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Non-beta-amyloid/tau cerebrospinal fluid markers inform staging and progression in Alzheimer's disease
Umesh Gangishetti, J Christina Howell, Richard J Perrin, Natalia Louneva, Kelly D Watts, Alexander Kollhoff, Murray Grossman, David A Wolk et al.. Alzheimer's research & therapy, 2018-09-25
Topic: Plasma and spinal-fluid biomarkers
Plain-language summary
Three biomarkers were identified to differ among the AD stages, including neurofilament light chain (NfL; p < 0.001), fatty acid binding protein 3 (Fabp3; p < 0.001), and interleukin (IL)-10 (p = 0.033). Increased NfL levels were most strongly associated with the dementia stage of AD, but increased Fabp3 levels were more sensitive to milder AD stages and correlated with both CSF tau markers. IL-10 levels did not correlate with tau biomarkers, but were associated with rates of longitudinal cognitive decline in mild cognitive impairment due to AD (p = 0.006). Prefreezing centrifugation did not influence measured CSF biomarker levels. CSF proteins associated with AD clinical stages and progression can complement Aβ and tau markers to inform neurodegeneration. A validated panel inclusive of multiple biomarker features (etiology, stage, progression) can improve AD phenotyping along the A/T/N framework.
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APA 7th
Gangishetti, U., Howell, J. C., Perrin, R. J., Louneva, N., Watts, K. D., Kollhoff, A., et al. (2018). Non-beta-amyloid/tau cerebrospinal fluid markers inform staging and progression in Alzheimer's disease. Alzheimer's research & therapy. https://doi.org/10.1186/s13195-018-0426-3
Vancouver
Gangishetti U, Howell JC, Perrin RJ, Louneva N, Watts KD, Kollhoff A, et al. Non-beta-amyloid/tau cerebrospinal fluid markers inform staging and progression in Alzheimer's disease. Alzheimer's research & therapy. 2018. doi:10.1186/s13195-018-0426-3. PMID: 30253800.
BibTeX
@article{gangishetti2018-30253800,
author = {Gangishetti, Umesh and Howell, J Christina and Perrin, Richard J and Louneva, Natalia and Watts, Kelly D and Kollhoff, Alexander and Grossman, Murray and Wolk, David A and others},
title = {{Non-beta-amyloid/tau cerebrospinal fluid markers inform staging and progression in Alzheimer's disease}},
journal = {Alzheimer's research \& therapy},
year = {2018},
doi = {10.1186/s13195-018-0426-3},
pmid = {30253800},
url = {https://doi.org/10.1186/s13195-018-0426-3}
}
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Key findings
- Three biomarkers were identified to differ among the AD stages, including neurofilament light chain (NfL; p < 0.001), fatty acid binding protein 3 (Fabp3; p < 0.001), and interleukin (IL)-10 (p = 0.033).
- Increased NfL levels were most strongly associated with the dementia stage of AD, but increased Fabp3 levels were more sensitive to milder AD stages and correlated with both CSF tau markers.
- IL-10 levels did not correlate with tau biomarkers, but were associated with rates of longitudinal cognitive decline in mild cognitive impairment due to AD (p = 0.006).
- Prefreezing centrifugation did not influence measured CSF biomarker levels.
- CSF proteins associated with AD clinical stages and progression can complement Aβ and tau markers to inform neurodegeneration.
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Study details
- Study designlongitudinal study
- Participants31
- Evidence strengthModerate
How this study scored 63/100
Published in a peer-reviewed journal, and it is a longitudinal study following the same people over time. Scored zero for effect reported and randomized / blinded because the record does not state it. We have no data on journal's citation record, times cited, citations per year, impact for its field and year, cited by studies here, still being cited, senior author's track record, institution's track record and free to read, so those were left out: it earned 37 of the 59 points we could judge it on, which is 63 out of 100.
| Component | Points | Why |
|---|---|---|
| Journal tier | 7 / 10 | Tier 3 — peer-reviewed journal (Alzheimer's research & therapy) |
| Journal's citation record | — / 4 | No journal record from OpenAlex — left out of this score |
| Study design | 7 / 12 | A longitudinal study following the same people over 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 | 2 / 5 | 2018 — within 10 year(s) of the newest study here |
| Sample size | 1 / 4 | 31 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 | — / 7 | No citation count (not found in OpenAlex) — left out of this score |
| Citations per year | — / 5 | No citation count or no year — left out of this score |
| Impact for its field and year | — / 6 | No field-weighted citation impact (OpenAlex has none yet) — left out of this score |
| Cited by studies here | — / 6 | Not yet checked against this library's citation graph — left out of this score |
| Still being cited | — / 4 | No yearly citation counts — left out of this score |
| Senior author's track record | — / 4 | Senior author's record not available — left out of this score |
| Institution's track record | — / 3 | No institution listed in OpenAlex — left out of this score |
| Multicenter collaboration | 2 / 3 | PubMed indexes it as a multicentre study |
| Indexed in PubMed | 2 / 2 | Indexed in PubMed (PMID 30253800) |
| Free to read | — / 2 | Access not recorded — left out of this score |
| Points | 37 / 59 | Scored on 11 of 20 parts. We have no data for the rest, so they are left out: 37 of the 59 points we could judge it on is 63 out of 100. |
| Total | 63 / 100 | — |
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