APOE ε4 influences cognitive decline positively in APP and negatively in PSEN1 mutation carriers with autosomal-dominant Alzheimer's disease
- PMID: 36039401
- PMCID: PMC9826049
- DOI: 10.1111/ene.15536
APOE ε4 influences cognitive decline positively in APP and negatively in PSEN1 mutation carriers with autosomal-dominant Alzheimer's disease
Abstract
Background and purpose: The aim was to investigate the effect of APOE ε4 allele on cognitive decline in adAD. Presence of the APOE ε4 allele reduces age of symptom onset, increases disease progression, and lowers cognitive performance in sporadic Alzheimer's disease (AD), while the impact of the APOE ε4 allele in autosomal-dominant AD (adAD) is incompletely known.
Methods: Mutation carriers (MCs; n = 39) and non-carriers (NCs; n = 40) from six adAD families harbouring a mutation in the APP (28 MCs and 25 NCs) or the PSEN1 genes (11 MCs and 15 NCs) underwent repeated cognitive assessments. A timeline of disease course was defined as years to expected age of clinical onset (YECO) based on history of disease onset in each family. The MC and NC groups were comparable with regard to demographics and prevalence of the APOE ε4 allele. The relationship between cognitive decline and YECO, YECO2 , education, APOE, and APOE-by-YECO interaction was analysed using linear mixed-effects models.
Results: The trajectory of cognitive decline was significantly predicted by linear and quadratic YECO and education in MCs and was determined by age and education in NCs. Adding APOE ε4 allele (presence/absence) as a predictor did not change the results in the MC and NC groups. The outcome also remained the same for MCs and NCs after adding the APOE-by-YECO interaction as a predictor. Analyses of APP and PSEN1 MCs separately showed favourable APOE-by-YECO interaction in APP (less steep decline) and unfavourable interaction in PSEN1 (steeper decline), linked to the APOE ε4 allele.
Conclusion: The APOE ε4 allele influences cognitive decline positively in APP and negatively in PSEN1 mutation carriers with adAD, indicating a possible antagonistic pleiotropy.
Keywords: APOE; APP/PSEN1; autosomal-dominant Alzheimer's disease; cognition; longitudinal.
© 2022 The Authors. European Journal of Neurology published by John Wiley & Sons Ltd on behalf of European Academy of Neurology.
Conflict of interest statement
None.
Figures

Similar articles
-
The APOE ε4 Allele Affects Cognitive Functions Differently in Carriers of APP Mutations Compared to Carriers of PSEN1 Mutations in Autosomal-Dominant Alzheimer's Disease.Genes (Basel). 2021 Dec 7;12(12):1954. doi: 10.3390/genes12121954. Genes (Basel). 2021. PMID: 34946903 Free PMC article.
-
Impact of APOE ε4 and ε2 on plasma neurofilament light chain and cognition in autosomal dominant Alzheimer's disease.Alzheimers Res Ther. 2024 Oct 1;16(1):208. doi: 10.1186/s13195-024-01572-y. Alzheimers Res Ther. 2024. PMID: 39354618 Free PMC article.
-
Odor Identification Across Time in Mutation Carriers and Non-Carriers in Autosomal-Dominant Alzheimer's Disease.J Alzheimers Dis. 2024;97(2):587-598. doi: 10.3233/JAD-230618. J Alzheimers Dis. 2024. PMID: 38160354 Free PMC article.
-
Cognitive Outcomes in Autosomal-Dominant Alzheimer's Disease: A Comprehensive Review from a Colombian Kindred with the Presenilin-1 E280A Mutation.J Alzheimers Dis. 2024;101(2):397-415. doi: 10.3233/JAD-240360. J Alzheimers Dis. 2024. PMID: 39213071 Free PMC article. Review.
-
Apolipoprotein E (APOE) ε4 and episodic memory decline in Alzheimer's disease: A review.Ageing Res Rev. 2016 May;27:15-22. doi: 10.1016/j.arr.2016.02.002. Epub 2016 Feb 11. Ageing Res Rev. 2016. PMID: 26876367 Free PMC article. Review.
Cited by
-
CTAD taskforce: genetic therapies in Alzheimer's disease.J Prev Alzheimers Dis. 2025 Sep;12(8):100269. doi: 10.1016/j.tjpad.2025.100269. Epub 2025 Jul 9. J Prev Alzheimers Dis. 2025. PMID: 40634156 Free PMC article. Review.
-
Pathological Functions of Lysosomal Ion Channels in the Central Nervous System.Int J Mol Sci. 2024 Jun 14;25(12):6565. doi: 10.3390/ijms25126565. Int J Mol Sci. 2024. PMID: 38928271 Free PMC article. Review.
-
Potential Modifying Effect of the APOEε4 Allele on Age of Onset and Clinical Manifestations in Patients with Early-Onset Alzheimer's Disease with and without a Pathogenic Variant in PSEN1 in a Sample of the Mexican Population.Int J Mol Sci. 2023 Oct 28;24(21):15687. doi: 10.3390/ijms242115687. Int J Mol Sci. 2023. PMID: 37958671 Free PMC article.
-
DAOA and APOEε4 as Modifiers of Age of Onset in Autosomal-Dominant Early-Onset Alzheimer's Disease Caused by the PSEN1 A431E Variant.Int J Mol Sci. 2025 Aug 16;26(16):7929. doi: 10.3390/ijms26167929. Int J Mol Sci. 2025. PMID: 40869250 Free PMC article.
-
Early- and Late-Onset Alzheimer's Disease: Two Sides of the Same Coin?Diseases. 2024 May 22;12(6):110. doi: 10.3390/diseases12060110. Diseases. 2024. PMID: 38920542 Free PMC article. Review.
References
-
- Corder EH, Saunders AM, Strittmatter WJ, et al. Gene dose of apolipoprotein E type 4 allele and the risk of Alzheimer's disease in late onset families. Science. 1993;261:921‐923. - PubMed
-
- Sudre CH, Cardoso MJ, Frost C, et al. APOE e4 status is associated with white matter hyperintensities volume accumulation rate independent of AD diagnosis. Neurobiol Aging. 2017;53:67‐75. - PubMed
-
- Kester MI, Blankenstein MA, Bouwman FH, van Elk EJ, Scheltens P, van der Flier WM. CSF biomarkers in Alzheimer's disease and controls: associations with APOE genotype are modified by age. J Alzheimers Dis. 2009;16:601‐607. - PubMed
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Medical
Miscellaneous