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 inJournal of medical genetics Vol. 43; no. 10; pp. 798 - 803
Main Authors Guo, Yan-fang, Xiong, Dong-hai, Shen, Hui, Zhao, Lan-juan, Xiao, Peng, Guo, Yan, Wang, Wei, Yang, Tie-lin, Recker, Robert R, Deng, Hong-wen
Format Journal Article
LanguageEnglish
Published London BMJ Publishing Group Ltd 01.10.2006
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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.
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
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– 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
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Issue 10
Keywords Human
Obesity
Family study
Nutrition disorder
Protein
Lipoprotein LDL
Phenotype
Association
Gene
Genetics
Nutritional status
Polymorphism
Biological receptor
Language English
License CC BY 4.0
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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
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These two authors contributed equally to this work.
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References 11719191 - Cell. 2001 Nov 16;107(4):513-23
16292600 - Osteoporos Int. 2005 Dec;16(12):2113-22
11029008 - Nature. 2000 Sep 28;407(6803):535-8
16130443 - Orv Hetil. 2005 Jul 10;146(28):1489-93
16222066 - Obes Res. 2005 Sep;13(9):1624-9
11741193 - Am J Hum Genet. 2002 Jan;70(1):11-9
16185158 - Expert Opin Ther Targets. 2005 Oct;9(5):1063-77
11731797 - Nat Genet. 2002 Jan;30(1):97-101
9126487 - Genomics. 1997 Apr 1;41(1):93-9
11454514 - Eur J Endocrinol. 2001 Aug;145(2):181-6
11244469 - Int J Obes Relat Metab Disord. 2001 Jan;25(1):132-7
11336703 - Mol Cell. 2001 Apr;7(4):801-9
12509515 - Proc Natl Acad Sci U S A. 2003 Jan 7;100(1):229-34
16025191 - Osteoporos Int. 2006 Jan;17(1):119-24
12452179 - Am J Hum Genet. 2002 Nov;71(5):1242-7
11313775 - Eur J Hum Genet. 2001 Apr;9(4):301-6
15829237 - Mutat Res. 2005 Jun 3;573(1-2):54-69
11748340 - J Clin Densitom. 2001 Winter;4(4):353-61
11029006 - Nature. 2000 Sep 28;407(6803):527-30
12029063 - Science. 2002 Jun 21;296(5576):2225-9
11275948 - Eur J Endocrinol. 2001 Apr;144(4):385-9
12509421 - J Biol Chem. 2003 Mar 28;278(13):11331-6
15067310 - J Clin Invest. 2004 Mar;113(6):805-6
10090903 - Am J Hum Genet. 1999 Apr;64(4):1177-85
15687398 - Obes Res. 2004 Dec;12(12):1967-73
15297300 - Bioinformatics. 2005 Jan 15;21(2):263-5
9714764 - Gene. 1998 Aug 17;216(1):103-11
12055200 - J Biol Chem. 2002 Aug 23;277(34):30998-1004
16082432 - Drugs Today (Barc). 2005 May;41(5):345-62
14691957 - Genet Epidemiol. 2004 Jan;26(1):61-9
11029007 - Nature. 2000 Sep 28;407(6803):530-5
12917706 - Int J Obes Relat Metab Disord. 2003 Sep;27(9):1020-7
15777745 - Bone. 2005 Apr;36(4):599-606
9634505 - Am J Hum Genet. 1998 Jul;63(1):259-66
15615112 - J Musculoskelet Neuronal Interact. 2004 Jun;4(2):135-8
12015390 - N Engl J Med. 2002 May 16;346(20):1513-21
15215394 - Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W273-9
11401438 - Genomics. 2001 Mar 15;72(3):231-42
15475226 - Clin Dermatol. 2004 Jul-Aug;22(4):276-80
11729172 - Genetics. 2001 Nov;159(3):1319-23
15067317 - J Clin Invest. 2004 Mar;113(6):846-55
10990489 - J Histochem Cytochem. 2000 Oct;48(10):1357-68
10739759 - Am J Hum Genet. 2000 Apr;66(4):1341-50
11256896 - Osteoporos Int. 2000;11(12):1043-50
16168727 - Bone. 2005 Dec;37(6):770-5
16293698 - Proc Natl Acad Sci U S A. 2005 Nov 29;102(48):17406-11
9535665 - N Engl J Med. 1998 Apr 9;338(15):1016-21
10937998 - Science. 2000 Aug 11;289(5481):950-3
16311223 - Best Pract Res Clin Endocrinol Metab. 2005 Dec;19(4):649-63
8841196 - Nat Genet. 1996 Oct;14(2):203-5
References_xml – reference: 11729172 - Genetics. 2001 Nov;159(3):1319-23
– reference: 11731797 - Nat Genet. 2002 Jan;30(1):97-101
– reference: 16293698 - Proc Natl Acad Sci U S A. 2005 Nov 29;102(48):17406-11
– reference: 15687398 - Obes Res. 2004 Dec;12(12):1967-73
– reference: 12029063 - Science. 2002 Jun 21;296(5576):2225-9
– reference: 11029006 - Nature. 2000 Sep 28;407(6803):527-30
– reference: 11748340 - J Clin Densitom. 2001 Winter;4(4):353-61
– reference: 10739759 - Am J Hum Genet. 2000 Apr;66(4):1341-50
– reference: 16082432 - Drugs Today (Barc). 2005 May;41(5):345-62
– reference: 16222066 - Obes Res. 2005 Sep;13(9):1624-9
– reference: 12917706 - Int J Obes Relat Metab Disord. 2003 Sep;27(9):1020-7
– reference: 16025191 - Osteoporos Int. 2006 Jan;17(1):119-24
– reference: 11741193 - Am J Hum Genet. 2002 Jan;70(1):11-9
– reference: 8841196 - Nat Genet. 1996 Oct;14(2):203-5
– reference: 15067317 - J Clin Invest. 2004 Mar;113(6):846-55
– reference: 11313775 - Eur J Hum Genet. 2001 Apr;9(4):301-6
– reference: 12509515 - Proc Natl Acad Sci U S A. 2003 Jan 7;100(1):229-34
– reference: 12055200 - J Biol Chem. 2002 Aug 23;277(34):30998-1004
– reference: 11029008 - Nature. 2000 Sep 28;407(6803):535-8
– reference: 11256896 - Osteoporos Int. 2000;11(12):1043-50
– reference: 15215394 - Nucleic Acids Res. 2004 Jul 1;32(Web Server issue):W273-9
– reference: 11275948 - Eur J Endocrinol. 2001 Apr;144(4):385-9
– reference: 11401438 - Genomics. 2001 Mar 15;72(3):231-42
– reference: 11719191 - Cell. 2001 Nov 16;107(4):513-23
– reference: 15475226 - Clin Dermatol. 2004 Jul-Aug;22(4):276-80
– reference: 11029007 - Nature. 2000 Sep 28;407(6803):530-5
– reference: 10090903 - Am J Hum Genet. 1999 Apr;64(4):1177-85
– reference: 9126487 - Genomics. 1997 Apr 1;41(1):93-9
– reference: 12015390 - N Engl J Med. 2002 May 16;346(20):1513-21
– reference: 10990489 - J Histochem Cytochem. 2000 Oct;48(10):1357-68
– reference: 12509421 - J Biol Chem. 2003 Mar 28;278(13):11331-6
– reference: 9535665 - N Engl J Med. 1998 Apr 9;338(15):1016-21
– reference: 10937998 - Science. 2000 Aug 11;289(5481):950-3
– reference: 14691957 - Genet Epidemiol. 2004 Jan;26(1):61-9
– reference: 15829237 - Mutat Res. 2005 Jun 3;573(1-2):54-69
– reference: 11454514 - Eur J Endocrinol. 2001 Aug;145(2):181-6
– reference: 15615112 - J Musculoskelet Neuronal Interact. 2004 Jun;4(2):135-8
– reference: 16130443 - Orv Hetil. 2005 Jul 10;146(28):1489-93
– reference: 16168727 - Bone. 2005 Dec;37(6):770-5
– reference: 9634505 - Am J Hum Genet. 1998 Jul;63(1):259-66
– reference: 16185158 - Expert Opin Ther Targets. 2005 Oct;9(5):1063-77
– reference: 9714764 - Gene. 1998 Aug 17;216(1):103-11
– reference: 15777745 - Bone. 2005 Apr;36(4):599-606
– reference: 11336703 - Mol Cell. 2001 Apr;7(4):801-9
– reference: 15067310 - J Clin Invest. 2004 Mar;113(6):805-6
– reference: 11244469 - Int J Obes Relat Metab Disord. 2001 Jan;25(1):132-7
– reference: 16292600 - Osteoporos Int. 2005 Dec;16(12):2113-22
– reference: 12452179 - Am J Hum Genet. 2002 Nov;71(5):1242-7
– reference: 15297300 - Bioinformatics. 2005 Jan 15;21(2):263-5
– reference: 16311223 - Best Pract Res Clin Endocrinol Metab. 2005 Dec;19(4):649-63
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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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