Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations

Michael Benzinou; Jean-Claude Chèvre; Kirsten J Ward; Cécile Lecoeur; Christian Dina; Stephane Lobbens; Emmanuelle Durand; Jérome Delplanque; Fritz F Horber; Barbara Heude; Beverley Balkau; Knut Borch-Johnsen; Torben Jørgensen; Torben Hansen; Oluf Pedersen; David Meyre; Philippe Froguel

doi:10.1093/hmg/ddn089

Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations

Michael Benzinou, Jean-Claude Chèvre, Kirsten J Ward, Cécile Lecoeur, Christian Dina, Stephane Lobbens, Emmanuelle Durand, Jérome Delplanque, Fritz F Horber, Barbara Heude, Beverley Balkau, Knut Borch-Johnsen, Torben Jørgensen, Torben Hansen, Oluf Pedersen, David Meyre, Philippe Froguel

76 Citations (Scopus)

Abstract

The therapeutic effects of cannabinoid receptor blockade on obesity-associated phenotypes underline the importance of the endocannabinoid pathway on the energy balance. Using a staged-approach, we examined the contribution of the endocannabinoid receptor 1 gene (CNR1) on obesity and body mass index (BMI) in the European population. With the input of CNR1 exons and 3' and 5' regions sequencing and HapMap database, we selected and genotyped 26 tagging single-nucleotide polymorphisms (SNPs) in 1932 obese cases and 1173 non-obese controls of French European origin. Variants that showed significant associations (P < 0.05) with obesity after correction for multiple testing were further tested in two additional European cohorts including 2645 individuals. For the identification of the potential causal variant(s), we further genotyped SNPs in high linkage disequilibrium (LD) with the obesity-associated variants. Of the 25 successfully genotyped CNR1 SNPs, 12 showed nominal evidence of association with childhood obesity, class I and II and/or class III adult obesity (1.16 < OR < 1.40, 0.00003 < P < 0.04). Intronic SNPs rs806381 and rs2023239, which resisted correction for multiple testing were further associated with higher BMI in both Swiss obese subjects and Danish individuals. The genotyping of all know variants in partial LD (r(2) > 0.5) with these two SNPs in the initial case-control study, identified two better associated SNPs (rs6454674 and rs10485170). Our study of 5750 subjects shows that CNR1 variations increase the risk for obesity and modulate BMI in our European population. As CB1 is a drug target for obesity, a pharmacogenetic analysis of the endocannabinoid blockade obesity treatment may be of interest to identify best responders.

Original language	English
Journal	Human Molecular Genetics
Volume	17
Issue number	13
Pages (from-to)	1916-21
Number of pages	5
ISSN	0964-6906
DOIs	https://doi.org/10.1093/hmg/ddn089
Publication status	Published - 2008

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

Access to Document

10.1093/hmg/ddn089

Cite this

Benzinou, M., Chèvre, J-C., Ward, K. J., Lecoeur, C., Dina, C., Lobbens, S., Durand, E., Delplanque, J., Horber, F. F., Heude, B., Balkau, B., Borch-Johnsen, K., Jørgensen, T., Hansen, T., Pedersen, O., Meyre, D., & Froguel, P. (2008). Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations. Human Molecular Genetics, 17(13), 1916-21. https://doi.org/10.1093/hmg/ddn089

Benzinou, M, Chèvre, J-C, Ward, KJ, Lecoeur, C, Dina, C, Lobbens, S, Durand, E, Delplanque, J, Horber, FF, Heude, B, Balkau, B, Borch-Johnsen, K, Jørgensen, T, Hansen, T, Pedersen, O, Meyre, D & Froguel, P 2008, 'Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations', Human Molecular Genetics, vol. 17, no. 13, pp. 1916-21. https://doi.org/10.1093/hmg/ddn089

@article{f6414d80ee1d11ddbf70000ea68e967b,

title = "Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations",

abstract = "The therapeutic effects of cannabinoid receptor blockade on obesity-associated phenotypes underline the importance of the endocannabinoid pathway on the energy balance. Using a staged-approach, we examined the contribution of the endocannabinoid receptor 1 gene (CNR1) on obesity and body mass index (BMI) in the European population. With the input of CNR1 exons and 3' and 5' regions sequencing and HapMap database, we selected and genotyped 26 tagging single-nucleotide polymorphisms (SNPs) in 1932 obese cases and 1173 non-obese controls of French European origin. Variants that showed significant associations (P < 0.05) with obesity after correction for multiple testing were further tested in two additional European cohorts including 2645 individuals. For the identification of the potential causal variant(s), we further genotyped SNPs in high linkage disequilibrium (LD) with the obesity-associated variants. Of the 25 successfully genotyped CNR1 SNPs, 12 showed nominal evidence of association with childhood obesity, class I and II and/or class III adult obesity (1.16 < OR < 1.40, 0.00003 < P < 0.04). Intronic SNPs rs806381 and rs2023239, which resisted correction for multiple testing were further associated with higher BMI in both Swiss obese subjects and Danish individuals. The genotyping of all know variants in partial LD (r(2) > 0.5) with these two SNPs in the initial case-control study, identified two better associated SNPs (rs6454674 and rs10485170). Our study of 5750 subjects shows that CNR1 variations increase the risk for obesity and modulate BMI in our European population. As CB1 is a drug target for obesity, a pharmacogenetic analysis of the endocannabinoid blockade obesity treatment may be of interest to identify best responders.",

author = "Michael Benzinou and Jean-Claude Ch{\`e}vre and Ward, {Kirsten J} and C{\'e}cile Lecoeur and Christian Dina and Stephane Lobbens and Emmanuelle Durand and J{\'e}rome Delplanque and Horber, {Fritz F} and Barbara Heude and Beverley Balkau and Knut Borch-Johnsen and Torben J{\o}rgensen and Torben Hansen and Oluf Pedersen and David Meyre and Philippe Froguel",

note = "Keywords: Adolescent; Adult; Body Mass Index; Case-Control Studies; Child; Cohort Studies; European Continental Ancestry Group; Female; Genotype; Humans; Linkage Disequilibrium; Male; Middle Aged; Obesity; Polymorphism, Single Nucleotide; Receptor, Cannabinoid, CB1; Risk Factors",

year = "2008",

doi = "10.1093/hmg/ddn089",

language = "English",

volume = "17",

pages = "1916--21",

journal = "Human Molecular Genetics",

issn = "0964-6906",

publisher = "Oxford University Press",

number = "13",

}

TY - JOUR

T1 - Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations

AU - Benzinou, Michael

AU - Chèvre, Jean-Claude

AU - Ward, Kirsten J

AU - Lecoeur, Cécile

AU - Dina, Christian

AU - Lobbens, Stephane

AU - Durand, Emmanuelle

AU - Delplanque, Jérome

AU - Horber, Fritz F

AU - Heude, Barbara

AU - Balkau, Beverley

AU - Borch-Johnsen, Knut

AU - Jørgensen, Torben

AU - Hansen, Torben

AU - Pedersen, Oluf

AU - Meyre, David

AU - Froguel, Philippe

N1 - Keywords: Adolescent; Adult; Body Mass Index; Case-Control Studies; Child; Cohort Studies; European Continental Ancestry Group; Female; Genotype; Humans; Linkage Disequilibrium; Male; Middle Aged; Obesity; Polymorphism, Single Nucleotide; Receptor, Cannabinoid, CB1; Risk Factors

PY - 2008

Y1 - 2008

N2 - The therapeutic effects of cannabinoid receptor blockade on obesity-associated phenotypes underline the importance of the endocannabinoid pathway on the energy balance. Using a staged-approach, we examined the contribution of the endocannabinoid receptor 1 gene (CNR1) on obesity and body mass index (BMI) in the European population. With the input of CNR1 exons and 3' and 5' regions sequencing and HapMap database, we selected and genotyped 26 tagging single-nucleotide polymorphisms (SNPs) in 1932 obese cases and 1173 non-obese controls of French European origin. Variants that showed significant associations (P < 0.05) with obesity after correction for multiple testing were further tested in two additional European cohorts including 2645 individuals. For the identification of the potential causal variant(s), we further genotyped SNPs in high linkage disequilibrium (LD) with the obesity-associated variants. Of the 25 successfully genotyped CNR1 SNPs, 12 showed nominal evidence of association with childhood obesity, class I and II and/or class III adult obesity (1.16 < OR < 1.40, 0.00003 < P < 0.04). Intronic SNPs rs806381 and rs2023239, which resisted correction for multiple testing were further associated with higher BMI in both Swiss obese subjects and Danish individuals. The genotyping of all know variants in partial LD (r(2) > 0.5) with these two SNPs in the initial case-control study, identified two better associated SNPs (rs6454674 and rs10485170). Our study of 5750 subjects shows that CNR1 variations increase the risk for obesity and modulate BMI in our European population. As CB1 is a drug target for obesity, a pharmacogenetic analysis of the endocannabinoid blockade obesity treatment may be of interest to identify best responders.

AB - The therapeutic effects of cannabinoid receptor blockade on obesity-associated phenotypes underline the importance of the endocannabinoid pathway on the energy balance. Using a staged-approach, we examined the contribution of the endocannabinoid receptor 1 gene (CNR1) on obesity and body mass index (BMI) in the European population. With the input of CNR1 exons and 3' and 5' regions sequencing and HapMap database, we selected and genotyped 26 tagging single-nucleotide polymorphisms (SNPs) in 1932 obese cases and 1173 non-obese controls of French European origin. Variants that showed significant associations (P < 0.05) with obesity after correction for multiple testing were further tested in two additional European cohorts including 2645 individuals. For the identification of the potential causal variant(s), we further genotyped SNPs in high linkage disequilibrium (LD) with the obesity-associated variants. Of the 25 successfully genotyped CNR1 SNPs, 12 showed nominal evidence of association with childhood obesity, class I and II and/or class III adult obesity (1.16 < OR < 1.40, 0.00003 < P < 0.04). Intronic SNPs rs806381 and rs2023239, which resisted correction for multiple testing were further associated with higher BMI in both Swiss obese subjects and Danish individuals. The genotyping of all know variants in partial LD (r(2) > 0.5) with these two SNPs in the initial case-control study, identified two better associated SNPs (rs6454674 and rs10485170). Our study of 5750 subjects shows that CNR1 variations increase the risk for obesity and modulate BMI in our European population. As CB1 is a drug target for obesity, a pharmacogenetic analysis of the endocannabinoid blockade obesity treatment may be of interest to identify best responders.

U2 - 10.1093/hmg/ddn089

DO - 10.1093/hmg/ddn089

M3 - Journal article

C2 - 18375449

SN - 0964-6906

VL - 17

SP - 1916

EP - 1921

JO - Human Molecular Genetics

JF - Human Molecular Genetics

IS - 13

ER -

Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations

Abstract

UN SDGs

Access to Document

Fingerprint

Cite this