Journal article
Circulating syndecan-1 is reduced in pregnancies with poor fetal growth and its secretion regulated by matrix metalloproteinases and the mitochondria
D Garcha, SP Walker, TM MacDonald, J Hyett, J Jellins, J Myers, SE Illanes, JK Nien, M Schepeler, E Keenan, CA Whigham, P Cannon, E Murray, TV Nguyen, M Kandel, J Masci, C Murphy, T Cruickshank, N Pritchard, NJ Hannan Show all
Scientific Reports | Published : 2021
Open access
Abstract
Fetal growth restriction is a leading cause of stillbirth that often remains undetected during pregnancy. Identifying novel biomarkers may improve detection of pregnancies at risk. This study aimed to assess syndecan-1 as a biomarker for small for gestational age (SGA) or fetal growth restricted (FGR) pregnancies and determine its molecular regulation. Circulating maternal syndecan-1 was measured in several cohorts; a large prospective cohort collected around 36 weeks’ gestation (n = 1206), a case control study from the Manchester Antenatal Vascular service (285 women sampled at 24–34 weeks’ gestation); two prospective cohorts collected on the day of delivery (36 + 3–41 + 3 weeks’ gestation,..
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Grants
Awarded by RANZCOG Research Foundation
Funding Acknowledgements
Funding for this work was provided by the National Health and Medical Research Council (#1065854, #1183854, #116071), an Australian Government Research Training Program Scholarship, and RANZCOG Taylor Hammond Scholarship to TM; National Health and Medical Research Council Fellowships to TKL (#1159261), NJH (#1146128), ST (#1136418). The funders played no role in study design or analysis.