4.7 Article

Effects of Gastric Bypass and Gastric Banding on Bone Remodeling in Obese Patients With Type 2 Diabetes

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出版社

ENDOCRINE SOC
DOI: 10.1210/jc.2015-3437

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资金

  1. National Institutes of Health [K23-DK093713, RC1-DK086918, R56-DK095451, P30-DK036836]
  2. Harvard Catalyst and The Harvard Clinical and Translational Science Center (National Center for Research Resources)
  3. Harvard Catalyst and The Harvard Clinical and Translational Science Center (National Center for Advancing Translational Sciences) [8UL1TR000170-05]
  4. Harvard Catalyst and The Harvard Clinical and Translational Science Center (KL2/MeRIT Program Award) [UL1 RR 025758]
  5. Harvard Catalyst and The Harvard Clinical and Translational Science Center (Harvard University and its affiliated academic healthcare centers)
  6. Joslin Clinical Research Center
  7. Marietta Blau Grant from the Osterreichischer Austausdienst [ICM-2010-02797]
  8. Herbert Graetz Fund
  9. Covidien
  10. Lifescan, a division of Johnson and Johnson
  11. Nestle
  12. NovoNordisk
  13. NNF Center for Basic Metabolic Research [Holst Group] Funding Source: researchfish

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Context: Roux-en-Y gastric bypass (RYGB) leads to high-turnover bone loss, but little is known about skeletal effects of laparoscopic adjustable gastric banding (LAGB) or mechanisms underlying bone loss after bariatric surgery. Objective: To evaluate effects of RYGB and LAGB on fasting and postprandial indices of bone remodeling. Design and Setting: Ancillary investigation of a prospective study at 2 academic institutions. Participants: Obese adults aged 21-65 years with type 2 diabetes who underwent RYGB (n = 11) or LAGB (n = 8). Outcomes: Serum C-terminal telopeptide (CTX), procollagen type 1 N-terminal propeptide (P1NP), and PTH were measured during a mixed meal tolerance test at baseline, 10 days and 1 year after surgery. Changes in 25-hydroxyvitamin D, polypeptide YY (PYY), glucagon-like peptide-1, glucose-dependent insulinotropic peptide, and insulin were also assessed. Results: Fasting CTX increased 10 days after RYGB but not LAGB (+69 +/- 23% vs +12 +/- 12%, P < .001), despite comparable weight loss at that time. By 1 year, fasting CTX and P1NP increased more after RYGB than LAGB (CTX +221 +/- 60% vs +15 +/- 6%, P < 0.001; P1NP +93 +/- 25% vs -9 +/- 10%, P < .001) and weight loss was greater with RYGB. Changes in CTX were independent of PTH and 25-hydroxyvitamin D but were associated with increases in fasting PYY. Postprandial suppression of CTX was more pronounced after RYGB than LAGB at 10 days and 1 year postoperatively. Conclusions: RYGB is accompanied by early increases in fasting indices of bone remodeling, independent of weight loss or changes in PTH or 25-hydroxyvitamin D. LAGB did not affect bone markers. PYY and other enterohormonal signals may play a role in RYGB-specific skeletal changes.

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