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Hierarchical Classes Analysis (HICLAS): A novel data reduction method to examine associations between biallelic SNPs and perceptual organization phenotypes in schizophrenia

机译:等级分类分析(HICLAS):一种新颖的数据归约方法用于检查精神分裂症中双等位基因SNP与知觉组织表型之间的关联

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摘要

The power of SNP association studies to detect valid relationships with clinical phenotypes in schizophrenia is largely limited by the number of SNPs selected and non-specificity of phenotypes. To address this, we first assessed performance on two visual perceptual organization tasks designed to avoid many generalized deficit confounds, Kanizsa shape perception and contour integration, in a schizophrenia patient sample. Then, to reduce the total number of candidate SNPs analyzed in association with perceptual organization phenotypes, we employed a two-stage strategy: first a priori SNPs from three candidate genes were selected (GAD1, NRG1 and DTNBP1); then a Hierarchical Classes Analysis (HICLAS) was performed to reduce the total number of SNPs, based on statistically related SNP clusters. HICLAS reduced the total number of candidate SNPs for subsequent phenotype association analyses from 6 to 3. MANCOVAs indicated that rs10503929 and rs1978340 were associated with the Kanizsa shape perception filling in metric but not the global shape detection metric. rs10503929 was also associated with altered contour integration performance. SNPs not selected by the HICLAS model were unrelated to perceptual phenotype indices. While the contribution of candidate SNPs to perceptual impairments requires further clarification, this study reports the first application of HICLAS as a hypothesis-independent mathematical method for SNP data reduction. HICLAS may be useful for future larger scale genotype-phenotype association studies.
机译:SNP关联研究检测与精神分裂症临床表型之间有效关系的能力在很大程度上受到所选SNP数量和表型非特异性的限制。为了解决这个问题,我们首先评估了在两个视觉感知组织任务上的性能,这些任务旨在避免精神分裂症患者样本中的许多广义缺陷混杂症,即卡尼萨形状感知和轮廓整合。然后,为了减少与感知组织表型相关的候选SNP总数,我们采用了两阶段策略:首先从三个候选基因(GAD1,NRG1和DTNBP1)中选择先验SNP;然后根据统计相关的SNP聚类进行层次分类分析(HICLAS),以减少SNP的总数。 HICLAS将用于后续表型关联分析的候选SNP总数从6个减少到3个。MANCOVAs指出rs10503929和rs1978340与填写指标的Kanizsa形状感知相关,但与总体形状检测指标无关。 rs10503929也与轮廓整合性能的改变有关。 HICLAS模型未选择的SNP与感知表型指数无关。尽管候选SNP对知觉障碍的贡献尚需进一步阐明,但本研究报告了HICLAS首次作为假设独立的数学方法用于SNP数据缩减的应用。 HICLAS可能对将来更大规模的基因型-表型关联研究有用。

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