Comprehensive molecular and morphological study of abortion material in missed abortion of the first trimester

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Abstract

BACKGROUND: Missed abortion is the main cause of reproductive loss in the first trimester, and genetic causes come first in the etiology of this disease. The immunological aspects of the mother-fetus system are currently widely discussed. In this regard, the study of the immunological relationship between the mother’s body and the fetus in missed abortion, depending on the chorion karyotype, as well as after suffering reproductive loss, is a topical task, as it can optimize the methods of examining patients with missed abortion and identify factors that contribute to the development of recurrent miscarriage.

AIM: The aim of this study was to investigate the morphological and immunohistochemical characteristics of abortion material in missed abortion, depending on the presence of chorionic chromosomal abnormalities and the patient’s history of reproductive losses.

MATERIALS AND METHODS: We performed a comprehensive morphological and immunohistochemical study (CD56, HLA-DR-II) of abortion material in 273 cases of missed abortion. Group 1 consisted of patients with different variants of chorionic chromosomal abnormalities (n = 169); group 2 included subjects with a normal karyotype of the chorion (n = 104). The data analysis was carried out taking into account the anamnesis of patients, depending on the presence of reproductive losses.

RESULTS: We revealed the morphological features of the abortion material in missed abortion in cases with chromosomal abnormalities of the chorion: pronounced edema, sclerosis, necrosis of chorionic villi, more pronounced inflammatory changes in the form of moderate and severe macrophage infiltration of the decidual tissue and endometrium, and accumulations of leukocytes as microabscesses. It has been proven that the severity of inflammatory changes in abortuses depends only on the chorion karyotype and does not depend on either the duration of the presence of an unviable fetal egg in the uterine cavity, or the patient’s history of reproductive losses. It was shown that the CD56 and HLA-DR-II expressions in the abortion material depend on the patient’s history of reproductive losses, regardless of the chorion karyotype.

CONCLUSIONS: In patients with an unburdened obstetric and gynecological history in the first missed abortion, it is advisable only to determine the chorion karyotype in order to identify the cause of missed abortion. The immunohistochemical study of the abortion material with the determination of the CD56 and HLA-DR-II expressions is important in repeated missed abortions, regardless of the chorion karyotype.

About the authors

Olga A. Romanova

North-Western State Medical University named after I.I. Mechnikov

Email: romanova-roa@yandex.ru
ORCID iD: 0000-0003-2637-5620
SPIN-code: 5740-7953
ResearcherId: ААВ-2136-2021

MD, obstetrician-gynecologist of the Department of Gynecology

Russian Federation, 41, Kirochnaya St., Saint Petersburg, 191015

Victoria A. Pechenikova

North-Western State Medical University named after I.I. Mechnikov

Author for correspondence.
Email: p-vikka@mail.ru
SPIN-code: 9603-5645
ResearcherId: ААВ-2105-2021

MD, Dr. Sci. (Med.), PhD, Professor of the Department of Obstetrics and Gynecology

Russian Federation, 41, Kirochnaya St., Saint Petersburg, 191015

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Supplementary files

Supplementary Files
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1. JATS XML
2. Fig. 1. Chorionic villi with chromosomal abnormalities: a combination of severe sclerosis and edema, trophoblast necrosis, and fibrinoid necrosis fields in the intervillous space. Staining with hematoxylin and eosin, magnified at ×100

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3. Fig. 2. Decidual tissue with a chorionic chromosomal abnormality (microabscess). Stained with hematoxylin and eosin, magnified at ×100

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4. Fig. 3. Microabscesses of the endometrium with a chorionic chromosomal abnormality o. Stained with hematoxylin and eosin, magnified at ×100

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5. Fig. 4. Immunohistochemical study of CD56 and HLA-DR class II in the endometrium and decidual tissue in missed miscarriage in patients with reproductive losses in history

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6. Fig. 5. Micrographs of the immunohistochemical study of CD56: a — in the endometrium of a patient with a first missed miscarriage; b — in the decidual tissue of a patient with the first missed miscarriage; c — in the endometrium of a patient with a history of reproductive losses; d — in the decidual tissue of a patient with a history of reproductive losses. The immunohistochemical study was magnified at ×400

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7. Fig. 6. Micrographs of the immunohistochemical study of HLA-DR class II: a — in the endometrium of a patient with a first missed miscarriage; b — in the decidual tissue of a patient with the first missed miscarriage; c — in the endometrium of a patient with a history of reproductive losses; d — in the decidual tissue of a patient with a history of reproductive losses. The immunohistochemical study was magnified at ×400

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