The Association Study of the LIPC -250G/A Polymorphism and High-carbohydrate/Low-fat Diet Induced Serum Lipid and Apolipoprotein Concentration Changes in Healthy Youth
Abstract
To investigate the role of the -250G/A polymorphism in the promoter region of hepatic lipase gene (LIPC) on serum lipid profile and its interactions with a high-carbohydrate/low-fat (HC/LF) diet on serum lipid profiles in a young healthy Chinese population. Methods After a stabilization diet for seven days, fifty-six young healthy subjects (27 mdles, 29 females) were given the HC/LF diet for six days. The serum lipid profiles were analyzed of the twelve-hour fasting venous blood samples collected in the mornings of the first, the eighth and the fourteenth days. The concentrations of serum apolipoproteins were measured. The LIPC -250G/A polymorphism were analyzed. Results At baseline, the female subjects with the GG genotype had significantly higher high-density lipoprotein cholesterol (HDL-C) (P=0.041) and apolipoprotein A-Ⅰ (Apo A-Ⅰ) (P=0.020) than the male subjects with the same genotype. After the stabilization diet, the females had significantly higher HDL-C (GG genotype:P=0.021, A carriers:P=0.014) and Apo A-Ⅰ (GG genotype:P=0.035, A carriers:P=0.006) than the males in all genotypes. After the HC/LF diet, the female A carriers had significantly higher total cholesterol (TC) (P=0.042) than the male A carriers, and the females had significantly higher Apo A-Ⅰ than the males in all genotypes (GG genotype:P=0.010, A carriers:P=0.009). Compared with those before the HC/LF diet, TC (males with GG genotype:P=0.013, male A carriers:P=0.000; females with GG genotype:P=0.025, female A carriers:P=0.048) and low-density lipoprotein cholesterol (LDL-C) (males with GG genotype:P=0.028, male A carriers:P=0.000; females with GG genotype:P=0.004, female A carriers:P=0.001) significantly decreased after the diet in all the subjects. Triglycerides (TAG) (GG genotype:P=0.006, A carriers:P=0.001) significantly increased in the females regardless of the genotype. However, only in the male A carriers, HDL-C (P=0.011) and Apo A-Ⅰ (P=0.041) significantly increased after the diet. Conclusion The A allele at the LIPC -250G/A polymorphism is associated with the HC/LF diet induced HDL-C and Apo A-Ⅰ concentration changes in the males.
Keywords: Hepatic lipase, Gene polymorphism, The high-carbohydrate/low-fat diet, Lipids, Apolipoproteins
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Lee MM, Wu-Williams A, Whittemore AS, et al. Comparison of dietary habits, physical activity and body size among Chinese in North America and China. Int J Epidemiol, 1994 ;23(5);984- 990.
Chen Z, Shu XO, Yang G, et al. Nutrient intake among Chinese women living in Shanghai, China. Br J Nutr,2006;96 (2):393-399.
Suzuki T, Yokota H, Yamazaki T, et al. Angiotensin converting enzyme polymorphism is associated with severity of coronary heart disease and serum lipids (total cholesterol and triglyceride levels) in Japanese patients. Coronary Artery Dis, 1996;7(5):371-375.
Oren I, Brook JG, Gershoni-Baruch R, et al. The D allele of the angiotensin-converting enzyme gene contributes towards blood LDL-cholesterol levels and the presence of hypertension. Atherosclerosis, 1999; 145(2):267-271.
Vaisi-Raygani A, Ghaneialvar H, Rahimi Z, et al. The angiotensin converting enzyme D allele is an independent risk factor for early onset coronary artery disease. Clin Biochem, 2010;43(15):1189-1194.
Nakauchi Y, AsuehiroT, Yamamoto M, elal. Significance of angiotensin I -converting enzyme and angiotensin Ц type 1 receptor gene polymorphisms as risk factors for coronary heart disease. Atherosclerosis, 1996; 125(2); 161-169.
Hubert C, Houot AM, Corvol P. et al. Structure of the angiotensin I -converting enzyme gene; two alternate promoters correspond to evolutionary steps of a duplicated gene. J Biol Chem, 1991;266(23); 15377-15383.
Tiret L. Rigat B, Visvikis S, et al. Evidence, from combined segregation and linkage analysis, that a variance of the angiotensin I -converting enzyme (ACE) gene controls plasma ACE levels. Am J Hum Genet, 1992; 51 (1); 197-205.
Nakai K, Itoh C, Miura Y, et al. Deletion polymorphism of the angiotensin I -converting enzyme gene as associates with increased risk for is chemic heart disease in the Japanese. Jpn J Rinsho Byori, 1994 ;42( 7):689-694.
Pietro DP. Sergio C, Salvatore P. Does angiotensin converting enzyme gene polymorphism affect blood pressure? Findings after 6 years of follow-up in healthy subjects. Eur J Heart Fail, 2004;6( 1 ) : 11-16.
Zhang JH, Kohara K, Yamamoto Y, et al. Genetic predisposition to neurological symptoms in lacunar infarction. Cerebrovasc Dis,2004 ; 17(4); 273-279.
Staessen JA, Wang JG, Giuliana G, et al. The deletion/ insertion polymorphism of the angiotensin converting enzyme gene and cardiovascular-renal risk. J Hypertens, 1997 ; 15(12); 1579-1592.
Panahloo A, Andres С, Mohamed-Ali V, et al. The insertion allele of the ACE gene 1/D polymorphism; a candidate gene for insulin resistance? Circulation, 1995 ;92(12):3390-3393.
Sultan S, Hynes N. Cardiovascular disease; primary prevention, disease modulation and regenerative therapy. Vascular,2012;20(5) ;243-250.
Baum SJ, Kris-Etherton PM, Willett WC, et al. Fatty acids in cardiovascular health and disease; a comprehensive update. J Clin Lipidol,2012;6(3):216-234.
Brunzell JDt Zambon A. Deeb SS. The effect of hepatic lipase on coronary artery disease in humans is influenced by the underlying lipoprotein phenotype. Biochim Biophys Acta,2012; 1821(3)s365-372.
Meng L, Ruixing Y, Yiyang L, et al. Association of LIPC 250G>A polymorphism and several environmental factors with serum lipid levels in the Guangxi Bai Ku Yao and Han populations. Lipids Health Dis, 2010; 9; 28. http;//www. lipidworld. com/content/9/1/28.
Holmes RS, Vandeberg JL, Cox LA. Vertebrate hepatic lipase genes and proteins: a review supported by bioinformatic studies. Open Access Bioinformatics,2011;2011(3):85-95.
Jimenez-Gomez Y, Perez-Jimenez F. Marin C, et al. The 250G/A polymorphism in the hepatic lipase gene promoter influences the postprandial lipemic response in healthy men. Nutr Metab Cardiovasc Dis,2008; 18(3): 173-181.
Leite ML. Nicolosi A. Dietary patterns and metabolic syndrome factors in a non-diabetic Italian population. Public Health Nutr, 2009;12(9):1494-1503.
Khor VK, Dhir R, Yin X, et al. Estrogen sulfotransferase regulates body fat and glucose homeostasis in female mice. Am J Physiol Endocrinol Metab,2010;299(4);E657-E664.
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