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Association of peripheral blood DNA methylation level with Alzheimer's disease progression
Li QS, Vasanthakumar A, Davis JW, Idler KB, Nho K, Waring JF, Saykin AJ, Alzheimer’s Disease Neuroimaging Initiative (ADNI).. Clinical epigenetics, 2021-10-15
Topic: Amyloid, tau and blood-test diagnosis
Plain-language summary
Background Identifying biomarkers associated with Alzheimer's disease (AD) progression may enable patient enrichment and improve clinical trial designs. Epigenome-wide association studies have revealed correlations between DNA methylation at cytosine-phosphate-guanine (CpG) sites and AD pathology and diagnosis. Here, we report relationships between peripheral blood DNA methylation profiles measured using Infinium® MethylationEPIC BeadChip and AD progression in participants from the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort.
What this study adds
Evidence grade: Moderate
The record lists 19 participants. This study looked at peripheral blood DNA methylation profiles in Alzheimer's Disease Neuroimaging Initiative participants to see if they were related to Alzheimer's disease progression. The rate of cognitive decline was estimated from the initial DNA sampling visit to subsequent visits, and correlations with methylation at specific sites were examined.
Taken from this record’s own fields, not from reading the paper. The grade is assigned from the abstract’s wording; what that means.
Cite this study APA, Vancouver, BibTeX · download .bib or .ris
APA 7th
Li, Q. S., Vasanthakumar, A., Davis, J. W., Idler, K. B., Nho, K., Waring, J. F., et al. (2021). Association of peripheral blood DNA methylation level with Alzheimer's disease progression. Clinical epigenetics. https://doi.org/10.1186/s13148-021-01179-2
Vancouver
Li QS, Vasanthakumar A, Davis JW, Idler KB, Nho K, Waring JF, et al. Association of peripheral blood DNA methylation level with Alzheimer's disease progression. Clinical epigenetics. 2021. doi:10.1186/s13148-021-01179-2. PMID: 34654479.
BibTeX
@article{li2021-34654479,
author = {Li, Q. S. and Vasanthakumar, A. and Davis, J. W. and Idler, K. B. and Nho, K. and Waring, J. F. and Saykin, A. J.},
title = {{Association of peripheral blood DNA methylation level with Alzheimer's disease progression}},
journal = {Clinical epigenetics},
year = {2021},
doi = {10.1186/s13148-021-01179-2},
pmid = {34654479},
url = {https://doi.org/10.1186/s13148-021-01179-2}
}
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 names 7 authors; APA and Vancouver show the first six, BibTeX and the downloads carry all of them. Check the citation against the original before you use it.
Key findings
- Epigenome-wide association studies have revealed correlations between DNA methylation at cytosine-phosphate-guanine (CpG) sites and AD pathology and diagnosis.
- Here, we report relationships between peripheral blood DNA methylation profiles measured using Infinium® MethylationEPIC BeadChip and AD progression in participants from the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort.
- Results The rate of cognitive decline from initial DNA sampling visit to subsequent visits was estimated by the slopes of the modified Preclinical Alzheimer Cognitive Composite (mPACC; mPACC digit and mPACC trailsB ) and Clinical Dementia Rating Scale Sum of Boxes (CDR-SB) plots using robust linear regression in cognitively normal (CN) participants and patients with mild cognitive impairment (MCI), respectively.
- In addition, diagnosis conversion status was assessed using a dichotomized endpoint.
Why it matters
This study looked at peripheral blood DNA methylation profiles in Alzheimer's Disease Neuroimaging Initiative participants to see if they were related to Alzheimer's disease progression. The rate of cognitive decline was estimated from the initial DNA sampling visit to subsequent visits, and correlations with methylation at specific sites were examined.
Study details
- Participants19
- Evidence strengthModerate
How this study scored 51/100
Published in a peer-reviewed journal. Scored zero for study design, effect reported and randomized / blinded because the record does not state it. We have no data on senior author's track record, so that was left out: it earned 49 of the 96 points we could judge it on, which is 51 out of 100.
| Component | Points | Why |
|---|---|---|
| Journal tier | 7 / 10 | Tier 3 — peer-reviewed journal (Clinical epigenetics) |
| Journal's citation record | 1 / 4 | Clinical Epigenetics: journal h-index 114 (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 | 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 | 3 / 5 | 2021 — within 6 year(s) of the newest study here |
| Sample size | 1 / 4 | 19 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 | 4 / 7 | Cited 70 times (OpenAlex, 2026-10-10) |
| Citations per year | 3 / 5 | 10.0 citations a year over 7 year(s) since 2021 |
| Impact for its field and year | 4 / 6 | Cited 8.1× the average for papers of its field and year (OpenAlex FWCI) |
| Cited by studies here | 1 / 6 | Cited by 2 other studies in this library |
| Still being cited | 2 / 4 | Cited 42 times in 2024–2026 (2026 still in progress; OpenAlex) |
| Senior author's track record | — / 4 | Senior author's record not available — left out of this score |
| Institution's track record | 1 / 3 | Indiana University School of Medicine: institution h-index 784 (OpenAlex) |
| Multicenter collaboration | 2 / 3 | OpenAlex lists 5 institution(s) in 1 country |
| Indexed in PubMed | 2 / 2 | Indexed in PubMed (PMID 34654479) |
| Free to read | 2 / 2 | Free to read |
| Points | 49 / 96 | Scored on 19 of 20 parts. We have no data for the rest, so they are left out: 49 of the 96 points we could judge it on is 51 out of 100. |
| Total | 51 / 100 | — |
What each of these 20 components measures, and what this score is not →
Read the original
- DOI: 10.1186/s13148-021-01179-2
- PubMed: 34654479
- Original source →
- Free full text: Clinical Epigenetics →
Full text: free to read — OpenAlex lists this copy as free to read: the link above (checked 6 Feb 1020).
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