Effects of Biliopancreatic Diversion on Bone Turnover Markers and Association with Hormonal Factors in Patients with Severe Obesity.


Journal

Obesity surgery
ISSN: 1708-0428
Titre abrégé: Obes Surg
Pays: United States
ID NLM: 9106714

Informations de publication

Date de publication:
03 2019
Historique:
pubmed: 28 11 2018
medline: 25 3 2020
entrez: 28 11 2018
Statut: ppublish

Résumé

This study evaluated early and medium-term changes in bone turnover markers, and their associations with weight loss, total bone mineral density (BMD), and hormonal changes after biliopancreatic diversion (BPD). Ancillary study from a one-year prospective cohort of 16 individuals assessed before, 3 days, 3 and 12 months after BPD. Bone turnover markers (C-terminal telopeptide (CTX), intact osteocalcin (OC), sclerostin, and osteoprotegerin (OPG)) and several hormones were measured at each visit. Total BMD by DXA was assessed at baseline, 3 and 12 months after BPD. Three participants were lost to follow-up. CTX increased significantly at 3 days (+ 66%), 3 months (+ 219%), and 12 months (+ 295%). OC decreased at 3 days (- 19%) then increased at 3 months (+ 69%) and 12 months (+ 164%). Change in sclerostin was only significant between 3 days and 3 months (+ 13%), while change in OPG was significant between baseline and 3 days (+ 48%) and baseline and 12 months (+ 45%). CTX increase correlated negatively with weight loss at 3 (r = - 0.63, p = 0.009) and 12 months (r = - 0.58, p = 0.039), and total BMD decrease (r = - 0.67, p = 0.033) at 12 months. Change in insulin and adiponectin correlated with changes in bone turnover markers independently of weight loss. BPD causes an earlier and greater increase in bone resorption over bone formation markers and a decrease in total BMD. Sclerostin did not increase as expected following extensive weight loss. Changes in insulin and adiponectin seem to play a role in the activation of bone remodeling after BPD.

Sections du résumé

BACKGROUND
This study evaluated early and medium-term changes in bone turnover markers, and their associations with weight loss, total bone mineral density (BMD), and hormonal changes after biliopancreatic diversion (BPD).
METHODS
Ancillary study from a one-year prospective cohort of 16 individuals assessed before, 3 days, 3 and 12 months after BPD. Bone turnover markers (C-terminal telopeptide (CTX), intact osteocalcin (OC), sclerostin, and osteoprotegerin (OPG)) and several hormones were measured at each visit. Total BMD by DXA was assessed at baseline, 3 and 12 months after BPD. Three participants were lost to follow-up.
RESULTS
CTX increased significantly at 3 days (+ 66%), 3 months (+ 219%), and 12 months (+ 295%). OC decreased at 3 days (- 19%) then increased at 3 months (+ 69%) and 12 months (+ 164%). Change in sclerostin was only significant between 3 days and 3 months (+ 13%), while change in OPG was significant between baseline and 3 days (+ 48%) and baseline and 12 months (+ 45%). CTX increase correlated negatively with weight loss at 3 (r = - 0.63, p = 0.009) and 12 months (r = - 0.58, p = 0.039), and total BMD decrease (r = - 0.67, p = 0.033) at 12 months. Change in insulin and adiponectin correlated with changes in bone turnover markers independently of weight loss.
CONCLUSION
BPD causes an earlier and greater increase in bone resorption over bone formation markers and a decrease in total BMD. Sclerostin did not increase as expected following extensive weight loss. Changes in insulin and adiponectin seem to play a role in the activation of bone remodeling after BPD.

Identifiants

pubmed: 30478790
doi: 10.1007/s11695-018-3617-x
pii: 10.1007/s11695-018-3617-x
doi:

Substances chimiques

ADIPOQ protein, human 0
Adiponectin 0
Biomarkers 0
Hormones 0
Osteoprotegerin 0
TNFRSF11B protein, human 0
Osteocalcin 104982-03-8

Types de publication

Journal Article Observational Study Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

990-998

Subventions

Organisme : CIHR
ID : MOP 97947
Pays : Canada

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Auteurs

Anne-Frédérique Turcotte (AF)

Endocrinology and Nephrology Unit, CHU de Québec Research Centre, 2705, Boulevard Laurier, Québec City, QC, G1V 4G2, Canada.

Thomas Grenier-Larouche (T)

CHU de Sherbrooke Research Centre, Sherbrooke, Canada.
Department of Medicine, Université de Sherbrooke, Sherbrooke, Canada.

Roth-Visal Ung (RV)

Endocrinology and Nephrology Unit, CHU de Québec Research Centre, 2705, Boulevard Laurier, Québec City, QC, G1V 4G2, Canada.

David Simonyan (D)

Clinical and Evaluative Research Platform, CHU de Québec-Université Laval Research Centre, Québec City, QC, Canada.

Anne-Marie Carreau (AM)

CHU de Sherbrooke Research Centre, Sherbrooke, Canada.
Department of Medicine, Université de Sherbrooke, Sherbrooke, Canada.

André C Carpentier (AC)

CHU de Sherbrooke Research Centre, Sherbrooke, Canada.
Department of Medicine, Université de Sherbrooke, Sherbrooke, Canada.

Fabrice Mac-Way (F)

Endocrinology and Nephrology Unit, CHU de Québec Research Centre, 2705, Boulevard Laurier, Québec City, QC, G1V 4G2, Canada.
Department of Medicine, Université Laval, Québec City, Canada.

Laetitia Michou (L)

Endocrinology and Nephrology Unit, CHU de Québec Research Centre, 2705, Boulevard Laurier, Québec City, QC, G1V 4G2, Canada.
Department of Medicine, Université Laval, Québec City, Canada.

André Tchernof (A)

Endocrinology and Nephrology Unit, CHU de Québec Research Centre, 2705, Boulevard Laurier, Québec City, QC, G1V 4G2, Canada.
Department of Medicine, Université Laval, Québec City, Canada.
Québec Heart and Lung Institute Research Centre, Québec City, Canada.
Institute of Nutrition and Functional Foods, Université Laval, Quebec City, QC, Canada.

Laurent Biertho (L)

Québec Heart and Lung Institute Research Centre, Québec City, Canada.
Department of Surgery, Université Laval, Québec City, Canada.

Stefane Lebel (S)

Québec Heart and Lung Institute Research Centre, Québec City, Canada.
Department of Surgery, Université Laval, Québec City, Canada.

Simon Marceau (S)

Québec Heart and Lung Institute Research Centre, Québec City, Canada.
Department of Surgery, Université Laval, Québec City, Canada.

Claudia Gagnon (C)

Endocrinology and Nephrology Unit, CHU de Québec Research Centre, 2705, Boulevard Laurier, Québec City, QC, G1V 4G2, Canada. claudia.gagnon@crchudequebec.ulaval.ca.
Department of Medicine, Université Laval, Québec City, Canada. claudia.gagnon@crchudequebec.ulaval.ca.
Québec Heart and Lung Institute Research Centre, Québec City, Canada. claudia.gagnon@crchudequebec.ulaval.ca.
Institute of Nutrition and Functional Foods, Université Laval, Quebec City, QC, Canada. claudia.gagnon@crchudequebec.ulaval.ca.

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