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Modulation of Renin-Angiotensin System May Slow Conversion from Mild Cognitive Impairment to Alzheimer's Disease
Wharton W, Goldstein FC, Zhao L, Steenland K, Levey AI, Hajjar I.. Journal of the American Geriatrics Society, 2015-09-01
Topic: Amyloid, tau and blood-test diagnosis
Plain-language summary
Objectives To assess the effect of modulation of the renin-angiotensin system (RAS) on conversion to Alzheimer's disease (AD) and cognitive decline in people with mild cognitive impairment (MCI) and the effect of the permeability of the blood-brain barrier (BBB) and race on the potential relationship between the RAS and AD. Design Analysis of data from AD centers funded by the National Alzheimer's Coordinating Center, National Institute on Aging. Setting Alzheimer's Disease Centers. Participants Individuals receiving antihypertensive medications who had MCI at baseline and had cognitive assessments on at least two follow-up visits (N = 784; mean age 75 l 48/% male). Measurements Conversion to AD and cognitive and functional decline. Results Four hundred eighty-eight participants were receiving RAS-acting antihypertensive medications. RAS-acting medication users were less likely to convert to AD (33% vs 40%; P = .04) and had slower decline on the Clinical Dementia Rating Sum of Boxes (CDR-SOB, P = .005) and Digit Span Forward (P = .02) than nonusers. BBB-crossing RAS-acting medications were associated with slower cognitive decline on the CDR-SOB, (P = .009), the Mini-Mental State Examination (MMSE), (P = .001), and the Boston Naming test (P = .002). RAS-acting medications were associated with cognitive benefits more in African Americans than in Caucasians (MMSE, P = .05; category fluency, P = .04; Digit Span Backward, P = .03). Conclusion RAS-acting medication users were less likely to convert to AD. BBB permeability may produce additional cognitive benefit, and African Americans may benefit more from RAS modulation than Caucasians. Results highlight the need for trials investigating RAS modulation during prodromal disease stages.
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APA 7th
Wharton, W., Goldstein, F. C., Zhao, L., Steenland, K., Levey, A. I., & Hajjar, I. (2015). Modulation of Renin-Angiotensin System May Slow Conversion from Mild Cognitive Impairment to Alzheimer's Disease. Journal of the American Geriatrics Society. https://doi.org/10.1111/jgs.13627
Vancouver
Wharton W, Goldstein FC, Zhao L, Steenland K, Levey AI, Hajjar I. Modulation of Renin-Angiotensin System May Slow Conversion from Mild Cognitive Impairment to Alzheimer's Disease. Journal of the American Geriatrics Society. 2015. doi:10.1111/jgs.13627. PMID: 26389987.
BibTeX
@article{wharton2015-26389987,
author = {Wharton, W. and Goldstein, F. C. and Zhao, L. and Steenland, K. and Levey, A. I. and Hajjar, I.},
title = {{Modulation of Renin-Angiotensin System May Slow Conversion from Mild Cognitive Impairment to Alzheimer's Disease}},
journal = {Journal of the American Geriatrics Society},
year = {2015},
doi = {10.1111/jgs.13627},
pmid = {26389987},
url = {https://doi.org/10.1111/jgs.13627}
}
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Key findings
- Results Four hundred eighty-eight participants were receiving RAS-acting antihypertensive medications.
- BBB-crossing RAS-acting medications were associated with slower cognitive decline on the CDR-SOB, (P = .009), the Mini-Mental State Examination (MMSE), (P = .001), and the Boston Naming test (P = .002).
- RAS-acting medications were associated with cognitive benefits more in African Americans than in Caucasians (MMSE, P = .05; category fluency, P = .04; Digit Span Backward, P = .03).
- Results highlight the need for trials investigating RAS modulation during prodromal disease stages.
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Study details
- Participants784
- Evidence strengthLow
How this study scored 45/100
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 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 multicenter collaboration, so those were left out: it earned 26 of the 58 points we could judge it on, which is 45 out of 100.
| Component | Points | Why |
|---|---|---|
| Journal tier | 7 / 10 | Tier 3 — peer-reviewed journal (Journal of the American Geriatrics Society) |
| Journal's citation record | — / 4 | No journal record from OpenAlex — left out of this score |
| 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 | 1 / 5 | 2015 — within 20 year(s) of the newest study here |
| Sample size | 2 / 4 | 784 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 | — / 3 | Institutions not listed — left out of this score |
| Indexed in PubMed | 2 / 2 | Indexed in PubMed (PMID 26389987) |
| Free to read | 0 / 2 | Behind a paywall — scores zero |
| Points | 26 / 58 | Scored on 11 of 20 parts. We have no data for the rest, so they are left out: 26 of the 58 points we could judge it on is 45 out of 100. |
| Total | 45 / 100 | — |
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