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Exploring the Paradoxical Relationship of a Creb 3 Regulatory Factor Missense Variant With Body Mass Index and Diabetes Among Samoans: Protocol for the Soifua Manuia (Good Health) Observational Cohort Study.
Hawley, Nicola L; Pomer, Alysa; Rivara, Anna C; Rosenthal, Samantha L; Duckham, Rachel L; Carlson, Jenna C; Naseri, Take; Reupena, Muagututia Sefuiva; Selu, Melania; Lupematisila, Vaimoana; Unasa, Folla; Vesi, Lupesina; Fatu, Tracy; Unasa, Seipepa; Faasalele-Savusa, Kima; Wetzel, Abigail I; Soti-Ulberg, Christina; Prescott, Angela T; Siufaga, Gloria; Penaia, Corina; To, Sophie B; LaMonica, Lauren C; Lameko, Viali; Choy, Courtney C; Crouter, Scott E; Redline, Susan; Deka, Ranjan; Kershaw, Erin E; Urban, Zsolt; Minster, Ryan L; Weeks, Daniel E; McGarvey, Stephen T.
Afiliación
  • Hawley NL; Department of Chronic Disease Epidemiology, Yale School of Public Health, New Haven, CT, United States.
  • Pomer A; Department of Chronic Disease Epidemiology, Yale School of Public Health, New Haven, CT, United States.
  • Rivara AC; Department of Chronic Disease Epidemiology, Yale School of Public Health, New Haven, CT, United States.
  • Rosenthal SL; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, United States.
  • Duckham RL; Institute of Physical Activity and Nutrition, Deakin University, Geelong, Australia.
  • Carlson JC; Australian Institute for Musculoskeletal Sciences, The University of Melbourne and Western Health, St Albans, Australia.
  • Naseri T; Department of Biostatistics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, United States.
  • Reupena MS; Ministry of Health, Apia, Samoa.
  • Selu M; Lutia I Puava Ae Mapu I Fagalele, Apia, Samoa.
  • Lupematisila V; Obesity, Lifestyle and Genetic Adaptations Study Group, Apia, Samoa.
  • Unasa F; Obesity, Lifestyle and Genetic Adaptations Study Group, Apia, Samoa.
  • Vesi L; Obesity, Lifestyle and Genetic Adaptations Study Group, Apia, Samoa.
  • Fatu T; Obesity, Lifestyle and Genetic Adaptations Study Group, Apia, Samoa.
  • Unasa S; Obesity, Lifestyle and Genetic Adaptations Study Group, Apia, Samoa.
  • Faasalele-Savusa K; Obesity, Lifestyle and Genetic Adaptations Study Group, Apia, Samoa.
  • Wetzel AI; Obesity, Lifestyle and Genetic Adaptations Study Group, Apia, Samoa.
  • Soti-Ulberg C; International Health Institute, Department of Epidemiology, School of Public Health, Brown University, Providence, RI, United States.
  • Prescott AT; Ministry of Health, Apia, Samoa.
  • Siufaga G; Department of Plastic and Reconstructive Surgery, University of Pittsburgh Medical Center, Pittsburgh, PA, United States.
  • Penaia C; Obesity, Lifestyle and Genetic Adaptations Study Group, Apia, Samoa.
  • To SB; Asian Pacific Islander Forward Movement, Los Angeles, CA, United States.
  • LaMonica LC; Department of Social and Behavioral Sciences, Yale School of Public Health, New Haven, CT, United States.
  • Lameko V; Department of Chronic Disease Epidemiology, Yale School of Public Health, New Haven, CT, United States.
  • Choy CC; Oceania University of Medicine, Apia, Samoa.
  • Crouter SE; International Health Institute, Department of Epidemiology, School of Public Health, Brown University, Providence, RI, United States.
  • Redline S; Department of Kinesiology, Recreation, and Sport Studies, The University of Tennessee Knoxville, Knoxville, TN, United States.
  • Deka R; Departments of Medicine, Brigham and Women's Hospital and Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, United States.
  • Kershaw EE; Department of Environmental Health, College of Medicine, University of Cincinnati, Cincinnati, OH, United States.
  • Urban Z; Division of Endocrinology, Department of Medicine, University of Pittsburgh, Pittsburgh, PA, United States.
  • Minster RL; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, United States.
  • Weeks DE; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, United States.
  • McGarvey ST; Department of Human Genetics, Graduate School of Public Health, University of Pittsburgh, Pittsburgh, PA, United States.
JMIR Res Protoc ; 9(7): e17329, 2020 Jul 23.
Article en En | MEDLINE | ID: mdl-32706746
BACKGROUND: The prevalence of obesity and diabetes in Samoa, like many other Pacific Island nations, has reached epidemic proportions. Although the etiology of these conditions can be largely attributed to the rapidly changing economic and nutritional environment, a recently identified genetic variant, rs373863828 (CREB 3 regulatory factor, CREBRF: c.1370G>A p.[R457Q]) is associated with increased odds of obesity, but paradoxically, decreased odds of diabetes. OBJECTIVE: The overarching goal of the Soifua Manuia (Good Health) study was to precisely characterize the association of the CREBRF variant with metabolic (body composition and glucose homeostasis) and behavioral traits (dietary intake, physical activity, sleep, and weight control behaviors) that influence energy homeostasis in 500 adults. METHODS: A cohort of adult Samoans who participated in a genome-wide association study of adiposity in Samoa in 2010 was followed up, based on the presence or absence of the CREBRF variant, between August 2017 and March 2019. Over a period of 7-10 days, each participant completed the main study protocol, which consisted of anthropometric measurements (weight, height, circumferences, and skinfolds), body composition assessment (bioelectrical impedance and dual-energy x-ray absorptiometry), point-of-care glycated hemoglobin measurement, a fasting blood draw and oral glucose tolerance test, urine collection, blood pressure measurement, hand grip strength measurement, objective physical activity and sleep apnea monitoring, and questionnaire measures (eg, health interview, cigarette and alcohol use, food frequency questionnaire, socioeconomic position, stress, social support, food and water insecurity, sleep, body image, and dietary preferences). In January 2019, a subsample of the study participants (n=118) completed a buttock fat biopsy procedure to collect subcutaneous adipose tissue samples. RESULTS: Enrollment of 519 participants was completed in March 2019. Data analyses are ongoing, with results expected in 2020 and 2021. CONCLUSIONS: While the genetic variant rs373863828, in CREBRF, has the largest known effect size of any identified common obesity gene, very little is currently understood about the mechanisms by which it confers increased odds of obesity but paradoxically lowered odds of type 2 diabetes. The results of this study will provide insights into how the gene functions on a whole-body level, which could provide novel targets to prevent or treat obesity, diabetes, and associated metabolic disorders. This study represents the human arm of a comprehensive and integrated approach involving humans as well as preclinical models that will provide novel insights into metabolic disease. INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): RR1-10.2196/17329.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: JMIR Res Protoc Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Canadá

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Etiology_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: JMIR Res Protoc Año: 2020 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Canadá