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| Content Provider | World Health Organization (WHO)-Global Index Medicus |
|---|---|
| Author | Harsløf, Laurine B. S. Damsgaard, Camilla T. Andersen, Anders D. Aakjær, Ditte L. Michaelsen, Kim F. Hellgren, Lars I. Frøkiær, Hanne Vogel, Ulla Lauritzen, Lotte |
| Description | Country affiliation: Denmark Author Affiliation: Harsløf LB ( Department of Nutrition, Exercise and Sports, Faculty of Science, University of Copenhagen, Frederiksberg, Denmark.); Damsgaard CT ( Department of Nutrition, Exercise and Sports, Faculty of Science, University of Copenhagen, Frederiksberg, Denmark.); Andersen AD ( Department of Nutrition, Exercise and Sports, Faculty of Science, University of Copenhagen, Frederiksberg, Denmark.); Aakjær DL ( Department of Nutrition, Exercise and Sports, Faculty of Science, University of Copenhagen, Frederiksberg, Denmark.); Michaelsen KF ( Department of Nutrition, Exercise and Sports, Faculty of Science, University of Copenhagen, Frederiksberg, Denmark.); Hellgren LI ( Department of Systems Biology, Center for Biological Sequence Analysis, Technical University of Denmark, Lyngby, Denmark.); Frøkiær H ( Department of Veterinary Disease Biology, Faculty of Health & Medical Sciences, University of Copenhagen, Frederiksberg, Denmark.); Vogel U ( National Research Centre for the Working Environment, Copenhagen, Denmark.); Lauritzen L ( Department of Nutrition, Exercise and Sports, Faculty of Science, University of Copenhagen, Frederiksberg, Denmark. Electronic address: ll@nexs.ku.dk.) |
| Abstract | We investigated whether n-3 LCPUFA affected immune function in late infancy and explored effect-modification by single nucleotide polymorphisms (SNPs) and links to intestinal microbiota. Infants (n=105) were randomized to fish oil (FO, 1.2g/d n-3 LCPUFA) or sunflower oil (SO)-supplements from age 9-18 months. Immune function was assessed by ex vivo cytokine production in stimulated blood and plasma immunoglobulin E (IgE). We genotyped functional SNPs in PPARG2 and COX2 and analyzed fecal microbiota by 16S-rRNA terminal restriction fragment length polymorphism. FO compared to SO reduced Lactobacillus paracasei-stimulated IL-6 at 18 months (P=0.03, n=104). This effect was most pronounced among infants wild-type for PPARG2-Pro12Ala and/or COX2-T8473C (P<0.05). Predominant bacterial fragments were associated with 18 months IgE in all infants (P=0.004) (bp100) and with IL-6 production among infants weaned before 9 months (P=0.047) (bp102). Thus, FO reduced IL-6 in a genotype-modified manner. The microbiota was partly linked to IL-6 and IgE, not directly to FO. |
| File Format | HTM / HTML |
| ISSN | 09523278 |
| Volume Number | 94 |
| e-ISSN | 15322823 |
| Journal | Prostaglandins, Leukotrienes and Essential Fatty Acids (PLEFA) |
| Language | English |
| Publisher | Elsevier |
| Publisher Date | 2015-03-01 |
| Publisher Place | Great Britain (UK) |
| Access Restriction | One Nation One Subscription (ONOS) |
| Subject Keyword | Discipline Endocrinology Cyclooxygenase 2 Genetics Fish Oils Administration & Dosage Interleukin-6 Metabolism Ppar Gamma Plant Oils Bacterial Infections Immunology Dietary Fats, Unsaturated Feces Microbiology Female Humans Immunoglobulin E Blood Infant Intestines Male Microbiota Drug Effects Polymorphism, Single Nucleotide Journal Article Randomized Controlled Trial |
| Content Type | Text |
| Resource Type | Article |
| Subject | Cell Biology Clinical Biochemistry |
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