Kaitlyn Marie Dybing, Thomas W. McAllister, Yu-Chien Wu, Brenna C. McDonald, Steven P. Broglio, Jason P. Mihalik, Kevin M. Guskiewicz, Joshua T. Goldman, Jonathan C. Jackson, Shannon L. Risacher, Andrew J. Saykin, Kelly N. H. Nudelman
{"title":"Association of Alzheimer's disease polygenic risk score with concussion severity and recovery metrics","authors":"Kaitlyn Marie Dybing, Thomas W. McAllister, Yu-Chien Wu, Brenna C. McDonald, Steven P. Broglio, Jason P. Mihalik, Kevin M. Guskiewicz, Joshua T. Goldman, Jonathan C. Jackson, Shannon L. Risacher, Andrew J. Saykin, Kelly N. H. Nudelman","doi":"10.1101/2024.07.10.24309042","DOIUrl":null,"url":null,"abstract":"Identification of genetic alleles associated with both Alzheimer's disease (AD) and concussion severity/recovery could help explain\nthe association between concussion and elevated dementia risk. However, there has been little investigation into whether AD risk\ngenes associate with concussion severity/recovery, and the limited findings are mixed. We used AD polygenic risk scores (PRS) and\nAPOE genotypes to investigate any such associations in the NCAA-DoD Grand Alliance CARE Consortium (CARE) dataset. We\nassessed six outcomes in 931 total participants. The outcomes were two concussion recovery measures (number of days to\nasymptomatic status, number of days to return to play (RTP)) and four concussion severity measures (scores on SAC and BESS,\nSCAT symptom severity, and total number of symptoms). We calculated PRS using a published score [1] and performed multiple\nlinear regression (MLR) to assess the relationship of PRS with the outcomes. We also used t-tests and chi-square tests to examine\noutcomes by APOE genotype, and MLR to analyze outcomes in European and African genetic ancestry subgroups. Higher PRS was\nassociated with longer injury to RTP in the normal RTP (<24 days) subgroup (p = 0.024), and one standard deviation increase in PRS\nresulted in a 9.89 hour increase to the RTP interval. There were no other consistently significant effects, suggesting that high AD\ngenetic risk is not strongly associated with more severe concussions or poor recovery in young adults. Future studies should attempt to\nreplicate these findings in larger samples with longer follow-up using PRS calculated from diverse populations.","PeriodicalId":501122,"journal":{"name":"medRxiv - Sports Medicine","volume":"5 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"medRxiv - Sports Medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.07.10.24309042","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Identification of genetic alleles associated with both Alzheimer's disease (AD) and concussion severity/recovery could help explain
the association between concussion and elevated dementia risk. However, there has been little investigation into whether AD risk
genes associate with concussion severity/recovery, and the limited findings are mixed. We used AD polygenic risk scores (PRS) and
APOE genotypes to investigate any such associations in the NCAA-DoD Grand Alliance CARE Consortium (CARE) dataset. We
assessed six outcomes in 931 total participants. The outcomes were two concussion recovery measures (number of days to
asymptomatic status, number of days to return to play (RTP)) and four concussion severity measures (scores on SAC and BESS,
SCAT symptom severity, and total number of symptoms). We calculated PRS using a published score [1] and performed multiple
linear regression (MLR) to assess the relationship of PRS with the outcomes. We also used t-tests and chi-square tests to examine
outcomes by APOE genotype, and MLR to analyze outcomes in European and African genetic ancestry subgroups. Higher PRS was
associated with longer injury to RTP in the normal RTP (<24 days) subgroup (p = 0.024), and one standard deviation increase in PRS
resulted in a 9.89 hour increase to the RTP interval. There were no other consistently significant effects, suggesting that high AD
genetic risk is not strongly associated with more severe concussions or poor recovery in young adults. Future studies should attempt to
replicate these findings in larger samples with longer follow-up using PRS calculated from diverse populations.