Choi, Kyu YeongLee, Jang JaeGunasekaran, Tamil IniyanKang, SarangLee, WoojeJeong, JanghoLim, Ho JaeZhang, XiaolingZhu, CongcongWon, So-YoonChoi, Yu YongSeo, Eun HyunLee, Seok CheolGim, JungsooChung, Ji YeonChong, AriByun, Min SooSeo, SujinKo, Pan-WooHan, Ji-WonMcLean, CatrionaFarrell, JohnLunetta, Kathryn L.Miyashita, AkinoriHara, NorikazuWon, SunghoChoi, Seong-MinHa, Jung-MinJeong, Jee HyangKuwano, RyozoSong, Min KyungAn, Seong Soo A.Lee, Young MinPark, Kyung WonLee, Ho-WonChoi, Seong HyeRhee, SangmyungSong, Woo KeunLee, Jung SupMayeux, RichardHaines, Jonathan L.Pericak-Vance, Margaret A.Choo, IL HanNho, KwangsikKim, Ki-WoongLee, Dong YoungKim, SangYunKim, Byeong C.Kim, HoowonJun, Gyungah R.Schellenberg, Gerard D.Ikeuchi, TakeshiFarrer, Lindsay A.Lee, Kun Ho2020-01-022020-01-022019-08-16Choi, K. Y., Lee, J. J., Gunasekaran, T. I., Kang, S., Lee, W., Jeong, J., … Neuroimaging Initative, A. D. (2019). APOE Promoter Polymorphism-219T/G is an Effect Modifier of the Influence of APOE ε4 on Alzheimer's Disease Risk in a Multiracial Sample. Journal of clinical medicine, 8(8), 1236. doi:10.3390/jcm8081236https://hdl.handle.net/1805/21685Variants in the APOE gene region may explain ethnic differences in the association of Alzheimer's disease (AD) with ε4. Ethnic differences in allele frequencies for three APOE region SNPs (single nucleotide polymorphisms) were identified and tested for association in 19,398 East Asians (EastA), including Koreans and Japanese, 15,836 European ancestry (EuroA) individuals, and 4985 African Americans, and with brain imaging measures of cortical atrophy in sub-samples of Koreans and EuroAs. Among ε4/ε4 individuals, AD risk increased substantially in a dose-dependent manner with the number of APOE promoter SNP rs405509 T alleles in EastAs (TT: OR (odds ratio) = 27.02, p = 8.80 × 10-94; GT: OR = 15.87, p = 2.62 × 10-9) and EuroAs (TT: OR = 18.13, p = 2.69 × 10-108; GT: OR = 12.63, p = 3.44 × 10-64), and rs405509-T homozygotes had a younger onset and more severe cortical atrophy than those with G-allele. Functional experiments using APOE promoter fragments demonstrated that TT lowered APOE expression in human brain and serum. The modifying effect of rs405509 genotype explained much of the ethnic variability in the AD/ε4 association, and increasing APOE expression might lower AD risk among ε4 homozygotes.en-USAPOEPromoter polymorphismAlzheimer’s diseaseEthnic variabilityBrain atrophyGenetic associationArticle