Evidence map›Paper›PMID 20517700›Full record

ReviewJournal of neural transmission (Vienna, Austria : 1996)2010

Macrophages in Alzheimer's disease: the blood-borne identity.

David Gate, Kavon Rezai-Zadeh, Dominique Jodry, Altan Rentsendorj, Terrence Town

Abstract readReview
In one paragraph

Review in Journal of neural transmission (Vienna, Austria : 1996), 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed
–field-weighted citation impact
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

77 citing papers in PubMed.

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17 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

5 authors.

David GateDepartment of Biomedical Sciences, Regenerative Medicine Institute, Cedars-Sinai Medical Center, 8700 Beverly Blvd., Steven Spielberg Building, Room 361, Los Angeles, CA 90048, USA.
Kavon Rezai-Zadeh
Dominique Jodry
Altan Rentsendorj
Terrence Town

Funding

Blocking TGF-Beta immune signaling as a therapeutic target for Alzheimer's diseasR00AG029726 · NIA · CEDARS-SINAI MEDICAL CENTER · PI TOWN, TERRENCE C · 2008 to 2010
$790k
NIA NIH HHS 5R00AG029726-03NIA NIH HHS 5R00AG029726-04NIA NIH HHS R00 AG029726
6 · The paper itself

Abstract

Alzheimer's disease (AD) is a progressive and incurable neurodegenerative disorder clinically characterized by cognitive decline involving loss of memory, reasoning and linguistic ability. The amyloid cascade hypothesis holds that mismetabolism and aggregation of neurotoxic amyloid-beta (Abeta) peptides, which are deposited as amyloid plaques, are the central etiological events in AD. Recent evidence from AD mouse models suggests that blood-borne mononuclear phagocytes are capable of infiltrating the brain and restricting beta-amyloid plaques, thereby limiting disease progression. These observations raise at least three key questions: (1) what is the cell of origin for macrophages in the AD brain, (2) do blood-borne macrophages impact the pathophysiology of AD and (3) could these enigmatic cells be therapeutically targeted to curb cerebral amyloidosis and thereby slow disease progression? This review begins with a historical perspective of peripheral mononuclear phagocytes in AD, and moves on to critically consider the controversy surrounding their identity as distinct from brain-resident microglia and their potential impact on AD pathology.

Indexed as

Alzheimer DiseaseAnimalsBlood-Brain BarrierBrainHumansMacrophagesModels, Biological

Identifiers

PMID20517700
PMCPMC2917548

What OpenQuestion holds

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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.