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      KCI등재 SCI SCIE SCOPUS

      DNA Polymorphisms and Haplotypes of Apolipoprotein A5's Attribution to the Plasma Triglyceride Levels in Koreans

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      https://www.riss.kr/link?id=A101618479

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      다국어 초록 (Multilingual Abstract)

      Purpose: Recent studies using human and mice reported that apolipoprotein A-V (APOA5) gene plays an important role in controlling triglyceride (TG) concentrations. The purpose of the present study was to investigate the correlation between single nucleotide polymorphisms (SNPs) and haplotypes in the APOA5 gene and TG in subjects and to search for possible associations of the APOA5 gene variants and common haplotypes with hypertriglyceridemia (HTG). Materials and Methods: We examined the case-control subjects including 100 HTG patients and 243 unrelated healthy control. The genes were screened for SNPs by direct sequencing in 48 genetically unrelated individuals. Six SNPs (-1390C>T, -1020G>A, -3A>G, V150M, G182C and 1259T>C) were genotyped in case and control populations. Results: In this study, our results indicated a strong association between APOA5 SNP -3A>G and G182C and elevated TG levels (p <0.001). Analysis of the SNPs from APOA5 gene has identified major haplotype showing very strong association with HTG, CGGGTT (p<0.001). Likelihood ratio test (LRT) of these six SNPs revealed that haplotypes were strong independent predictors of HTG (p<0.001). Haplotype-trend logistic regression (HTR) analysis revealed a significant association between the CGGGGC (haplotype 2) and CGGGTT (haplotype 4) and HTG (OR=2.48, 95% CI=1.06-5.76 and OR=8.54, 95% CI=2.66-27.42, respectively). Conclusion: We confirm that the APOA5 variants are associated with triglyceride levels and the haplotype may be strong independent predictors of HTG among Koreans.
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      Purpose: Recent studies using human and mice reported that apolipoprotein A-V (APOA5) gene plays an important role in controlling triglyceride (TG) concentrations. The purpose of the present study was to investigate the correlation between single nucl...

      Purpose: Recent studies using human and mice reported that apolipoprotein A-V (APOA5) gene plays an important role in controlling triglyceride (TG) concentrations. The purpose of the present study was to investigate the correlation between single nucleotide polymorphisms (SNPs) and haplotypes in the APOA5 gene and TG in subjects and to search for possible associations of the APOA5 gene variants and common haplotypes with hypertriglyceridemia (HTG). Materials and Methods: We examined the case-control subjects including 100 HTG patients and 243 unrelated healthy control. The genes were screened for SNPs by direct sequencing in 48 genetically unrelated individuals. Six SNPs (-1390C>T, -1020G>A, -3A>G, V150M, G182C and 1259T>C) were genotyped in case and control populations. Results: In this study, our results indicated a strong association between APOA5 SNP -3A>G and G182C and elevated TG levels (p <0.001). Analysis of the SNPs from APOA5 gene has identified major haplotype showing very strong association with HTG, CGGGTT (p<0.001). Likelihood ratio test (LRT) of these six SNPs revealed that haplotypes were strong independent predictors of HTG (p<0.001). Haplotype-trend logistic regression (HTR) analysis revealed a significant association between the CGGGGC (haplotype 2) and CGGGTT (haplotype 4) and HTG (OR=2.48, 95% CI=1.06-5.76 and OR=8.54, 95% CI=2.66-27.42, respectively). Conclusion: We confirm that the APOA5 variants are associated with triglyceride levels and the haplotype may be strong independent predictors of HTG among Koreans.

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      참고문헌 (Reference)

      1 Zhao SP, "of human serum apolipoprotein A5 with lipid profiles affected by gender" 376 : 68-71, 2007

      2 Pennacchio LA, "Two independent apolipoprotein A5 haplotypes influence human plasma triglyceride levels" 11 : 3031-3038, 2002

      3 Jang Y, "The -1131T″C polymorphism in the apolipoprotein A5 gene is associated with postprandial hypertriacylglycerolemia; elevated small, dense LDL concentrations; and oxidative stress nonobese Korean men" 80 : 832-840, 2004

      4 Wright WT, "SNPs at the APOA5 gene account for the strong association with hypertriglyceridaemia at the APOA5/A4/C3/A1 locus on chromosome 11q23 in the Northern Irish population" 185 : 353-360, 2006

      5 Szalai C, "Polymorphism in the promoter region of the apolipoprotein A5 gene is associated with an increased susceptibility for coronary artery disease" 173 : 109-114, 2004

      6 Hubcek JA, "New variants in the apolipoprotein AV gene in individuals with extreme triglyceride levels" 53 : 225-228, 2004

      7 Zhao JH, "Model-free analysis and permutation tests for allelic associations" 50 : 133-139, 2000

      8 Jiang YD, "Interaction of the G182C polymorphism in the APOA5 gene and fasting plasma glucose on plasma triglycerides in Type 2 diabetic subjects" 22 : 1690-1695, 2005

      9 Dallongeville J, "Impact of APOA5/A4/C3 genetic polymorphisms on lipid variables and cardiovascular disease risk in French men" 106 : 152-156, 2006

      10 Hsu LA, "Genetic variations of apolipoprotein A5 gene is associated with the risk of coronary artery disease among Chinese in Taiwan" 185 : 143-149, 2006

      1 Zhao SP, "of human serum apolipoprotein A5 with lipid profiles affected by gender" 376 : 68-71, 2007

      2 Pennacchio LA, "Two independent apolipoprotein A5 haplotypes influence human plasma triglyceride levels" 11 : 3031-3038, 2002

      3 Jang Y, "The -1131T″C polymorphism in the apolipoprotein A5 gene is associated with postprandial hypertriacylglycerolemia; elevated small, dense LDL concentrations; and oxidative stress nonobese Korean men" 80 : 832-840, 2004

      4 Wright WT, "SNPs at the APOA5 gene account for the strong association with hypertriglyceridaemia at the APOA5/A4/C3/A1 locus on chromosome 11q23 in the Northern Irish population" 185 : 353-360, 2006

      5 Szalai C, "Polymorphism in the promoter region of the apolipoprotein A5 gene is associated with an increased susceptibility for coronary artery disease" 173 : 109-114, 2004

      6 Hubcek JA, "New variants in the apolipoprotein AV gene in individuals with extreme triglyceride levels" 53 : 225-228, 2004

      7 Zhao JH, "Model-free analysis and permutation tests for allelic associations" 50 : 133-139, 2000

      8 Jiang YD, "Interaction of the G182C polymorphism in the APOA5 gene and fasting plasma glucose on plasma triglycerides in Type 2 diabetic subjects" 22 : 1690-1695, 2005

      9 Dallongeville J, "Impact of APOA5/A4/C3 genetic polymorphisms on lipid variables and cardiovascular disease risk in French men" 106 : 152-156, 2006

      10 Hsu LA, "Genetic variations of apolipoprotein A5 gene is associated with the risk of coronary artery disease among Chinese in Taiwan" 185 : 143-149, 2006

      11 Levy RT, "Fredrickson DS. Estimation of the concentration of low-density lipoprotein cholesterol in plasma without use of the preparative ultracentrifuge. Clin Chem 1972" 449-502,

      12 Cordell HJ, "Estimation and testing of genotype and haplotype effects in case-control studies: comparison of weighted regression and multiple imputation procedures" 30 : 259-275, 2006

      13 Austin MA, "Association of apolipoprotein A5 variants with LDL particle size and triglyceride in Japanese Americans" 1688 : 1-9, 2004

      14 Liu H, "Association between DNA variant sites in the apolipoprotein A5 gene and coronary heart disease in Chinese" 54 : 568-572, 2005

      15 Charlton-Menys V, "Apolipoprotein A5 and hypertriglyceridemia" 51 : 295-297, 2005

      16 Pennacchio LA, "An apolipoprotein influencing triglycerides in humans and mice revealed by comparative sequencing" 294 : 169-173, 2001

      17 Kao JT, "A novel genetic variant in the apolipoprotein A5 gene is associated with hypertriglyceridemia" 12 : 2533-2539, 2003

      18 Tang Y, "A genetic variant c.553G>T in the apolipoprotein A5 gene is associated with an increased risk of coronary artery disease and altered triglyceride levels in a Chinese population" 185 : 433-437, 2006

      19 Devlin B, "A comparison of linkage disequilibrium measures for fine-scale mapping" 29 : 311-322, 1995

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      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
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      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-05-31 학술지등록 한글명 : Yonsei Medical Journal
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      2002-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2000-01-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.42 0.3 0.99
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.83 0.72 0.546 0.08
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