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ABSTRACT: Background
Human twin studies and other studies have indicated that chronic pain has heritability that ranges from 30% to 70%. We aimed to identify potential genetic variants that contribute to the susceptibility to chronic pain and efficacy of administered drugs. We conducted genome-wide association studies (GWASs) using whole-genome genotyping arrays with more than 700,000 markers in 191 chronic pain patients and a subgroup of 89 patients with postherpetic neuralgia (PHN) in addition to 282 healthy control subjects in several genetic models, followed by additional gene-based and gene-set analyses of the same phenotypes. We also performed a GWAS for the efficacy of drugs for the treatment of pain.Results
Although none of the single-nucleotide polymorphisms (SNPs) were foun
SUBMITTER: Nishizawa D
PROVIDER: S-EPMC8822450 | biostudies-literature | 2021 Jan-Dec
REPOSITORIES: biostudies-literature