African-American TOMM40'523-APOE haplotypes are admixture of West African and Caucasian alleles

نویسندگان

  • Allen D. Roses
  • Michael W. Lutz
  • Ann M. Saunders
  • Dmitry Goldgaber
  • Robert Saul
  • Scott S. Sundseth
  • P. Anthony Akkari
  • Stephanie M. Roses
  • W. Kirby Gottschalk
  • Keith E. Whitfield
  • Alexander A. Vostrov
  • Michael A. Hauser
  • R. Rand Allingham
  • Daniel K. Burns
  • Ornit Chiba-Falek
  • Kathleen A. Welsh-Bohmer
چکیده

BACKGROUND Several studies have demonstrated a lower apolipoprotein E4 (APOE ε4) allele frequency in African-Americans, but yet an increased age-related prevalence of AD. An algorithm for prevention clinical trials incorporating TOMM40'523 (Translocase of Outer Mitochondria Membrane) and APOE depends on accurate TOMM40'523-APOE haplotypes. METHODS We have compared the APOE and TOMM40'523 phased haplotype frequencies of a 9.5 kb TOMM40/APOE genomic region in West African, Caucasian, and African-American cohorts. RESULTS African-American haplotype frequency scans of poly-T lengths connected in phase with either APOE ε4 or APOE ε3 differ from both West Africans and Caucasians and represent admixture of several distinct West African and Caucasian haplotypes. A new West African TOMM40'523 haplotype, with APOE ε4 connected to a short TOMM40'523 allele, is observed in African-Americans but not Caucasians. CONCLUSION These data have therapeutic implications for the age of onset risk algorithm estimates and the design of a prevention trial for African-Americans or other mixed ethnic populations.

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عنوان ژورنال:
  • Alzheimer's & Dementia

دوره 10  شماره 

صفحات  -

تاریخ انتشار 2014