Evidence map›Paper›PMID 34436747›Full record

ReviewMetabolic brain disease2022

Unravelling the potential neuroprotective facets of erythropoietin for the treatment of Alzheimer's disease.

Dapinder Kaur, Tapan Behl, Aayush Sehgal, Sukhbir Singh, Neelam Sharma, Vishnu Nayak Badavath, Syed Shams Ul Hassan, Mohammad Mehedi Hasan, Saurabh Bhatia, Ahmed Al-Harassi and 2 more

Abstract readReview
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In one paragraph

Review in Metabolic brain disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
2.9field-weighted citation impact, top 8% 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

15 citing papers in PubMed, 26 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. Article
  5. Review
  6. Article
  7. Cognitive Impairment in Multiple Sclerosis.Bioengineering (Basel, Switzerland) · 2023
    Review
  8. Review
  9. Review
  10. Natural coumarins fromFrontiers in pharmacology · 2023
    Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
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

12 authors at 7 institutions in 6 countries.

Dapinder Kaur *Chitkara College of Pharmacy, Chitkara University, Rajpura, Punjab, India.
Tapan Behl *Chitkara College of Pharmacy, Chitkara University, Rajpura, Punjab, India. tapanbehl31@gmail.com.ORCID 0000-0003-0993-7708
Aayush SehgalChitkara College of Pharmacy, Chitkara University, Rajpura, Punjab, India.
Sukhbir SinghChitkara College of Pharmacy, Chitkara University, Rajpura, Punjab, India.
Neelam SharmaChitkara College of Pharmacy, Chitkara University, Rajpura, Punjab, India.
Vishnu Nayak BadavathChitkara College of Pharmacy, Chitkara University, Rajpura, Punjab, India.
Syed Shams Ul HassanSchool of Medicine and Pharmaceutical Sciences, Zhejiang University, Hangzhou, China.
Mohammad Mehedi HasanDepartment of Biochemistry and Molecular Biology, Faculty of Life Science, Mawlana Bhashani Science and Technology University, Tangail, Bangladesh.
Saurabh BhatiaNatural & Medical Sciences Research Centre, University of Nizwa, Nizwa, Oman.
Ahmed Al-HarassiNatural & Medical Sciences Research Centre, University of Nizwa, Nizwa, Oman.
Haroon KhanDepartment of Pharmacy, Abdul Wali Khan University Mardan, Mardan, Pakistan.
Simona BungauDepartment of Pharmacy, Faculty of Medicine and Pharmacy, University of Oradea, Oradea, Romania.
Chitkara University · INAbdul Wali Khan University Mardan · PKAmity University · INMawlana Bhashani Science and Technology University · BDUniversity of Nizwa · OMUniversity of Oradea · ROZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

During the last three decades, recombinant DNA technology has produced a wide range of hematopoietic and neurotrophic growth factors, including erythropoietin (EPO), which has emerged as a promising protein drug in the treatment of several diseases. Cumulative studies have recently indicated the neuroprotective role of EPO in preclinical models of acute and chronic neurodegenerative disorders, including Alzheimer's disease (AD). AD is one of the most prevalent neurodegenerative illnesses in the elderly, characterized by the accumulation of extracellular amyloid-ß (Aß) plaques and intracellular neurofibrillary tangles (NFTs), which serve as the disease's two hallmarks. Unfortunately, AD lacks a successful treatment strategy due to its multifaceted and complex pathology. Various clinical studies, both in vitro and in vivo, have been conducted to identify the various mechanisms by which erythropoietin exerts its neuroprotective effects. The results of clinical trials in patients with AD are also promising. Herein, it is summarized and reviews all such studies demonstrating erythropoietin's potential therapeutic benefits as a pleiotropic neuroprotective agent in the treatment of Alzheimer's disease.

Indexed as

Alzheimer DiseaseErythropoietinNeuroprotective AgentsAgedAmyloid beta-PeptidesHumansPlaque, AmyloidAmyloid beta-PeptidesErythropoietinNeuroprotective AgentsErythropoietinNeurodegenerationNeuroinflammationNeuroprotectionOxidative stress

Identifiers

PMID34436747
OpenAlexW3194985744

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.