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Cross-sectional associations of plasma vitamin D with plasma phosphorylated tau-181 and plasma neurofilament light chain in older adults with memory complaints
Claudie Hooper, Emmanuel González, Nicola Coley, Bruno Vellas, Sophie Guyonnet. Neurobiology of Disease, 2025-07-22
Topic: Brain proteins, microglia and lab models
Lack of vitamin D is associated with cognitive decline and Alzheimer's disease. Therefore, we examined the relationship between plasma 25 hydroxyvitamin D [25(OH)D] and plasma phosphorylated-tau 181 (p-tau 181) and neurofilament light chain (NfL) in older adults with memory complaints. This is a cross-sectional analysis of ‘Multidomain Alzheimer Preventive Trial’ baseline data. Subjects were 519 French community-dwelling adults aged 70 + years at risk of dementia with baseline data on plasma 25(OH)D and plasma p-tau 181 and 311 individuals with baseline data on plasma 25(OH)D and plasma NfL. Plasma 25(OH)D, p-tau 181 and NfL were measured using high-sensitivity immune-based assays and associations were explored using adjusted regression analyses. Subjects had a mean (SD) age of 75.2 years (4.3) and 67.6 % were female. The mean (SD) plasma 25(OH)D concentration was 23.5 ng/ml (11.3). The mean (SD) concentrations of plasma p-tau 181 and plasma NfL were 9.9 pg/ml (4.5) and 81.1 pg/ml (34.1) respectively. We did not find significant cross-sectional associations between baseline plasma 25(OH)D and plasma p-tau 181 (Model 3: β-coefficient, 0.0003, 95 % CI: −0.0036, 0.0042, p = 0.879) or plasma 25(OH)D and plasma NfL (Model 3: β-coefficient, −0.0012, 95 % CI: −0.0055, 0.0032, p = 0.599). Age, cognitive status, sex, cardiovascular risk or apolipoprotein ε4 genotype did not modify these non-significant associations. These findings provide evidence that plasma 25(OH)D is not associated with plasma p-tau 181 or plasma NfL in older adults with heightened dementia risk. Longitudinal replication studies are essential to validate these cross-sectional results. • Vitamin D deficiency is associated with an increased risk of Alzheimer's disease. • This is a secondary analysis of the Multidomain Alzheimer Preventive Trial (MAPT). • There were no associations between plasma vitamin D and phosphorylated-tau 181. • There were no associations between plasma vitamin D and neurofilament light chain. • Longitudinal studies are required to validate these cross-sectional findings.
Cite this study APA, Vancouver, BibTeX · download .bib or .ris
APA 7th
Hooper, C., González, E., Coley, N., Vellas, B., & Guyonnet, S. (2025). Cross-sectional associations of plasma vitamin D with plasma phosphorylated tau-181 and plasma neurofilament light chain in older adults with memory complaints. Neurobiology of Disease. https://doi.org/10.1016/j.nbd.2025.107041
Vancouver
Hooper C, González E, Coley N, Vellas B, Guyonnet S. Cross-sectional associations of plasma vitamin D with plasma phosphorylated tau-181 and plasma neurofilament light chain in older adults with memory complaints. Neurobiology of Disease. 2025. doi:10.1016/j.nbd.2025.107041. PMID: 40706903.
BibTeX
@article{hooper2025-40706903,
author = {Hooper, Claudie and González, Emmanuel and Coley, Nicola and Vellas, Bruno and Guyonnet, Sophie},
title = {{Cross-sectional associations of plasma vitamin D with plasma phosphorylated tau-181 and plasma neurofilament light chain in older adults with memory complaints}},
journal = {Neurobiology of Disease},
year = {2025},
doi = {10.1016/j.nbd.2025.107041},
pmid = {40706903},
url = {https://doi.org/10.1016/j.nbd.2025.107041}
}
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Key findings
- Lack of vitamin D is associated with cognitive decline and Alzheimer's disease.
- We did not find significant cross-sectional associations between baseline plasma 25(OH)D and plasma p-tau 181 (Model 3: β-coefficient, 0.0003, 95 % CI: −0.0036, 0.0042, p = 0.879) or plasma 25(OH)D and plasma NfL (Model 3: β-coefficient, −0.0012, 95 % CI: −0.0055, 0.0032, p = 0.599).
- Age, cognitive status, sex, cardiovascular risk or apolipoprotein ε4 genotype did not modify these non-significant associations.
- These findings provide evidence that plasma 25(OH)D is not associated with plasma p-tau 181 or plasma NfL in older adults with heightened dementia risk.
- Longitudinal replication studies are essential to validate these cross-sectional results. • Vitamin D deficiency is associated with an increased risk of Alzheimer's disease. • This is a secondary analysis of the Multidomain Alzheimer Preventive Trial (MAPT). • There were no associations between plasma vitamin D and phosphorylated-tau 181. • There were no associations between plasma vitamin D and neurofilament light chain. • Longitudinal studies are required to validate these cross-sectional findings.
Why it matters
In older adults with memory complaints, the study found no significant cross-sectional associations between plasma vitamin D and either plasma p-tau181 or plasma NfL. This means the data did not show a link between vitamin D levels and these Alzheimer's-related blood markers.
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Study details
- Study designcross-sectional
- Participants311
- Evidence strengthModerate
How this study scored 45/100
Published in a peer-reviewed journal, and it is a snapshot of people at one point in time. Scored zero for effect reported and randomized / blinded because the record does not state it.
| Component | Points | Why |
|---|---|---|
| Journal tier | 7 / 10 | Tier 3 — peer-reviewed journal (Neurobiology of Disease) |
| Journal's citation record | 2 / 4 | Neurobiology of Disease: journal h-index 225 (OpenAlex, 2026-10-29) |
| Study design | 4 / 12 | A snapshot of people at one point in time |
| Strength of evidence | 3 / 5 | Rated “moderate” in our summary |
| Peer-review validation | 10 / 10 | Peer-reviewed. Published as an article in a named peer-reviewed journal. |
| How recent | 4 / 5 | 2025 — within 3 year(s) of the newest study here |
| Sample size | 2 / 4 | 311 participants |
| Effect reported | 0 / 3 | No effect size reported — scores zero (not stated in the record — scored 0) |
| Studied in people | 3 / 3 | Studied in people (participant count stated) |
| Randomized / blinded | 0 / 2 | No randomization or blinding stated — scores zero (not stated in the record — scored 0) |
| Times cited | 0 / 7 | Cited 0 times (OpenAlex, 2026-10-10) |
| Citations per year | 0 / 5 | 0.0 citations a year over 3 year(s) since 2025 |
| Impact for its field and year | 0 / 6 | Cited 0.0× the average for papers of its field and year (OpenAlex FWCI) |
| Cited by studies here | 0 / 6 | No other study in this library cites it |
| Still being cited | 0 / 4 | Cited 0 times in 2024–2026 (2026 still in progress; OpenAlex) |
| Senior author's track record | 2 / 4 | Last-listed author Sophie Guyonnet: h-index 38 (OpenAlex, whole career) |
| Institution's track record | 2 / 3 | Inserm: institution h-index 1,988 (OpenAlex) |
| Multicenter collaboration | 2 / 3 | OpenAlex lists 4 institution(s) in 1 country |
| Indexed in PubMed | 2 / 2 | Indexed in PubMed (PMID 40706903) |
| Free to read | 2 / 2 | Free to read |
| Total | 45 / 100 | — |
What each of these 20 components measures, and what this score is not →
Read the original
- DOI: 10.1016/j.nbd.2025.107041
- PubMed: 40706903
- Original source →
- Free full text: Neurobiology of Disease →
Full text: free to read — OpenAlex lists this copy as free to read: the link above (checked 6 Feb 1020).
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