Aaron J Gorelik, Sarah E Paul, Nicole R Karcher, Emma C Johnson, Isha Nagella, Lauren Blaydon, Hailey Modi, Isabella S Hansen, Sarah M C Colbert, David A A Baranger, Sara A Norton, Isaiah Spears, Brian Gordon, Wei Zhang, Patrick L Hill, Thomas F Oltmanns, Janine D Bijsterbosch, Arpana Agrawal, Alexander S Hatoum, Ryan Bogdan
{"title":"欧洲血统儿童中晚期阿尔茨海默病遗传风险的全表型关联研究 (PheWAS):ABCD 研究的结果","authors":"Aaron J Gorelik, Sarah E Paul, Nicole R Karcher, Emma C Johnson, Isha Nagella, Lauren Blaydon, Hailey Modi, Isabella S Hansen, Sarah M C Colbert, David A A Baranger, Sara A Norton, Isaiah Spears, Brian Gordon, Wei Zhang, Patrick L Hill, Thomas F Oltmanns, Janine D Bijsterbosch, Arpana Agrawal, Alexander S Hatoum, Ryan Bogdan","doi":"10.1007/s10519-023-10140-3","DOIUrl":null,"url":null,"abstract":"<p><p>Genetic risk for Late Onset Alzheimer Disease (AD) has been associated with lower cognition and smaller hippocampal volume in healthy young adults. However, whether these and other associations are present during childhood remains unclear. Using data from 5556 genomically-confirmed European ancestry youth who completed the baseline session of the ongoing the Adolescent Brain Cognitive Development<sup>SM</sup> Study (ABCD Study®), our phenome-wide association study estimating associations between four indices of genetic risk for late-onset AD (i.e., AD polygenic risk scores (PRS), APOE rs429358 genotype, AD PRS with the APOE region removed (AD<sub>PRS-APOE</sub>), and an interaction between AD<sub>PRS-APOE</sub> and APOE genotype) and 1687 psychosocial, behavioral, and neural phenotypes revealed no significant associations after correction for multiple testing (all ps > 0.0002; all p<sub>fdr</sub> > 0.07). These data suggest that AD genetic risk may not phenotypically manifest during middle-childhood or that effects are smaller than this sample is powered to detect.</p>","PeriodicalId":8715,"journal":{"name":"Behavior Genetics","volume":"53 3","pages":"249-264"},"PeriodicalIF":2.6000,"publicationDate":"2023-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10309061/pdf/","citationCount":"0","resultStr":"{\"title\":\"A Phenome-Wide Association Study (PheWAS) of Late Onset Alzheimer Disease Genetic Risk in Children of European Ancestry at Middle Childhood: Results from the ABCD Study.\",\"authors\":\"Aaron J Gorelik, Sarah E Paul, Nicole R Karcher, Emma C Johnson, Isha Nagella, Lauren Blaydon, Hailey Modi, Isabella S Hansen, Sarah M C Colbert, David A A Baranger, Sara A Norton, Isaiah Spears, Brian Gordon, Wei Zhang, Patrick L Hill, Thomas F Oltmanns, Janine D Bijsterbosch, Arpana Agrawal, Alexander S Hatoum, Ryan Bogdan\",\"doi\":\"10.1007/s10519-023-10140-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Genetic risk for Late Onset Alzheimer Disease (AD) has been associated with lower cognition and smaller hippocampal volume in healthy young adults. However, whether these and other associations are present during childhood remains unclear. Using data from 5556 genomically-confirmed European ancestry youth who completed the baseline session of the ongoing the Adolescent Brain Cognitive Development<sup>SM</sup> Study (ABCD Study®), our phenome-wide association study estimating associations between four indices of genetic risk for late-onset AD (i.e., AD polygenic risk scores (PRS), APOE rs429358 genotype, AD PRS with the APOE region removed (AD<sub>PRS-APOE</sub>), and an interaction between AD<sub>PRS-APOE</sub> and APOE genotype) and 1687 psychosocial, behavioral, and neural phenotypes revealed no significant associations after correction for multiple testing (all ps > 0.0002; all p<sub>fdr</sub> > 0.07). These data suggest that AD genetic risk may not phenotypically manifest during middle-childhood or that effects are smaller than this sample is powered to detect.</p>\",\"PeriodicalId\":8715,\"journal\":{\"name\":\"Behavior Genetics\",\"volume\":\"53 3\",\"pages\":\"249-264\"},\"PeriodicalIF\":2.6000,\"publicationDate\":\"2023-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10309061/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Behavior Genetics\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1007/s10519-023-10140-3\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2023/4/18 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"BEHAVIORAL SCIENCES\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Behavior Genetics","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s10519-023-10140-3","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2023/4/18 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BEHAVIORAL SCIENCES","Score":null,"Total":0}
A Phenome-Wide Association Study (PheWAS) of Late Onset Alzheimer Disease Genetic Risk in Children of European Ancestry at Middle Childhood: Results from the ABCD Study.
Genetic risk for Late Onset Alzheimer Disease (AD) has been associated with lower cognition and smaller hippocampal volume in healthy young adults. However, whether these and other associations are present during childhood remains unclear. Using data from 5556 genomically-confirmed European ancestry youth who completed the baseline session of the ongoing the Adolescent Brain Cognitive DevelopmentSM Study (ABCD Study®), our phenome-wide association study estimating associations between four indices of genetic risk for late-onset AD (i.e., AD polygenic risk scores (PRS), APOE rs429358 genotype, AD PRS with the APOE region removed (ADPRS-APOE), and an interaction between ADPRS-APOE and APOE genotype) and 1687 psychosocial, behavioral, and neural phenotypes revealed no significant associations after correction for multiple testing (all ps > 0.0002; all pfdr > 0.07). These data suggest that AD genetic risk may not phenotypically manifest during middle-childhood or that effects are smaller than this sample is powered to detect.
期刊介绍:
Behavior Genetics - the leading journal concerned with the genetic analysis of complex traits - is published in cooperation with the Behavior Genetics Association. This timely journal disseminates the most current original research on the inheritance and evolution of behavioral characteristics in man and other species. Contributions from eminent international researchers focus on both the application of various genetic perspectives to the study of behavioral characteristics and the influence of behavioral differences on the genetic structure of populations.