Evidence map›Paper›PMID 24760112›Full record

ReviewJournal of clinical immunology2014

Clinical trials of intravenous immunoglobulin for Alzheimer's disease.

Norman Relkin

Abstract readReview
PubMed Publisher
In one paragraph

Review in Journal of clinical immunology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
6.1field-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

34 citing papers in PubMed, 67 citations in OpenAlex.

  1. Genetic evidence suggests a protective role of immunoglobulin M in Alzheimer's disease.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2026
    Article
  2. Review
  3. Article
  4. Review
  5. Review
  6. Review
  7. Review
  8. Review
  9. Linalool Alleviates AOxidative medicine and cellular longevity · 2021
    Article
  10. Review
  11. Review
  12. Plasma-Based Strategies for Therapeutic Modulation of Brain Aging.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2019
    Review
  13. Article
  14. Review
  15. Article
  16. Review
  17. Article
  18. Intense Focus Yet Many Setbacks for Alzheimer's Disease Drug Development.P & T : a peer-reviewed journal for formulary management · 2018
    Article
  19. Article
  20. 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

1 author at 1 institution in 1 country.

Norman RelkinDepartment of Neurology and Brain Mind Research Institute, Weill Cornell Medical College, New York, NY, USA, nrelkin@med.cornell.edu.
Cornell University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The human polyclonal IgG antibody preparation known as Intravenous Immunoglobulin (IVIG) has been under study as a potential treatment for Alzheimer's disease (AD) since 2002. Preclinical and clinical studies have shown that IVIG has anti-amyloid and immune modulatory properties relevant to treating neurodegenerative disorders. In early stage AD clinical trials, IVIG was found to reduce cognitive decline and increase brain glucose metabolism. Unfortunately, IVIG failed to meet primary outcome objectives in the North American Phase 3 clinical trial in mild to moderate AD. However, positive cognitive signals were observed in pre-planned subgroup analyses among APOE-ε4 carriers and moderately impaired AD patients. Biomarker studies revealed dose dependent increases in plasma and CSF immunoglobulins and decreases in beta amyloid-42 levels. In addition, IVIG treatment was generally safe and well-tolerated. These findings suggest that naturally occurring human anti-amyloid antibodies may play a physiologic role in the clearance of aggregated amyloid proteins. While the results of clinical trials to date do not provide support for the use of IVIG to treat AD at the doses tested, additional studies of IVIG's mechanisms are warranted and may guide the development of more effective therapies for AD in the future.

Indexed as

Alzheimer DiseaseAmyloid beta-PeptidesAnimalsApolipoprotein E4Clinical Trials as TopicCognitionDisease ProgressionHumansImmunity, HumoralImmunoglobulinsImmunoglobulins, IntravenousImmunotherapyNeurogenic InflammationProtein DenaturationProtein MultimerizationAmyloid beta-PeptidesApolipoprotein E4ImmunoglobulinsImmunoglobulins, Intravenous

Identifiers

PMID24760112
OpenAlexW2058049534

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.