Evidence map›Paper›PMID 38918983›Full record

ReviewCurrent molecular medicine2025

siRNA Treatments for Diabetic Neuropathy: Obstacles and Delivery Techniques.

Mohammad Shabib Akhtar, Nehal Mohsin, Ahmad Zahak, Khalid Altigani Awad Alkarem Ahmed, Yasir Alhazmi, Mohamad Taleuzzaman

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current molecular medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Review
  3. 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

6 authors.

Mohammad Shabib AkhtarDepartment of Clinical Pharmacy, College of Pharmacy, Najran University, Najran, 11001, Kingdom of Saudi Arabia.ORCID 0000-0001-5629-9783
Nehal MohsinDepartment of Clinical Pharmacy, College of Pharmacy, Najran University, Najran, 11001, Kingdom of Saudi Arabia.ORCID 0009-0004-2261-0712
Ahmad ZahakSchool of Pharmacy, Al-Karim University, Katihar, Bihar, 854109, India.
Khalid Altigani Awad Alkarem AhmedDepartment of Clinical Pharmacy, College of Pharmacy, Najran University, Najran, 11001, Kingdom of Saudi Arabia.ORCID 0000-0001-9698-2448
Yasir AlhazmiDepartment of Clinical Pharmacy, College of Pharmacy, Najran University, Najran, 11001, Kingdom of Saudi Arabia.ORCID 0009-0001-8004-9327
Mohamad TaleuzzamanDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Maulana Azad University, Village Bujhawar, Tehsil Luni, Jodhpur, Rajasthan, 342008, India.ORCID 0000-0002-5201-3503

Funding

Deanship of Scientific Research at Najran University NU/NRP/MRC/12/14
6 · The paper itself

Abstract

Targeting genes using siRNA shows promise as an approach to alleviate symptoms of diabetic neuropathy. It focuses on neuropathies and distal symmetric polyneuropathy (DSPN) to explore the potential use of small interfering RNA (siRNA) as a treatment for diabetic neuropathy. Timely identification and management of neuropathy play a critical role in mitigating potential complications. RNAi success depends on understanding factors affecting small interfering RNA (siRNA) functionality and specificity. These include sequence space restrictions, structural and sequence features, mechanisms for nonspecific gene modulation, and chemical modifications. Addressing these factors enhances siRNA performance for efficient gene silencing and confidence in RNAi-mediated genomic studies. Diabetic retinopathy, particularly in South Asian, African, Latin American, and indigenous populations, is a significant concern due to its association with diabetes. Ethnicity plays a crucial role in its development and progression. Despite declining rates in the US, global trends remain concerning, and further research is needed to understand regional differences and reinforce ethnicity-based screening and treatment protocols. In this regard, siRNA emerges as a valuable instrument for early intervention strategies. While presenting promising therapeutic applications, siRNA utilization encounters challenges within insect pest control contexts, thereby providing insights into enhancing its delivery mechanisms for neuropathy treatment purposes. Recent advancements in delivery modalities, such as nanoparticles, allow for the controlled release of siRNA. More investigation is necessary to grasp the safety and efficacy of siRNA technology fully. It holds promise in transforming the treatment of diabetic neuropathy by honing in on particular genes and tackling issues such as inflammation and oxidative stress. Continuous advancements in delivery techniques have the potential to enhance patient results significantly. SiRNA targets genes in diabetic neuropathy, curbing nerve damage and pain and potentially preventing or delaying the condition. Customized treatments based on genetic variations hold promise for symptom management and enhancing quality of life.

Indexed as

Diabetic NeuropathiesGene Transfer TechniquesRNA, Small InterferingAnimalsGenetic TherapyHumansRNA InterferenceRNA, Small Interferingdiabetic neuropathydistal symmetricnerve cells.Small interfering RNA (siRNA)targeting genes using siRNAtherapeutic applications

Identifiers

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.