Intake levels of dietary long-chain PUFAs modify the association between genetic variation in FADS and LDL-C[S]

Autor: Elisabet Wirfält, Bo Hedblad, Sophie Hellstrand, Bo Gullberg, Emily Sonestedt, Marju Orho-Melander, Ulrika Ericson
Jazyk: angličtina
Rok vydání: 2012
Předmět:
Fatty Acid Desaturases
Male
medicine.medical_specialty
Linoleic acid
Blood lipids
QD415-436
Endocrinology and Diabetes
Polymorphism
Single Nucleotide

Biochemistry
low density lipoprotein cholesterol
chemistry.chemical_compound
Endocrinology
Diet and cancer
Dietary Fats
Unsaturated

Internal medicine
medicine
Humans
Cardiac and Cardiovascular Systems
Alleles
Triglycerides
chemistry.chemical_classification
Nutrition and Dietetics
Triglyceride
biology
fatty acid desaturase
business.industry
Cholesterol
Cholesterol
HDL

cholesterol
Cholesterol
LDL

Cell Biology
cohort
Middle Aged
Fatty acid desaturase
chemistry
Genetic Loci
Fatty Acids
Unsaturated

biology.protein
Female
lipids (amino acids
peptides
and proteins)

epidemiology
Patient-Oriented and Epidemiological Research
business
diet
Lipoprotein
Polyunsaturated fatty acid
polyunsaturated fatty acids
Zdroj: Journal of Lipid Research, Vol 53, Iss 6, Pp 1183-1189 (2012)
Journal of Lipid Research
Journal of Lipid Research; 53(6), pp 1183-1189 (2012)
ISSN: 0022-2275
1183-1189
1539-7262
Popis: Polymorphisms of the FA desaturase (FADS) gene cluster have been associated with LDL, HDL, and triglyceride concentrations. Because FADS converts alpha-linolenic acid (ALA) and linoleic acid into PUFAs, we investigated the interaction between different PUFA intakes and the FADS polymorphism rs174547 (T>C) on fasting blood lipid and lipoprotein concentrations. We included 4,635 individuals (60% females, 45-68 years) from the Swedish population-based Malmo Diet and Cancer cohort. Dietary intakes were assessed by a modified diet history method including 7-day registration of cooked meals. The C-allele of rs174547 was associated with lower LDL concentration (P = 0.03). We observed significant interaction between rs174547 and long-chain omega-3 PUFA intakes on LDL (P = 0.01); the C-allele was only associated with lower LDL among individuals in the lowest tertile of long-chain omega-3 PUFA intakes (P < 0.001). In addition, significant interaction was observed between rs174547 and the ratio of ALA and linoleic FA intakes on HDL (P = 0.03). However, no significant associations between the C-allele and HDL were detected within the intake tertiles of the ratio. Our findings suggest that dietary intake levels of different PUFAs modify the associated effect of genetic variation in FADS on LDL and HDL.-Hellstrand, S., E. Sonestedt, U. Ericson, B. Gullberg, E. Wirfalt, B. Hedblad, and M. Orho-Melander. Intake levels of dietary PUFAs modify the association between genetic variation in FADS and LDL-C. J. Lipid Res. 2012. 53: 1183-1189.
Databáze: OpenAIRE