Evidence map›Paper›PMID 31451729›Full record

ArticleScientific reports2019

Effect of Protease Inhibitors in Healing of the Vaginal Wall.

Maria Florian-Rodriguez, Kathleen Chin, Jennifer Hamner, Jesus Acevedo, Patrick Keller, R Ann Word

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 16% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Chapter 4.5: New Proposed Treatments for Pelvic Organ Prolapse.International urogynecology journal · 2026
    Review
  4. Current practice in animal models for pelvic floor dysfunction.International urogynecology journal · 2023
    Review
  5. Article
  6. Biaxial Murine Vaginal Remodeling With Reproductive Aging.Journal of biomechanical engineering · 2022
    Article
  7. 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 1 institution in 1 country.

Maria Florian-RodriguezDepartment of Obstetrics and Gynecology Division of Female Pelvic Medicine and Reconstructive Surgery, University of Texas Southwestern Medical Center, Dallas, Texas, USA. maria.florian-rodriguez@UTSouthwestern.edu.
Kathleen ChinDepartment of Obstetrics and Gynecology Division of Female Pelvic Medicine and Reconstructive Surgery, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Jennifer HamnerDepartment of Obstetrics and Gynecology Division of Female Pelvic Medicine and Reconstructive Surgery, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Jesus AcevedoCecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
Patrick KellerCecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
R Ann WordCecil H. and Ida Green Center for Reproductive Biology Sciences, University of Texas Southwestern Medical Center, Dallas, Texas, USA.
The University of Texas Southwestern Medical Center · US

Funding

Elastic Fiber Homeostasis in the Vaginal WallR01AG028048 · NIA · UT SOUTHWESTERN MEDICAL CENTER · PI WORD, RUTH A · 2007 to 2017
$3.2M
CORE--RECOMBINANT PROTEINP30HD028048 · NICHD · NORTHWESTERN UNIVERSITY · PI WOODRUFF, TERESA K · 1991 to 1999
–
NIA NIH HHS R01 AG028048
6 · The paper itself

Abstract

Impaired elastogenesis and increased degradation of elastic fibers has been implicated in the pathogenesis of pelvic organ prolapse. Loss of the elastogenic organizer, fibulin-5 (FBLN5), leads to pelvic organ prolapse in mice. The objective of this study was to investigate the regulation of FBLN5 after surgical injury of the vaginal wall using the rat as a preclinical animal model. Both endogenous and recombinant FBLN5 were degraded after surgical injury. Estrogen did not alter the dramatic loss of vaginal FBLN5 in the acute phase after injury (12-48 h), but resulted in rescue of the poor recovery of FBLN5 levels in the late phase (7 d) of healing in ovariectomized animals. In contrast with estrogen, the general MMP inhibitor, actinonin, abrogated injury-induced degradation of FBLN5 significantly. Further, actinonin rescued the negative effects of injury on biomechanics, histomorphology, and elastic fibers. Control of excessive matrix degradation by local application of actinonin at the time of surgery may lead to improved elastic fiber regeneration and wound healing, thereby potentially enhancing pelvic floor recovery after reconstructive surgery for prolapse.

Indexed as

AnimalsBiomechanical PhenomenaElasticityEstrogensExtracellular Matrix ProteinsFemaleHydroxamic AcidsProtease InhibitorsRats, Sprague-DawleyVaginaWound HealingactinoninEstrogensExtracellular Matrix ProteinsHydroxamic AcidsProtease Inhibitors

Identifiers

PMID31451729
PMCPMC6710245
OpenAlexW2971024356

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.