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Gene-Environment Interactions of Circadian-Related Genes for Cardiometabolic Traits
OBJECTIVE: Common circadian-related gene variants associate with increased risk for metabolic alterations including type 2 diabetes. However, little is known about whether diet and sleep could modify associations between circadian-related variants (CLOCK-rs1801260, CRY2-rs11605924, MTNR1B-rs1387153,...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Diabetes Association
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4512139/ https://www.ncbi.nlm.nih.gov/pubmed/26084345 http://dx.doi.org/10.2337/dc14-2709 |
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author | Dashti, Hassan S. Follis, Jack L. Smith, Caren E. Tanaka, Toshiko Garaulet, Marta Gottlieb, Daniel J. Hruby, Adela Jacques, Paul F. Kiefte-de Jong, Jessica C. Lamon-Fava, Stefania Scheer, Frank A.J.L. Bartz, Traci M. Kovanen, Leena Wojczynski, Mary K. Frazier-Wood, Alexis C. Ahluwalia, Tarunveer S. Perälä, Mia-Maria Jonsson, Anna Muka, Taulant Kalafati, Ioanna P. Mikkilä, Vera Ordovás, José M. Lemaitre, Rozenn N. Partonen, Timo Ebeling, Tapani Hopkins, Paul N. Paternoster, Lavinia Lahti, Jari Hernandez, Dena G. Toft, Ulla Saxena, Richa Vitezova, Anna Kanoni, Stavroula Raitakari, Olli T. Psaty, Bruce M. Perola, Markus Männistö, Satu Straka, Robert J. Hansen, Torben Räikkönen, Katri Ferrucci, Luigi Grarup, Niels Johnson, W. Craig Rallidis, Loukianos Kähönen, Mika Siscovick, David S. Havulinna, Aki S. Astrup, Arne Jørgensen, Torben Chen, Tzu-An Hofman, Albert Deloukas, Panos Viikari, Jorma S.A. Mozaffarian, Dariush Pedersen, Oluf Rotter, Jerome I. Uitterlinden, André G. Seppälä, Ilkka Tiemeier, Henning Salomaa, Veikko Gharib, Sina A. Borecki, Ingrid B. Arnett, Donna K. Sørensen, Thorklid I.A. Eriksson, Johan G. Bandinelli, Stefania Linneberg, Allan Rich, Stephen S. Franco, Oscar H. Dedoussis, George Lehtimäki, Terho |
author_facet | Dashti, Hassan S. Follis, Jack L. Smith, Caren E. Tanaka, Toshiko Garaulet, Marta Gottlieb, Daniel J. Hruby, Adela Jacques, Paul F. Kiefte-de Jong, Jessica C. Lamon-Fava, Stefania Scheer, Frank A.J.L. Bartz, Traci M. Kovanen, Leena Wojczynski, Mary K. Frazier-Wood, Alexis C. Ahluwalia, Tarunveer S. Perälä, Mia-Maria Jonsson, Anna Muka, Taulant Kalafati, Ioanna P. Mikkilä, Vera Ordovás, José M. Lemaitre, Rozenn N. Partonen, Timo Ebeling, Tapani Hopkins, Paul N. Paternoster, Lavinia Lahti, Jari Hernandez, Dena G. Toft, Ulla Saxena, Richa Vitezova, Anna Kanoni, Stavroula Raitakari, Olli T. Psaty, Bruce M. Perola, Markus Männistö, Satu Straka, Robert J. Hansen, Torben Räikkönen, Katri Ferrucci, Luigi Grarup, Niels Johnson, W. Craig Rallidis, Loukianos Kähönen, Mika Siscovick, David S. Havulinna, Aki S. Astrup, Arne Jørgensen, Torben Chen, Tzu-An Hofman, Albert Deloukas, Panos Viikari, Jorma S.A. Mozaffarian, Dariush Pedersen, Oluf Rotter, Jerome I. Uitterlinden, André G. Seppälä, Ilkka Tiemeier, Henning Salomaa, Veikko Gharib, Sina A. Borecki, Ingrid B. Arnett, Donna K. Sørensen, Thorklid I.A. Eriksson, Johan G. Bandinelli, Stefania Linneberg, Allan Rich, Stephen S. Franco, Oscar H. Dedoussis, George Lehtimäki, Terho |
author_sort | Dashti, Hassan S. |
collection | PubMed |
description | OBJECTIVE: Common circadian-related gene variants associate with increased risk for metabolic alterations including type 2 diabetes. However, little is known about whether diet and sleep could modify associations between circadian-related variants (CLOCK-rs1801260, CRY2-rs11605924, MTNR1B-rs1387153, MTNR1B-rs10830963, NR1D1-rs2314339) and cardiometabolic traits (fasting glucose [FG], HOMA-insulin resistance, BMI, waist circumference, and HDL-cholesterol) to facilitate personalized recommendations. RESEARCH DESIGN AND METHODS: We conducted inverse-variance weighted, fixed-effect meta-analyses of results of adjusted associations and interactions between dietary intake/sleep duration and selected variants on cardiometabolic traits from 15 cohort studies including up to 28,190 participants of European descent from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. RESULTS: We observed significant associations between relative macronutrient intakes and glycemic traits and short sleep duration (<7 h) and higher FG and replicated known MTNR1B associations with glycemic traits. No interactions were evident after accounting for multiple comparisons. However, we observed nominally significant interactions (all P < 0.01) between carbohydrate intake and MTNR1B-rs1387153 for FG with a 0.003 mmol/L higher FG with each additional 1% carbohydrate intake in the presence of the T allele, between sleep duration and CRY2-rs11605924 for HDL-cholesterol with a 0.010 mmol/L higher HDL-cholesterol with each additional hour of sleep in the presence of the A allele, and between long sleep duration (≥9 h) and MTNR1B-rs1387153 for BMI with a 0.60 kg/m(2) higher BMI with long sleep duration in the presence of the T allele relative to normal sleep duration (≥7 to <9 h). CONCLUSIONS: Our results suggest that lower carbohydrate intake and normal sleep duration may ameliorate cardiometabolic abnormalities conferred by common circadian-related genetic variants. Until further mechanistic examination of the nominally significant interactions is conducted, recommendations applicable to the general population regarding diet—specifically higher carbohydrate and lower fat composition—and normal sleep duration should continue to be emphasized among individuals with the investigated circadian-related gene variants. |
format | Online Article Text |
id | pubmed-4512139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American Diabetes Association |
record_format | MEDLINE/PubMed |
spelling | pubmed-45121392016-08-01 Gene-Environment Interactions of Circadian-Related Genes for Cardiometabolic Traits Dashti, Hassan S. Follis, Jack L. Smith, Caren E. Tanaka, Toshiko Garaulet, Marta Gottlieb, Daniel J. Hruby, Adela Jacques, Paul F. Kiefte-de Jong, Jessica C. Lamon-Fava, Stefania Scheer, Frank A.J.L. Bartz, Traci M. Kovanen, Leena Wojczynski, Mary K. Frazier-Wood, Alexis C. Ahluwalia, Tarunveer S. Perälä, Mia-Maria Jonsson, Anna Muka, Taulant Kalafati, Ioanna P. Mikkilä, Vera Ordovás, José M. Lemaitre, Rozenn N. Partonen, Timo Ebeling, Tapani Hopkins, Paul N. Paternoster, Lavinia Lahti, Jari Hernandez, Dena G. Toft, Ulla Saxena, Richa Vitezova, Anna Kanoni, Stavroula Raitakari, Olli T. Psaty, Bruce M. Perola, Markus Männistö, Satu Straka, Robert J. Hansen, Torben Räikkönen, Katri Ferrucci, Luigi Grarup, Niels Johnson, W. Craig Rallidis, Loukianos Kähönen, Mika Siscovick, David S. Havulinna, Aki S. Astrup, Arne Jørgensen, Torben Chen, Tzu-An Hofman, Albert Deloukas, Panos Viikari, Jorma S.A. Mozaffarian, Dariush Pedersen, Oluf Rotter, Jerome I. Uitterlinden, André G. Seppälä, Ilkka Tiemeier, Henning Salomaa, Veikko Gharib, Sina A. Borecki, Ingrid B. Arnett, Donna K. Sørensen, Thorklid I.A. Eriksson, Johan G. Bandinelli, Stefania Linneberg, Allan Rich, Stephen S. Franco, Oscar H. Dedoussis, George Lehtimäki, Terho Diabetes Care Epidemiology/Health Services Research OBJECTIVE: Common circadian-related gene variants associate with increased risk for metabolic alterations including type 2 diabetes. However, little is known about whether diet and sleep could modify associations between circadian-related variants (CLOCK-rs1801260, CRY2-rs11605924, MTNR1B-rs1387153, MTNR1B-rs10830963, NR1D1-rs2314339) and cardiometabolic traits (fasting glucose [FG], HOMA-insulin resistance, BMI, waist circumference, and HDL-cholesterol) to facilitate personalized recommendations. RESEARCH DESIGN AND METHODS: We conducted inverse-variance weighted, fixed-effect meta-analyses of results of adjusted associations and interactions between dietary intake/sleep duration and selected variants on cardiometabolic traits from 15 cohort studies including up to 28,190 participants of European descent from the Cohorts for Heart and Aging Research in Genomic Epidemiology (CHARGE) Consortium. RESULTS: We observed significant associations between relative macronutrient intakes and glycemic traits and short sleep duration (<7 h) and higher FG and replicated known MTNR1B associations with glycemic traits. No interactions were evident after accounting for multiple comparisons. However, we observed nominally significant interactions (all P < 0.01) between carbohydrate intake and MTNR1B-rs1387153 for FG with a 0.003 mmol/L higher FG with each additional 1% carbohydrate intake in the presence of the T allele, between sleep duration and CRY2-rs11605924 for HDL-cholesterol with a 0.010 mmol/L higher HDL-cholesterol with each additional hour of sleep in the presence of the A allele, and between long sleep duration (≥9 h) and MTNR1B-rs1387153 for BMI with a 0.60 kg/m(2) higher BMI with long sleep duration in the presence of the T allele relative to normal sleep duration (≥7 to <9 h). CONCLUSIONS: Our results suggest that lower carbohydrate intake and normal sleep duration may ameliorate cardiometabolic abnormalities conferred by common circadian-related genetic variants. Until further mechanistic examination of the nominally significant interactions is conducted, recommendations applicable to the general population regarding diet—specifically higher carbohydrate and lower fat composition—and normal sleep duration should continue to be emphasized among individuals with the investigated circadian-related gene variants. American Diabetes Association 2015-08 2015-06-17 /pmc/articles/PMC4512139/ /pubmed/26084345 http://dx.doi.org/10.2337/dc14-2709 Text en © 2015 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. |
spellingShingle | Epidemiology/Health Services Research Dashti, Hassan S. Follis, Jack L. Smith, Caren E. Tanaka, Toshiko Garaulet, Marta Gottlieb, Daniel J. Hruby, Adela Jacques, Paul F. Kiefte-de Jong, Jessica C. Lamon-Fava, Stefania Scheer, Frank A.J.L. Bartz, Traci M. Kovanen, Leena Wojczynski, Mary K. Frazier-Wood, Alexis C. Ahluwalia, Tarunveer S. Perälä, Mia-Maria Jonsson, Anna Muka, Taulant Kalafati, Ioanna P. Mikkilä, Vera Ordovás, José M. Lemaitre, Rozenn N. Partonen, Timo Ebeling, Tapani Hopkins, Paul N. Paternoster, Lavinia Lahti, Jari Hernandez, Dena G. Toft, Ulla Saxena, Richa Vitezova, Anna Kanoni, Stavroula Raitakari, Olli T. Psaty, Bruce M. Perola, Markus Männistö, Satu Straka, Robert J. Hansen, Torben Räikkönen, Katri Ferrucci, Luigi Grarup, Niels Johnson, W. Craig Rallidis, Loukianos Kähönen, Mika Siscovick, David S. Havulinna, Aki S. Astrup, Arne Jørgensen, Torben Chen, Tzu-An Hofman, Albert Deloukas, Panos Viikari, Jorma S.A. Mozaffarian, Dariush Pedersen, Oluf Rotter, Jerome I. Uitterlinden, André G. Seppälä, Ilkka Tiemeier, Henning Salomaa, Veikko Gharib, Sina A. Borecki, Ingrid B. Arnett, Donna K. Sørensen, Thorklid I.A. Eriksson, Johan G. Bandinelli, Stefania Linneberg, Allan Rich, Stephen S. Franco, Oscar H. Dedoussis, George Lehtimäki, Terho Gene-Environment Interactions of Circadian-Related Genes for Cardiometabolic Traits |
title | Gene-Environment Interactions of Circadian-Related Genes for Cardiometabolic Traits |
title_full | Gene-Environment Interactions of Circadian-Related Genes for Cardiometabolic Traits |
title_fullStr | Gene-Environment Interactions of Circadian-Related Genes for Cardiometabolic Traits |
title_full_unstemmed | Gene-Environment Interactions of Circadian-Related Genes for Cardiometabolic Traits |
title_short | Gene-Environment Interactions of Circadian-Related Genes for Cardiometabolic Traits |
title_sort | gene-environment interactions of circadian-related genes for cardiometabolic traits |
topic | Epidemiology/Health Services Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4512139/ https://www.ncbi.nlm.nih.gov/pubmed/26084345 http://dx.doi.org/10.2337/dc14-2709 |
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