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An autosomal genomic screen for dementia in an extended Amish family.

Publication ,  Journal Article
Ashley-Koch, AE; Shao, Y; Rimmler, JB; Gaskell, PC; Welsh-Bohmer, KA; Jackson, CE; Scott, WK; Haines, JL; Pericak-Vance, MA
Published in: Neurosci Lett
May 13, 2005

Apolipoprotein E (APOE) is the only universally confirmed susceptibility gene for late-onset Alzheimer disease (LOAD), although many loci are believed to modulate LOAD risk. The genetic homogeneity of isolated populations, such as the Amish, potentially provide increased power to identify LOAD susceptibility genes. Population homogeneity in these special populations may reduce the total number of susceptibility genes contributing to the complex disorder, thereby increasing the ability to identify any one susceptibility gene. Dementia in the Amish is clinically indistinguishable from LOAD in the general population. Previous studies in the Amish demonstrated a significantly decreased frequency of the APOE-4 susceptibility allele, but significant familial clustering of dementia [M.A. Pericak-Vance, C.C. Johnson, J.B. Rimmler, A.M. Saunders, L.C. Robinson, E.G. D'Hondt, C.E. Jackson, J.L. Haines, Alzheimer's disease and apolipoprotein E-4 allele in an Amish population, Ann. Neurol. 39 (1996) 700-704]. These data suggested that a genetic etiology independent of APOE may underlie the dementia observed in this population. In the present analysis, we focused on a large, multiplex, inbred Amish family (24 sampled individuals; 10 of whom are affected). We completed a genomic screen to identify novel LOAD loci (n=316 genetic markers), using both model-dependent "affecteds-only" analysis (dominant and recessive) and model-independent affected relative pair analysis. Interesting results (lod>1.5 or p<0.01) were obtained for markers on eight chromosomes (2q, 5q, 6q, 7p, 8p, 8q, 11p, 18p, 18q, and 19q). The highest overall score was a multipoint lod score of 3.1 on chromosome 11p. Most regions we identified were not previously detected by genomic screens of outbred populations and may represent population-specific susceptibilities to LOAD. These loci are currently under further investigation in a study of LOAD including additional Amish families.

Duke Scholars

Published In

Neurosci Lett

DOI

ISSN

0304-3940

Publication Date

May 13, 2005

Volume

379

Issue

3

Start / End Page

199 / 204

Location

Ireland

Related Subject Headings

  • Pedigree
  • Models, Molecular
  • Lod Score
  • Humans
  • Genetic Testing
  • Genetic Predisposition to Disease
  • Genetic Linkage
  • Female
  • Family Health
  • Ethnicity
 

Citation

APA
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ICMJE
MLA
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Ashley-Koch, A. E., Shao, Y., Rimmler, J. B., Gaskell, P. C., Welsh-Bohmer, K. A., Jackson, C. E., … Pericak-Vance, M. A. (2005). An autosomal genomic screen for dementia in an extended Amish family. Neurosci Lett, 379(3), 199–204. https://doi.org/10.1016/j.neulet.2004.12.065
Ashley-Koch, A. E., Y. Shao, J. B. Rimmler, P. C. Gaskell, K. A. Welsh-Bohmer, C. E. Jackson, W. K. Scott, J. L. Haines, and M. A. Pericak-Vance. “An autosomal genomic screen for dementia in an extended Amish family.Neurosci Lett 379, no. 3 (May 13, 2005): 199–204. https://doi.org/10.1016/j.neulet.2004.12.065.
Ashley-Koch AE, Shao Y, Rimmler JB, Gaskell PC, Welsh-Bohmer KA, Jackson CE, et al. An autosomal genomic screen for dementia in an extended Amish family. Neurosci Lett. 2005 May 13;379(3):199–204.
Ashley-Koch, A. E., et al. “An autosomal genomic screen for dementia in an extended Amish family.Neurosci Lett, vol. 379, no. 3, May 2005, pp. 199–204. Pubmed, doi:10.1016/j.neulet.2004.12.065.
Ashley-Koch AE, Shao Y, Rimmler JB, Gaskell PC, Welsh-Bohmer KA, Jackson CE, Scott WK, Haines JL, Pericak-Vance MA. An autosomal genomic screen for dementia in an extended Amish family. Neurosci Lett. 2005 May 13;379(3):199–204.
Journal cover image

Published In

Neurosci Lett

DOI

ISSN

0304-3940

Publication Date

May 13, 2005

Volume

379

Issue

3

Start / End Page

199 / 204

Location

Ireland

Related Subject Headings

  • Pedigree
  • Models, Molecular
  • Lod Score
  • Humans
  • Genetic Testing
  • Genetic Predisposition to Disease
  • Genetic Linkage
  • Female
  • Family Health
  • Ethnicity