The 15-Epilipoxin-A4 Pathway with Prophylactic Aspirin in Preventing Preeclampsia: A Longitudinal Cohort Study

Author:

Shanmugalingam Renuka1234ORCID,Wang XiaoSuo56,Motum Penelope37,Fulcher Ian8,Lee Gaksoo38,Kumar Roshika9,Hennessy Annemarie1234,Makris Angela12349

Affiliation:

1. Department of Renal Medicine, South Western Sydney Local Health District, NSW, Australia

2. School of Medicine, Western Sydney University, NSW, Australia

3. Women’s Health Initiative Translational Unit (WHITU), Ingham Institute For Applied Medical Research and South Western Sydney Local Health District, NSW, Australia

4. Vascular Immunology Research Group, Heart Research Institute (HRI), Sydney, NSW, Australia

5. Bosch Mass Spectrometry Faculty, University of Sydney, NSW, Australia

6. Freedman Foundation Metabolomics Facility, Innovation Centre, Victor Chang Cardiac Research Institute, NSW, Australia

7. Department of Haematology, South Western Sydney Local Health District, NSW, Australia

8. Department of Obstetrics and Gynaecology, South Western Sydney Local Health District, NSW, Australia

9. South Western Sydney Clinical School, University of New South Wales (UNSW), NSW, Australia

Abstract

Abstract Introduction The benefit of aspirin in preventing preeclampsia is increasingly recognized; however, its mechanism of action remains unclear. Nonobstetric studies have described an anti-inflammatory effect of aspirin through the 15-epilipoxin-A4 pathway (aspirin-triggered lipoxin [ATL]). However, the anti-inflammatory mechanism of aspirin in the prevention of preeclampsia remains unknown. Objective/Hypothesis To examine (1) the difference in longitudinal endogenous lipoxin-A4 (En-Lipoxin-A4) concentration in low-risk (LR) and high-risk (HR) pregnancies, and (2) the effect of aspirin on endogenous ATL concentration and the associated effect on cytokine profile of HR women. Methods Plasma from 220 HR women was collected at 12, 16, 20, 24, 28, 32, and 36 weeks of gestation. Adherence to aspirin was biochemically verified. Plasma En-Lipoxin-A4 and ATL concentrations were analyzed using liquid chromatography mass spectrometry, and cytokines, interleukin (IL)-10, tumor necrosis factor-α, interferon-γ, IL-8, and IL-1β, with the high-sensitivity multibead Luminex® assay. Results HR women have up to 70% lower plasma concentration of En-Lipoxin-A4 (P < 0.001) than LR women. HR women with adequate aspirin adherence (HR-AA) (n = 82) had higher plasma concentration of ATL (P < .001), lower concentration of IL-8 from 16 to 36 weeks of gestation (P < .001), and increased IL-10 concentration from 16 to 28 weeks of gestation (P = .03) compared with high-risk women who were not on aspirin (HR-NA). HR-AA who did not develop preeclampsia had higher plasma En-lipoxin-A4 (P < .001), ATL (P = .02), and IL-10 concentrations (P < .001) with lower IL-8 concentration (P = .004) than HR women who developed preeclampsia. Discussion Plasma concentration of En-Lipoxin-A4 is lower in HR women than in LR controls. Adequate adherence with aspirin results in an increase in ATL and IL-10 with reduced IL-8 plasma concentration. This study suggests a potential anti-inflammatory role of aspirin through the ATL pathway with prophylactic aspirin in HR pregnant women.

Funder

PEARLS Foundation

SWSLHD funded Women’s Health Initiate Translational Unit

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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