Gene × Physical Activity Interactions in Obesity: Combined Analysis of 111,421 Individuals of European AncestrySkåne University Hospital, Lund University, Sweden; Umeå University, Sweden.
Brigham and Women's Hospital and Harvard Medical School, USA.
Brigham and Women's Hospital and Harvard Medical School, USA.
Karolinska Institutet, Sweden.
Harvard School of Public Health, USA.
University of Eastern Finland, Finland.
University of Copenhagen, Denmark.
Addenbrooke's Hospital, UK.
Harvard School of Public Health, Boston, USA; Brigham and Women's Hospital and Harvard Medical School, USA.
Harvard School of Public Health, Boston, USA; Brigham and Women's Hospital and Harvard Medical School, USA.
University of Copenhagen, Denmark.
Glostrup University Hospital, Denmark.
Addenbrooke's Hospital, UK.
Addenbrooke's Hospital, UK.
Glostrup University Hospital, Denmark.
Glostrup University Hospital, Denmark.
McMaster University, Canada; Population Health Research Institute, Canada.
Karolinska Institutet, Sweden.
Harvard Medical School, USA.
Addenbrooke's Hospital, USA.
Uppsala University, Sweden.
Kuopio University Hospital, Finland.
Karolinska Institutet, Sweden.
Harvard School of Public Health, USA; Brigham and Women's Hospital and Harvard Medical School, USA.
Addenbrooke's Hospital, UK.
Harvard School of Public Health, USA; Brigham and Women's Hospital and Harvard Medical School, USA.
Skåne University Hospital, Lund University, Sweden.
Skåne University Hospital, Lund University, Sweden.
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2013 (English)In: PLOS Genetics, ISSN 1553-7390, E-ISSN 1553-7404, Vol. 9, no 7, article id e1003607
Article in journal (Refereed) Published
Abstract [en]
Numerous obesity loci have been identified using genome-wide association studies. A UK study indicated that physical activity may attenuate the cumulative effect of 12 of these loci, but replication studies are lacking. Therefore, we tested whether the aggregate effect of these loci is diminished in adults of European ancestry reporting high levels of physical activity. Twelve obesity-susceptibility loci were genotyped or imputed in 111,421 participants. A genetic risk score (GRS) was calculated by summing the BMI-associated alleles of each genetic variant. Physical activity was assessed using self-administered questionnaires. Multiplicative interactions between the GRS and physical activity on BMI were tested in linear and logistic regression models in each cohort, with adjustment for age, age2, sex, study center (for multicenter studies), and the marginal terms for physical activity and the GRS. These results were combined using meta-analysis weighted by cohort sample size. The meta-analysis yielded a statistically significant GRS × physical activity interaction effect estimate (Pinteraction = 0.015). However, a statistically significant interaction effect was only apparent in North American cohorts (n = 39,810, Pinteraction = 0.014 vs. n = 71,611, Pinteraction = 0.275 for Europeans). In secondary analyses, both the FTO rs1121980 (Pinteraction = 0.003) and the SEC16B rs10913469 (Pinteraction = 0.025) variants showed evidence of SNP × physical activity interactions. This meta-analysis of 111,421 individuals provides further support for an interaction between physical activity and a GRS in obesity disposition, although these findings hinge on the inclusion of cohorts from North America, indicating that these results are either population-specific or non-causal.
Place, publisher, year, edition, pages
Public Library of Science (PLoS), 2013. Vol. 9, no 7, article id e1003607
National Category
Public Health, Global Health and Social Medicine
Identifiers
URN: urn:nbn:se:sh:diva-55093DOI: 10.1371/journal.pgen.1003607ISI: 000322321100013PubMedID: 23935507Scopus ID: 2-s2.0-84880838336OAI: oai:DiVA.org:sh-55093DiVA, id: diva2:1907787
2024-10-232024-10-232025-10-07Bibliographically approved