Related Experiment Video
Updated: Jan 2, 2026

Noninvasive Sampling of Mucosal Lining Fluid for the Quantification of In Vivo Upper Airway Immune-mediator Levels
Published on: August 7, 2017
Prenatal polyunsaturated fatty acids and child asthma: Effect modification by maternal asthma and child sex
Maria José Rosa1, Terryl J Hartman2, Margaret Adgent3
1Department of Environmental Medicine and Public Health, Icahn School of Medicine at Mount Sinai, New York, NY.
Insights
Prenatal exposure to omega-6 polyunsaturated fatty acids (PUFAs) increased childhood asthma risk, while omega-3 PUFAs showed a protective effect. These associations were significantly modified by maternal asthma history and child sex, highlighting key risk factors.
Area of Science:
- Environmental Health
- Pediatric Allergy
- Nutritional Epidemiology
Background:
- Inconsistent findings exist regarding prenatal polyunsaturated fatty acid (PUFA) intake and childhood wheeze/asthma.
- Investigating the influence of specific PUFA types and their ratios is crucial for understanding respiratory health outcomes in children.
Purpose of the Study:
- To examine the association between prenatal polyunsaturated fatty acid (PUFA) status and the risk of wheeze and asthma in children.
- To investigate the modifying effects of maternal asthma/atopy, child sex, and maternal race on these associations.
Main Methods:
- Analyzed plasma omega-3 (n-3) and omega-6 (n-6) PUFAs from 1019 mother-child dyads during the second trimester.
- Assessed child wheeze/asthma outcomes at ages 4-6 years using physician diagnoses, symptoms, and medication use.
- Employed modified Poisson regression with interaction terms to analyze PUFA indicators and outcomes, considering potential modifiers.
Main Results:
- Higher prenatal omega-6 PUFAs correlated with increased risk of ever and current diagnosed asthma (RR 1.70).
- Higher prenatal omega-3 PUFAs were associated with a reduced risk of current diagnosed asthma (RR 0.59).
- Maternal asthma history amplified the risk of respiratory outcomes with higher n-6 PUFAs; a significant 3-way interaction revealed highest risk in male children of asthmatic mothers with high n-6/n-3 ratios.
Conclusions:
- Prenatal PUFA status significantly influences childhood wheeze and asthma risk.
- Maternal asthma history and child sex are critical modifiers of the relationship between prenatal PUFA exposure and respiratory health outcomes.
- Targeted interventions focusing on PUFA balance during pregnancy may be beneficial for preventing childhood asthma, particularly in high-risk groups.
Background:
Findings on prenatal polyunsaturated fatty acid (PUFA) intake and child wheeze and asthma have been inconsistent.
Objective:
We sought to examine associations between prenatal PUFA status and child wheeze/asthma and modifying effects of maternal asthma/atopy, child sex, and maternal race.
Methods:
Analyses included 1019 mother-child dyads with omega-3 (n-3) and omega-3 (n-6) PUFAs measured in second-trimester plasma; n-6/n-3 ratios were calculated. Child wheeze/asthma outcomes ascertained at age 4 to 6 years included ever physician-diagnosed asthma, current wheeze (symptoms past 12 months), current asthma (diagnosis and medication and/or symptoms past 12 months), and current diagnosed asthma. Each PUFA indicator and outcome was analyzed in separate models using modified Poisson regression with interaction terms.
Results:
In quartile (Q) analyses, higher n-6 PUFAs were associated with increased risk of ever (risk ratio [RR] high vs low [RR Q4 vs Q1], 1.70; 95% CI, 1.07-2.71) and current (RR Q4 vs Q1, 1.70; 95% CI, 1.07-2.71) diagnosed asthma, whereas n-3 PUFAs were associated with lower risk (RR Q4 vs Q1, 0.59; 95% CI, 0.33-1.03) of current diagnosed asthma (Ptrend < .05 for all). Higher n-6 PUFAs were associated with a higher risk of all respiratory outcomes among children born to women with asthma (Pinteraction < .05 for all outcomes). A significant 3-way interaction between child sex, maternal asthma, and n-6/n-3 PUFA indicated that male children born to women with asthma and a higher ratio had the highest risk across wheeze/asthma outcomes (Pinteraction < .05).
Conclusions:
Associations between prenatal PUFA status and childhood wheeze/asthma were modified by maternal history of asthma and child sex.
More Related Videos
03:19Author Spotlight: Studying the Impact of Maternal Dietary Deficiencies on Long-Term Offspring Health Outcomes
Published on: June 28, 2024
05:55Stable Isotope In-Vivo Labeling for Mass-Spectrometry Identification of Paternal Metabolites Transferred from Sperm to Oocyte During Fertilization
Published on: June 17, 2025
Related Concept Videos
Asthma-I: Introduction
Antiasthma Drugs: Leukotriene Modifiers
Leukotriene modifiers work through two distinct mechanisms:
Upper Respiratory Drugs: Antitussives, Expectorants, and Mucolytics
Antitussives include codeine, dextromethorphan (Robitussin), and benzonatate (Tessalon). Codeine and dextromethorphan exert their effects centrally by suppressing the cough reflex center in the medulla. Benzonatate operates peripherally within the respiratory tract by...
Asthma: Pathogenesis and Management
Asthma is classified as allergic and non-allergic. Allergens such as dust mites, pollen, and pet dander trigger allergic asthma, while factors like cold air, intense emotions, or exercise can induce non-allergic asthma.
Asthma-II: Pathophysiology and Classification
Additionally, environmental and genetic factors play crucial roles in determining an individual's susceptibility to asthma and the severity of their condition.
Critical processes in asthma pathophysiology include:
Antiasthma Drugs: Mast Cell Stabilizers and Anti-IgE Drugs
Mast cell stabilizers, such as cromolyn (also known as sodium cromoglycate) and nedocromil (Tilade), are effective drugs in asthma management. These stabilizers hinder histamine release by skillfully obstructing the activation of mast cells and other cellular entities. Notably, they navigate this task without...