Evidence mapPaperPMID 41734041Full record

ArticlePain2026

Fibromyalgia Analog Model index analysis demonstrates the predictive validity of the Dahl S rat as a model of fibromyalgia.

Luiz F Ferrari, Ashley Wilkinson, Anna Ramirez, James Kuchenbecker, Jay Neitz, Matthew Mauck, Norman E Taylor

Abstract read
In one paragraph

Article in Pain, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Luiz F FerrariDepartment of Anesthesiology, University of Utah, School of Medicine, Salt Lake City, UT, United States.ORCID 0000-0002-3831-6428
Ashley WilkinsonDepartment of Anesthesiology, University of Utah, School of Medicine, Salt Lake City, UT, United States.
Anna RamirezDepartment of Anesthesiology, University of Utah, School of Medicine, Salt Lake City, UT, United States.
James KuchenbeckerDepartment of Ophthalmology, University of Washington, School of Medicine, Seattle, WA, United States.
Jay NeitzDepartment of Ophthalmology, University of Washington, School of Medicine, Seattle, WA, United States.
Matthew MauckDepartment of Anesthesiology, University of North Carolina at Chapel Hill, School of Medicine, Chapel Hill, NC United States.
Norman E TaylorDepartment of Anesthesiology, University of Utah, School of Medicine, Salt Lake City, UT, United States.ORCID 0000-0001-5961-6641

Funding

NIH HHS 1RM1NS140200NIH-NINDS R33NS123758NIH-NINDS R61NS123758NINDS NIH HHS R33 NS123758NINDS NIH HHS R61 NS123758NINDS NIH HHS RM1 NS140200
6 · The paper itself

Abstract

abstractAnimal models of disease are frequently used to test the safety and efficacy of new treatments and to explore mechanistic insights. The most useful models are those that accurately predict therapeutic success in humans of both pharmacologic and nonpharmacologic interventions. Here, we tested the predictive validity of the Dahl salt-sensitive (SS) rat strain as a model of fibromyalgia syndrome (FMS), a chronic disorder characterized by widespread musculoskeletal pain, fatigue, and mood disorders. Using the Fibromyalgia Analog Model (FAM) index, a multivariate statistical tool that quantifies the magnitude of fibromyalgia traits in an animal, we assessed the effectiveness of both established and investigational pharmacologic and nonpharmacologic therapies in SS rats. FAM scores were higher in female SS rats than males ( P < 0.0001), indicating more robust fibromyalgia-like traits, matching the higher prevalence of FMS in women. When compared to controls, treatments with the FDA-approved drugs for FMS milnacipran and pregabalin (both P < 0.0001, in males and females), as well as the investigational therapies metformin ( P < 0.0001) and green light exposure ( P = 0.0034 and P = 0.0002 for males and females, respectively) effectively decreased the FAM scores, showing reduction of FMS-like symptoms in SS rats. In contrast, indomethacin and the mu-opioid agonist DAMGO displayed limited efficacy ( P = 0.0239 and P = 0.0523, respectively), matching the relative effectiveness of these treatments in humans, justifying why they are not usually prescribed for patients with FMS. The results validate the SS rat as a predictive model in testing pharmacologic and nonpharmacologic therapies for FMS treatment, illustrating the utility of the FAM index in assessing treatment outcomes.

Indexed as

Disease Models, AnimalFibromyalgiaAnalgesicsAnimalsFemaleMalePain MeasurementPredictive Value of TestsRatsRats, Inbred DahlReproducibility of ResultsAnalgesicsChronic painDahl SS ratFAM indexFibromyalgiaGreen light therapyRodent pain model

Identifiers

PMID41734041
PMCPMC13383937

What Socratic holds

Textmetadata
LicenceTDM
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 Socratic graph.