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Impact of chronic endometritis on endometrial receptivity analysis results and pregnancy outcomes.


ABSTRACT: BACKGROUND:The aim of this study is to evaluate the relationship between chronic endometritis (CE) and a personalized window of implantation (WOI), identified by results of endometrial receptivity analysis (ERA), and pregnancy outcomes following embryo transfer (ET) based on the ERA outcomes. METHODS:The single-center, cross-sectional study was designed. The study population consisted of 101 infertile women who underwent endometrial sampling between June 2018 and February 2020. We recruited 88 patients who underwent ERA testing and immunohistochemistry of the plasma cell marker CD138 to diagnose CE within 3 months of testing. Subjects were divided into three groups as follows: 33 without CE (non-CE group); 19 with untreated CE at ERA testing (CE group); and 36 successfully treated for CE before ERA testing (cured-CE group). CE diagnosis was defined as ?5 CD138-positive plasma cells per 10 random stromal areas at ×400 magnification. RESULTS:In non-CE, CE, and cured-CE groups, the numbers of CD138-positive cells were 0.7?±?1.0, 28.5?±?30.4, and 1.3?±?1.3, respectively (p?

SUBMITTER: Kuroda K 

PROVIDER: S-EPMC7654412 | biostudies-literature | 2020 Dec

REPOSITORIES: biostudies-literature

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Impact of chronic endometritis on endometrial receptivity analysis results and pregnancy outcomes.

Kuroda Keiji K   Horikawa Takashi T   Moriyama Azusa A   Nakao Kazuki K   Juen Hiroyasu H   Takamizawa Satoru S   Ojiro Yuko Y   Nakagawa Koji K   Sugiyama Rikikazu R  

Immunity, inflammation and disease 20200923 4


<h4>Background</h4>The aim of this study is to evaluate the relationship between chronic endometritis (CE) and a personalized window of implantation (WOI), identified by results of endometrial receptivity analysis (ERA), and pregnancy outcomes following embryo transfer (ET) based on the ERA outcomes.<h4>Methods</h4>The single-center, cross-sectional study was designed. The study population consisted of 101 infertile women who underwent endometrial sampling between June 2018 and February 2020. We  ...[more]

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