Clinical chorioamnionitis at term is characterized by changes in the plasma concentration of CHCHD2/MNRR1, a mitochondrial protein
dc.contributor.author | Bosco M. | |
dc.contributor.author | Romero R. | |
dc.contributor.author | Gallo D.M. | |
dc.contributor.author | Suksai M. | |
dc.contributor.author | Gotsch F. | |
dc.contributor.author | Jung E. | |
dc.contributor.author | Chaemsaithong P. | |
dc.contributor.author | Tarca A.L. | |
dc.contributor.author | Gomez-Lopez N. | |
dc.contributor.author | Arenas-Hernandez M. | |
dc.contributor.author | Meyyazhagan A. | |
dc.contributor.author | Al Qasem M. | |
dc.contributor.author | Franchi M.P. | |
dc.contributor.author | Grossman L.I. | |
dc.contributor.author | Aras S. | |
dc.contributor.author | Chaiworapongsa T. | |
dc.contributor.other | Mahidol University | |
dc.date.accessioned | 2023-07-07T18:01:59Z | |
dc.date.available | 2023-07-07T18:01:59Z | |
dc.date.issued | 2023-12-01 | |
dc.description.abstract | OBJECTIVE: Mitochondrial dysfunction was observed in acute systemic inflammatory conditions such as sepsis and might be involved in sepsis-induced multi-organ failure. Coiled-Coil-Helix-Coiled-Coil-Helix Domain Containing 2 (CHCHD2), also known as Mitochondrial Nuclear Retrograde Regulator 1 (MNRR1), a bi-organellar protein located in the mitochondria and the nucleus, is implicated in cell respiration, survival, and response to tissue hypoxia. Recently, the reduction of the cellular CHCHD2/MNRR1 protein, as part of mitochondrial dysfunction, has been shown to play a role in the amplification of inflammatory cytokines in a murine model of lipopolysaccharide-induced systemic inflammation. The aim of this study was to determine whether the plasma concentration of CHCHD2/MNRR1 changed during human normal pregnancy, spontaneous labor at term, and clinical chorioamnionitis at term. METHODS: We conducted a cross-sectional study that included the following groups: 1) non-pregnant women (n = 17); 2) normal pregnant women at various gestational ages from the first trimester until term (n = 110); 3) women at term with spontaneous labor (n = 50); and 4) women with clinical chorioamnionitis at term in labor (n = 25). Plasma concentrations of CHCHD2/MNRR1 were assessed by an enzyme-linked immunosorbent assay. RESULTS: 1) Pregnant women at term in labor with clinical chorioamnionitis had a significantly higher plasma CHCHD2/MNRR1 concentration than those in labor without chorioamnionitis (p = .003); 2) CHCHD2/MNRR1 is present in the plasma of healthy non-pregnant and normal pregnant women without significant differences in its plasma concentrations between the two groups; 3) there was no correlation between maternal plasma CHCHD2/MNRR1 concentration and gestational age at venipuncture; and 4) plasma CHCHD2/MNRR1 concentration was not significantly different in women at term in spontaneous labor compared to those not in labor. CONCLUSIONS: CHCHD2/MNRR1 is physiologically present in the plasma of healthy non-pregnant and normal pregnant women, and its concentration does not change with gestational age and parturition at term. However, plasma CHCHD2/MNRR1 is elevated in women at term with clinical chorioamnionitis. CHCHD2/MNRR1, a novel bi-organellar protein located in the mitochondria and the nucleus, is released into maternal plasma during systemic inflammation. | |
dc.identifier.citation | The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians Vol.36 No.2 (2023) , 2222333 | |
dc.identifier.doi | 10.1080/14767058.2023.2222333 | |
dc.identifier.eissn | 14764954 | |
dc.identifier.pmid | 37349086 | |
dc.identifier.scopus | 2-s2.0-85162740813 | |
dc.identifier.uri | https://repository.li.mahidol.ac.th/handle/20.500.14594/87787 | |
dc.rights.holder | SCOPUS | |
dc.subject | Medicine | |
dc.title | Clinical chorioamnionitis at term is characterized by changes in the plasma concentration of CHCHD2/MNRR1, a mitochondrial protein | |
dc.type | Article | |
mu.datasource.scopus | https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85162740813&origin=inward | |
oaire.citation.issue | 2 | |
oaire.citation.title | The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians | |
oaire.citation.volume | 36 | |
oairecerif.author.affiliation | Inje University Paik Hospital | |
oairecerif.author.affiliation | Universidad del Valle, Cali | |
oairecerif.author.affiliation | Azienda Ospedaliera Universitaria Integrata Verona | |
oairecerif.author.affiliation | Mutah University | |
oairecerif.author.affiliation | University of Michigan Medical School | |
oairecerif.author.affiliation | Michigan State University | |
oairecerif.author.affiliation | Faculty of Medicine, Prince of Songkia University | |
oairecerif.author.affiliation | Wayne State University School of Medicine | |
oairecerif.author.affiliation | National Institute of Child Health and Human Development (NICHD) | |
oairecerif.author.affiliation | Mahidol University | |
oairecerif.author.affiliation | Wayne State University | |
oairecerif.author.affiliation | Università degli Studi di Perugia |