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Elevated fasting and postprandial C-terminal telopeptide after Roux-en-Y gastric bypass.
Maghsoodi, Negar; Alaghband-Zadeh, Jamshid; Cross, Gemma F; Werling, Malin; Fändriks, Lars; Docherty, Neil G; Olbers, Torsten; Dew, Tracy; Sherwood, Roy A; Vincent, Royce P; le Roux, Carel W.
Afiliação
  • Maghsoodi N; 1 Department of Clinical Biochemistry, King's College Hospital NHS Foundation Trust, London, UK.
  • Alaghband-Zadeh J; 2 Department of Chemical Pathology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Cross GF; 2 Department of Chemical Pathology, Guy's and St Thomas' NHS Foundation Trust, London, UK.
  • Werling M; 1 Department of Clinical Biochemistry, King's College Hospital NHS Foundation Trust, London, UK.
  • Fändriks L; 3 Department of Gastrosurgical Research and Education, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Docherty NG; 4 Department of Surgery, Sahlgrenska University Hospital/Sahlgrenska, Gothenburg, Sweden.
  • Olbers T; 3 Department of Gastrosurgical Research and Education, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Dew T; 4 Department of Surgery, Sahlgrenska University Hospital/Sahlgrenska, Gothenburg, Sweden.
  • Sherwood RA; 3 Department of Gastrosurgical Research and Education, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
  • Vincent RP; 4 Department of Surgery, Sahlgrenska University Hospital/Sahlgrenska, Gothenburg, Sweden.
  • le Roux CW; 5 Diabetes Complications Research Centre, Conway Institute, University College Dublin, Ireland.
Ann Clin Biochem ; 54(4): 495-500, 2017 Jul.
Article em En | MEDLINE | ID: mdl-27555664
Background Roux-en-Y gastric bypass increases circulating bile acid concentrations, known mediators of postprandial suppression of markers of bone resorption. Long-term data, however, indicate that Roux-en-Y gastric bypass confers an increased risk of bone loss on recipients. Methods Thirty-six obese individuals, median age 44 (26-64) with median body mass index at baseline of 42.5 (40.4-46) were studied before and 15 months after Roux-en-Y gastric bypass. After an overnight fast, patients received a 400 kcal mixed meal. Blood samples were collected premeal then at 30-min periods for 120 min. Pre and postmeal samples were analysed for total bile acids, parathyroid hormone and C-terminal telopeptide. Results Body weight loss post Roux-en-Y gastric bypass was associated with a median 4.9-fold increase in peak postprandial total bile acid concentration, and a median 2.4-fold increase in cumulative food evoked bile acid response. Median fasting parathyroid hormone, postprandial reduction in parathyroid hormone and total parathyroid hormone release over 120 min remained unchanged after surgery. After surgery, median fasting C-terminal telopeptide increased 2.3-fold, peak postprandial concentrations increased 3.8-fold and total release was increased 1.9-fold. Conclusions Fasting and postprandial total bile acids and C-terminal telopeptide are increased above reference range after Roux-en-Y gastric bypass. These changes occur in spite of improved vitamin D status with supplementation. These results suggest that post-Roux-en-Y gastric bypass increases in total bile acids do not effectively oppose an ongoing resorptive signal operative along the gut-bone axis. Serial measurement of C-terminal telopeptide may be of value as a risk marker for long-term skeletal pathology in patients post Roux-en-Y gastric bypass.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeos / Reabsorção Óssea / Obesidade Mórbida / Derivação Gástrica / Colágeno Tipo I Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Clin Biochem Ano de publicação: 2017 Tipo de documento: Article País de publicação: Reino Unido

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Peptídeos / Reabsorção Óssea / Obesidade Mórbida / Derivação Gástrica / Colágeno Tipo I Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Ann Clin Biochem Ano de publicação: 2017 Tipo de documento: Article País de publicação: Reino Unido