Evidence map›Paper›PMID 33910450›Full record

ReviewPrion2021

Development of molecular tools for diagnosis of Alzheimer's disease that are based on detection of amyloidogenic proteins.

Konstantin Y Kulichikhin, Sergei A Fedotov, Maria S Rubel, Natalia M Zalutskaya, Anastasia E Zobnina, Oksana A Malikova, Nikolay G Neznanov, Yury O Chernoff, Aleksandr A Rubel

Open access · goldAbstract readReview
In one paragraph

Review in Prion, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed, 3 pooled it
2.3field-weighted citation impact, top 12% 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

11 citing papers in PubMed, 3 syntheses or guidelines pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Review
  5. Review
  6. Biofluid biomarkers for Alzheimer's disease.Frontiers in aging neuroscience · 2024
    Review
  7. Review
  8. Review
  9. Article
  10. Prostate cancer treatment and the relationship of androgen deprivation therapy to cognitive function.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2022
    Review
  11. 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

9 authors at 4 institutions in 2 countries.

Konstantin Y KulichikhinLaboratory of Amyloid Biology, St. Petersburg State University, St. Petersburg, Russia.ORCID 0000-0002-7443-4560
Sergei A FedotovLaboratory of Amyloid Biology, St. Petersburg State University, St. Petersburg, Russia.ORCID 0000-0002-7428-120X
Maria S RubelSCAMT Institute, ITMO University, St. Petersburg, Russia.
Natalia M ZalutskayaV.M. Bekhterev National Research Medical Center for Psychiatry and Neurology, St. Petersburg, Russia.
Anastasia E ZobninaLaboratory of Amyloid Biology, St. Petersburg State University, St. Petersburg, Russia.ORCID 0000-0002-1234-1342
Oksana A MalikovaLaboratory of Amyloid Biology, St. Petersburg State University, St. Petersburg, Russia.ORCID 0000-0003-4203-1158
Nikolay G NeznanovV.M. Bekhterev National Research Medical Center for Psychiatry and Neurology, St. Petersburg, Russia.
Yury O ChernoffLaboratory of Amyloid Biology, St. Petersburg State University, St. Petersburg, Russia.ORCID 0000-0002-8934-9051
Aleksandr A RubelLaboratory of Amyloid Biology, St. Petersburg State University, St. Petersburg, Russia.ORCID 0000-0001-6203-2006
St Petersburg University · RUSt.Petersburg V.M.Bekhterev Psychoneurological Research Institute · RUGeorgia Institute of Technology · USITMO University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Alzheimer's disease (AD) is the most common form of dementia that usually occurs among older people. AD results from neuronal degeneration that leads to the cognitive impairment and death. AD is incurable, typically develops over the course of many years and is accompanied by a loss of functional autonomy, making a patient completely dependent on family members and/or healthcare workers. Critical features of AD are pathological polymerization of Aβ peptide and microtubule-associated protein tau, accompanied by alterations of their conformations and resulting in accumulation of cross-β fibrils (amyloids) in human brains. AD apparently progresses asymptomatically for years or even decades before the appearance of symptoms. Therefore, development of the early AD diagnosis at a pre-symptomatic stage is essential for potential therapies. This review is focused on current and potential molecular tools (including non-invasive methods) that are based on detection of amyloidogenic proteins and can be applicable to early diagnosis of AD.

Indexed as

Alzheimer DiseaseAgedAmyloid beta-PeptidesAmyloidogenic ProteinsAmyloid Precursor Protein SecretasesAspartic Acid EndopeptidasesBiomarkersHumansPositron-Emission Tomographytau ProteinsAmyloid beta-PeptidesAmyloidogenic ProteinsAmyloid Precursor Protein SecretasesAspartic Acid EndopeptidasesBiomarkerstau ProteinsAlzheimer’s diseaseamyloid betaAβ oligomersbloodearly diagnostics

Identifiers

PMID33910450
PMCPMC8096329
OpenAlexW3158470085

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.