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MicroRNA analysis in maternal blood of pregnancies with preterm premature rupture of membranes reveals a distinct expression profile.
Spiliopoulos, Michail; Haddad, Andrew; Al-Kouatly, Huda B; Haleema, Saeed; Paidas, Michael J; Iqbal, Sara N; Glazer, Robert I.
Afiliación
  • Spiliopoulos M; Department of Obstetrics, Gynecology and Reproductive Sciences, Division of Maternal Fetal Medicine and Genetics, University of Miami, Miami, Florida, United States of America.
  • Haddad A; Department of Obstetrics, Gynecology & Women's Health, Division of Maternal Fetal Medicine & Surgery, Hackensack Meridian School of Medicine, Hackensack University Medical Center, Hackensack, New Jersey, United States of America.
  • Al-Kouatly HB; Department of Obstetrics and Gynecology, Division of Maternal Fetal Medicine, Thomas Jefferson University, Philadelphia, Pennsylvania, United States of America.
  • Haleema S; Department of Obstetrics, Gynecology and Reproductive Sciences, Division of Maternal Fetal Medicine, MedStar Washington Hospital Center, Washington, DC, United States of America.
  • Paidas MJ; Department of Obstetrics, Gynecology and Reproductive Sciences, Division of Maternal Fetal Medicine and Genetics, University of Miami, Miami, Florida, United States of America.
  • Iqbal SN; Department of Obstetrics, Gynecology and Reproductive Sciences, Division of Maternal Fetal Medicine, MedStar Washington Hospital Center, Washington, DC, United States of America.
  • Glazer RI; Department of Oncology and Lombardi Comprehensive Cancer Center, Georgetown University, Washington, DC, United States of America.
PLoS One ; 17(11): e0277098, 2022.
Article en En | MEDLINE | ID: mdl-36327243
OBJECTIVE: To determine the expression profile of microRNAs in the peripheral blood of pregnant women with preterm premature rupture of membranes (PPROM) compared to that of healthy pregnant women. STUDY DESIGN: This was a pilot study with case-control design in pregnant patients enrolled between January 2017 and June 2019. Patients with healthy pregnancies and those affected by PPROM between 20- and 33+6 weeks of gestation were matched by gestational age and selected for inclusion to the study. Patients were excluded for multiple gestation and presence of a major obstetrical complication such as preeclampsia, diabetes, fetal growth restriction and stillbirth. A total of ten (n = 10) controls and ten (n = 10) patients with PPROM were enrolled in the study. Specimens were obtained before administration of betamethasone or intravenous antibiotics. MicroRNA expression was analyzed for 800 microRNAs in each sample using the NanoString nCounter Expression Assay. Differential expression was calculated after normalization and log2- transformation using the false discovery rate (FDR) method at an alpha level of 5%. RESULTS: Demographic characteristics were similar between the two groups. Of the 800 miRNAs analyzed, 116 were differentially expressed after normalization. However, only four reached FDR-adjusted statistical significance. Pregnancies affected by PPROM were characterized by upregulation of miR-199a-5p, miR-130a-3p and miR-26a-5p and downregulation of miR-513b-5p (FDR adjusted p-values <0.05). The differentially expressed microRNAs participate in pathways associated with altered collagen and matrix metalloprotease expression in the extracellular matrix. CONCLUSION: Patients with PPROM have a distinct peripheral blood microRNA profile compared to healthy pregnancies as measured by the NanoString Expression Assay.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Rotura Prematura de Membranas Fetales / MicroARNs Límite: Female / Humans / Newborn / Pregnancy Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Rotura Prematura de Membranas Fetales / MicroARNs Límite: Female / Humans / Newborn / Pregnancy Idioma: En Revista: PLoS One Asunto de la revista: CIENCIA / MEDICINA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Estados Unidos