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APOE ɛ4 allele and TOMM40-APOC1 variants jointly contribute to survival to older ages.

Publication ,  Journal Article
Kulminski, AM; Jain-Washburn, E; Philipp, I; He, L; Loika, Y; Loiko, E; Bagley, O; Ukraintseva, S; Yashin, A; Arbeev, K; Stallard, E ...
Published in: Aging cell
December 2022

Age-related diseases characteristic of post-reproductive life, aging, and life span are the examples of polygenic non-Mendelian traits with intricate genetic architectures. Polygenicity of these traits implies that multiple variants can impact their risks independently or jointly as combinations of specific variants. Here, we examined chances to live to older ages, 85 years and older, for carriers of compound genotypes comprised of combinations of genotypes of rs429358 (APOE ɛ4 encoding polymorphism), rs2075650 (TOMM40), and rs12721046 (APOC1) polymorphisms using data from four human studies. The choice of these polymorphisms was motivated by our prior results showing that the ɛ4 carriers having minor alleles of the other two polymorphisms were at exceptionally high risk of Alzheimer's disease (AD), compared with non-carriers of the minor alleles. Consistent with our prior findings for AD, we show here that the adverse effect of the ɛ4 allele on survival to older ages is significantly higher in carriers of minor alleles of rs2075650 and/or rs12721046 polymorphisms compared with their non-carriers. The exclusion of AD cases made this effect stronger. Our results provide compelling evidence that AD does not mediate the associations of the same compound genotypes with chances to survive until older ages, indicating the existence of genetically heterogeneous mechanisms. The survival chances can be mainly associated with lipid- and immunity-related mechanisms, whereas the AD risk, can be driven by the AD-biomarker-related mechanism, among others. Targeting heterogeneous polygenic profiles of individuals at high risks of complex traits is promising for the translation of genetic discoveries to health care.

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Published In

Aging cell

DOI

EISSN

1474-9726

ISSN

1474-9718

Publication Date

December 2022

Volume

21

Issue

12

Start / End Page

e13730

Related Subject Headings

  • Mitochondrial Precursor Protein Import Complex Proteins
  • Middle Aged
  • Humans
  • Heterozygote
  • Genotype
  • Developmental Biology
  • Apolipoproteins E
  • Apolipoprotein E4
  • Alzheimer Disease
  • Alleles
 

Citation

APA
Chicago
ICMJE
MLA
NLM
Kulminski, A. M., Jain-Washburn, E., Philipp, I., He, L., Loika, Y., Loiko, E., … Culminskaya, I. (2022). APOE ɛ4 allele and TOMM40-APOC1 variants jointly contribute to survival to older ages. Aging Cell, 21(12), e13730. https://doi.org/10.1111/acel.13730
Kulminski, Alexander M., Ethan Jain-Washburn, Ian Philipp, Liang He, Yury Loika, Elena Loiko, Olivia Bagley, et al. “APOE ɛ4 allele and TOMM40-APOC1 variants jointly contribute to survival to older ages.Aging Cell 21, no. 12 (December 2022): e13730. https://doi.org/10.1111/acel.13730.
Kulminski AM, Jain-Washburn E, Philipp I, He L, Loika Y, Loiko E, et al. APOE ɛ4 allele and TOMM40-APOC1 variants jointly contribute to survival to older ages. Aging cell. 2022 Dec;21(12):e13730.
Kulminski, Alexander M., et al. “APOE ɛ4 allele and TOMM40-APOC1 variants jointly contribute to survival to older ages.Aging Cell, vol. 21, no. 12, Dec. 2022, p. e13730. Epmc, doi:10.1111/acel.13730.
Kulminski AM, Jain-Washburn E, Philipp I, He L, Loika Y, Loiko E, Bagley O, Ukraintseva S, Yashin A, Arbeev K, Stallard E, Feitosa MF, Schupf N, Christensen K, Culminskaya I. APOE ɛ4 allele and TOMM40-APOC1 variants jointly contribute to survival to older ages. Aging cell. 2022 Dec;21(12):e13730.
Journal cover image

Published In

Aging cell

DOI

EISSN

1474-9726

ISSN

1474-9718

Publication Date

December 2022

Volume

21

Issue

12

Start / End Page

e13730

Related Subject Headings

  • Mitochondrial Precursor Protein Import Complex Proteins
  • Middle Aged
  • Humans
  • Heterozygote
  • Genotype
  • Developmental Biology
  • Apolipoproteins E
  • Apolipoprotein E4
  • Alzheimer Disease
  • Alleles