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Furan fatty acid metabolite in newborns predicts risk of asthma
Gözde Gürdeniz1,2, Min Kim1, Nicklas Brustad1
1COPSAC, Copenhagen Prospective Studies on Asthma in Childhood, Herlev and Gentofte Hospital, University of Copenhagen, Gentofte, Denmark.
Insights
Newborn blood biomarkers, like CMPF, can indicate prenatal fish oil intake and predict lower childhood asthma risk. This discovery may help in early asthma screening for newborns.
Area of Science:
- Perinatal nutrition and its impact on child health outcomes.
- Metabolomics and biomarker discovery in newborns.
- Epidemiology of childhood asthma and environmental risk factors.
Background:
- Prenatal intake of fish oil and fatty fish is linked to reduced childhood asthma risk.
- Biomarkers for quantifying prenatal fish oil or fatty fish consumption are currently lacking.
Purpose of the Study:
- To identify biomarkers of prenatal fish oil exposure using newborn blood metabolomics.
- To evaluate the identified biomarkers' utility in stratifying childhood asthma risk.
Main Methods:
- Utilized the Danish COPSAC2010 mother-child cohort (n=677) for a randomized controlled trial of fish oil supplementation.
- Analyzed newborn dry blood spot metabolomics profiles using liquid chromatography-mass spectrometry.
- Replicated findings in the independent COPSAC2000 cohort (n=387) using observational data.
Main Results:
- Newborn metabolomics profiles significantly differed between fish oil and placebo groups (AUC=0.94).
- The fish oil biomarker, 3-carboxy-4-methyl-5-propyl-2-furan propanoic acid (CMPF), and the overall fish oil profile were associated with decreased asthma risk by age 6.
- In both cohorts, higher newborn CMPF levels correlated with lower asthma risk, fewer respiratory symptoms, and fewer infections in early childhood.
Conclusions:
- Newborn CMPF levels serve as a reliable biomarker for prenatal fish oil and fatty fish intake.
- Elevated CMPF in newborns is associated with a reduced risk of developing childhood asthma.
- This biomarker could potentially be used for newborn screening to identify children at lower risk for asthma.
Background:
Intake of fish-oil and fatty fish during pregnancy has been shown to reduce the risk of childhood asthma but biomarkers of such intake are lacking.
Objective:
To establish biomarkers of prenatal fish-oil exposure from newborn dry blood spot metabolomics profiles and assess their relevance for childhood asthma risk stratification.
Methods:
The Danish COPSAC2010 mother-child cohort was utilized to investigate the effect of a double-blinded randomized controlled trial of fish-oil supplementation during pregnancy on dry blood spot liquid-chromatography mass spectrometry-based metabolomics profiles of 677 newborns. We thereafter investigated the association between fish-oil associated biomarkers in the newborn and development of asthma-related outcomes. Replication was sought in the independent observational COPSAC2000 cohort with 387 newborn metabolomics profiles.
Results:
The newborn metabolomics profiles differed between children in the fish-oil vs. placebo group in COPSAC2010 (area under the receiver operator curve = 0.94 ± 0.03, p < .001). The fish-oil metabolomics profile and the top biomarker, 3-carboxy-4-methyl-5-propyl-2-furan propanoic acid (CMPF) were both associated with a decreased risk of asthma by age 6 years (HR = 0.89, p = .002 and HR = 0.67, p = .005, respectively). In COPSAC2000 , newborn CMPF level was also inversely associated with asthma risk by age 6 years (HR = 0.69, p = .01). Troublesome lung symptoms and common infections in the first 3 years were also inversely associated with newborn CMPF levels in both cohorts.
Conclusions:
Newborn children's blood levels of the furan fatty acid metabolite CMPF reflect fish-oil and fatty fish intake during pregnancy and are associated with a lower risk of asthma across two cohorts, which could aid newborn screening for childhood asthma.
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