Evidence map›Paper›PMID 30059802›Full record

ArticleActa biomaterialia2018

The mechanical response of the mouse cervix to tensile cyclic loading in term and preterm pregnancy.

C Jayyosi, N Lee, A Willcockson, S Nallasamy, M Mahendroo, K Myers

Open access · greenAbstract read
In one paragraph

Article in Acta biomaterialia, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

18 citing papers in PubMed, 25 citations in OpenAlex.

  1. Biomechanical function of the murine cervix with elastic fiber deficiency.Journal of the mechanical behavior of biomedical materials · 2026
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  10. Novel regulatory roles of small leucine-rich proteoglycans in remodeling of the uterine cervix in pregnancy.Matrix biology : journal of the International Society for Matrix Biology · 2022
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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 2 institutions in 1 country.

C JayyosiDepartment of Mechanical Engineering, Columbia University, New York, NY 10027, USA.
N LeeDepartment of Mechanical Engineering, Columbia University, New York, NY 10027, USA.
A WillcocksonDepartment of Obstetrics and Gynecology and Green Center for Reproductive Biological Sciences, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
S NallasamyDepartment of Obstetrics and Gynecology and Green Center for Reproductive Biological Sciences, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
M MahendrooDepartment of Obstetrics and Gynecology and Green Center for Reproductive Biological Sciences, University of Texas Southwestern Medical Center, Dallas, TX 75390, USA.
K MyersDepartment of Mechanical Engineering, Columbia University, New York, NY 10027, USA. Electronic address: kmm2233@columbia.edu.
Columbia University · USThe University of Texas Southwestern Medical Center · US

Funding

Mechanisms of infection-mediated cervical ripeningR01HD084695 · NICHD · UT SOUTHWESTERN MEDICAL CENTER · PI MAHENDROO, MALA S. · 2016 to 2020
$2.0M
Mechanisms by which steroid hormones modulate cervical extracellular matrix structure and function during pregnancy and provide therapeutic protection against preterm birthR01HD088481 · NICHD · UT SOUTHWESTERN MEDICAL CENTER · PI MAHENDROO, MALA S., MYERS, KRISTIN MARIE · 2016 to 2020
$1.8M
NICHD NIH HHS R01 HD084695NICHD NIH HHS R01 HD088481
6 · The paper itself

Abstract

A well-timed modification of both the collagen and elastic fiber network in the cervix during pregnancy accompanies the evolution of tissue mechanical parameters that are key to a successful pregnancy. Understanding of the cervical mechanical behaviour along normal and abnormal pregnancy is crucial to define the molecular events that regulate remodeling in term and preterm birth (PTB). In this study, we measured the mechanical response of mouse cervical tissue to a history of cyclic loading and quantified the tissue's ability to recover from small and large deformations. Assessments were made in nonpregnant, pregnant (gestation days 6, 12, 15 and 18) and mouse models of infection mediated PTB treated with lipopolysaccharide on gestation d15 (LPS treated) and hormone withdrawal mediated PTB on gestation d15 (RU486 treated). The current study uncovers the contributions of collagen and elastic fiber networks to the progressive change in mechanical function of the cervix through pregnancy. Premature cervical remodeling induced on gestation day 15 in the LPS infection model is characterized by distinct mechanical properties that are similar but not identical to mechanical properties at term ripening on day 18. Remodeling in the LPS infection model results in a weaker cervix, unable to withstand high loads. In contrast, the RU486 preterm model resembles the cyclic mechanical behaviour seen for term d18 cervix, where the extremely compliant tissue is able to withstand multiple cycles under large deformations without breaking. The distinct material responses to load-unload cycles in the two PTB models matches the differing microstructural changes in collagen and elastic fibers in these two models of preterm birth. Improved understanding of the impact of microstructural changes to mechanical performance of the cervix will provide insights to aid in the development of therapies for prevention of preterm birth. STATEMENT OF SIGNIFICANCE: Preterm Birth (PTB) still represents a serious challenge to be overcome, considering its implications on infant mortality and lifelong health consequences. While the causes and etiologies of PTB are diverse and yet to be fully elucidated, a common pathway leading to a preterm delivery is premature cervical remodeling. Throughout pregnancy, the cervix remodels through changes of its microstructure, thus altering its mechanical properties. An appropriate timing for these transformations is critical for a healthy pregnancy and avoidance of PTB. Hence, this study aims at understanding how the mechanical function of the cervix evolves during a normal and preterm pregnancy. By performing cyclic mechanical testing on cervix samples from animal models, we assess the cervix's ability to recover from moderate and severe loading. The developed methodology links mechanical parameters to specific microstructural components. This work identifies a distinct biomechanical signature associated with inflammation mediated PTB that differs from PTB induced by hormone withdrawal and from normal term remodeling.

Indexed as

AnimalsBiomechanical PhenomenaCervix UteriElastic ModulusFemaleMice, Inbred C57BLPregnancyRuptureTensile StrengthWeight-BearingCervical remodelingCyclic tensile testLPSPreterm birthRU486

Identifiers

PMID30059802
PMCPMC6336396
OpenAlexW2883465300

What OpenQuestion 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 OpenQuestion graph.