Fernandez-Gonzalez Sergi, Ortiz-Arrabal Olimpia, Torrecillas Ariadna, Pérez-Cruz Miriam, Chueca Natalia, Gómez-Roig María D, Gómez-Llorente Carolina
Hospital de Sant Joan de Déu. D'Esplugues de Llobregat, Passeig Sant Joan de Déu 2. Esplugues, Barcelona.
Biochemistry and Molecular Biology II Department, School of Pharmacy, University of Granada, Campus de Cartuja s/n.
Medicine (Baltimore). 2020 Nov 13;99(46):e22722. doi: 10.1097/MD.0000000000022722.
In general terms, fetal growth restriction (FGR) is considered the impossibility of achieving the genetically determined potential size. In the vast majority of cases, it is related to uteroplacental insufficiency. Although its origin remains unknown and causes are only known in 30% of cases, it is believed to be related to an interaction of environmental and genetic factors with either a fetal or maternal origin. One hypothesis is that alterations in the gastrointestinal microbiota composition, and thus alteration in the immune response, could play a role in FGR development. We performed an observational, prospective study in a subpopulation affected with FGR to elucidate the implications of this microbiota on the FGR condition.A total of 63 fetuses with FGR diagnosed in the third trimester as defined by the Delphi consensus, and 63 fetuses with fetal growth appropriate for gestational age will be recruited. Obstetric and nutritional information will be registered by means of specific questionnaires. We will collect maternal fecal samples between 30 to 36 weeks, intrapartum samples (maternal feces, maternal and cord blood) and postpartum samples (meconium and new-born feces at 6 weeks of life). Samples will be analyzed in the Department of Biochemistry and Molecular Biology II, Nutrition and Food Technology Institute of the University of Granada (UGR), for the determination of the gastrointestinal microbiota composition and its relationship with inflammatory biomarkers.This study will contribute to a better understanding of the influence of gastrointestinal microbiota and related inflammatory biomarkers in the development of FGR.Trial registration: NCT04047966. Registered August 7, 2019, during the recruitment stage. Retrospectively registered. Ongoing research.
一般来说,胎儿生长受限(FGR)被认为是无法达到基因决定的潜在大小。在绝大多数情况下,它与子宫胎盘功能不全有关。尽管其起源尚不清楚,仅在30%的病例中已知病因,但人们认为它与环境和遗传因素的相互作用有关,这些因素可能源于胎儿或母体。一种假说认为,胃肠道微生物群组成的改变,进而免疫反应的改变,可能在FGR的发生发展中起作用。我们对受FGR影响的亚人群进行了一项观察性前瞻性研究,以阐明这种微生物群对FGR病情的影响。将招募63例根据德尔菲共识定义在孕晚期诊断为FGR的胎儿,以及63例胎儿生长与孕周相符的胎儿。产科和营养信息将通过特定问卷进行记录。我们将在30至36周之间收集母体粪便样本、分娩时样本(母体粪便、母体和脐带血)以及产后样本(胎粪和出生6周时的新生儿粪便)。样本将在格拉纳达大学(UGR)营养与食品技术研究所生物化学与分子生物学II系进行分析,以确定胃肠道微生物群组成及其与炎症生物标志物的关系。本研究将有助于更好地理解胃肠道微生物群和相关炎症生物标志物在FGR发生发展中的影响。试验注册:NCT04047966。于2019年8月7日在招募阶段注册。回顾性注册。正在进行的研究。