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Plasma protein biomarker model for screening Alzheimer disease using multiple reaction monitoring-mass spectrometry
Kim Y, Kim J, Son M, Lee J, Yeo I, Choi KY, Kim H, Kim BC et al.. Scientific reports, 2022-01-24
Topic: Amyloid, tau and blood-test diagnosis
Alzheimer disease (AD) is a leading cause of dementia that has gained prominence in our aging society. Yet, the complexity of diagnosing AD and measuring its invasiveness poses an obstacle. To this end, blood-based biomarkers could mitigate the inconveniences that impede an accurate diagnosis. We developed models to diagnose AD and measure the severity of neurocognitive impairment using blood protein biomarkers. Multiple reaction monitoring-mass spectrometry, a highly selective and sensitive approach for quantifying targeted proteins in samples, was used to analyze blood samples from 4 AD groups: cognitive normal control, asymptomatic AD, prodromal AD), and AD dementia. Multimarker models were developed using 10 protein biomarkers and apolipoprotein E genotypes for amyloid beta and 10 biomarkers with Korean Mini-Mental Status Examination (K-MMSE) score for predicting Alzheimer disease progression. The accuracies for the AD classification model and AD progression monitoring model were 84.9% (95% CI 82.8 to 87.0) and 79.1% (95% CI 77.8 to 80.5), respectively. The models were more accurate in diagnosing AD, compared with single APOE genotypes and the K-MMSE score. Our study demonstrates the possibility of predicting AD with high accuracy by blood biomarker analysis as an alternative method of screening for AD.
Key findings
- The models were more accurate in diagnosing AD, compared with single APOE genotypes and the K-MMSE score.
Why it matters
Blood protein models using mass spectrometry classified Alzheimer disease with about 85% accuracy and monitored progression with about 79% accuracy, doing better than APOE genotype alone or a cognitive score. This is a screening approach and does not treat, cure or prevent the disease.
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Study details
- Effect size84.9%; 79.1%
- Evidence strengthLow
How this study scored 45/100
Published in a peer-reviewed journal. Scored zero for study design, sample size, studied in people and randomised / blinded because the record does not state it.
| Component | Points | Why |
|---|---|---|
| Journal tier | 7 / 10 | Tier 3 — peer-reviewed journal (Scientific reports) |
| Journal's citation record | 3 / 4 | Scientific Reports: journal h-index 463 (OpenAlex, 2026-10-29) |
| Study design | 0 / 12 | No study design recorded — scores zero, not guessed (not stated in the record — scored 0) |
| Strength of evidence | 1 / 5 | Rated “low” in our summary |
| Peer-review validation | 10 / 10 | Peer-reviewed. Published as an article in a named peer-reviewed journal. |
| How recent | 3 / 5 | 2022 — within 6 year(s) of the newest study here |
| Sample size | 0 / 4 | Participant count not stated — scores zero (not stated in the record — scored 0) |
| Effect reported | 2 / 3 | Effect reported as a number, without an interval or test |
| Studied in people | 0 / 3 | Not stated whether this was studied in people — scores zero (not stated in the record — scored 0) |
| Randomised / blinded | 0 / 2 | No randomisation or blinding stated — scores zero (not stated in the record — scored 0) |
| Times cited | 3 / 7 | Cited 29 times (OpenAlex, 2026-10-10) |
| Citations per year | 2 / 5 | 4.8 citations a year over 6 year(s) since 2022 |
| Impact for its field and year | 3 / 6 | Cited 3.8× 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 | 2 / 4 | Cited 21 times in 2024–2026 (2026 still in progress; OpenAlex) |
| Senior author's track record | 2 / 4 | Last-listed author Youngsoo Kim: h-index 43 (OpenAlex, whole career) |
| Institution's track record | 1 / 3 | Seoul National University: institution h-index 1,053 (OpenAlex) |
| Multi-centre collaboration | 2 / 3 | OpenAlex lists 5 institution(s) in 1 country |
| Indexed in PubMed | 2 / 2 | Indexed in PubMed (PMID 35075217) |
| 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: 10.1038/s41598-022-05384-8
- PubMed: 35075217
- Original source →
- Free full text: Scientific Reports →
Full text: free to read — OpenAlex lists this copy as free to read: the link above (checked 6 Feb 1020).
Cite this study APA, Vancouver, BibTeX · download .bib or .ris
Built from the record alzhub holds for this paper, not looked up. Volume, issue and page numbers are not held in the record. The record's author list ends in “et al.”, so not every author is named. Check the citation against the original before you use it.
APA 7th
Kim, Y., Kim, J., Son, M., Lee, J., Yeo, I., Choi, K. Y., et al. (2022). Plasma protein biomarker model for screening Alzheimer disease using multiple reaction monitoring-mass spectrometry. Scientific reports. https://doi.org/10.1038/s41598-022-05384-8
Vancouver
Kim Y, Kim J, Son M, Lee J, Yeo I, Choi KY, et al. Plasma protein biomarker model for screening Alzheimer disease using multiple reaction monitoring-mass spectrometry. Scientific reports. 2022. doi:10.1038/s41598-022-05384-8. PMID: 35075217.
BibTeX
@article{kim2022-35075217,
author = {Kim, Y. and Kim, J. and Son, M. and Lee, J. and Yeo, I. and Choi, K. Y. and Kim, H. and Kim, B. C. and others},
title = {{Plasma protein biomarker model for screening Alzheimer disease using multiple reaction monitoring-mass spectrometry}},
journal = {Scientific reports},
year = {2022},
doi = {10.1038/s41598-022-05384-8},
pmid = {35075217},
url = {https://doi.org/10.1038/s41598-022-05384-8}
}
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