Title | Lower mortality risk in APOE4 carriers with normal cognitive ageing. |
Publication Type | Journal Article |
Year of Publication | 2023 |
Authors | Pirraglia E, Glodzik L, Shao Y |
Journal | Sci Rep |
Volume | 13 |
Issue | 1 |
Pagination | 15089 |
Date Published | 2023 Sep 12 |
ISSN | 2045-2322 |
Keywords | Aging, Alzheimer Disease, Apolipoprotein E4, Cognition, Humans, Late Onset Disorders, Risk Factors |
Abstract | Abnormal cognitive ageing, including dementia, poses serious challenges to health and social systems in ageing populations. As such, characterizing factors associated with abnormal cognitive ageing and developing needed preventive measures are of great importance. The ε4 allele of the Apolipoprotein E gene (APOE4) is a well-known genetic risk factor for late-onset Alzheimer's disease. APOE4 carriers are also at elevated risk of cardiovascular diseases which are associated with increased risk of cognitive impairment. On the other hand, APOE4 is known to be associated with reduced risk of multiple common types of cancer-a major age-related disease and leading cause of mortality. We conducted the first-ever study of APOE4's opposing effects on cognitive decline and mortality using competing risk models considering two types of death-death with high-amounts versus low-amounts of autopsy-assessed Alzheimer's neuropathology. We observed that APOE4 was associated with decreased mortality risk in people who died with low amounts of Alzheimer's-type neuropathology, but APOE4 was associated with increased mortality risk in people who died with high amounts of Alzheimer's-type neuropathology, a major risk factor of cognitive impairment. Possible preventive measures of abnormal cognitive ageing are also discussed. |
DOI | 10.1038/s41598-023-41078-5 |
Alternate Journal | Sci Rep |
PubMed ID | 37699966 |
PubMed Central ID | PMC10497512 |
Grant List | P20 AG068053 / AG / NIA NIH HHS / United States P30 AG062421 / AG / NIA NIH HHS / United States P30 AG066508 / AG / NIA NIH HHS / United States P30 AG066519 / AG / NIA NIH HHS / United States P30 AG072973 / AG / NIA NIH HHS / United States P30 AG066462 / AG / NIA NIH HHS / United States P30 AG066530 / AG / NIA NIH HHS / United States P01 AG060882 / AG / NIA NIH HHS / United States P30 AG066509 / AG / NIA NIH HHS / United States P20 AG068077 / AG / NIA NIH HHS / United States P30 AG066546 / AG / NIA NIH HHS / United States P30 AG072972 / AG / NIA NIH HHS / United States P30 AG072979 / AG / NIA NIH HHS / United States P20 AG068082 / AG / NIA NIH HHS / United States P30 AG072975 / AG / NIA NIH HHS / United States P30 AG066444 / AG / NIA NIH HHS / United States P30 AG066507 / AG / NIA NIH HHS / United States P30 AG072946 / AG / NIA NIH HHS / United States P30 AG066518 / AG / NIA NIH HHS / United States P30 AG066511 / AG / NIA NIH HHS / United States U24 AG072122 / AG / NIA NIH HHS / United States P30 AG066512 / AG / NIA NIH HHS / United States U01 OH012486 / OH / NIOSH CDC HHS / United States P30 AG066515 / AG / NIA NIH HHS / United States P30 AG072978 / AG / NIA NIH HHS / United States P30 AG062429 / AG / NIA NIH HHS / United States P30 AG062422 / AG / NIA NIH HHS / United States R01 AG079280 / AG / NIA NIH HHS / United States P30 AG072977 / AG / NIA NIH HHS / United States P30 AG062677 / AG / NIA NIH HHS / United States P20 AG068024 / AG / NIA NIH HHS / United States P30 AG072958 / AG / NIA NIH HHS / United States P30 AG062715 / AG / NIA NIH HHS / United States P30 AG066506 / AG / NIA NIH HHS / United States P30 AG066468 / AG / NIA NIH HHS / United States P30 AG072976 / AG / NIA NIH HHS / United States P30 AG072947 / AG / NIA NIH HHS / United States P30 AG072931 / AG / NIA NIH HHS / United States P30 AG066514 / AG / NIA NIH HHS / United States P30 AG072959 / AG / NIA NIH HHS / United States |
Related Institute:
Brain Health Imaging Institute (BHII)