Evidence map›Paper›PMID 42193936›Full record

ReviewCells2026

Emerging Therapeutic Strategies for Neurodegenerative Diseases: A Comprehensive Review of Recent Advances and Future Directions.

Masood Sepehrimanesh, Sarah Victoria Melen, Fatima Yeasmin, Victor Adeleke Ojo, Francisca Walden, Humaira Urmee, Jenna Etheridge, Aruna Kumari Nasu

Abstract readReview
In one paragraph

Review in Cells, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Dysregulation of mitochondrial bioenergetics, RNA processing, and cellular stress responses in FUS-ALS: a multi-dataset transcriptomic perspective.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Article
  2. Review
  3. Review
  4. 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

8 authors.

Masood SepehrimaneshSchool of Biological Sciences, College of Applied and Natural Sciences, Louisiana Tech University, Ruston, LA 71272, USA.
Sarah Victoria MelenSchool of Biological Sciences, College of Applied and Natural Sciences, Louisiana Tech University, Ruston, LA 71272, USA.
Fatima YeasminSchool of Biological Sciences, College of Applied and Natural Sciences, Louisiana Tech University, Ruston, LA 71272, USA.
Victor Adeleke OjoSchool of Biological Sciences, College of Applied and Natural Sciences, Louisiana Tech University, Ruston, LA 71272, USA.ORCID 0009-0000-9427-5328
Francisca WaldenSchool of Biological Sciences, College of Applied and Natural Sciences, Louisiana Tech University, Ruston, LA 71272, USA.
Humaira UrmeeSchool of Biological Sciences, College of Applied and Natural Sciences, Louisiana Tech University, Ruston, LA 71272, USA.
Jenna EtheridgeSchool of Biological Sciences, College of Applied and Natural Sciences, Louisiana Tech University, Ruston, LA 71272, USA.
Aruna Kumari NasuSchool of Biological Sciences, College of Applied and Natural Sciences, Louisiana Tech University, Ruston, LA 71272, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Neurodegenerative diseases, including Alzheimer's disease (AD), Parkinson's disease (PD), and amyotrophic lateral sclerosis (ALS; Lou Gehrig's disease), represent a growing global health burden characterized by progressive neuronal loss and functional decline. Despite decades of intensive research, effective disease-modifying therapies remain limited, underscoring the urgent need for innovative therapeutic strategies. This review highlights recent advances in the understanding of disease etiology and emerging treatment approaches, with a particular focus on modalities with translational potential. We discussed novel disease-modifying interventions, including gene and cell therapies, RNA-targeting strategies, and immunotherapies aimed at clearing misfolded proteins such as amyloid-β, tau, and α-synuclein. In parallel, we examined the evolving recognition of neuroinflammation and mitochondrial dysfunction as actionable therapeutic targets, alongside progress in precision medicine and biomarker-guided approaches that enable early diagnosis and individualized treatment. Additionally, we summarized developments in repurposed pharmacological agents, neuroprotective compounds, and lifestyle interventions, emphasizing the importance of integrative, multimodal strategies. Across AD, PD, and ALS, convergent molecular mechanisms, including protein misfolding, oxidative stress, and disrupted proteostasis, present opportunities for cross-disease therapeutic targeting. Finally, we addressed key challenges and future directions, including translating preclinical efficacy into clinical success, optimizing CNS-targeted delivery systems, and navigating ethical considerations surrounding gene editing and stem cell therapies.

Indexed as

Neurodegenerative DiseasesAnimalsGenetic TherapyHumansNeuroprotective AgentsNeuroprotective AgentsAlzheimer’s diseaseamyotrophic lateral sclerosisneuroinflammationParkinson’s diseaseprotein aggregation

Identifiers

PMID42193936
PMCPMC13204815

What OpenQuestion holds

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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.