Evidence map›Paper›PMID 40945635›Full record

ArticleThe journal of pain2025

A cautionary tale: Non-steroidal anti-inflammatory drug use and localized provoked vulvodynia.

Emanuelle Chrysilla, Sarah Fischer, Ji-Mi Jang, Krishna Rao Maddipati, Tanzy M T Love, Mitchell A Linder, Megan L Falsetta

Abstract read
In one paragraph

Article in The journal of pain, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. 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

7 authors.

Emanuelle ChrysillaDepartment of Pharmacology and Physiology, University of Rochester, Rochester, NY, United States.
Sarah FischerDepartment of Obstetrics and Gynecology, University of Rochester, Rochester, NY, United States.
Ji-Mi JangDepartment of Obstetrics and Gynecology, University of Rochester, Rochester, NY, United States.
Krishna Rao MaddipatiLipidomics Core Facility and Bioactive Lipids Research Program, Wayne State University, Detroit, MI, United States.
Tanzy M T LoveDepartment of Biostatistics and Computational Biology, University of Rochester, Rochester, NY, United States.
Mitchell A LinderDepartment of Obstetrics and Gynecology, University of Rochester, Rochester, NY, United States.
Megan L FalsettaDepartment of Pharmacology and Physiology, University of Rochester, Rochester, NY, United States; Department of Obstetrics and Gynecology, University of Rochester, Rochester, NY, United States. Electronic address: Megan_Falsetta@URMC.rochester.edu.

Funding

Mechanisms of vulvodynia involving dysregulation of pro-resolving lipidsR01HD092334 · NICHD · UNIVERSITY OF ROCHESTER · PI HAIDARIS, CONSTANTINE G, WOOD, MEGAN LINDSAY FALSETTA · 2018 to 2022
$2.4M
Transient Vanilloid Receptors and Vulvar Pain: New Therapeutic Targets for VulvodyniaR01HD108173 · NICHD · UNIVERSITY OF ROCHESTER · PI Megan Lindsay Falsetta Wood · 2023 to 2026
$2.3M
NICHD NIH HHS R01 HD092334NICHD NIH HHS R01 HD108173
6 · The paper itself

Abstract

Localized provoked vulvodynia (LPV) is characterized by chronic vulvar pain upon light touch to the vulvar vestibule, a specialized ring of tissue immediately surrounding the vaginal opening. LPV affects ∼14 million people in the US. Current treatments for LPV include nonsteroidal anti-inflammatory drugs (NSAIDs), but clinical evidence has demonstrated that they are ineffective for vulvar pain. Here, the effects of NSAID treatment on inflammation and resolution in an in vitro model of LPV were explored using enzyme-linked immunosorbent assays (ELISAs), calcium imaging, and metabololipidomics. Additionally, the effectiveness of NSAID treatment on mitigating chronic vulvar pain was assessed using a validated LPV mouse model that mimics key features of vulvodynia. These findings indicate that although NSAID treatment reduced pro-inflammatory eicosanoid production in vulvar fibroblasts, lipidomic analysis revealed that COX inhibition also downregulated levels of pro-resolving lipids, namely epoxyeicosatrienoic acids (EETs), lipoxins (LXs), and resolvin E-series (RvEs). In vivo, NSAID treatment did not restore vulvar pain thresholds back to baseline levels in mice. Overall, this study offers one possible explanation for previous reports of the ineffectiveness of NSAIDs on managing LPV-associated vulvar pain. PERSPECTIVE: Taking NSAIDs to manage chronic vulvar pain may downregulate levels of specialized pro-resolving lipid mediators, thereby resulting in prolonged pain and delayed inflammation resolution. This study provides one possible explanation for clinical reports of the ineffectiveness of NSAIDs in the mitigation of vulvodynia-associated pain.

Indexed as

Anti-Inflammatory Agents, Non-SteroidalVulvodyniaAnimalsDisease Models, AnimalFemaleMiceMice, Inbred C57BLAnti-Inflammatory Agents, Non-SteroidalChronic painInflammationNon-steroidal anti-inflammatory drugsSpecialized pro-resolving lipid mediatorsVulvodynia

Identifiers

PMID40945635
PMCPMC12458989

What Socratic holds

Textmetadata
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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.