Physical Activity and Sex Modulate Obesity Risk Linked to 3111T C Gene Variant of the CLOCK Gene in an Elderly Population: The SUN Project
Genetic factors may interact with physical activity levels to modify obesity risk. Our aim was to explore the influence of rs1801260 single-nucleotide polymorphism (SNP) (3111T C) of CLOCK gene on obesity risk, and to examine its potential interaction with lifestyle factors in an elderly population...
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Published in | Chronobiology international Vol. 29; no. 10; pp. 1397 - 1404 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Informa Healthcare
01.12.2012
Taylor & Francis |
Subjects | |
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Abstract | Genetic factors may interact with physical activity levels to modify obesity risk. Our aim was to explore the influence of rs1801260 single-nucleotide polymorphism (SNP) (3111T C) of CLOCK gene on obesity risk, and to examine its potential interaction with lifestyle factors in an elderly population within the SUN ("Seguimiento Universidad de Navarra") Project. Subjects (n = 903, aged 69 ± 6 yrs) were recruited from the SUN Project. DNA was obtained from saliva, whereas lifestyle and dietary data were collected by validated self-report questionnaires. Genotype was assessed by reverse transcriptase-polymerase chain reaction (RT-PCR) plus allele discrimination. A significant interaction was observed between the 3111T C SNP of CLOCK gene and sex for overweight obesity risk (p for sex × CLOCK interaction <.001). Our results showed that women carrying the C allele of CLOCK gene had a marginally significant lower risk of overweight obesity compared with noncarrier-TT-subjects (odds ratio [OR]: .61, 95% confidence interval [CI]: .36-1.04; p = .069). Moreover, this association of the C allele with a decreased overweight obesity risk might be enhanced in those women with a high physical activity level. Women practicing more than 16.8 metabolic equivalent tasks (hours per week) had a significantly lower overweight obesity risk (OR: .36, 95% CI: .17-.79; p = .011). Furthermore, a significant interaction between the 3111T C gene variant and physical activity (PA) for overweight obesity risk was observed but only in women (p for PA × CLOCK interaction <.050). In conclusion, it appears that physical activity levels may act by modifying the association of the 3111T C SNP (rs1801260) of the CLOCK gene with overweight obesity risk in elderly women in the SUN Project. |
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AbstractList | Genetic factors may interact with physical activity levels to modify obesity risk. Our aim was to explore the influence of rs1801260 single-nucleotide polymorphism (SNP) (3111T/C) of CLOCK gene on obesity risk, and to examine its potential interaction with lifestyle factors in an elderly population within the SUN ("Seguimiento Universidad de Navarra") Project. Subjects (n = 903, aged 69 ± 6 yrs) were recruited from the SUN Project. DNA was obtained from saliva, whereas lifestyle and dietary data were collected by validated self-report questionnaires. Genotype was assessed by reverse transcriptase-polymerase chain reaction (RT-PCR) plus allele discrimination. A significant interaction was observed between the 3111T/C SNP of CLOCK gene and sex for overweight/obesity risk (p for sex × CLOCK interaction <.001). Our results showed that women carrying the C allele of CLOCK gene had a marginally significant lower risk of overweight/obesity compared with noncarrier-TT-subjects (odds ratio [OR]: .61, 95% confidence interval [CI]: .36-1.04; p = .069). Moreover, this association of the C allele with a decreased overweight/obesity risk might be enhanced in those women with a high physical activity level. Women practicing more than 16.8 metabolic equivalent tasks (hours per week) had a significantly lower overweight/obesity risk (OR: .36, 95% CI: .17-.79; p = .011). Furthermore, a significant interaction between the 3111T/C gene variant and physical activity (PA) for overweight/obesity risk was observed but only in women (p for PA × CLOCK interaction <.050). In conclusion, it appears that physical activity levels may act by modifying the association of the 3111T/C SNP (rs1801260) of the CLOCK gene with overweight/obesity risk in elderly women in the SUN Project.Genetic factors may interact with physical activity levels to modify obesity risk. Our aim was to explore the influence of rs1801260 single-nucleotide polymorphism (SNP) (3111T/C) of CLOCK gene on obesity risk, and to examine its potential interaction with lifestyle factors in an elderly population within the SUN ("Seguimiento Universidad de Navarra") Project. Subjects (n = 903, aged 69 ± 6 yrs) were recruited from the SUN Project. DNA was obtained from saliva, whereas lifestyle and dietary data were collected by validated self-report questionnaires. Genotype was assessed by reverse transcriptase-polymerase chain reaction (RT-PCR) plus allele discrimination. A significant interaction was observed between the 3111T/C SNP of CLOCK gene and sex for overweight/obesity risk (p for sex × CLOCK interaction <.001). Our results showed that women carrying the C allele of CLOCK gene had a marginally significant lower risk of overweight/obesity compared with noncarrier-TT-subjects (odds ratio [OR]: .61, 95% confidence interval [CI]: .36-1.04; p = .069). Moreover, this association of the C allele with a decreased overweight/obesity risk might be enhanced in those women with a high physical activity level. Women practicing more than 16.8 metabolic equivalent tasks (hours per week) had a significantly lower overweight/obesity risk (OR: .36, 95% CI: .17-.79; p = .011). Furthermore, a significant interaction between the 3111T/C gene variant and physical activity (PA) for overweight/obesity risk was observed but only in women (p for PA × CLOCK interaction <.050). In conclusion, it appears that physical activity levels may act by modifying the association of the 3111T/C SNP (rs1801260) of the CLOCK gene with overweight/obesity risk in elderly women in the SUN Project. Genetic factors may interact with physical activity levels to modify obesity risk. Our aim was to explore the influence of rs1801260 single-nucleotide polymorphism (SNP) (3111T/C) of CLOCK gene on obesity risk, and to examine its potential interaction with lifestyle factors in an elderly population within the SUN ("Seguimiento Universidad de Navarra") Project. Subjects (n = 903, aged 69 ± 6 yrs) were recruited from the SUN Project. DNA was obtained from saliva, whereas lifestyle and dietary data were collected by validated self-report questionnaires. Genotype was assessed by reverse transcriptase-polymerase chain reaction (RT-PCR) plus allele discrimination. A significant interaction was observed between the 3111T/C SNP of CLOCK gene and sex for overweight/obesity risk (p for sex × CLOCK interaction <.001). Our results showed that women carrying the C allele of CLOCK gene had a marginally significant lower risk of overweight/obesity compared with noncarrier-TT-subjects (odds ratio [OR]: .61, 95% confidence interval [CI]: .36-1.04; p = .069). Moreover, this association of the C allele with a decreased overweight/obesity risk might be enhanced in those women with a high physical activity level. Women practicing more than 16.8 metabolic equivalent tasks (hours per week) had a significantly lower overweight/obesity risk (OR: .36, 95% CI: .17-.79; p = .011). Furthermore, a significant interaction between the 3111T/C gene variant and physical activity (PA) for overweight/obesity risk was observed but only in women (p for PA × CLOCK interaction <.050). In conclusion, it appears that physical activity levels may act by modifying the association of the 3111T/C SNP (rs1801260) of the CLOCK gene with overweight/obesity risk in elderly women in the SUN Project. |
Author | Martínez, J. Alfredo Galbete, Cecilia Martínez-González, Miguel Ángel Marti, Amelia Guillén-Grima, Francisco Contreras, Rafael |
Author_xml | – sequence: 1 givenname: Cecilia surname: Galbete fullname: Galbete, Cecilia email: amarti@unav.es, amarti@unav.es organization: University of Navarra – sequence: 2 givenname: Rafael surname: Contreras fullname: Contreras, Rafael email: amarti@unav.es, amarti@unav.es organization: University of Navarra – sequence: 3 givenname: J. Alfredo surname: Martínez fullname: Martínez, J. Alfredo email: amarti@unav.es, amarti@unav.es organization: University of Navarra – sequence: 4 givenname: Miguel Ángel surname: Martínez-González fullname: Martínez-González, Miguel Ángel email: amarti@unav.es, amarti@unav.es organization: University of Navarra – sequence: 5 givenname: Francisco surname: Guillén-Grima fullname: Guillén-Grima, Francisco email: amarti@unav.es, amarti@unav.es organization: University of Navarra Clinic – sequence: 6 givenname: Amelia surname: Marti fullname: Marti, Amelia email: amarti@unav.es, amarti@unav.es organization: University of Navarra |
BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23131019$$D View this record in MEDLINE/PubMed |
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SubjectTerms | Aged Aged, 80 and over Aging Alleles Body mass index CLOCK CLOCK Proteins - genetics Cross-sectional study Female Gene Frequency - genetics Genetic Predisposition to Disease Genotype Humans Male Middle Aged Motor Activity - genetics Mutation - genetics Obesity - genetics Obesity risk Overweight - genetics Polymorphism, Single Nucleotide - genetics rs1801260 Sex Factors |
Title | Physical Activity and Sex Modulate Obesity Risk Linked to 3111T C Gene Variant of the CLOCK Gene in an Elderly Population: The SUN Project |
URI | https://www.tandfonline.com/doi/abs/10.3109/07420528.2012.728657 https://www.ncbi.nlm.nih.gov/pubmed/23131019 https://www.proquest.com/docview/1221132504 |
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