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FADS1 FADS2 Gene Cluster, PUFA Intake and Blood Lipids in Children: Results from the GINIplus and LISAplus Studies
by
Drogies, Tim
, Schaaf, Beate
, Krämer, Ursula
, Thiery, Joachim
, Buyken, Anette
, Berdel, Dietrich
, Bauer, Carl-Peter
, Lattka, Eva
, Standl, Marie
, Heinrich, Joachim
, Stach, Barbara
, Röder, Stefan
, von Berg, Andrea
, Koletzko, Berthold
, Herbarth, Olf
, Koletzko, Sibylle
in
Adults
/ Alleles
/ Analysis
/ Biology
/ Blood
/ Blood levels
/ Breastfeeding & lactation
/ Cardiovascular diseases
/ Child
/ Children
/ Children & youth
/ Cholesterol
/ Cholesterol, HDL - blood
/ Cholesterol, HDL - genetics
/ Cholesterol, LDL - blood
/ Cholesterol, LDL - genetics
/ Clusters
/ Cohort analysis
/ Cohort Studies
/ Desaturase
/ Diet
/ Dietary intake
/ Environmental health
/ Epidemiology
/ Fatty Acid Desaturases - genetics
/ Fatty acids
/ Fatty Acids, Unsaturated - administration & dosage
/ Female
/ Food intake
/ Genes
/ Genetic aspects
/ Genetic Association Studies
/ Genotype
/ Germany
/ Health risks
/ Heart diseases
/ High density lipoprotein
/ Hospitals
/ Humans
/ Immunoglobulins
/ Laboratories
/ Lipids
/ Lipoproteins (high density)
/ Lipoproteins (low density)
/ Low density lipoprotein
/ Low density lipoproteins
/ Male
/ Medicine
/ Metabolism
/ Metabolites
/ Multigene Family
/ Omega 3 fatty acids
/ Pediatrics
/ Polymorphism, Single Nucleotide
/ Polyunsaturated fatty acids
/ Prospective Studies
/ Regression analysis
/ Risk factors
/ Single nucleotide polymorphisms
/ Single-nucleotide polymorphism
/ Studies
/ Surveys and Questionnaires
/ Triglycerides
/ Triglycerides - blood
/ Triglycerides - genetics
2012
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FADS1 FADS2 Gene Cluster, PUFA Intake and Blood Lipids in Children: Results from the GINIplus and LISAplus Studies
by
Drogies, Tim
, Schaaf, Beate
, Krämer, Ursula
, Thiery, Joachim
, Buyken, Anette
, Berdel, Dietrich
, Bauer, Carl-Peter
, Lattka, Eva
, Standl, Marie
, Heinrich, Joachim
, Stach, Barbara
, Röder, Stefan
, von Berg, Andrea
, Koletzko, Berthold
, Herbarth, Olf
, Koletzko, Sibylle
in
Adults
/ Alleles
/ Analysis
/ Biology
/ Blood
/ Blood levels
/ Breastfeeding & lactation
/ Cardiovascular diseases
/ Child
/ Children
/ Children & youth
/ Cholesterol
/ Cholesterol, HDL - blood
/ Cholesterol, HDL - genetics
/ Cholesterol, LDL - blood
/ Cholesterol, LDL - genetics
/ Clusters
/ Cohort analysis
/ Cohort Studies
/ Desaturase
/ Diet
/ Dietary intake
/ Environmental health
/ Epidemiology
/ Fatty Acid Desaturases - genetics
/ Fatty acids
/ Fatty Acids, Unsaturated - administration & dosage
/ Female
/ Food intake
/ Genes
/ Genetic aspects
/ Genetic Association Studies
/ Genotype
/ Germany
/ Health risks
/ Heart diseases
/ High density lipoprotein
/ Hospitals
/ Humans
/ Immunoglobulins
/ Laboratories
/ Lipids
/ Lipoproteins (high density)
/ Lipoproteins (low density)
/ Low density lipoprotein
/ Low density lipoproteins
/ Male
/ Medicine
/ Metabolism
/ Metabolites
/ Multigene Family
/ Omega 3 fatty acids
/ Pediatrics
/ Polymorphism, Single Nucleotide
/ Polyunsaturated fatty acids
/ Prospective Studies
/ Regression analysis
/ Risk factors
/ Single nucleotide polymorphisms
/ Single-nucleotide polymorphism
/ Studies
/ Surveys and Questionnaires
/ Triglycerides
/ Triglycerides - blood
/ Triglycerides - genetics
2012
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FADS1 FADS2 Gene Cluster, PUFA Intake and Blood Lipids in Children: Results from the GINIplus and LISAplus Studies
by
Drogies, Tim
, Schaaf, Beate
, Krämer, Ursula
, Thiery, Joachim
, Buyken, Anette
, Berdel, Dietrich
, Bauer, Carl-Peter
, Lattka, Eva
, Standl, Marie
, Heinrich, Joachim
, Stach, Barbara
, Röder, Stefan
, von Berg, Andrea
, Koletzko, Berthold
, Herbarth, Olf
, Koletzko, Sibylle
in
Adults
/ Alleles
/ Analysis
/ Biology
/ Blood
/ Blood levels
/ Breastfeeding & lactation
/ Cardiovascular diseases
/ Child
/ Children
/ Children & youth
/ Cholesterol
/ Cholesterol, HDL - blood
/ Cholesterol, HDL - genetics
/ Cholesterol, LDL - blood
/ Cholesterol, LDL - genetics
/ Clusters
/ Cohort analysis
/ Cohort Studies
/ Desaturase
/ Diet
/ Dietary intake
/ Environmental health
/ Epidemiology
/ Fatty Acid Desaturases - genetics
/ Fatty acids
/ Fatty Acids, Unsaturated - administration & dosage
/ Female
/ Food intake
/ Genes
/ Genetic aspects
/ Genetic Association Studies
/ Genotype
/ Germany
/ Health risks
/ Heart diseases
/ High density lipoprotein
/ Hospitals
/ Humans
/ Immunoglobulins
/ Laboratories
/ Lipids
/ Lipoproteins (high density)
/ Lipoproteins (low density)
/ Low density lipoprotein
/ Low density lipoproteins
/ Male
/ Medicine
/ Metabolism
/ Metabolites
/ Multigene Family
/ Omega 3 fatty acids
/ Pediatrics
/ Polymorphism, Single Nucleotide
/ Polyunsaturated fatty acids
/ Prospective Studies
/ Regression analysis
/ Risk factors
/ Single nucleotide polymorphisms
/ Single-nucleotide polymorphism
/ Studies
/ Surveys and Questionnaires
/ Triglycerides
/ Triglycerides - blood
/ Triglycerides - genetics
2012
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FADS1 FADS2 Gene Cluster, PUFA Intake and Blood Lipids in Children: Results from the GINIplus and LISAplus Studies
Journal Article
FADS1 FADS2 Gene Cluster, PUFA Intake and Blood Lipids in Children: Results from the GINIplus and LISAplus Studies
2012
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Overview
Elevated cholesterol levels in children can be a risk factor for cardiovascular diseases in later life. In adults, it has been shown that blood lipid levels are strongly influenced by polymorphisms in the fatty acid desaturase (FADS) gene cluster in addition to nutritional and other exogenous and endogenous determinants. Our aim was to investigate whether lipid levels are determined by the FADS genotype already in children and whether this association interacts with dietary intake of n-3 fatty acids.
The analysis was based on data of 2006 children from two German prospective birth cohort studies. Total cholesterol, HDL, LDL and triglycerides were measured at 10 years of age. Six single nucleotide polymorphisms (SNPs) of the FADS gene cluster were genotyped. Dietary n-3 fatty acid intake was assessed by food frequency questionnaire. Linear regression modeling was used to assess the association between lipid levels, n-3 fatty acid intake and FADS genotype.
Individuals carrying the homozygous minor allele had lower levels of total cholesterol [means ratio (MR) ranging from 0.96 (p = 0.0093) to 0.98 (p = 0.2949), depending on SNPs] and LDL [MR between 0.94 (p = 0.0179) and 0.97 (p = 0.2963)] compared to homozygous major allele carriers. Carriers of the heterozygous allele showed lower HDL levels [β between -0.04 (p = 0.0074) to -0.01 (p = 0.3318)] and higher triglyceride levels [MR ranging from 1.06 (p = 0.0065) to 1.07 (p = 0.0028)] compared to homozygous major allele carriers. A higher n-3 PUFA intake was associated with higher concentrations of total cholesterol, LDL, HDL and lower triglyceride levels, but these associations did not interact with the FADS1 FADS2 genotype.
Total cholesterol, HDL, LDL and triglyceride concentrations may be influenced by the FADS1 FADS2 genotype already in 10 year old children. Genetically determined blood lipid levels during childhood might differentially predispose individuals to the development of cardiovascular diseases later in life.
Publisher
Public Library of Science,Public Library of Science (PLoS)
Subject
/ Alleles
/ Analysis
/ Biology
/ Blood
/ Child
/ Children
/ Clusters
/ Diet
/ Fatty Acid Desaturases - genetics
/ Fatty Acids, Unsaturated - administration & dosage
/ Female
/ Genes
/ Genotype
/ Germany
/ Humans
/ Lipids
/ Male
/ Medicine
/ Polymorphism, Single Nucleotide
/ Single nucleotide polymorphisms
/ Single-nucleotide polymorphism
/ Studies
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