Evidence map›Paper›PMID 38775852›Full record

ReviewNaunyn-Schmiedeberg's archives of pharmacology2024

In vivo and ex vivo gene therapy for neurodegenerative diseases: a promise for disease modification.

Pouya Ebrahimi, Elham Davoudi, Razieh Sadeghian, Amin Zaki Zadeh, Emran Razmi, Reza Heidari, Mohammad Hossein Morowvat, Issa Sadeghian

Abstract readReview
PubMed Publisher
In one paragraph

Review in Naunyn-Schmiedeberg's archives of pharmacology, 2024. 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. Review
  2. Review
  3. Article
  4. Ethics and healthcare in the older adult population.Journal of medical ethics and history of medicine · 2024
    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

8 authors.

Pouya EbrahimiAhvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Elham DavoudiDepartment of Biomedical and Nutritional Sciences, University of Massachusetts Lowell, Lowell, MA, USA.
Razieh SadeghianAhvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Amin Zaki ZadehAhvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Emran RazmiArak University of Medical Sciences, Arak, Iran.
Reza HeidariPharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Mohammad Hossein MorowvatPharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. mhmorowvat@sums.ac.ir.
Issa SadeghianPharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran. sadeghian_i@sums.ac.ir.

Funding

Shiraz University of Medical Sciences 29849
6 · The paper itself

Abstract

Neurodegenerative diseases (NDDs), including AD, PD, HD, and ALS, represent a growing public health concern linked to aging and lifestyle factors, characterized by progressive nervous system damage leading to motor and cognitive deficits. Current therapeutics offer only symptomatic management, highlighting the urgent need for disease-modifying treatments. Gene therapy has emerged as a promising approach, targeting the underlying pathology of diseases with diverse strategies including gene replacement, gene silencing, and gene editing. This innovative therapeutic approach involves introducing functional genetic material to combat disease mechanisms, potentially offering long-term efficacy and disease modification. With advancements in genomics, structural biology, and gene editing tools such as CRISPR/Cas9, gene therapy holds significant promise for addressing the root causes of NDDs. Significant progress in preclinical and clinical studies has demonstrated the potential of in vivo and ex vivo gene therapy to treat various NDDs, offering a versatile and precise approach in comparison to conventional treatments. The current review describes various gene therapy approaches employed in preclinical and clinical studies for the treatment of NDDs, including AD, PD, HD, and ALS, and addresses some of the key translational challenges in this therapeutic approach.

Indexed as

Genetic TherapyNeurodegenerative DiseasesAnimalsGene EditingHumansADALSGene therapyHDNeurodegenerative diseasesPD

Identifiers

PMID38775852

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.