Evidence map›Paper›PMID 40705707›Full record

SynthesisPain2025

Enhancing clinical translation of analgesics for neuropathic pain: a systematic review and meta-analysis on the role of non-evoked pain assessment in preclinical trials.

Miguel Á Huerta, Patricia Roza, Elsa Cisneros, Matilde Alique, Carolina Roza

Abstract readSystematic ReviewMeta-Analysis
In one paragraph

Synthesis in Pain, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. 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

5 authors.

Miguel Á HuertaDepartment of Pharmacology, Faculty of Medicine, University of Granada, Granada, Spain.ORCID 0000-0003-2842-0085
Patricia RozaDepartment of Ecology, University of Málaga, Málaga, Spain.ORCID 0009-0003-6420-263
Elsa CisnerosHealth Sciences School, Centro Universitario Internacional de Madrid (CUNIMAD), Madrid, Spain.ORCID 0000-0002-9784-9240
Matilde AliqueDepartment of System's Biology, Medical School, University of Alcala de Henares, Alcalá de Henares, Spain.ORCID 0000-0002-7912-1133
Carolina RozaHealth Sciences School, Universidad Internacional de La Rioja (UNIR), Logroño, Spain.ORCID 0000-0001-5757-9066

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

abstractCurrent therapies for neuropathic pain are often inadequate and several promising preclinical drugs have failed in clinical trials. This may stem from an overreliance on reflex-based outcomes, which do not accurately reflect the spontaneous or non-evoked pain (NEP) characteristic of neuropathic pain. To bridge this gap, we evaluated the preclinical efficacy of standard analgesics in relieving NEP associated with neuropathic pain, thereby providing valuable insights that could optimize preclinical testing. A comprehensive search was performed in PubMed, Scopus, and Web of Science (July 2023). A random-effects model evaluated the effect of the intervention, with subgroup analyses exploring variability sources. Of the 91 included studies, 65 were eligible for meta-analysis, yielding 196 drug evaluations. Most evaluations involved traumatic nerve injury (91%) in male animals, although fewer were nontraumatic neuropathies (6%) or spinal cord injuries (4%). Standard pharmacotherapy for neuropathic pain relieved NEP with efficacy patterns closely matching clinical results. Tricyclic antidepressants and selective serotonin reuptake inhibitors showed the highest efficacy, followed by gabapentinoids and strong opioids, whereas nonsteroidal anti-inflammatory drugs and mild opioids had no significant effect. Next, we confirmed that all the NEP-related behaviors were significantly alleviated by standard analgesics, validating that they are indeed pain associated. Moreover, drug efficacy was greater in traumatic nerve injury models compared with nontraumatic neuropathy models. In conclusion, standard analgesics demonstrated robust preclinical efficacy in alleviating NEP, mirroring their clinical performance. These findings underscore the importance of incorporating assessments of spontaneous pain into classical tests in preclinical studies to enhance the clinical translation of investigational analgesics.

Indexed as

AnalgesicsNeuralgiaPain MeasurementTranslational Research, BiomedicalAnimalsDrug Evaluation, PreclinicalHumansAnalgesicsAnalgesiaBehaviorDrug discoveryNeuropathyPharmacologyPreclinical researchSpontaneous pain

Identifiers

PMID40705707
PMCPMC12519534

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Registered trials

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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.