Changes in Lipid Profiles with the Progression of Pregnancy in Black Women

Author:

Saadat Nadia1ORCID,Aguate Fernando2,Nowak Alexandra3ORCID,Hyer Suzanne4ORCID,Lin Anna5ORCID,Decot Hannah5ORCID,Koch Hannah5,Walker Deborah6ORCID,Lydic Todd5ORCID,Padmanabhan Vasantha1ORCID,Campos Gustavo2,Misra Dawn2,Giurgescu Carmen4

Affiliation:

1. Department of Pediatrics, University of Michigan, Ann Arbor, MI 48019, USA

2. Department of Epidemiology and Biostatistics, Michigan State University, East Lansing, MI 48824, USA

3. School of Nursing, Loyola University, Maywood, IL 60153, USA

4. College of Nursing, University of Central Florida, Orlando, FL 32826, USA

5. Molecular Metabolism and Disease Mass Spectrometry Core, Michigan State University, East Lansing, MI 48824, USA

6. College of Nursing, Wayne State University, Detroit, MI 48202, USA

Abstract

Background/Objectives: Lipid metabolism plays an important role in maternal health and fetal development. There is a gap in the knowledge of how lipid metabolism changes during pregnancy for Black women who are at a higher risk of adverse outcomes. We hypothesized that the comprehensive lipidome profiles would show variation across pregnancy indicative of requirements during gestation and fetal development. Methods: Black women were recruited at prenatal clinics. Plasma samples were collected at 8–18 weeks (T1), 22–29 weeks (T2), and 30–36 weeks (T3) of pregnancy. Samples from 64 women who had term births (≥37 weeks gestation) were subjected to “shotgun” Orbitrap mass spectrometry. Mixed-effects models were used to quantify systematic changes and dimensionality reduction models were used to visualize patterns and identify reliable lipid signatures. Results: Total lipids and major lipid classes showed significant increases with the progression of pregnancy. Phospholipids and glycerolipids exhibited a gradual increase from T1 to T2 to T3, while sphingolipids and total sterol lipids displayed a more pronounced increase from T2 to T3. Acylcarnitines, hydroxy acylcarnitines, and Lyso phospholipid levels significantly decreased from T1 to T3. A deviation was that non-esterified fatty acids decreased from T1 to T2 and increased again from T2 to T3, suggestive of a potential role for these lipids during the later stages of pregnancy. The fatty acids showing this trend included key fatty acids—non-esterified Linoleic acid, Arachidonic acid, Alpha-linolenic acid, Eicosapentaenoic acid, Docosapentaenoic acid, and Docosahexaenoic acid. Conclusions: Mapping lipid patterns and identifying lipid signatures would help develop intervention strategies to reduce perinatal health disparities among pregnant Black women.

Funder

Amendt Heller Award for Newborn Research

Publisher

MDPI AG

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