PERIOD2 variants are associated with abdominal obesity, psycho-behavioral factors, and attrition in the dietary treatment of obesity
Open accessAbstract
The purpose of this research was to test for association between polymorphisms in the circadian clock-related gene PERIOD2 (PER2) and attrition in patients prone to withdrawal from a behavioral weight-reduction program based on the Mediterranean diet. A total of 454 overweight/obese participants (women=380, men=74), aged 20 to 65 years, who attended outpatient clinics specializing in obesity between January and December 2008, were studied. Anthropometric, biochemical, and dietary-intake variables were analyzed. Effectiveness of the program was assessed, and a questionnaire of barriers to weight loss was considered. Multivariate analysis and logistic regression models were performed. Results indicate that PER2 polymorphisms rs2304672C>G and rs4663302C>T were associated with abdominal obesity (P<0.05). Participants who withdrew from treatment were significantly more obese and had more barriers to lose weight (P<0.05). They also displayed a lower likelihood of planning eating in advance and experiencing stress with dieting than those who completed treatment. Frequency of rs4663307 minor allele was significantly greater in withdrawers than in those who successfully completed treatment (P<0.05). Logistic regression analysis showed that rs2304672 C>G minor allele carriers had a greater probability of dropping out, displaying extreme snacking, experiencing stress with dieting, eating when bored, and skipping breakfast than noncarriers. PER2 is implicated in attrition in weight-loss treatment and may modulate eating-behavior-related phenotypes. These findings could represent a step toward personalized health care and nutrition based on a combination of genotyping and psycho-behavioral characterization.
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PER2 SNPs rs2304672 and rs4663302 were associated with abdominal obesity.
“Our results show that PER2 SNPs rs2304672 and rs4663302 were associated with abdominal obesity.”
From Circadian rhythms, metabolism, and chrononutrition in rodents and humans (2016) · cites this paper as [60]
Carriers of the minor allele at PER2 SNPs rs2304672 and rs4663302 had a greater probability of dropping out from the weight-loss program and displaying extreme snacking, experiencing stress with dieting, eating when bored, and skipping breakfast than noncarriers.
“Moreover, carriers of the minor allele at these PER2 SNPs had a greater probability of dropping out from the weight-loss program as well as displaying extreme snacking, experiencing stress with dieting, eating when bored, and skipping breakfast than noncarriers.”
From Circadian rhythms, metabolism, and chrononutrition in rodents and humans (2016) · cites this paper as [60]
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References 26 · Cited by 111
Research works printed but not linked: 1
- [21]Caucasian European Utah data International HapMap Project Web site http://hapmap.ncbi.nlm.nih.gov/cgi-perl/gbrowse/hapmap27_B36/?ref=chr2;start=238812418;stop=238871946;version= Accessed June 25, 2008
- Authors
- Garaulet, M., Corbalán-Tutau, M. D., Madrid, J. A., Baraza, J. C., Parnell, L. D., Lee, Y.-C., & Ordovas, J. M.
- Affiliations
- Universidad de Murcia (ES)
- Tufts University (US)
- Corresponding author
- Garaulet, Marta
- Venue
- Journal of the American Dietetic Association
- Publisher
- Elsevier BV
- Published
- 2010-06
- Volume
- 110
- Issue
- 6
- Pages
- 917-921
- ISSN
- 0002-8223 (ISSN-L)
- PMC
- PMC4428932
- OpenAlex
- W2083550508
- Cited by
- 111
- References
- 26
- Citations by year
- 2026: 1 · 2025: 6 · 2024: 9 · 2023: 7 · 2022: 9 · 2021: 2 · 2020: 4 · 2019: 2 · 2018: 4 · 2017: 3 · 2016: 12 · 2015: 7 · 2014: 11 · 2013: 9 · 2012: 11
- FWCI
- 6.12
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Journal of the American Dietetic Association (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- Government of Education, Science, and Research of Murcia (BIO/FFA 07/01-0004)
- Spanish Government of Science and Innovation (AGL2008-01655/ALI)
- National Institute of Diabetes and Digestive and Kidney Diseases (DK075030)
- US Department of Agriculture Research Service (53-K06-5-10, 58-1950-9-001)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Nutrition, Genetics, and Disease
- Life Sciences › Neuroscience › Endocrine and Autonomic Systems › Circadian rhythm and melatonin
- Social Sciences › Psychology › Clinical Psychology › Eating Disorders and Behaviors
- Keywords
- clock genes, genetic polymorphism, abdominal obesity, Mediterranean diet, dietary habits, snacking, barriers to weight loss, personalized nutrition
- MeSH terms
- Adult, Aged, Behavior Therapy, Diet, Reducing, Feeding Behavior, Female, Humans, Male, Middle Aged, Obesity, Patient Dropouts, Polymorphism, Genetic, Weight Loss, Cognitive Behavioral Therapy, Logistic Models, Treatment Outcome, Genetic Predisposition to Disease, Self Efficacy, Diet, Mediterranean, Young Adult, Obesity, Abdominal, Period Circadian Proteins
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