Exploring effect of known Alzheimer disease genetic loci in the Peruvian population

Background Native American populations are substantially underrepresented in Alzheimer disease (AD) genetic studies. The Peruvian (PE) population with up to ∼80 of Amerindian ancestry (AI) provides a unique opportunity to assess the role of AI ancestry in AD. We performed whole‐genome sequencing in...

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Veröffentlicht in:Alzheimer's & dementia 2022-12, Vol.18 (S3), p.n/a
Hauptverfasser: Cornejo‐Olivas, Mario, Rajabli, Farid, Kushch, Nicholas A., Mena, Pedro Ramon, Illanes‐Manrique, Maryenela, Adams, Larry D., Whitehead, Patrice L., Hamilton‐Nelson, Kara L., Milla‐Neyra, Karina, Marca, Victoria, Sarapura‐Castro, Elison, Manrique‐Enciso, Carla, Mejía, Koni K., Isasi, Rosario, Castro‐Suarez, Sheila, Araujo‐Aliaga, Ismael, Custodio, Nilton, Montesinos, Rosa, Griswold, Anthony J., Dalgard, Clifton L., Beecham, Gary W., Cuccaro, Michael L., Vance, Jeffery M., Pericak‐Vance, Margaret A.
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Sprache:eng
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Zusammenfassung:Background Native American populations are substantially underrepresented in Alzheimer disease (AD) genetic studies. The Peruvian (PE) population with up to ∼80 of Amerindian ancestry (AI) provides a unique opportunity to assess the role of AI ancestry in AD. We performed whole‐genome sequencing in PE case‐control study to assess the effect of the known AD loci in PE population. Methods Whole‐genome sequencing was performed in 96 AD cases and 145 unrelated cognitive healthy controls from PE population. We calculated the global ancestry (principal components) using the EIGENSTRAT approach. We tested 21 AD lead variants from the recent large non‐Hispanic White (NHW) GWAS of AD (Kunkle et al. 2019). We performed association analyses using logistic regression model with accounting for age, gender, and population substructure (first three principal components). We used Bonferroni approach for multiple test correction. Results Logistic regression analysis confirmed association of APOE with AD (rs429358, OR=3.6, CI:1.9‐7.0; pv < 8.4e‐05) in PE population. CLU loci (rs9331896, pv=9.3e‐04) passed the significance threshold after Bonferroni multiple test correction. Two AD loci demonstrated nominal associations (pv
ISSN:1552-5260
1552-5279
DOI:10.1002/alz.068028