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Three genes associated with anterior and posterior cruciate ligament injury: a genome-wide association analysis

AIMS: The aim of this study was to screen the entire genome for genetic markers associated with risk for anterior cruciate ligament (ACL) and posterior cruciate ligament (PCL) injury. METHODS: Genome-wide association (GWA) analyses were performed using data from the Kaiser Permanente Research Board...

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Autores principales: Kim, Stuart K., Nguyen, Condor, Avins, Andrew L., Abrams, Geoffrey D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The British Editorial Society of Bone & Joint Surgery 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8244791/
https://www.ncbi.nlm.nih.gov/pubmed/34169730
http://dx.doi.org/10.1302/2633-1462.26.BJO-2021-0040.R1
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author Kim, Stuart K.
Nguyen, Condor
Avins, Andrew L.
Abrams, Geoffrey D.
author_facet Kim, Stuart K.
Nguyen, Condor
Avins, Andrew L.
Abrams, Geoffrey D.
author_sort Kim, Stuart K.
collection PubMed
description AIMS: The aim of this study was to screen the entire genome for genetic markers associated with risk for anterior cruciate ligament (ACL) and posterior cruciate ligament (PCL) injury. METHODS: Genome-wide association (GWA) analyses were performed using data from the Kaiser Permanente Research Board (KPRB) and the UK Biobank. ACL and PCL injury cases were identified based on electronic health records from KPRB and the UK Biobank. GWA analyses from both cohorts were tested for ACL and PCL injury using a logistic regression model adjusting for sex, height, weight, age at enrolment, and race/ethnicity using allele counts for single nucleotide polymorphisms (SNPs). The data from the two GWA studies were combined in a meta-analysis. Candidate genes previously reported to show an association with ACL injury in athletes were also tested for association from the meta-analysis data from the KPRB and the UK Biobank GWA studies. RESULTS: There was a total of 2,214 cases of ACL and PCL injury and 519,869 controls within the two cohorts, with three loci demonstrating a genome-wide significant association in the meta-analysis: INHBA, AEBP2, and LOC101927869. Of the eight candidate genes previously studied in the literature, six were present in the current dataset, and only COL3A1 (rs1800255) showed a significant association (p = 0.006). CONCLUSION: Genetic markers in three novel loci in this study and one previously-studied candidate gene were identified as potential risk factors for ACL and PCL injury and deserve further validation and investigation of molecular mechanisms. Cite this article: Bone Jt Open 2021;2(6):414–421.
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spelling pubmed-82447912021-07-14 Three genes associated with anterior and posterior cruciate ligament injury: a genome-wide association analysis Kim, Stuart K. Nguyen, Condor Avins, Andrew L. Abrams, Geoffrey D. Bone Jt Open Knee AIMS: The aim of this study was to screen the entire genome for genetic markers associated with risk for anterior cruciate ligament (ACL) and posterior cruciate ligament (PCL) injury. METHODS: Genome-wide association (GWA) analyses were performed using data from the Kaiser Permanente Research Board (KPRB) and the UK Biobank. ACL and PCL injury cases were identified based on electronic health records from KPRB and the UK Biobank. GWA analyses from both cohorts were tested for ACL and PCL injury using a logistic regression model adjusting for sex, height, weight, age at enrolment, and race/ethnicity using allele counts for single nucleotide polymorphisms (SNPs). The data from the two GWA studies were combined in a meta-analysis. Candidate genes previously reported to show an association with ACL injury in athletes were also tested for association from the meta-analysis data from the KPRB and the UK Biobank GWA studies. RESULTS: There was a total of 2,214 cases of ACL and PCL injury and 519,869 controls within the two cohorts, with three loci demonstrating a genome-wide significant association in the meta-analysis: INHBA, AEBP2, and LOC101927869. Of the eight candidate genes previously studied in the literature, six were present in the current dataset, and only COL3A1 (rs1800255) showed a significant association (p = 0.006). CONCLUSION: Genetic markers in three novel loci in this study and one previously-studied candidate gene were identified as potential risk factors for ACL and PCL injury and deserve further validation and investigation of molecular mechanisms. Cite this article: Bone Jt Open 2021;2(6):414–421. The British Editorial Society of Bone & Joint Surgery 2021-06-25 /pmc/articles/PMC8244791/ /pubmed/34169730 http://dx.doi.org/10.1302/2633-1462.26.BJO-2021-0040.R1 Text en © 2021 Author(s) et al. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial No Derivatives (CC BY-NC-ND 4.0) licence, which permits the copying and redistribution of the work only, and provided the original author and source are credited. See https://creativecommons.org/licenses/by-nc-nd/4.0/
spellingShingle Knee
Kim, Stuart K.
Nguyen, Condor
Avins, Andrew L.
Abrams, Geoffrey D.
Three genes associated with anterior and posterior cruciate ligament injury: a genome-wide association analysis
title Three genes associated with anterior and posterior cruciate ligament injury: a genome-wide association analysis
title_full Three genes associated with anterior and posterior cruciate ligament injury: a genome-wide association analysis
title_fullStr Three genes associated with anterior and posterior cruciate ligament injury: a genome-wide association analysis
title_full_unstemmed Three genes associated with anterior and posterior cruciate ligament injury: a genome-wide association analysis
title_short Three genes associated with anterior and posterior cruciate ligament injury: a genome-wide association analysis
title_sort three genes associated with anterior and posterior cruciate ligament injury: a genome-wide association analysis
topic Knee
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8244791/
https://www.ncbi.nlm.nih.gov/pubmed/34169730
http://dx.doi.org/10.1302/2633-1462.26.BJO-2021-0040.R1
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