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Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record

机译:评估phecode,临床分类软件和ICD-9-CM代码,用于电子健康记录中的全基因组关联研究

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摘要

To compare three groupings of Electronic Health Record (EHR) billing codes for their ability to represent clinically meaningful phenotypes and to replicate known genetic associations. The three tested coding systems were the International Classification of Diseases, Ninth Revision, Clinical Modification (ICD-9-CM) codes, the Agency for Healthcare Research and Quality Clinical Classification Software for ICD-9-CM (CCS), and manually curated "phecodes" designed to facilitate phenome-wide association studies (PheWAS) in EHRs. We selected 100 disease phenotypes and compared the ability of each coding system to accurately represent them without performing additional groupings. The 100 phenotypes included 25 randomly-chosen clinical phenotypes pursued in prior genome-wide association studies (GWAS) and another 75 common disease phenotypes mentioned across free-text problem lists from 189,289 individuals. We then evaluated the performance of each coding system to replicate known associations for 440 SNP-phenotype pairs. Out of the 100 tested clinical phenotypes, phecodes exactly matched 83, compared to 53 for ICD-9-CM and 32 for CCS. ICD-9-CM codes were typically too detailed (requiring custom groupings) while CCS codes were often not granular enough. Among 440 tested known SNP-phenotype associations, use of phecodes replicated 153 SNP-phenotype pairs compared to 143 for ICD-9-CM and 139 for CCS. Phecodes also generally produced stronger odds ratios and lower p-values for known associations than ICD-9-CM and CCS. Finally, evaluation of several SNPs via PheWAS identified novel potential signals, some seen in only using the phecode approach. Among them, rs7318369 in PEPD was associated with gastrointestinal hemorrhage. Our results suggest that the phecode groupings better align with clinical diseases mentioned in clinical practice or for genomic studies. ICD-9-CM, CCS, and phecode groupings all worked for PheWAS-type studies, though the phecode groupings produced superior results
机译:比较三组电子健康记录(EHR)计费代码的功能,以表示临床上有意义的表型和复制已知的遗传关联。这三个经过测试的编码系统分别是国际疾病分类,第九修订版,临床修改(ICD-9-CM)编码,医疗保健研究机构和ICD-9-CM的质量临床分类软件(CCS),并手动制定了“ phecodes”,旨在促进EHR中的全现象组关联研究(PheWAS)。我们选择了100种疾病表型,并比较了每个编码系统准确代表它们的能力,而无需执行其他分组。这100种表型包括在先前的全基因组关联研究(GWAS)中追求的25种随机选择的临床表型,以及从189,289个人的自由文本问题列表中提到的另外75种常见疾病表型。然后,我们评估了每个编码系统复制440个SNP表型对的已知关联的性能。在100种经过测试的临床表型中,密码与83种精确匹配,而ICD-9-CM为53种,CCS为32种。 ICD-9-CM代码通常过于详细(需要自定义分组),而CCS代码通常不够精细。在440个已知的SNP表型关联中,使用phecodes复制了153个SNP表型对,而ICD-9-CM为143个,CCS为139个。与ICD-9-CM和CCS相比,对于已知的关联,Phecode通常还产生更强的优势比和更低的p值。最后,通过PheWAS对几个SNP的评估确定了新颖的潜在信号,其中一些信号仅在使用phecode方法时才能看到。其中,PEPD中的rs7318369与胃肠道出血有关。我们的结果表明phecode分组与临床实践或基因组研究中提到的临床疾病更好地吻合。 ICD-9-CM,CCS和phecode分组均适用于PheWAS型研究,尽管phecode分组产生了更好的结果

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