Evidence map›Paper›PMID 38102484›Full record

SynthesisMolecular psychiatry2024

Peripheral immune function and Alzheimer's disease: a living systematic review and critical appraisal.

Chihua Li, Rebecca C Stebbins, Grace A Noppert, Constanza X Carney, Chunyu Liu, Ashley R M Sapp, Elijah J Watson, Allison E Aiello

Open access · greenAbstract readSystematic Review
In one paragraph

Synthesis in Molecular psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
2.6field-weighted citation impact, top 9% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 15 citations in OpenAlex.

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  15. Crosstalk between bone and brain in Alzheimer's disease: Mechanisms, applications, and perspectives.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Review
  16. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

8 authors at 7 institutions in 3 countries.

Chihua Li *Social Environment and Health Program, Institute for Social Research, University of Michigan, Ann Arbor, MI, USA. chihuali@umich.edu.ORCID 0000-0002-0933-8425
Rebecca C Stebbins *Robert N. Butler Columbia Aging Center, Mailman School of Public Health, Columbia University, New York City, NY, USA.
Grace A Noppert *Social Environment and Health Program, Institute for Social Research, University of Michigan, Ann Arbor, MI, USA.ORCID 0000-0002-2040-960X
Constanza X CarneyDepartment of Epidemiology, Milken Institute School of Public Health, The George Washington University, Washington, DC, USA.
Chunyu LiuDepartment of Mental Health, Bloomberg School of Public Health, Johns Hopkins University, Baltimore, MD, USA.
Ashley R M SappCarolina Population Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Elijah J WatsonDepartment of Anthropology, Northwestern University, Evanston, IL, USA.ORCID 0000-0003-3808-0424
Allison E AielloRobert N. Butler Columbia Aging Center, Mailman School of Public Health, Columbia University, New York City, NY, USA.
Johns Hopkins University · USCity University of New York · USColumbia University · USMilken Institute · USNorthwestern University · USUniversity of Michigan · USUniversity of North Carolina at Chapel Hill · US

Funding

Socioeconomic, Cardiovascular, and Psychosocial Sources of Cross-National Variation in Cognitive Health Among Older AdultsR01AG070953 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Alden L. Gross, Lindsay C Kobayashi · 2021 to 2026
$4.6M
Immunosenescence, socioeconomic disadvantage and dementia in the US aging populationR01AG075719 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Allison E Aiello, Grace A Noppert · 2022 to 2026
$3.6M
Social Disadvantage and Its Impact on Pathogen Burden and Immune Dysfunction Across the Life CourseR00AG062749 · NIA · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI NOPPERT, GRACE A · 2021 to 2023
$747k
NIA NIH HHS R00 AG062749NIA NIH HHS R01 AG070953NIA NIH HHS R01 AG075719U.S. Department of Health & Human Services | NIH | National Institute on Aging (U.S. National Institute on Aging) R01AG075719
6 · The paper itself

Abstract

backgroundA growing body of literature examines the relationship between peripheral immune function and Alzheimer's Disease (AD) in human populations. Our living systematic review summarizes the characteristics and findings of these studies, appraises their quality, and formulates recommendations for future research.

methodsWe searched the electronic databases PubMed, PsycINFO, and Web of Science, and reviewed references of previous reviews and meta-analyses to identify human studies examining the relationship between any peripheral immune biomarkers and AD up to September 7th, 2023. We examined patterns of reported statistical associations (positive, negative, and null) between each biomarker and AD across studies. Evidence for each biomarker was categorized into four groups based on the proportion of studies reporting different associations: corroborating a positive association with AD, a negative association, a null association, and presenting contradictory findings. A modified Newcastle-Ottawa scale (NOS) was employed to assess the quality of the included studies.

findingsIn total, 286 studies were included in this review. The majority were cross-sectional (n = 245, 85.7%) and hospital-based (n = 248, 86.7%), examining relationships between 187 different peripheral immune biomarkers and AD. Cytokines were the most frequently studied group of peripheral immune biomarkers. Evidence supported a positive association with AD for six biomarkers, including IL-6, IL-1β, IFN-γ, ACT, IL-18, and IL-12, and a negative association for two biomarkers, including lymphocytes and IL-6R. Only a small proportion of included studies (n = 22, 7.7%) were deemed to be of high quality based on quality assessment.

interpretationExisting research on peripheral immune function and AD exhibits substantial methodological variations and limitations, with a notable lack of longitudinal, population-based studies investigating a broad range of biomarkers with prospective AD outcomes. The extent and manner in which peripheral immune function can contribute to AD pathophysiology remain open questions. Given the biomarkers that we identified to be associated with AD, we posit that targeting peripheral immune dysregulation may present a promising intervention point to reduce the burden of AD.

Indexed as

Alzheimer DiseaseBiomarkersCross-Sectional StudiesCytokinesHumansBiomarkersCytokines

Identifiers

PMID38102484
PMCPMC11483233
OpenAlexW4389792732

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.