此在 26%的易感性综合征病例中检测到第二个事件并不奇怪。尽管在世界各地的大多数实验室中,为确定变异的遗传情况,调查 VUS 的遗传情况是常见做法,但我们的结果表明这种方法的成本效益极低,并强烈表明在预算有限的情况下,不优先对 VUS 携带者的父母进行 CMA 调查。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1293/9452501/17289923f1cc/41598_2022_19274_Fig1_HTML.jpg

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