@article{1906,
  author = {Brian W. Kunkle and Michael Schmidt and Hans-Ulrich Klein and Adam C. Naj and Kara L. Hamilton-Nelson and Eric B. Larson and Denis A. Evans and Phil L. De Jager and Paul K. Crane and Joe D. Buxbaum and Nilufer Ertekin-Taner and Lisa L. Barnes and M. Daniele Fallin and Jennifer J. Manly and Rodney C. P. Go and Thomas O. Obisesan and M. Ilyas Kamboh and David A. Bennett and Kathleen S. Hall and Alison M. Goate and Tatiana M. Foroud and Eden R. Martin and Li-San Wang and Goldie S. Byrd and Lindsay A. Farrer and Jonathan L. Haines and Gerard D. Schellenberg and Richard Mayeux and Margaret A. Pericak-Vance and Christiane Reitz and Writing Group for the Alzheimer’s Disease Genetics Consortium (ADGC)},
  title = {Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis},
  abstract = {Compared with non-Hispanic White individuals, African American individuals from the same community are approximately twice as likely to develop Alzheimer disease. Despite this disparity, the largest Alzheimer disease genome-wide association studies to date have been conducted in non-Hispanic White individuals. In the largest association analyses of Alzheimer disease in African American individuals, ABCA7, TREM2, and an intergenic locus at 5q35 were previously implicated.To identify additional risk loci in African American individuals by increasing the sample size and using the African Genome Resource panel.This genome-wide association meta-analysis used case-control and family-based data sets from the Alzheimer Disease Genetics Consortium. There were multiple recruitment sites throughout the United States that included individuals with Alzheimer disease and controls of African American ancestry. Analysis began October 2018 and ended September 2019.Diagnosis of Alzheimer disease.A total of 2784 individuals with Alzheimer disease (1944 female [69.8%]) and 5222 controls (3743 female [71.7%]) were analyzed (mean [SD] age at last evaluation, 74.2 [13.6] years). Associations with 4 novel common loci centered near the intracellular glycoprotein trafficking gene EDEM1 (3p26; P = 8.9 × 10−7), near the immune response gene ALCAM (3q13; P = 9.3 × 10−7), within GPC6 (13q31; P = 4.1 × 10−7), a gene critical for recruitment of glutamatergic receptors to the neuronal membrane, and within VRK3 (19q13.33; P = 3.5 × 10−7), a gene involved in glutamate neurotoxicity, were identified. In addition, several loci associated with rare variants, including a genome-wide significant intergenic locus near IGF1R at 15q26 (P = 1.7 × 10−9) and 6 additional loci with suggestive significance (P ≤ 5 × 10−7) such as API5 at 11p12 (P = 8.8 × 10−8) and RBFOX1 at 16p13 (P = 5.4 × 10−7) were identified. Gene expression data from brain tissue demonstrate association of ALCAM, ARAP1, GPC6, and RBFOX1 with brain β-amyloid load. Of 25 known loci associated with Alzheimer disease in non-Hispanic White individuals, only APOE, ABCA7, TREM2, BIN1, CD2AP, FERMT2, and WWOX were implicated at a nominal significance level or stronger in African American individuals. Pathway analyses strongly support the notion that immunity, lipid processing, and intracellular trafficking pathways underlying Alzheimer disease in African American individuals overlap with those observed in non-Hispanic White individuals. A new pathway emerging from these analyses is the kidney system, suggesting a novel mechanism for Alzheimer disease that needs further exploration.While the major pathways involved in Alzheimer disease etiology in African American individuals are similar to those in non-Hispanic White individuals, the disease-associated loci within these pathways differ.},
  year = {2021},
  journal = {JAMA Neurology},
  volume = {78},
  pages = {102-113},
  month = {2021-01-01},
  issn = {2168-6149},
  url = {https://doi.org/10.1001/jamaneurol.2020.3536},
  doi = {10.1001/jamaneurol.2020.3536},
}