4.7 Review

Do FADS genotypes enhance our knowledge about fatty acid related phenotypes?

期刊

CLINICAL NUTRITION
卷 29, 期 3, 页码 277-287

出版社

CHURCHILL LIVINGSTONE
DOI: 10.1016/j.clnu.2009.11.005

关键词

Delta-6 desaturase; Delta-5 desaturase; Single nucleotide polymorphism; Brain development; Coronary artery disease; Metabolic syndrome

资金

  1. Commission of the European Communities [Food-CT-2005-007036, FP6-036196-2, FP7-212652]
  2. German Federal Ministry of Education and Research [01GS0485]
  3. Bristol-Myers-Squibb Foundation, New York, NY, USA

向作者/读者索取更多资源

Several physiological processes, such as visual and cognitive development in early life, are dependent on the availability of long-chain polyunsaturated fatty acids (LC-PUFAs). Furthermore, the concentration of LC-PUFAs in phospholipids has been associated with numerous complex diseases like cardiovascular disease, atopic disease and metabolic syndrome. The level and composition of LC-PUFAs in the human body is mainly dependent on their dietary intake or on the intake of fatty acid precursors, which are endogenously elongated and desaturated to physiologically active LC-PUFAs. The delta-5 and delta-6 desaturase are the most important enzymes in this reaction cascade. In the last few years, several studies have reported an association between single nucleotide polymorphisms (SNPs) in the two desaturase encoding genes (FADS! and FADS2) and the concentration of omega-6 and omega-3 fatty acids. This shows that beside nutrition, genetic factors play an important role in the regulation of LC-PUFAs as well. This review focuses on current knowledge of the impact of FADS genotypes on LC-PUFA and lipid metabolism and discusses their influence on infant intellectual development, neurological conditions, metabolic disease as well as cardiovascular disease. (c) 2009 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism. All rights reserved.

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