Maternal plasma fatty acid patterns in mid-pregnancy and offspring epigenetic gestational age at birth

• Published in: Epigenetics Vol. 17; no. 11; pp. 1562 - 1572
• Main Authors: Monasso, Giulietta S., Voortman, Trudy, Felix, Janine F.
• Format: Journal Article
• Language: English
• Published: United States Taylor & Francis 02.11.2022; Taylor & Francis Group
• Subjects: Child; cohort study; DNA Methylation; Epigenesis, Genetic; epigenetic age; epigenetic clock; Fatty Acids; Fatty Acids, Omega-3; Fatty Acids, Unsaturated; Female; Gestational Age; gestational age acceleration; Humans; Infant, Newborn; Pregnancy; Research Paper; cohort study; epigenetic age; gestational age acceleration; pregnancy; DNA methylation; Fatty acids; child; epigenetic clock
• ISSN: 1559-2294; 1559-2308; 1559-2308
• DOI: 10.1080/15592294.2022.2076051

Maternal pregnancy fatty acid status is associated with child health. Epigenetic gestational age acceleration, referring to a discrepancy between chronological and epigenetic gestational age, may underlie these associations. Previous research suggests that analysing fatty acid patterns rather than individual fatty acids may overcome the caveat of missing synergistic or additive effects. Among 1226 mother-newborn pairs from the population-based Generation R Study, we examined the associations of three maternal plasma mid-pregnancy fatty acid patterns, identified by principal component analysis, with offspring epigenetic gestational age acceleration. This was estimated from cord blood DNA methylation data using the method developed by Bohlin. As a secondary analysis, we used the method developed by Knight to estimate epigenetic gestational age. The identified 'high n-6 polyunsaturated fatty acid,' 'monounsaturated and saturated fatty acid' and 'high n-3 polyunsaturated fatty acid' patterns were not associated with epigenetic gestational age acceleration in the main analyses. In sensitivity analyses restricted to 337 children born to mothers with more accurate pregnancy dating based on a regular menstrual cycle, a one standard-deviation-score higher maternal plasma 'high n-3 polyunsaturated fatty acid' pattern was associated with an epigenetic gestational age acceleration of 0.20 weeks (95% CI 0.06, 0.33), but only when using the Knight method. Thus, we found some evidence that a maternal plasma fatty acid pattern characterized by higher concentrations of n-3 polyunsaturated fatty acids may be associated with accelerated epigenetic gestational ageing. These findings depended on the method used and the accuracy of pregnancy dating and therefore need confirmation.