Document Type

Journal Article

Publication Title

Free Radical Research

Publisher

Taylor and Francis

School

School of Medical and Health Sciences

RAS ID

30802

Comments

This is an Accepted Manuscript of an article published by Taylor & Francis in Free Radical Research on 9 December 2019, available online: http://www.tandfonline.com/10.1080/10715762.2019.1685668.

Anto, E. O., Roberts, P., Coall, D. A., Adua, E., Turpin, C. A., Tawiah, A., ... & Wang, W. (2020). Suboptimal health pregnant women are associated with increased oxidative stress and unbalanced pro-and antiangiogenic growth mediators: A cross-sectional study in a Ghanaian population. Free Radical Research, 54(1), 27-42. https://doi.org/10.1080/10715762.2019.1685668

Abstract

Optimal oxidative stress (OS) is important throughout pregnancy; however, an increased OS may alter placental angiogenesis culminating in an imbalanced of angiogenic growth mediators (AGMs). Suboptimal Health Status (SHS), a physical state between health and disease, may be associated with increased OS and unbalanced AGMs. In this study, we explored the association between SHS, biomarkers of OS (BOS) and AGMs among normotensive pregnant women (NTN-PW) in a Ghanaian Suboptimal Health Cohort Study (GHOACS). This comparative GHOACS recruited 593 NTN-PW from the Komfo Anokye Teaching Hospital, Ghana. SHS was measured using a Suboptimal Health Status Questionnaire-25 (SHSQ-25). Along with the subjective SHS measure, objective BOS: 8-hydroxy-2-deoxyguanosine (8-OHdG), 8-epiprostaglandinF2 alpha (8-epi-PGF2α), total antioxidant capacity (TAC), and AGMs: vascular endothelial growth factor-A (VEGF-A), soluble fms-like tyrosine kinase receptor 1 (sFlt-1), placental growth factor (PIGF) and soluble endoglin (sEng) were evaluated. Compared to optimal health NTN-PW, levels of PlGF, VEGF-A and TAC were significantly (p < 0.05) reduced and negatively associated with SHS whilst sEng, sFlt-1, 8-epiPGF2α, 8-OHdG, and combined ratios of sFlt-1/PlGF, 8-epiPGF2α/PlGF, 8-OHdG/PlGF, and sEng/PlGF were significantly increased and positively associated with SHS. The first quartile for PIGF (2.79-fold) and VEGF-A (5.35-fold), and the fourth quartile for sEng (4.31-fold), sFlt-1 (1.84-fold), 8-epiPGF2α (2.23-fold), 8-OHdG (1.90-fold) and urinary 8-OHdG (1.95-fold) were independently associated with SHS (p < 0.05). SHS is associated with increased OS and unbalanced AGMs. Early identification of SHS-related OS and unbalanced AGMs may inform clinicians of the need for therapeutic options.

DOI

10.1080/10715762.2019.1685668

Available for download on Wednesday, December 09, 2020

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