Evidence map›Paper›PMID 37371715›Full record

ReviewBiomedicines2023

Opiate Antagonists for Chronic Pain: A Review on the Benefits of Low-Dose Naltrexone in Arthritis versus Non-Arthritic Diseases.

Praneet Dara, Zeba Farooqui, Fackson Mwale, Chungyoul Choe, Andre J van Wijnen, Hee-Jeong Im

Open access · goldAbstract readReview
In one paragraph

Review in Biomedicines, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.3field-weighted citation impact, top 12% 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

8 citing papers in PubMed, 13 citations in OpenAlex.

  1. Opioid Signaling in Multiple Sclerosis: Emerging Targets for Repair.International journal of molecular sciences · 2026
    Review
  2. Article
  3. Review
  4. [Clinical pharmacology of opioid analgesics].Schmerz (Berlin, Germany) · 2025
    Review
  5. Article
  6. Article
  7. Article
  8. 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

6 authors at 4 institutions in 3 countries.

Praneet DaraOsteopathic Medical School, Des Moines University (DMU), Des Moines, IA 50312, USA.
Zeba FarooquiDepartment of Biomedical Engineering, University of Illinois at Chicago (UIC), Chicago, IL 60607, USA.
Fackson MwaleLady Davis Institute for Medical Research, SMBD-Jewish General Hospital, 3755 Cote Ste-Catherine Road, Room F-602, Montreal, QC H3T 1E2, Canada.
Chungyoul ChoeMedical Research Institute, School of Medicine, Sungkyunkwan University (SKKU), Suwon 16419, Republic of Korea.
Andre J van WijnenDepartment of Biomedical Engineering, University of Illinois at Chicago (UIC), Chicago, IL 60607, USA.ORCID 0000-0002-4458-0946
Hee-Jeong ImDepartment of Biomedical Engineering, University of Illinois at Chicago (UIC), Chicago, IL 60607, USA.ORCID 0000-0001-7672-269X
University of Illinois Chicago · USJewish General Hospital · CASungkyunkwan University · KRUniversity of Vermont · US

Funding

Validation of Novel Target for OA TreatmentR01AR077890 · NIAMS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ROYSTON, THOMAS J · 2020 to 2020
$4.2M
NIAMS NIH HHS R01 AR077890NIH HHS AR077890
6 · The paper itself

Abstract

Chronic pain conditions create major financial and emotional burdens that can be devastating for individuals and society. One primary source of pain is arthritis, a common inflammatory disease of the joints that causes persistent pain in affected people. The main objective of pharmacological treatments for either rheumatoid arthritis (RA) or osteoarthritis (OA) is to reduce pain. Non-steroidal anti-inflammatory drugs, opioids, and opioid antagonists have each been considered in the management of chronic pain in arthritis patients. Naltrexone is an oral-activated opioid antagonist with biphasic dose-dependent pharmacodynamic effects. The molecule acts as a competitive inhibitor of opioid receptors at high doses. However, naltrexone at low doses has been shown to have hormetic effects and provides relief for chronic pain conditions such as fibromyalgia, multiple sclerosis (MS), and inflammatory bowel disorders. Current knowledge of naltrexone suggests that low-dose treatments may be effective in the treatment of pain perception in chronic inflammatory conditions observed in patients with either RA or OA. In this review, we evaluated the therapeutic benefits of low-dose naltrexone (LDN) on arthritis-related pain conditions.

Indexed as

arthritiscartilagenaltrexoneopiateosteoarthritispainregenerative medicine

Identifiers

PMID37371715
PMCPMC10296090
OpenAlexW4379233502

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.