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      혈중 지질 농도와 관련한 양적 형질 유전자의 연관 불균형 분석 = Linkage Disequilibrium Analysis of Quantitative Trait Locus Associated with Lipid Profiles

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      https://www.riss.kr/link?id=A104687214

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      다국어 초록 (Multilingual Abstract)

      Background and Objectives:The common methods of genetic association analysis are sensitive to population stratification, which may easily lead to a spurious association result. We used a regression approach based for linkage disequilibrium to perform a high resolution genetic association analysis. Subjects and Methods:We applied a regression approach that can increase the resolution of quantitative traits that are related with cardiovascular diseases.
      The population data was composed of 543 males and 876 females without cardiovascular diseases, and it was obtained from a cardiovascular genome center. We used information about linkage disequilibrium between the marker and trait locus, and we added the covariates to model their effects. Results:We found that this regression approach has the merit of analyzing genetic association based on linkage disequilibrium. In the analysis of the male group, the total cholesterol was significantly in linkage disequilibrium with CETP3 (p=0.002), and triglyceride was significantly in linkage disequilibrium with ACE8 (p=0.037), APOA1-1 (p=0.031), APOA5-1 (p=0.001), APOA5- 2 (p=0.001) and LIPC4 (p=0.022). HDL-cholesterol was significantly in linkage disequilibrium with ACE7 (p= 0.002), ACE8 (p=0.008), ACE10 (p=0.003), APOA5-2 (p=0.022), and MTP1 (p=0.001). In the female group, total cholesterol was significantly associated with APOA5-1 (p=0.020), APOA5-2 (p=0.001), and LIPC1 (p= 0.016), and triglyceride was significantly associated with APOA5-1 (p=0.009), APOA5-2 (p=0.001), and CETP5 (p=0.049). LDL-cholesterol was significantly associated with APOA5-2 (p=0.004), and HDL-cholesterol was significantly associated with LIPC1 (p=0.004). Conclusion:We used a regression-based method to perform high resolution linkage disequilibrium analysis of a quantitative trait locus that’s associated with lipid profiles. This method of using a single marker, as applied in this paper, was well suited for analysis of genetic association. Because of the simplicity, the method can also be easily performed by routine statistical analysis software. (Korean Circulation J 2006;36:688-694)
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      Background and Objectives:The common methods of genetic association analysis are sensitive to population stratification, which may easily lead to a spurious association result. We used a regression approach based for linkage disequilibrium to perfor...

      Background and Objectives:The common methods of genetic association analysis are sensitive to population stratification, which may easily lead to a spurious association result. We used a regression approach based for linkage disequilibrium to perform a high resolution genetic association analysis. Subjects and Methods:We applied a regression approach that can increase the resolution of quantitative traits that are related with cardiovascular diseases.
      The population data was composed of 543 males and 876 females without cardiovascular diseases, and it was obtained from a cardiovascular genome center. We used information about linkage disequilibrium between the marker and trait locus, and we added the covariates to model their effects. Results:We found that this regression approach has the merit of analyzing genetic association based on linkage disequilibrium. In the analysis of the male group, the total cholesterol was significantly in linkage disequilibrium with CETP3 (p=0.002), and triglyceride was significantly in linkage disequilibrium with ACE8 (p=0.037), APOA1-1 (p=0.031), APOA5-1 (p=0.001), APOA5- 2 (p=0.001) and LIPC4 (p=0.022). HDL-cholesterol was significantly in linkage disequilibrium with ACE7 (p= 0.002), ACE8 (p=0.008), ACE10 (p=0.003), APOA5-2 (p=0.022), and MTP1 (p=0.001). In the female group, total cholesterol was significantly associated with APOA5-1 (p=0.020), APOA5-2 (p=0.001), and LIPC1 (p= 0.016), and triglyceride was significantly associated with APOA5-1 (p=0.009), APOA5-2 (p=0.001), and CETP5 (p=0.049). LDL-cholesterol was significantly associated with APOA5-2 (p=0.004), and HDL-cholesterol was significantly associated with LIPC1 (p=0.004). Conclusion:We used a regression-based method to perform high resolution linkage disequilibrium analysis of a quantitative trait locus that’s associated with lipid profiles. This method of using a single marker, as applied in this paper, was well suited for analysis of genetic association. Because of the simplicity, the method can also be easily performed by routine statistical analysis software. (Korean Circulation J 2006;36:688-694)

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      참고문헌 (Reference)

      1 "Transmission/disequilibriumtests for quantitative traits" 64 : 555-565, 2000

      2 "Transmission test forlinkage disequilibrium:the insulin gene region and insulin-dependentdiabetes melitus(IDDM)" 52 : 506-16, 1993

      3 "Transmission disequilibrium tests for quantitativetraits" 60 : 676-690, 1997

      4 "The impact of apolipoproteinA1 polymorphisms on the lipid profiles in middle aged healthymen and women" 34 : 1158-1166, 2004

      5 "The future of genetic studies of complexhuman diseases" 273 : 1516-1517, 1996

      6 "TDT statistics for mappingquantitative trait loci" 62 : 431-452, 1998

      7 "Multipoint analysis of human quantitative geneticvariation" 47 : 957-67, 1990

      8 "Models and tests of linkage and associationstudies of QTL for multi-allele marker loci" 53 : 130-145, 2002

      9 "Microsomaltriglyceride transfer protein -493T variant reduces IDL plus LDLapoB production and the plasma concentration of large LDLparticles" 290 : 739-745, 2006

      10 "Mathematical and statistical methods for genetic analysis" Springer 2002

      1 "Transmission/disequilibriumtests for quantitative traits" 64 : 555-565, 2000

      2 "Transmission test forlinkage disequilibrium:the insulin gene region and insulin-dependentdiabetes melitus(IDDM)" 52 : 506-16, 1993

      3 "Transmission disequilibrium tests for quantitativetraits" 60 : 676-690, 1997

      4 "The impact of apolipoproteinA1 polymorphisms on the lipid profiles in middle aged healthymen and women" 34 : 1158-1166, 2004

      5 "The future of genetic studies of complexhuman diseases" 273 : 1516-1517, 1996

      6 "TDT statistics for mappingquantitative trait loci" 62 : 431-452, 1998

      7 "Multipoint analysis of human quantitative geneticvariation" 47 : 957-67, 1990

      8 "Models and tests of linkage and associationstudies of QTL for multi-allele marker loci" 53 : 130-145, 2002

      9 "Microsomaltriglyceride transfer protein -493T variant reduces IDL plus LDLapoB production and the plasma concentration of large LDLparticles" 290 : 739-745, 2006

      10 "Mathematical and statistical methods for genetic analysis" Springer 2002

      11 "Linkage and association" 15 : 565-576, 1998

      12 "Introduction to quantitative genetics" Longman House 1996

      13 "Insertion/deletion polymorphismof angiotensin Iconverting enzyme gene in Korean patentswith ischemic heart disease" 26 : 5-13, 1996

      14 "Hepatic lipase C-514Tpolymorphism and its association with high-density lipoproteincholesterol level in Tehran" 13 : 101-103, 2006

      15 "Genetics and analysis of quantitative traits" Sinauer Associates 1998

      16 "Genetic variations of apolipoproteinA5 gene is associated with the risk of coronary arterydisease among Chinese in Taiwan" 185 : 143-149, 2006

      17 "Genetic variation in thehepatic lipase gene is associated with combined hyperlipidemia,plasma lipid concentrations,and lipid-lowering drug response" 150 : 1154-1162, 2005

      18 "Genetic linkage methods for quantitativetraits" 10 : 3-25, 2001

      19 "Effects of cholesterylester transfer protein inhibition on high-density lipoproteinsubspecies,apolipoprotein A-I metabolism,and fecal sterol excretion" 25 : 1057-1064, 2005

      20 "Comparison of linkage disequilibrium methodsfor localization of genes influencing quantitative trait in humans" 64 : 1194-1205, 1999

      21 "Combined linkage and linkage disequilibriummapping for genome screens" 19 : 211-234, 2000

      22 "Association study designs for complex diseases" 2 : 91-99, 2001

      23 "Association studies of QTL for multi-allele markersby mixed models" 54 : 132-150, 2002

      24 "Association between I/D,G14480C,A22982G polymorphisms of Angiotesin I-converting enzyme geneand essential hypertension in the Korean population" 34 : 1137-1147, 2004

      25 "An I/D polymorphismin angiotensin-converting enzyme gene in myocardialinfarction" 26 : 465-472, 1996

      26 "A transmission disequilibrium test for quantitativetrait loci" 47 : 342-350, 1997

      27 "A genetic variant in the apolipoproteinA5 gene is associated with an increased risk of coronaryartery disease and altered triglyceride levels in a Chinese popu694" 36 : 688-694, 2006

      28 "A general test of associationfor quantitative traits in nuclear families" 66 : 279-292, 2000

      29 "A general model for the genetic analysis ofpedigree data" 21 : 523-42, 1971

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      학술지 이력

      학술지 이력
      연월일 이력구분 이력상세 등재구분
      2023 평가예정 해외DB학술지평가 신청대상 (해외등재 학술지 평가)
      2020-01-01 평가 등재학술지 유지 (해외등재 학술지 평가) KCI등재
      2011-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2009-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2008-05-15 학회명변경 한글명 : 대한순환기학회 -> 대한심장학회
      영문명 : The Korean Society Of Circulation -> The Korean Society of Cardiology
      KCI등재
      2007-01-01 평가 등재학술지 유지 (등재유지) KCI등재
      2005-08-02 학술지등록 한글명 : Korean Circulation Journal
      외국어명 : Korean Circulation Journal
      KCI등재
      2004-01-01 평가 등재학술지 선정 (등재후보2차) KCI등재
      2003-01-01 평가 등재후보 1차 PASS (등재후보1차) KCI등재후보
      2001-07-01 평가 등재후보학술지 선정 (신규평가) KCI등재후보
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      학술지 인용정보

      학술지 인용정보
      기준연도 WOS-KCI 통합IF(2년) KCIF(2년) KCIF(3년)
      2016 1.13 0.34 0.71
      KCIF(4년) KCIF(5년) 중심성지수(3년) 즉시성지수
      0.45 0.36 0.52 0.12
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