Evidence map›Paper›PMID 36396603›Full record

ArticleAlzheimer's & dementia : the journal of the Alzheimer's Association2023

Blood levels of MCP-1 modulate the genetic risks of Alzheimer's disease mediated by HLA-DRB1 and APOE for Alzheimer's disease.

Jinghan Huang, Thor D Stein, Yixuan Wang, Ting Fang Alvin Ang, Qiushan Tao, Kathryn L Lunetta, Joseph Massaro, Samia C Akhter-Khan, Jesse Mez, Rhoda Au and 4 more

Open access · greenAbstract read
In one paragraph

Article in Alzheimer's & dementia : the journal of the Alzheimer's Association, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.4field-weighted citation impact, top 18% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 14 citations in OpenAlex.

  1. Pooled it
  2. Immune dysfunction in Alzheimer disease.Nature reviews. Neuroscience · 2026
    Review
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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

14 authors at 2 institutions in 3 countries.

Jinghan HuangDepartment of Medicine (Biomedical Genetics), Boston University School of Medicine, Boston, Massachusetts, USA.ORCID 0000-0003-0628-6022
Thor D SteinDepartment of Pathology and Laboratory Medicine, Boston University School of Medicine, Boston, Massachusetts, USA.
Yixuan WangDepartment of Medicine (Biomedical Genetics), Boston University School of Medicine, Boston, Massachusetts, USA.
Ting Fang Alvin AngDepartment of Anatomy & Neurobiology, Boston University School of Medicine, Boston, Massachusetts, USA.
Qiushan TaoDepartment of Pharmacology & Experimental Therapeutics, Boston University School of Medicine, Boston, Massachusetts, USA.
Kathryn L LunettaDepartments of Biostatistics, Boston University School of Public Health, Boston, Massachusetts, USA.
Joseph MassaroDepartments of Biostatistics, Boston University School of Public Health, Boston, Massachusetts, USA.
Samia C Akhter-KhanFramingham Heart Study, Boston University School of Medicine, Framingham, Massachusetts, USA.
Jesse MezAlzheimer's Disease Research Center, Boston University School of Medicine, Boston, Massachusetts, USA.
Rhoda AuAlzheimer's Disease Research Center, Boston University School of Medicine, Boston, Massachusetts, USA.
Lindsay A FarrerDepartment of Medicine (Biomedical Genetics), Boston University School of Medicine, Boston, Massachusetts, USA.
Xiaoling ZhangDepartment of Medicine (Biomedical Genetics), Boston University School of Medicine, Boston, Massachusetts, USA.
Wei Qiao QiuAlzheimer's Disease Research Center, Boston University School of Medicine, Boston, Massachusetts, USA.
Alzheimer's Disease Neuroimaging InitiativeDepartment of Medicine (Biomedical Genetics), Boston University School of Medicine, Boston, Massachusetts, USA.
Boston University · USKing's College London · GB

Funding

Alzheimer's Disease Neuroimaging Initiative - SupplementU01AG024904 · NIA · NORTHERN CALIFORNIA INSTITUTE RES &EDUC · PI WEINER, MICHAEL W · 2004 to 2015
$121.0M
TBDU19AG068753 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Lindsay A. Farrer · 2020 to 2026
$42.4M
Alzheimer Disease Genetic Architecture in African AmericansR01AG048927 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI Lindsay A. Farrer · 2015 to 2026
$8.4M
Multi-center development of a novel diagnostic test for Alzheimer's diseaseR01AG059424 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FARLOW, MARTIN RHYS, KOWALL, NEIL W. · 2018 to 2022
$6.4M
Identification and characterization of the CD31-ApoE-mCRP pathway for Alzheimer's disease in humans.RF1AG075832 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI EMILI, ANDREW, QIU, WEI QIAO WENDY · 2023 to 2023
$2.4M
Genomic and Biological Studies of APOE ε2 in Alzheimer DiseaseRF1AG057519 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI FARRER, LINDSAY A., JUN, GYUNGAH · 2017 to 2017
$2.4M
NIA NIH HHS R01 AG048927NIA NIH HHS R01 AG059424NIA NIH HHS RF1 AG057519NIA NIH HHS RF1 AG075832NIA NIH HHS U01 AG024904NIA NIH HHS U19 AG068753
6 · The paper itself

Abstract

introductionC-Reactive protein (CRP) and monocyte chemoattractant protein-1 (MCP-1) are both implicated in the peripheral proinflammatory cascade and blood-brain barrier (BBB) disruption. Since the blood CRP level increases Alzheimer's disease (AD) risk depending on the apolipoprotein E (APOE) genotype, we hypothesized that the blood MCP-1 level exerts different effects on the AD risk depending on the genotypes.

methodsUsing multiple regression analyses, data from the Framingham Heart Study (n = 2884) and Alzheimer's Disease Neuroimaging Initiative study (n = 231) were analyzed.

resultsAn elevated blood MCP-1 level was associated with AD risk in major histocompatibility complex, Class II, DR beta 1 (HLA-DRB1) rs9271192-AC/CC (hazard ratio [HR] = 3.07, 95% confidence interval [CI] = 1.50-6.28, p = 0.002) and in APOE ε4 carriers (HR = 3.22, 95% CI = 1.59-6.53, p = 0.001). In contrast, among HLA-DRB1 rs9271192-AA and APOE ε4 noncarriers, blood MCP-1 levels were not associated with these phenotypes. DISCUSSION: Since HLA-DRB1 and APOE are expressed in the BBB, blood MCP-1 released in the peripheral inflammatory cascade may function as a mediator of the effects of HLA-DRB1 rs9271192-AC/CC and APOE ε4 genotypes on AD pathogenesis in the brain via the BBB pathways.

Indexed as

Alzheimer DiseaseApolipoproteins EChemokine CCL2HLA-DRB1 ChainsApolipoprotein E4GenotypeHumansApolipoprotein E4Apolipoproteins EChemokine CCL2HLA-DRB1 ChainsAlzheimer's diseasebloodgenotypesMCP-1

Identifiers

PMID36396603
PMCPMC10182187
OpenAlexW4309261576

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.