Association of plasma phosphor-tau181 with Aβ levels may vary by APOE ε4 status and sex among non-demented old adults. (1st April 2023)
- Record Type:
- Journal Article
- Title:
- Association of plasma phosphor-tau181 with Aβ levels may vary by APOE ε4 status and sex among non-demented old adults. (1st April 2023)
- Main Title:
- Association of plasma phosphor-tau181 with Aβ levels may vary by APOE ε4 status and sex among non-demented old adults
- Authors:
- Cai, Yan
Fu, Pan
Zhang, Xin - Abstract:
- Highlights: In the APOE ɛ4 carriers, both females and males demonstrated a stronger significant correlation between plasma p-tau181 and Aβ levels. Our study showed a significant three-way interaction between sex, APOE, and plasma p-tau181 for Aβ levels in non-demented older individuals. Abstract: Background: To evaluate the relationship between blood tau phosphorylated at threonine 181 (p-tau181) levels and β-amyloid (Aβ) levels, this study took the potential role of sex differences and apolipoprotein E (APOE)-ε4 status into account. Methods: We examined 620 participants with normal cognition (n = 178) and mild cognitive impairment (n = 442). Three-way interactions between sex, APOE ε4 status, and the levels of plasma p-tau181 were examined with linear regression models for Aβ levels adjusting for age, education, and diagnosis. The correlation analysis was performed to detect the association of the levels of plasma p-tau181 with brain Aβ stratified for APOE status and sex. Results: Blood p-tau181 levels were higher in APOE ε4+ participants as compared to APOE ε4 – participants ( p < 0.001). A comparison of APOE ε4 status within each gender showed that APOE ε4 carriers had higher levels of plasma p-tau181 and amyloid-β than APOE ε4 noncarriers in both men and women ( p < 0.001). In sex/APOE-stratified analyses, individuals with the APOE ε4 allele showed stronger correlations between plasma p-tau181 and brain Aβ levels in both females (r = 0.49, p < 0.001 for APOE ε4Highlights: In the APOE ɛ4 carriers, both females and males demonstrated a stronger significant correlation between plasma p-tau181 and Aβ levels. Our study showed a significant three-way interaction between sex, APOE, and plasma p-tau181 for Aβ levels in non-demented older individuals. Abstract: Background: To evaluate the relationship between blood tau phosphorylated at threonine 181 (p-tau181) levels and β-amyloid (Aβ) levels, this study took the potential role of sex differences and apolipoprotein E (APOE)-ε4 status into account. Methods: We examined 620 participants with normal cognition (n = 178) and mild cognitive impairment (n = 442). Three-way interactions between sex, APOE ε4 status, and the levels of plasma p-tau181 were examined with linear regression models for Aβ levels adjusting for age, education, and diagnosis. The correlation analysis was performed to detect the association of the levels of plasma p-tau181 with brain Aβ stratified for APOE status and sex. Results: Blood p-tau181 levels were higher in APOE ε4+ participants as compared to APOE ε4 – participants ( p < 0.001). A comparison of APOE ε4 status within each gender showed that APOE ε4 carriers had higher levels of plasma p-tau181 and amyloid-β than APOE ε4 noncarriers in both men and women ( p < 0.001). In sex/APOE-stratified analyses, individuals with the APOE ε4 allele showed stronger correlations between plasma p-tau181 and brain Aβ levels in both females (r = 0.49, p < 0.001 for APOE ε4 carriers vs r = 0.28, p < 0.001 for APOE ε4 noncarrier.) and males (r = 0.34, p < 0.001 for APOE ε4 carriers vs r = 0.21, p = 0.04 for APOE ε4 noncarriers.). In interactive analysis, the association of plasma p-tau181 and Aβ levels was significant in the female APOE ε4 carriers ( p < 0.003). Discussion: APOE ε4 status and female sex interact to impact the correlation between plasma p-tau181 and Aβ levels. Although the APOE ε4 genotype is one of the most important risky genes for AD, sex differences may also modify the degree of risk at critical times among non-demented older adults. … (more)
- Is Part Of:
- Neuroscience letters. Volume 802(2023)
- Journal:
- Neuroscience letters
- Issue:
- Volume 802(2023)
- Issue Display:
- Volume 802, Issue 2023 (2023)
- Year:
- 2023
- Volume:
- 802
- Issue:
- 2023
- Issue Sort Value:
- 2023-0802-2023-0000
- Page Start:
- Page End:
- Publication Date:
- 2023-04-01
- Subjects:
- Blood biomarker -- Apolipoprotein E ε4 -- β-Amyloid -- Plasma phosphorylated tau181 -- Sex differences
Neurology -- Periodicals
Neurology -- Periodicals
Research -- Periodicals
Neurologie -- Périodiques
Neuroanatomie -- Périodiques
Neuropharmacologie -- Périodiques
Neurophysiologie -- Périodiques
Neurology
Periodicals
Electronic journals
617.48 - Journal URLs:
- http://www.sciencedirect.com/science/journal/03043940 ↗
http://www.elsevier.com/journals ↗ - DOI:
- 10.1016/j.neulet.2023.137161 ↗
- Languages:
- English
- ISSNs:
- 0304-3940
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6081.562000
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