The Center for Gene Therapy, The Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.
The Departments of Pediatrics, The Ohio State University, Columbus, OH, USA.
Eur J Hum Genet. 2023 Jun;31(6):663-673. doi: 10.1038/s41431-023-01329-5. Epub 2023 Mar 20.
The major determinant of disease severity in Duchenne muscular dystrophy (DMD) or milder Becker muscular dystrophy (BMD) is whether the dystrophin gene (DMD) mutation truncates the mRNA reading frame or allows expression of a partially functional protein. However, even in the complete absence of dystrophin, variability in disease severity is observed, and candidate gene studies have implicated several genes as modifiers. Here we present the largest genome-wide search to date for loci influencing severity in N = 419 DMD patients. Availability of subjects for such studies is quite limited, leading to modest sample sizes, which present a challenge for GWAS design. We have therefore taken special steps to minimize heterogeneity within our dataset at the DMD locus itself, taking a novel approach to mutation classification to effectively exclude the possibility of residual dystrophin expression, and utilized statistical methods that are well adapted to smaller sample sizes, including the use of a novel linear regression-like residual for time to ambulatory loss and the application of evidential statistics for the GWAS approach. Finally, we applied an unbiased in silico pipeline, utilizing functional genomic datasets to explore the potential impact of the best supported SNPs. In all, we obtained eight SNPs (out of 1,385,356 total) with posterior probability of trait-marker association (PPLD) ≥ 0.4, representing six distinct loci. Our analysis prioritized likely non-coding SNP regulatory effects on six genes (ETAA1, PARD6G, GALNTL6, MAN1A1, ADAMTS19, and NCALD), each with plausibility as a DMD modifier. These results support both recurrent and potentially new pathways for intervention in the dystrophinopathies.
杜氏肌营养不良症(DMD)或轻度贝克肌营养不良症(BMD)的疾病严重程度的主要决定因素是肌营养不良蛋白基因(DMD)突变是否截断 mRNA 阅读框或允许表达部分功能蛋白。然而,即使完全缺乏肌营养不良蛋白,也会观察到疾病严重程度的可变性,候选基因研究表明几个基因是修饰基因。在这里,我们提出了迄今为止最大的全基因组搜索,以寻找影响 N = 419 名 DMD 患者严重程度的基因座。此类研究的受试者可用性非常有限,导致样本量较小,这对 GWAS 设计提出了挑战。因此,我们采取了特殊措施来最大限度地减少 DMD 基因座本身数据集中的异质性,采用了一种新的突变分类方法来有效地排除残留肌营养不良蛋白表达的可能性,并利用了非常适合较小样本量的统计方法,包括使用新的线性回归样残差来分析行走能力丧失的时间和为 GWAS 方法应用证据统计学。最后,我们应用了一个无偏的计算管道,利用功能基因组数据集来探索最佳支持 SNP 的潜在影响。总之,我们获得了 8 个 SNP(在 1385356 个总 SNP 中),其特征与标记关联的后验概率(PPLD)≥0.4,代表 6 个不同的基因座。我们的分析优先考虑了 6 个基因(ETAA1、PARD6G、GALNTL6、MAN1A1、ADAMTS19 和 NCALD)上可能的非编码 SNP 调节效应,每个基因都有可能作为 DMD 修饰基因。这些结果支持了在肌营养不良蛋白病中干预的反复出现的和潜在的新途径。