Evidence map›Paper›PMID 37287674›Full record

ArticleAging medicine (Milton (N.S.W))2023

Quantification of senescence-associated secretory phenotype proteins in the vaginal secretions of pre- and postmenopausal women with and without prolapse.

Polina Sawyer, Haolin Shi, Patrick Keller, Steven Brown, Maria Florian-Rodriguez

Open access · diamondAbstract read
In one paragraph

Article in Aging medicine (Milton (N.S.W)), 2023. 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
0.7field-weighted citation impact, top 27% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Chapter 4.5: New Proposed Treatments for Pelvic Organ Prolapse.International urogynecology journal · 2026
    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

5 authors at 3 institutions in 1 country.

Polina SawyerDivision of Female Pelvic Medicine and Reconstructive Surgery, Department of Obstetrics and Gynecology University of Texas Southwestern Medical Center Dallas Texas USA.
Haolin ShiDepartment of Obstetrics and Gynecology University of Texas Southwestern Medical Center Dallas Texas USA.
Patrick KellerDepartment of Obstetrics and Gynecology University of Texas Southwestern Medical Center Dallas Texas USA.
Steven BrownParkland Memorial Hospital Dallas Texas USA.
Maria Florian-RodriguezDivision of Female Pelvic Medicine and Reconstructive Surgery, Department of Obstetrics and Gynecology University of Texas Southwestern Medical Center Dallas Texas USA.ORCID https://orcid.org/0000-0002-5835-2266
Institute for Female Pelvic Medicine and Reconstructive Surgery · USThe University of Texas Southwestern Medical Center · USParkland Memorial Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Cellular senescence has been proposed as a pathophysiologic driver in the development of pelvic organ prolapse (POP), especially during aging. In this study, we aimed to determine if markers of cell senescence can be quantified from vaginal secretions collected from pre- and postmenopausal women with and without POP. Methods: Vaginal swabs were collected from 81 women in four groups: premenopausal with (pre-P) and without prolapse (pre-NP), and postmenopausal with (post-P) and without prolapse (post-NP). Multiplex immunoassays (MagPix) were then used to detect and quantify the presence of 10 SASP proteins in vaginal secretions. Results: The total protein concentration of vaginal secretions differed significantly among the four groups ( Conclusions: In this study, we found that SASP proteins can be detected and quantified in vaginal secretions. Several of these markers were differentially expressed among the four groups studied, with the highest normalized concentrations of SASP markers found among postmenopausal women with prolapse. Overall, the data support the theory that senescence is associated with prolapse during aging but that other factors may be important in younger women who develop POP before menopause.

Indexed as

agingcellular senescenceinflammationmenopausepelvic organ prolapse

Identifiers

PMID37287674
PMCPMC10242250
OpenAlexW4379768017

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.