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Bone structural changes after gastric bypass surgery evaluated by HR-pQCT: a two-year longitudinal study

OBJECTIVE, DESIGN AND METHODS: Roux-en-Y gastric bypass (RYGB) has proved successful in attaining sustained weight loss but may lead to metabolic bone disease. To assess impact on bone mass and structure, we measured a real bone mineral density at the hip and spine by dual-energy X-ray absorptiometr...

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Autores principales: Shanbhogue, Vikram V, Støving, René Klinkby, Frederiksen, Katrine Hartmund, Hanson, Stine, Brixen, Kim, Gram, Jeppe, Jørgensen, Niklas Rye, Hansen, Stinus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Bioscientifica Ltd 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5425940/
https://www.ncbi.nlm.nih.gov/pubmed/28289103
http://dx.doi.org/10.1530/EJE-17-0014
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author Shanbhogue, Vikram V
Støving, René Klinkby
Frederiksen, Katrine Hartmund
Hanson, Stine
Brixen, Kim
Gram, Jeppe
Jørgensen, Niklas Rye
Hansen, Stinus
author_facet Shanbhogue, Vikram V
Støving, René Klinkby
Frederiksen, Katrine Hartmund
Hanson, Stine
Brixen, Kim
Gram, Jeppe
Jørgensen, Niklas Rye
Hansen, Stinus
author_sort Shanbhogue, Vikram V
collection PubMed
description OBJECTIVE, DESIGN AND METHODS: Roux-en-Y gastric bypass (RYGB) has proved successful in attaining sustained weight loss but may lead to metabolic bone disease. To assess impact on bone mass and structure, we measured a real bone mineral density at the hip and spine by dual-energy X-ray absorptiometry, and volumetric BMD (vBMD) and bone microarchitecture at the distal radius and tibia by high-resolution peripheral quantitative CT in 25 morbidly obese subjects (15 females, 10 males) at 0, 12 and 24 months after RYGB. Bone turnover markers (BTMs), calciotropic and gut hormones and adipokines were measured at the same time points. RESULTS: After a 24.1% mean weight loss from baseline to month 12 (P < 0.001), body weight plateaued from month 12 to 24 (−0.9%, P = 0.50). However, cortical and trabecular vBMD and microarchitecture deteriorated through the 24 months, such that there was a 5 and 7% reduction in estimated bone strength at the radius and tibia respectively (both P < 0.001). The declines observed in the first 12 months were matched or exceeded by declines in the 12- to 24-month period. While a significant increase in BTMs and decrease in leptin and insulin were seen at 24 months, these changes were maximal at month 12 and stabilized from month 12 to 24. CONCLUSIONS: Despite weight stabilization and maintenance of metabolic parameters, bone loss and deterioration in bone strength continued and were substantial in the second year. The clinical importance of these changes in terms of increased risk of developing osteoporosis and fragility fractures remain an important concern.
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spelling pubmed-54259402017-05-15 Bone structural changes after gastric bypass surgery evaluated by HR-pQCT: a two-year longitudinal study Shanbhogue, Vikram V Støving, René Klinkby Frederiksen, Katrine Hartmund Hanson, Stine Brixen, Kim Gram, Jeppe Jørgensen, Niklas Rye Hansen, Stinus Eur J Endocrinol Clinical Study OBJECTIVE, DESIGN AND METHODS: Roux-en-Y gastric bypass (RYGB) has proved successful in attaining sustained weight loss but may lead to metabolic bone disease. To assess impact on bone mass and structure, we measured a real bone mineral density at the hip and spine by dual-energy X-ray absorptiometry, and volumetric BMD (vBMD) and bone microarchitecture at the distal radius and tibia by high-resolution peripheral quantitative CT in 25 morbidly obese subjects (15 females, 10 males) at 0, 12 and 24 months after RYGB. Bone turnover markers (BTMs), calciotropic and gut hormones and adipokines were measured at the same time points. RESULTS: After a 24.1% mean weight loss from baseline to month 12 (P < 0.001), body weight plateaued from month 12 to 24 (−0.9%, P = 0.50). However, cortical and trabecular vBMD and microarchitecture deteriorated through the 24 months, such that there was a 5 and 7% reduction in estimated bone strength at the radius and tibia respectively (both P < 0.001). The declines observed in the first 12 months were matched or exceeded by declines in the 12- to 24-month period. While a significant increase in BTMs and decrease in leptin and insulin were seen at 24 months, these changes were maximal at month 12 and stabilized from month 12 to 24. CONCLUSIONS: Despite weight stabilization and maintenance of metabolic parameters, bone loss and deterioration in bone strength continued and were substantial in the second year. The clinical importance of these changes in terms of increased risk of developing osteoporosis and fragility fractures remain an important concern. Bioscientifica Ltd 2017-03-13 /pmc/articles/PMC5425940/ /pubmed/28289103 http://dx.doi.org/10.1530/EJE-17-0014 Text en © 2017 The authors http://creativecommons.org/licenses/by/3.0/ This work is licensed under a Creative Commons Attribution 3.0 International Licensev. (http://creativecommons.org/licenses/by/3.0/) .
spellingShingle Clinical Study
Shanbhogue, Vikram V
Støving, René Klinkby
Frederiksen, Katrine Hartmund
Hanson, Stine
Brixen, Kim
Gram, Jeppe
Jørgensen, Niklas Rye
Hansen, Stinus
Bone structural changes after gastric bypass surgery evaluated by HR-pQCT: a two-year longitudinal study
title Bone structural changes after gastric bypass surgery evaluated by HR-pQCT: a two-year longitudinal study
title_full Bone structural changes after gastric bypass surgery evaluated by HR-pQCT: a two-year longitudinal study
title_fullStr Bone structural changes after gastric bypass surgery evaluated by HR-pQCT: a two-year longitudinal study
title_full_unstemmed Bone structural changes after gastric bypass surgery evaluated by HR-pQCT: a two-year longitudinal study
title_short Bone structural changes after gastric bypass surgery evaluated by HR-pQCT: a two-year longitudinal study
title_sort bone structural changes after gastric bypass surgery evaluated by hr-pqct: a two-year longitudinal study
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5425940/
https://www.ncbi.nlm.nih.gov/pubmed/28289103
http://dx.doi.org/10.1530/EJE-17-0014
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