Evidence map›Paper›PMID 20847045›Full record

ArticleThe Journal of biological chemistry2010

Overexpression of human apolipoprotein A-I preserves cognitive function and attenuates neuroinflammation and cerebral amyloid angiopathy in a mouse model of Alzheimer disease.

Terry L Lewis, Dongfeng Cao, Hailin Lu, Robert A Mans, Yan Ru Su, Lisa Jungbauer, MacRae F Linton, Sergio Fazio, Mary Jo LaDu, Ling Li

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 126 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
126citing papers in PubMed, 2 pooled it
5.7field-weighted citation impact, top 3% 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

126 citing papers in PubMed, 2 syntheses or guidelines pooled it, 207 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Associations of plasma HDL subclasses with incident dementia risk in older adults.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
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  6. Review
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  8. CETP Renaissance with Obicetrapib.Current atherosclerosis reports · 2026
    Review
  9. Immune-proteo-metabolomic changes link to Aβ and tau pathology in Alzheimer disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  10. Review
  11. Vascular contribution to cognitive impairment and dementia (VCID): proceedings of 2025 workshop of the Jackson Laboratory.Mammalian genome : official journal of the International Mammalian Genome Society · 2026
    Article
  12. Review
  13. Article
  14. Apolipoprotein A (ApoA) in Neurological Disorders: Connections and Insights.International journal of molecular sciences · 2025
    Review
  15. Article
  16. Review
  17. Article
  18. Review
  19. Article
  20. Article

66 more citing papers are in PubMed but not listed here.

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

10 authors at 4 institutions in 1 country.

Terry L LewisDepartment of Medicine, University of Alabama at Birmingham, Birmingham, Alabama 35294, USA.
Dongfeng Cao
Hailin Lu
Robert A Mans
Yan Ru Su
Lisa Jungbauer
MacRae F Linton
Sergio Fazio
Mary Jo LaDu
Ling Li
University of Illinois Chicago · USUniversity of Alabama at Birmingham · USUniversity of Minnesota · USVanderbilt University Medical Center · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR029879 · NCRR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI MAZZONE, THEODORE · 2009 to 2011
$11.0M
TRANSGENIC MOUSE COREP01AG030128 · NIA · UNIVERSITY OF ILLINOIS AT CHICAGO · PI WEEBER, EDWIN JOHN · 2009 to 2013
$9.4M
MACROPHAGE EXPRESSION OF APOAI AND ATHEROSCLEROSISR01HL065709 · NHLBI · VANDERBILT UNIVERSITY · PI FAZIO, SERGIO · 2000 to 2008
$3.2M
ApoE and SR-BI as Determinants of HDL and Macrophage Function in AtherogenesisR01HL086988 · NHLBI · VANDERBILT UNIVERSITY · PI LINTON, MACRAE F · 2007 to 2010
$1.5M
Protective Mechanisms of Statins in Alzheimer's DiseaseR01AG031846 · NIA · UNIVERSITY OF MINNESOTA · PI LI, LING · 2008 to 2012
$1.5M
NCRR NIH HHS UL1 RR029879NCRR NIH HHS UL1RR029879NHLBI NIH HHS HL086988NHLBI NIH HHS HL65709NHLBI NIH HHS R01 HL065709NHLBI NIH HHS R01 HL086988NIA NIH HHS AG03012801NIA NIH HHS AG031846NIA NIH HHS P01 AG030128NIA NIH HHS R01 AG031846
6 · The paper itself

Abstract

To date there is no effective therapy for Alzheimer disease (AD). High levels of circulating high density lipoprotein (HDL) and its main protein, apolipoprotein A-I (apoA-I), reduce the risk of cardiovascular disease. Clinical studies show that plasma HDL cholesterol and apoA-I levels are low in patients with AD. To investigate if increasing plasma apoA-I/HDL levels ameliorates AD-like memory deficits and amyloid-β (Aβ) deposition, we generated a line of triple transgenic (Tg) mice overexpressing mutant forms of amyloid-β precursor protein (APP) and presenilin 1 (PS1) as well as human apoA-I (AI). Here we show that APP/PS1/AI triple Tg mice have a 2-fold increase of plasma HDL cholesterol levels. When tested in the Morris water maze for spatial orientation abilities, whereas APP/PS1 mice develop age-related learning and memory deficits, APP/PS1/AI mice continue to perform normally during aging. Interestingly, no significant differences were found in the total level and deposition of Aβ in the brains of APP/PS1 and APP/PS1/AI mice, but cerebral amyloid angiopathy was reduced in APP/PS1/AI mice. Also, consistent with the anti-inflammatory properties of apoA-I/HDL, glial activation was reduced in the brain of APP/PS1/AI mice. In addition, Aβ-induced production of proinflammatory chemokines/cytokines was decreased in mouse organotypic hippocampal slice cultures expressing human apoA-I. Therefore, we conclude that overexpression of human apoA-I in the circulation prevents learning and memory deficits in APP/PS1 mice, partly by attenuating neuroinflammation and cerebral amyloid angiopathy. These findings suggest that elevating plasma apoA-I/HDL levels may be an effective approach to preserve cognitive function in patients with AD.

Indexed as

Disease Models, AnimalAmyloid beta-PeptidesAmyloid beta-Protein PrecursorAnimalsApolipoprotein A-IBehavior, AnimalBlotting, WesternBrainCells, CulturedCerebral Amyloid AngiopathyCholesterolCognition DisordersEmbryo, MammalianEnzyme-Linked Immunosorbent AssayHumansImmunoenzyme TechniquesAmyloid beta-PeptidesAmyloid beta-Protein PrecursorAPOA1 protein, humanApolipoprotein A-IAPP protein, humanCholesterolInflammasomesLipoproteinsPresenilin-1RNA, Messenger

Identifiers

PMID20847045
PMCPMC2978624
OpenAlexW2005031405

What OpenQuestion holds

Textmetadata
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.