| Title: | Genome-Wide Association Analysis Identified ANXA1 Associated with Shoulder Impingement Syndrome in UK Biobank Samples |
| Journal: | G3: Genes, Genomes, Genetics |
| Published: | 1 Sep 2020 |
| Pubmed: | https://pubmed.ncbi.nlm.nih.gov/32690583/ |
| DOI: | https://doi.org/10.1534/g3.120.401257 |
| Citations: | 5 (1 in last 2 years) as of 8 Aug 2024 |
Publication 5004
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Abstract
Shoulder impingement syndrome (SIS) is a common shoulder disorder with unclear genetic mechanism. In this study, Genome-wide Association Study (GWAS) was conducted to identify the candidate loci associated with SIS by using the UK Biobank samples (including 3,626 SIS patients and 3,626 control subjects). Based on the GWAS results, gene set enrichment analysis was further performed to detect the candidate gene ontology and pathways associated with SIS. We identified multiple risk loci associated with SIS, such as rs750968 (P = 4.82 × 10-8), rs754832 (P = 4.83 × 10-8) and rs1873119 (P = 6.39 × 10-8) of ANXA1 gene. Some candidate pathways have been identified related to SIS, including those linked to infection response and hypoxia, "ZHOU_INFLAMMATORY_RESPONSE_FIMA_DN" (P = 0.012) and "MANALO_HYPOXIA_UP" (P = 5.00 × 10-5). Our results provide novel clues for understanding the genetic mechanism of SIS.</p>
11 Authors
- Bolun Cheng
- Yujie Ning
- Chujun Liang
- Ping Li
- Li Liu
- Shiqiang Cheng
- Mei Ma
- Lu Zhang
- Xin Qi
- Yan Wen
- Feng Zhang
Enabling scientific discoveries that improve human health