Acute Placental Inflammation Is Associated with Reduced Progesterone Receptor Density in the Basal Decidua in Spontaneous Preterm Birth.

IF 1.2 4区 医学 Q3 OBSTETRICS & GYNECOLOGY American journal of perinatology Pub Date : 2026-01-01 Epub Date: 2025-02-24 DOI:10.1055/a-2524-4053
Sunitha Suresh, Alexa Freedman, Emmet Hirsch, Linda M Ernst
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Abstract

A functional progesterone withdrawal has been thought to contribute to the pathophysiology of spontaneous preterm birth (PTB). The density of the progesterone receptor (PR) in gestational tissues could play a role in functional progesterone withdrawal. We sought to understand the relationship between placental pathology and the density of PR in the basal decidua in the setting of spontaneous preterm delivery.This is a secondary analysis of a retrospective cohort study of 40 patients with spontaneous PTB < 37 weeks from a prior study at NorthShore University HealthSystem previously described. Placental pathology was categorized according to the Amsterdam criteria into acute inflammation (AI), chronic inflammation (CI), maternal vascular malperfusion (MVM), and fetal vascular malperfusion (FVM). Slides containing basal decidua were stained for PR. Ten distinct images were obtained from the basal plate of each placenta. The positive cell detection program in QuPath image analysis software was used to estimate the percentage of cells positive for PR (%PR + ). The mean %PR+ cells were calculated from the ten representative images and were correlated with patterns of placental injury using t-tests. Models were adjusted for gestational age at delivery.The median gestational age at delivery was 32.5 weeks (interquartile range: 30.5, 34.1). There was a lower density of %PR+ cells among those with AI (12.9%PR+ without AI vs. 9.1%PR +  with AI, p = 0.03). There were no differences in the percent of %PR+ cells based on CI, MVM, or FVM. Models adjusted for gestational at delivery demonstrated persistent association with PR density and AI and no difference in the other pathologies.The presence of AI is associated with the lower density of PR expression in the basal decidua by quantitative immunohistochemical analysis. Further research is needed to investigate these findings in the context of spontaneous PTL and the prevention of PTB. · AI is associated with a lower density of PR expression.. · PR is expressed in the basal decidua in the placenta.. · Further research is needed to investigate findings in the context of PTB..

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自发性早产中,急性胎盘炎症与基底蜕膜中孕酮受体密度降低有关。
目的:功能性黄体酮戒断被认为与自发性早产(PTB)的病理生理有关。孕激素受体(PR)的密度在孕激素功能性戒断中起重要作用。我们试图了解自发性早产背景下胎盘病理与基底蜕膜PR密度之间的关系。研究设计:这是对40例自发性肺结核患者进行回顾性队列研究的二次分析。模型根据分娩时的胎龄进行调整。结果:分娩时中位胎龄为32.5周(四分位数范围:30.5,34.1)。AI组%PR+细胞密度较低(未AI组12.9%PR+, AI组9.1%PR +, p = 0.03)。基于CI、MVM或FVM的%PR+细胞百分比没有差异。经分娩妊娠期调整的模型显示,PR密度和AI持续存在关联,其他病理无差异。结论:AI的存在与基底蜕膜中PR表达密度较低有关。需要进一步的研究来调查这些发现在自发性PTL和PTB预防的背景下。·AI与PR表达密度较低相关。·PR在胎盘基底蜕膜中表达。·需要进一步的研究来调查在肺结核背景下的发现。
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来源期刊
American journal of perinatology
American journal of perinatology 医学-妇产科学
CiteScore
5.90
自引率
0.00%
发文量
302
审稿时长
4-8 weeks
期刊介绍: The American Journal of Perinatology is an international, peer-reviewed, and indexed journal publishing 14 issues a year dealing with original research and topical reviews. It is the definitive forum for specialists in obstetrics, neonatology, perinatology, and maternal/fetal medicine, with emphasis on bridging the different fields. The focus is primarily on clinical and translational research, clinical and technical advances in diagnosis, monitoring, and treatment as well as evidence-based reviews. Topics of interest include epidemiology, diagnosis, prevention, and management of maternal, fetal, and neonatal diseases. Manuscripts on new technology, NICU set-ups, and nursing topics are published to provide a broad survey of important issues in this field. All articles undergo rigorous peer review, with web-based submission, expedited turn-around, and availability of electronic publication. The American Journal of Perinatology is accompanied by AJP Reports - an Open Access journal for case reports in neonatology and maternal/fetal medicine.
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