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      The consequences of a weight‐centric approach to healthcare: A case for a paradigm shift in how clinicians address body weight

      1 , 2 , 3 , 4 , 5
      Nutrition in Clinical Practice
      Wiley

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          Diagnostic and Statistical Manual of Mental Disorders

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            Reduction in the incidence of type 2 diabetes with lifestyle intervention or metformin.

            Type 2 diabetes affects approximately 8 percent of adults in the United States. Some risk factors--elevated plasma glucose concentrations in the fasting state and after an oral glucose load, overweight, and a sedentary lifestyle--are potentially reversible. We hypothesized that modifying these factors with a lifestyle-intervention program or the administration of metformin would prevent or delay the development of diabetes. We randomly assigned 3234 nondiabetic persons with elevated fasting and post-load plasma glucose concentrations to placebo, metformin (850 mg twice daily), or a lifestyle-modification program with the goals of at least a 7 percent weight loss and at least 150 minutes of physical activity per week. The mean age of the participants was 51 years, and the mean body-mass index (the weight in kilograms divided by the square of the height in meters) was 34.0; 68 percent were women, and 45 percent were members of minority groups. The average follow-up was 2.8 years. The incidence of diabetes was 11.0, 7.8, and 4.8 cases per 100 person-years in the placebo, metformin, and lifestyle groups, respectively. The lifestyle intervention reduced the incidence by 58 percent (95 percent confidence interval, 48 to 66 percent) and metformin by 31 percent (95 percent confidence interval, 17 to 43 percent), as compared with placebo; the lifestyle intervention was significantly more effective than metformin. To prevent one case of diabetes during a period of three years, 6.9 persons would have to participate in the lifestyle-intervention program, and 13.9 would have to receive metformin. Lifestyle changes and treatment with metformin both reduced the incidence of diabetes in persons at high risk. The lifestyle intervention was more effective than metformin.
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              Genetic studies of body mass index yield new insights for obesity biology.

              Obesity is heritable and predisposes to many diseases. To understand the genetic basis of obesity better, here we conduct a genome-wide association study and Metabochip meta-analysis of body mass index (BMI), a measure commonly used to define obesity and assess adiposity, in up to 339,224 individuals. This analysis identifies 97 BMI-associated loci (P  20% of BMI variation. Pathway analyses provide strong support for a role of the central nervous system in obesity susceptibility and implicate new genes and pathways, including those related to synaptic function, glutamate signalling, insulin secretion/action, energy metabolism, lipid biology and adipogenesis.
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                Author and article information

                Contributors
                (View ORCID Profile)
                (View ORCID Profile)
                Journal
                Nutrition in Clinical Practice
                Nut in Clin Prac
                Wiley
                0884-5336
                1941-2452
                December 2022
                July 12 2022
                December 2022
                : 37
                : 6
                : 1291-1306
                Affiliations
                [1 ]Department of Nutrition, Food Science, and Packaging San José State University San José California USA
                [2 ]Department of Clinical Nutrition Stanford Health Care Stanford California USA
                [3 ]Am I Hungry? Mindful Eating Programs and Training USA
                [4 ]Department of Psychology Arizona State University Tempe Arizona USA
                [5 ]Department of Health Sciences Northern Arizona University Flagstaff Arizona USA
                Article
                10.1002/ncp.10885
                35819360
                0ba1ffc1-cc85-4a90-a0f7-ee574b42f5ac
                © 2022

                http://onlinelibrary.wiley.com/termsAndConditions#vor

                http://doi.wiley.com/10.1002/tdm_license_1.1

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