Evidence map›Paper›PMID 19903022›Full record

ReviewExpert review of neurotherapeutics2009

Can peripheral leukocytes be used as Alzheimer's disease biomarkers?

Kavon Rezai-Zadeh, David Gate, Christine A Szekely, Terrence Town

Open access · greenAbstract readReview
In one paragraph

Review in Expert review of neurotherapeutics, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
1.4field-weighted citation impact, top 17% 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

20 citing papers in PubMed, 37 citations in OpenAlex.

  1. Article
  2. Leukocyte surface biomarkers implicate deficits of innate immunity in sporadic Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2023
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Dysregulation of Systemic Immunity in Aging and Dementia.Frontiers in cellular neuroscience · 2021
    Review
  8. Observational
  9. Article
  10. Article
  11. Review
  12. Review
  13. Increased AβAlzheimer's research & therapy · 2017
    Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Macrophages in Alzheimer's disease: the blood-borne identity.Journal of neural transmission (Vienna, Austria : 1996) · 2010
    Review
  20. Impact of the CD40-CD40L dyad in Alzheimer's disease.CNS & neurological disorders drug targets · 2010
    Review
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

4 authors at 2 institutions in 1 country.

Kavon Rezai-ZadehDepartment of Biomedical Sciences, Cedars-Sinai Medical Center, Los Angeles, CA 90048, USA. rezaik@cshs.org
David Gate
Christine A Szekely
Terrence Town
Cedars-Sinai Medical Center · USNeuroSpine Institute · US

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 R00 AG029726
6 · The paper itself

Abstract

Alzheimer's disease (AD) is the leading cause of dementia in elderly populations throughout the world and its incidence is on the rise. Current clinical diagnosis of AD requires intensive examination that includes neuropsychological testing and costly brain imaging techniques, and a definitive diagnosis can only be made upon postmortem neuropathological examination. Additionally, antemortem clinical AD diagnosis is typically administered following onset of cognitive and behavioral symptoms. As these symptoms emerge relatively late in disease progression, therapeutic intervention occurs after significant neurodegeneration, thereby limiting efficacy. The identification of noninvasive diagnostic biomarkers of AD is becoming increasingly important to make diagnosis more widely available to clinics with limited access to neuropsychological testing or state-of-the-art brain imaging, reduce the cost of clinical diagnosis, provide a biological measure to track the course of therapeutic intervention, and most importantly, allow for earlier diagnosis--possibly even during the prodromal phase--with hopes of therapeutic intervention prior to appreciable neurodegeneration. Circulating leukocytes are attractive candidate AD biomarkers as they can be obtained in a minimally invasive manner and are easily analyzed by widely available flow cytometry techniques. In this review, we critically analyze the potential utility of peripheral leukocytes as biological markers for AD.

Indexed as

Alzheimer DiseaseAnimalsBiomarkersHumansLeukocytesPhenotypeBiomarkers

Identifiers

PMID19903022
PMCPMC2828773
OpenAlexW2171653890

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.