Polymorphisms of the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with obesity phenotypes in a large family-based association study
Background: The low-density lipoprotein receptor-related protein 5 (LRP5) gene, essential for glucose and cholesterol metabolism, may have a role in the aetiology of obesity, an important risk factor for diabetes. Participants and methods: To investigate the association between LRP5 polymorphisms an...
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Published in | Journal of medical genetics Vol. 43; no. 10; pp. 798 - 803 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
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London
BMJ Publishing Group Ltd
01.10.2006
BMJ BMJ Publishing Group LTD BMJ Group |
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Abstract | Background: The low-density lipoprotein receptor-related protein 5 (LRP5) gene, essential for glucose and cholesterol metabolism, may have a role in the aetiology of obesity, an important risk factor for diabetes. Participants and methods: To investigate the association between LRP5 polymorphisms and obesity, 27 single-nucleotide polymorphisms (SNPs), spacing about 5 kb apart on average and covering the full transcript length of the LRP5 gene, were genotyped in 1873 Caucasian people from 405 nuclear families. Obesity (defined as body mass index (BMI) >30 kg/m2) and three obesity-related phenotypes (BMI, fat mass and percentage of fat mass (PFM)) were investigated. Results: Single markers (12 tagging SNPs and 4 untaggable SNPs) and haplotypes (5 blocks) were tested for associations, using family-based designs. SNP4 (rs4988300) and SNP6 (rs634008) located in block 2 (intron 1) showed significant associations with obesity and BMI after Bonferroni correction (SNP4: p<0.001 and p = 0.001, respectively; SNP6: p = 0.002 and 0.003, respectively). The common allele A for SNP4 and minor allele G for SNP6 were associated with an increased risk of obesity. Significant associations were also observed between common haplotype A–G–G–G of block 2 with obesity, BMI, fat mass and PFM with global empirical values p<0.001, p<0.001, p = 0.003 and p = 0.074, respectively. Subsequent sex-stratified analyses showed that the association in the total sample between block 2 and obesity may be mainly driven by female subjects. Conclusion: Intronic variants of the LRP5 gene are markedly associated with obesity. We hypothesise that such an association may be due to the role of LRP5 in the WNT signalling pathway or lipid metabolism. Further functional studies are needed to elucidate the exact molecular mechanism underlying our finding. |
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AbstractList | BACKGROUND: The low-density lipoprotein receptor-related protein 5 (LRP5) gene, essential for glucose and cholesterol metabolism, may have a role in the aetiology of obesity, an important risk factor for diabetes. Participants and methods: To investigate the association between LRP5 polymorphisms and obesity, 27 single-nucleotide polymorphisms (SNPs), spacing about 5 kb apart on average and covering the full transcript length of the LRP5 gene, were genotyped in 1873 Caucasian people from 405 nuclear families. Obesity (defined as body mass index (BMI) >30 kg/m super(2)) and three obesity-related phenotypes (BMI, fat mass and percentage of fat mass (PFM)) were investigated. RESULTS: Single markers (12 tagging SNPs and 4 untaggable SNPs) and haplotypes (5 blocks) were tested for associations, using family-based designs. SNP4 (rs4988300) and SNP6 (rs634008) located in block 2 (intron 1) showed significant associations with obesity and BMI after Bonferroni correction (SNP4: p<0.001 and p = 0.001, respectively; SNP6: p = 0.002 and 0.003, respectively). The common allele A for SNP4 and minor allele G for SNP6 were associated with an increased risk of obesity. Significant associations were also observed between common haplotype A-G-G-G of block 2 with obesity, BMI, fat mass and PFM with global empirical values p<0.001, p<0.001, p = 0.003 and p = 0.074, respectively. Subsequent sex-stratified analyses showed that the association in the total sample between block 2 and obesity may be mainly driven by female subjects. CONCLUSION: Intronic variants of the LRP5 gene are markedly associated with obesity. We hypothesise that such an association may be due to the role of LRP5 in the WNT signalling pathway or lipid metabolism. Further functional studies are needed to elucidate the exact molecular mechanism underlying our finding. Background: The low-density lipoprotein receptor-related protein 5 (LRP5) gene, essential for glucose and cholesterol metabolism, may have a role in the aetiology of obesity, an important risk factor for diabetes. Participants and methods: To investigate the association between LRP5 polymorphisms and obesity, 27 single-nucleotide polymorphisms (SNPs), spacing about 5 kb apart on average and covering the full transcript length of the LRP5 gene, were genotyped in 1873 Caucasian people from 405 nuclear families. Obesity (defined as body mass index (BMI) >30 kg/m2) and three obesity-related phenotypes (BMI, fat mass and percentage of fat mass (PFM)) were investigated. Results: Single markers (12 tagging SNPs and 4 untaggable SNPs) and haplotypes (5 blocks) were tested for associations, using family-based designs. SNP4 (rs4988300) and SNP6 (rs634008) located in block 2 (intron 1) showed significant associations with obesity and BMI after Bonferroni correction (SNP4: p<0.001 and p = 0.001, respectively; SNP6: p = 0.002 and 0.003, respectively). The common allele A for SNP4 and minor allele G for SNP6 were associated with an increased risk of obesity. Significant associations were also observed between common haplotype A–G–G–G of block 2 with obesity, BMI, fat mass and PFM with global empirical values p<0.001, p<0.001, p = 0.003 and p = 0.074, respectively. Subsequent sex-stratified analyses showed that the association in the total sample between block 2 and obesity may be mainly driven by female subjects. Conclusion: Intronic variants of the LRP5 gene are markedly associated with obesity. We hypothesise that such an association may be due to the role of LRP5 in the WNT signalling pathway or lipid metabolism. Further functional studies are needed to elucidate the exact molecular mechanism underlying our finding. The low-density lipoprotein receptor-related protein 5 (LRP5) gene, essential for glucose and cholesterol metabolism, may have a role in the aetiology of obesity, an important risk factor for diabetes.BACKGROUNDThe low-density lipoprotein receptor-related protein 5 (LRP5) gene, essential for glucose and cholesterol metabolism, may have a role in the aetiology of obesity, an important risk factor for diabetes.To investigate the association between LRP5 polymorphisms and obesity, 27 single-nucleotide polymorphisms (SNPs), spacing about 5 kb apart on average and covering the full transcript length of the LRP5 gene, were genotyped in 1873 Caucasian people from 405 nuclear families. Obesity (defined as body mass index (BMI) >30 kg/m(2)) and three obesity-related phenotypes (BMI, fat mass and percentage of fat mass (PFM)) were investigated.PARTICIPANTS AND METHODSTo investigate the association between LRP5 polymorphisms and obesity, 27 single-nucleotide polymorphisms (SNPs), spacing about 5 kb apart on average and covering the full transcript length of the LRP5 gene, were genotyped in 1873 Caucasian people from 405 nuclear families. Obesity (defined as body mass index (BMI) >30 kg/m(2)) and three obesity-related phenotypes (BMI, fat mass and percentage of fat mass (PFM)) were investigated.Single markers (12 tagging SNPs and 4 untaggable SNPs) and haplotypes (5 blocks) were tested for associations, using family-based designs. SNP4 (rs4988300) and SNP6 (rs634008) located in block 2 (intron 1) showed significant associations with obesity and BMI after Bonferroni correction (SNP4: p<0.001 and p = 0.001, respectively; SNP6: p = 0.002 and 0.003, respectively). The common allele A for SNP4 and minor allele G for SNP6 were associated with an increased risk of obesity. Significant associations were also observed between common haplotype A-G-G-G of block 2 with obesity, BMI, fat mass and PFM with global empirical values p<0.001, p<0.001, p = 0.003 and p = 0.074, respectively. Subsequent sex-stratified analyses showed that the association in the total sample between block 2 and obesity may be mainly driven by female subjects.RESULTSSingle markers (12 tagging SNPs and 4 untaggable SNPs) and haplotypes (5 blocks) were tested for associations, using family-based designs. SNP4 (rs4988300) and SNP6 (rs634008) located in block 2 (intron 1) showed significant associations with obesity and BMI after Bonferroni correction (SNP4: p<0.001 and p = 0.001, respectively; SNP6: p = 0.002 and 0.003, respectively). The common allele A for SNP4 and minor allele G for SNP6 were associated with an increased risk of obesity. Significant associations were also observed between common haplotype A-G-G-G of block 2 with obesity, BMI, fat mass and PFM with global empirical values p<0.001, p<0.001, p = 0.003 and p = 0.074, respectively. Subsequent sex-stratified analyses showed that the association in the total sample between block 2 and obesity may be mainly driven by female subjects.Intronic variants of the LRP5 gene are markedly associated with obesity. We hypothesise that such an association may be due to the role of LRP5 in the WNT signalling pathway or lipid metabolism. Further functional studies are needed to elucidate the exact molecular mechanism underlying our finding.CONCLUSIONIntronic variants of the LRP5 gene are markedly associated with obesity. We hypothesise that such an association may be due to the role of LRP5 in the WNT signalling pathway or lipid metabolism. Further functional studies are needed to elucidate the exact molecular mechanism underlying our finding. The low-density lipoprotein receptor-related protein 5 (LRP5) gene, essential for glucose and cholesterol metabolism, may have a role in the aetiology of obesity, an important risk factor for diabetes. To investigate the association between LRP5 polymorphisms and obesity, 27 single-nucleotide polymorphisms (SNPs), spacing about 5 kb apart on average and covering the full transcript length of the LRP5 gene, were genotyped in 1873 Caucasian people from 405 nuclear families. Obesity (defined as body mass index (BMI) >30 kg/m(2)) and three obesity-related phenotypes (BMI, fat mass and percentage of fat mass (PFM)) were investigated. Single markers (12 tagging SNPs and 4 untaggable SNPs) and haplotypes (5 blocks) were tested for associations, using family-based designs. SNP4 (rs4988300) and SNP6 (rs634008) located in block 2 (intron 1) showed significant associations with obesity and BMI after Bonferroni correction (SNP4: p<0.001 and p = 0.001, respectively; SNP6: p = 0.002 and 0.003, respectively). The common allele A for SNP4 and minor allele G for SNP6 were associated with an increased risk of obesity. Significant associations were also observed between common haplotype A-G-G-G of block 2 with obesity, BMI, fat mass and PFM with global empirical values p<0.001, p<0.001, p = 0.003 and p = 0.074, respectively. Subsequent sex-stratified analyses showed that the association in the total sample between block 2 and obesity may be mainly driven by female subjects. Intronic variants of the LRP5 gene are markedly associated with obesity. We hypothesise that such an association may be due to the role of LRP5 in the WNT signalling pathway or lipid metabolism. Further functional studies are needed to elucidate the exact molecular mechanism underlying our finding. |
Author | Recker, Robert R Deng, Hong-wen Guo, Yan-fang Guo, Yan Wang, Wei Xiao, Peng Xiong, Dong-hai Shen, Hui Yang, Tie-lin Zhao, Lan-juan |
AuthorAffiliation | Y Guo , W Wang , T‐l Yang , Key Laboratory of Biomedical Information Engineering of Ministry of Education and Institute of Molecular Genetics, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an, P R China Y‐f Guo , H‐w Deng , Laboratory of Molecular and Statistical Genetics, College of Life Sciences, Hunan Normal University, Changsha, Hunan, P R China H Shen , Departments of Orthopedic Surgery and Basic Medical Sciences, University of Missouri–Kansas City, Kansas City, Missouri, USA D‐h Xiong , L‐j Zhao , P Xiao , R R Recker , Osteoporosis Research Center, Department of Biomedical Sciences, Creighton University, Omaha, Nebrasksa, USA |
AuthorAffiliation_xml | – name: Y‐f Guo , H‐w Deng , Laboratory of Molecular and Statistical Genetics, College of Life Sciences, Hunan Normal University, Changsha, Hunan, P R China – name: D‐h Xiong , L‐j Zhao , P Xiao , R R Recker , Osteoporosis Research Center, Department of Biomedical Sciences, Creighton University, Omaha, Nebrasksa, USA – name: H Shen , Departments of Orthopedic Surgery and Basic Medical Sciences, University of Missouri–Kansas City, Kansas City, Missouri, USA – name: Y Guo , W Wang , T‐l Yang , Key Laboratory of Biomedical Information Engineering of Ministry of Education and Institute of Molecular Genetics, School of Life Science and Technology, Xi'an Jiaotong University, Xi'an, P R China |
Author_xml | – sequence: 1 givenname: Yan-fang surname: Guo fullname: Guo, Yan-fang organization: Departments of Orthopedic Surgery and Basic Medical Sciences, University of Missouri–Kansas City, Kansas City, Missouri, USA – sequence: 2 givenname: Dong-hai surname: Xiong fullname: Xiong, Dong-hai organization: Departments of Orthopedic Surgery and Basic Medical Sciences, University of Missouri–Kansas City, Kansas City, Missouri, USA – sequence: 3 givenname: Hui surname: Shen fullname: Shen, Hui organization: Departments of Orthopedic Surgery and Basic Medical Sciences, University of Missouri–Kansas City, Kansas City, Missouri, USA – sequence: 4 givenname: Lan-juan surname: Zhao fullname: Zhao, Lan-juan organization: Departments of Orthopedic Surgery and Basic Medical Sciences, University of Missouri–Kansas City, Kansas City, Missouri, USA – sequence: 5 givenname: Peng surname: Xiao fullname: Xiao, Peng organization: Departments of Orthopedic Surgery and Basic Medical Sciences, University of Missouri–Kansas City, Kansas City, Missouri, USA – sequence: 6 givenname: Yan surname: Guo fullname: Guo, Yan organization: Departments of Orthopedic Surgery and Basic Medical Sciences, University of Missouri–Kansas City, Kansas City, Missouri, USA – sequence: 7 givenname: Wei surname: Wang fullname: Wang, Wei organization: Departments of Orthopedic Surgery and Basic Medical Sciences, University of Missouri–Kansas City, Kansas City, Missouri, USA – sequence: 8 givenname: Tie-lin surname: Yang fullname: Yang, Tie-lin organization: Departments of Orthopedic Surgery and Basic Medical Sciences, University of Missouri–Kansas City, Kansas City, Missouri, USA – sequence: 9 givenname: Robert R surname: Recker fullname: Recker, Robert R organization: Departments of Orthopedic Surgery and Basic Medical Sciences, University of Missouri–Kansas City, Kansas City, Missouri, USA – sequence: 10 givenname: Hong-wen surname: Deng fullname: Deng, Hong-wen organization: Departments of Orthopedic Surgery and Basic Medical Sciences, University of Missouri–Kansas City, Kansas City, Missouri, USA |
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Keywords | Human Obesity Family study Nutrition disorder Protein Lipoprotein LDL Phenotype Association Gene Genetics Nutritional status Polymorphism Biological receptor |
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Notes | Correspondence to:
H-W Deng
Departments of Orthopedic Surgery and Basic Medical Sciences, University of Missouri–Kansas City, 2411 Holmes Street, Room M3-C03, Kansas City, MO 64108-2792, USA;dengh@umkc.edu PMID:16723389 istex:A45DC73AA5DEF976EE6509FA6343E1071D888F99 ark:/67375/NVC-K8DD9BMZ-7 local:0430798 href:jmedgenet-43-798.pdf ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 These two authors contributed equally to this work. |
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Snippet | Background: The low-density lipoprotein receptor-related protein 5 (LRP5) gene, essential for glucose and cholesterol metabolism, may have a role in the... The low-density lipoprotein receptor-related protein 5 (LRP5) gene, essential for glucose and cholesterol metabolism, may have a role in the aetiology of... Background: The low-density lipoprotein receptor-related protein 5 (LRP5 ) gene, essential for glucose and cholesterol metabolism, may have a role in the... BACKGROUND: The low-density lipoprotein receptor-related protein 5 (LRP5) gene, essential for glucose and cholesterol metabolism, may have a role in the... |
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SubjectTerms | Adult Aged Biological and medical sciences BMI Body Composition Body Mass Index Bone density Child Confidence intervals Diabetes family-based association analysis FBAT Female Fundamental and applied biological sciences. Psychology General aspects. Genetic counseling generalised linear model Genes Genetic Linkage Genetics of eukaryotes. Biological and molecular evolution GLM haplotype version of FBAT Haplotypes HBAT Humans LDL-Receptor Related Proteins - genetics Linkage Disequilibrium Lipoproteins Low Density Lipoprotein Receptor-Related Protein-5 low-density lipoprotein receptor-related protein 5 gene LRP5 gene MAF Male Medical genetics Medical sciences Metabolic diseases Middle Aged minor allele frequencies Molecular and cellular biology Nuclear Family Obesity Obesity - genetics Original Osteoporosis percentage of fat mass PFM Phenotype Polymorphism, Genetic Polymorphism, Single Nucleotide Sex Characteristics single-nucleotide polymorphism SNP Studies |
Title | Polymorphisms of the low-density lipoprotein receptor-related protein 5 (LRP5) gene are associated with obesity phenotypes in a large family-based association study |
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