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Record W4391682383 · doi:10.3389/fphar.2024.1372317

Editorial: Repurposing β-blockers for non-cardiovascular diseases

2024· editorial· en· W4391682383 on OpenAlexaff
Ayaz Shahid, Jeffrey Wang, Bradley T. Andresen, S. R. Wayne Chen, Ying Huang

Bibliographic record

VenueFrontiers in Pharmacology · 2024
Typeeditorial
Languageen
FieldMedicine
TopicCancer, Stress, Anesthesia, and Immune Response
Canadian institutionsUniversity of Calgary
FundersNational Cancer InstituteNational Institutes of Health
KeywordsRepurposingMedicinePharmacologyInternal medicineTraditional medicineBiology

Abstract

fetched live from OpenAlex

Editorial on the Research Topic Repurposing β-blockers for non-cardiovascular diseases β-Blockers are a class of drugs that have been approved by the FDA for the treatment of cardiovascular diseases.However, Some β-blockers have been found to be effective in treating other disorders beyond the cardiovascular system, such as CNS conditions, diabetes, cancer, and organ toxicities (Alaskar et al., 2023;Beaman et al., 2023;Chen et al., 2023;Shahid et al., 2023).Furthermore, β-blockers are proposed to act as immunomodulators due to the role of β-adrenergic receptors in immunity (Fjaestad et al., 2022).Regarding the protection against organ toxicity, non-selective β-blockers, such as carvedilol and propranolol, have been found to protect against renal toxicity (Rodrigues et al., 2010;Rezayat et al., 2017).The effects of β-blockers on diseases outside of the cardiovascular system may not necessarily be related to their β-blocking activity.This issue compiles preclinical and clinical studies, along with a review article, on the use of βblockers for non-cardiovascular diseases.These studies provide evidence for repurposing these FDA-approved drugs for other diseases and identifying new mechanisms for their use beyond β-adrenergic receptor blockade.According to Massalee and Coa, β-blockers could be a possible treatment for cancer by blocking β-adrenergic receptor signaling, which is associated with tumor growth and immune system suppression.β-Blockers may also work well in combination with chemotherapy by enhancing anti-proliferative, antimitotic, and antimitochondrial properties, leading to better control of tumors and improved therapy outcomes.β-Blockers could also improve cancer immunotherapy by blocking immunosuppressive signaling and boosting the functionality of immune cells such as CD8 + T cells.Nonselective β-blockers, which inhibit both β1-and β2-adrenergic receptors, may be more effective in decreasing tumor proliferation and improving overall survival compared to selective β-blockers.More preclinical and clinical studies are needed to confirm the synergistic potential of combining β-blockers with conventional cancer therapies and/or immunotherapies.There are still challenges in understanding the mechanisms underlying the non-cardiovascular effects of β-blockers and how to use these drugs to improve clinical outcomes in non-cardiovascular diseases.Yang et al. aimed to evaluate the potential association between β-blockers and reduced mortality in patients with sepsis.The study involved analyzing data from two large ICU databases comprising 61,751 sepsis patients, out of which 43.8% received β-blockers.The data set included both selective and non-selective β-blockers administered by intravenous

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.008
metaresearch head score (Gemma)0.022
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Not applicable · Consensus signal: Not applicable
GenreCandidate signal: Editorial · Consensus signal: Editorial
Teacher disagreement score0.023
Threshold uncertainty score0.078

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0080.022
Meta-epidemiology (narrow)0.0060.001
Meta-epidemiology (broad)0.0060.004
Bibliometrics0.0040.002
Science and technology studies0.0030.003
Scholarly communication0.0070.006
Open science0.0050.002
Research integrity0.0160.019
Insufficient payload (model declined to judge)0.0230.022

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.006
GPT teacher head0.292
Teacher spread0.286 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designNot applicable
Domainnot available
GenreEditorial

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations2
Published2024
Admission routes1
Has abstractyes

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