4.4 Article

Effects of Roux-en-Y Gastric Bypass on Osteoclast Activity and Bone Density in Morbidly Obese Patients with Type 2 Diabetes

Journal

OBESITY SURGERY
Volume 30, Issue 1, Pages 290-295

Publisher

SPRINGER
DOI: 10.1007/s11695-019-04154-2

Keywords

Osteoclast; Bone loss; Roux-en-Y gastric bypass; Bariatric surgery; Bone mineral density

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Funding

  1. NIDDK NIH HHS [K23 DK075907] Funding Source: Medline

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Introduction Roux-en-Y gastric bypass (RYGB) is a well-established treatment for morbid obesity and type 2 diabetes. The effects of RYGB on bone metabolism and bone health are largely unknown. Objective Determine the changes in osteoclast function and bone density 1 year after RYGB as compared with a control group undergoing a diabetes support and education program (DSE). Design A prospective cohort study with patients matched for weight and age assigned to RYGB or DSE. Setting Large academic institution. Patients or Other Participants Patients with type 2 diabetes mellitus and morbid obesity (body mass index greater than 35 kg/m(2)). Intervention Subjects either received laparoscopic RYBG or DSE, which consisted of nutritional, exercise, and dietary counseling performed by a certified diabetic educator and a nutritionist three times over a year. Main Outcome Measure Osteoclast activity, bone mineral density. Results One year after, intervention subjects undergoing RYGB have a 280% increase in osteoclast activity as compared with a 7.6% increase in the DSE control group (P < 0.001). Furthermore, there was a statistically significant increase in sclerostin levels in subjects undergoing RYGB compared with an increase in the control group. The total bone mineral density was statistically unchanged within 1 year of intervention in both groups. A statistically significant decrease in bone mineral density in the left ribs (decrease of 6.8%, P < 0.05) and lumbar spine (decrease of 4.0%, P < 0.05) was seen 1 year after RYGB. Conclusions There is a significant increase in osteoclast activity observed 1 year after RYGB; the long-term clinical implications of this increased bone metabolism are unknown.

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