Improvements in glucose metabolism early after gastric bypass surgery are not explained by increases in total bile acids and fibroblast growth factor 19 concentrations

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Standard

Improvements in glucose metabolism early after gastric bypass surgery are not explained by increases in total bile acids and fibroblast growth factor 19 concentrations. / Jørgensen, Nils B; Dirksen, Carsten; Bojsen-Møller, Kirstine N; Kristiansen, Viggo B; Wulff, Birgitte S; Rainteau, Dominique; Humbert, Lydie; Rehfeld, Jens F; Holst, Jens Juul; Madsbad, Sten; Clausen, Trine R.

In: The Journal of clinical endocrinology and metabolism, Vol. 100, No. 3, 03.2015, p. E396-406.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Jørgensen, NB, Dirksen, C, Bojsen-Møller, KN, Kristiansen, VB, Wulff, BS, Rainteau, D, Humbert, L, Rehfeld, JF, Holst, JJ, Madsbad, S & Clausen, TR 2015, 'Improvements in glucose metabolism early after gastric bypass surgery are not explained by increases in total bile acids and fibroblast growth factor 19 concentrations', The Journal of clinical endocrinology and metabolism, vol. 100, no. 3, pp. E396-406. https://doi.org/10.1210/jc.2014-1658

APA

Jørgensen, N. B., Dirksen, C., Bojsen-Møller, K. N., Kristiansen, V. B., Wulff, B. S., Rainteau, D., Humbert, L., Rehfeld, J. F., Holst, J. J., Madsbad, S., & Clausen, T. R. (2015). Improvements in glucose metabolism early after gastric bypass surgery are not explained by increases in total bile acids and fibroblast growth factor 19 concentrations. The Journal of clinical endocrinology and metabolism, 100(3), E396-406. https://doi.org/10.1210/jc.2014-1658

Vancouver

Jørgensen NB, Dirksen C, Bojsen-Møller KN, Kristiansen VB, Wulff BS, Rainteau D et al. Improvements in glucose metabolism early after gastric bypass surgery are not explained by increases in total bile acids and fibroblast growth factor 19 concentrations. The Journal of clinical endocrinology and metabolism. 2015 Mar;100(3):E396-406. https://doi.org/10.1210/jc.2014-1658

Author

Jørgensen, Nils B ; Dirksen, Carsten ; Bojsen-Møller, Kirstine N ; Kristiansen, Viggo B ; Wulff, Birgitte S ; Rainteau, Dominique ; Humbert, Lydie ; Rehfeld, Jens F ; Holst, Jens Juul ; Madsbad, Sten ; Clausen, Trine R. / Improvements in glucose metabolism early after gastric bypass surgery are not explained by increases in total bile acids and fibroblast growth factor 19 concentrations. In: The Journal of clinical endocrinology and metabolism. 2015 ; Vol. 100, No. 3. pp. E396-406.

Bibtex

@article{27c8d46fd3394abdb879bde9779b2a61,
title = "Improvements in glucose metabolism early after gastric bypass surgery are not explained by increases in total bile acids and fibroblast growth factor 19 concentrations",
abstract = "Context: Bile acids and fibroblast growth factor 19 (FGF19) have been suggested as key mediators of the improvements in glucose metabolism after Roux-en-Y gastric bypass (RYGB). Objective: To describe fasting and postprandial state total bile acid (TBA) and FGF19 concentrations before and after RYGB and relate them to parameters of glucose metabolism, glucagon-like peptide-1, cholecystokinin, and cholesterol fractions. Design and Setting: A prospective descriptive study was performed at the Department of Endocrinology, Hvidovre Hospital, Hvidovre, Denmark.Patients: Thirteen type 2 diabetic (T2D) patients and 12 normal glucose tolerant (NGT) subjects participated in the study. Intervention: A 4-hour liquid meal test was performed before and 1 week, 3 months, and 1 year after RYGB. Main Outcome Measures: We measured fasting and postprandial TBA and FGF19 concentrations. Results: Fasting TBA concentrations decreased in NGT subjects (P < .001) and were unchanged in T2D patients 1 week after surgery, but then increased gradually in both groups with time from surgery (ANOVA Ptime < .001). Area under the curve (AUC) TBA was decreased in NGT subjects 1 week after RYGB (before surgery, 567 mmol * min/L [interquartile range, 481–826]; 1 wk, 419 [381–508]; P = .009) and was unchanged in T2D patients (894 [573–1002]; 695 [349–1147]; P = .97) but then increased with time from surgery in both groups (Ptime < .001). Fasting FGF19 concentrations were unchanged acutely after RYGB (NGT, 140 pg/mL [100–162], 134 [119–204], P = .42; T2D, 162 [130–196], 154 [104–164], P = .68) and remained unchanged throughout the follow-up period. AUC FGF19 increased gradually with time after surgery (Ptime < .001), resembling the changes seen with AUC TBA. One week after RYGB, glucose metabolism improved, low-density lipoprotein-cholesterol and high-density lipoprotein-cholesterol decreased, and cholecystokinin and glucagon-like peptide-1 secretion increased, whereas FFA concentrations were unchanged. Conclusion: TBA and FGF19 do not explain acute changes in glucose metabolism, cholesterol fractions, and gut hormone secretion after RYGB.",
author = "J{\o}rgensen, {Nils B} and Carsten Dirksen and Bojsen-M{\o}ller, {Kirstine N} and Kristiansen, {Viggo B} and Wulff, {Birgitte S} and Dominique Rainteau and Lydie Humbert and Rehfeld, {Jens F} and Holst, {Jens Juul} and Sten Madsbad and Clausen, {Trine R}",
year = "2015",
month = mar,
doi = "10.1210/jc.2014-1658",
language = "English",
volume = "100",
pages = "E396--406",
journal = "Journal of Clinical Endocrinology and Metabolism",
issn = "0021-972X",
publisher = "Oxford University Press",
number = "3",

}

RIS

TY - JOUR

T1 - Improvements in glucose metabolism early after gastric bypass surgery are not explained by increases in total bile acids and fibroblast growth factor 19 concentrations

AU - Jørgensen, Nils B

AU - Dirksen, Carsten

AU - Bojsen-Møller, Kirstine N

AU - Kristiansen, Viggo B

AU - Wulff, Birgitte S

AU - Rainteau, Dominique

AU - Humbert, Lydie

AU - Rehfeld, Jens F

AU - Holst, Jens Juul

AU - Madsbad, Sten

AU - Clausen, Trine R

PY - 2015/3

Y1 - 2015/3

N2 - Context: Bile acids and fibroblast growth factor 19 (FGF19) have been suggested as key mediators of the improvements in glucose metabolism after Roux-en-Y gastric bypass (RYGB). Objective: To describe fasting and postprandial state total bile acid (TBA) and FGF19 concentrations before and after RYGB and relate them to parameters of glucose metabolism, glucagon-like peptide-1, cholecystokinin, and cholesterol fractions. Design and Setting: A prospective descriptive study was performed at the Department of Endocrinology, Hvidovre Hospital, Hvidovre, Denmark.Patients: Thirteen type 2 diabetic (T2D) patients and 12 normal glucose tolerant (NGT) subjects participated in the study. Intervention: A 4-hour liquid meal test was performed before and 1 week, 3 months, and 1 year after RYGB. Main Outcome Measures: We measured fasting and postprandial TBA and FGF19 concentrations. Results: Fasting TBA concentrations decreased in NGT subjects (P < .001) and were unchanged in T2D patients 1 week after surgery, but then increased gradually in both groups with time from surgery (ANOVA Ptime < .001). Area under the curve (AUC) TBA was decreased in NGT subjects 1 week after RYGB (before surgery, 567 mmol * min/L [interquartile range, 481–826]; 1 wk, 419 [381–508]; P = .009) and was unchanged in T2D patients (894 [573–1002]; 695 [349–1147]; P = .97) but then increased with time from surgery in both groups (Ptime < .001). Fasting FGF19 concentrations were unchanged acutely after RYGB (NGT, 140 pg/mL [100–162], 134 [119–204], P = .42; T2D, 162 [130–196], 154 [104–164], P = .68) and remained unchanged throughout the follow-up period. AUC FGF19 increased gradually with time after surgery (Ptime < .001), resembling the changes seen with AUC TBA. One week after RYGB, glucose metabolism improved, low-density lipoprotein-cholesterol and high-density lipoprotein-cholesterol decreased, and cholecystokinin and glucagon-like peptide-1 secretion increased, whereas FFA concentrations were unchanged. Conclusion: TBA and FGF19 do not explain acute changes in glucose metabolism, cholesterol fractions, and gut hormone secretion after RYGB.

AB - Context: Bile acids and fibroblast growth factor 19 (FGF19) have been suggested as key mediators of the improvements in glucose metabolism after Roux-en-Y gastric bypass (RYGB). Objective: To describe fasting and postprandial state total bile acid (TBA) and FGF19 concentrations before and after RYGB and relate them to parameters of glucose metabolism, glucagon-like peptide-1, cholecystokinin, and cholesterol fractions. Design and Setting: A prospective descriptive study was performed at the Department of Endocrinology, Hvidovre Hospital, Hvidovre, Denmark.Patients: Thirteen type 2 diabetic (T2D) patients and 12 normal glucose tolerant (NGT) subjects participated in the study. Intervention: A 4-hour liquid meal test was performed before and 1 week, 3 months, and 1 year after RYGB. Main Outcome Measures: We measured fasting and postprandial TBA and FGF19 concentrations. Results: Fasting TBA concentrations decreased in NGT subjects (P < .001) and were unchanged in T2D patients 1 week after surgery, but then increased gradually in both groups with time from surgery (ANOVA Ptime < .001). Area under the curve (AUC) TBA was decreased in NGT subjects 1 week after RYGB (before surgery, 567 mmol * min/L [interquartile range, 481–826]; 1 wk, 419 [381–508]; P = .009) and was unchanged in T2D patients (894 [573–1002]; 695 [349–1147]; P = .97) but then increased with time from surgery in both groups (Ptime < .001). Fasting FGF19 concentrations were unchanged acutely after RYGB (NGT, 140 pg/mL [100–162], 134 [119–204], P = .42; T2D, 162 [130–196], 154 [104–164], P = .68) and remained unchanged throughout the follow-up period. AUC FGF19 increased gradually with time after surgery (Ptime < .001), resembling the changes seen with AUC TBA. One week after RYGB, glucose metabolism improved, low-density lipoprotein-cholesterol and high-density lipoprotein-cholesterol decreased, and cholecystokinin and glucagon-like peptide-1 secretion increased, whereas FFA concentrations were unchanged. Conclusion: TBA and FGF19 do not explain acute changes in glucose metabolism, cholesterol fractions, and gut hormone secretion after RYGB.

U2 - 10.1210/jc.2014-1658

DO - 10.1210/jc.2014-1658

M3 - Journal article

C2 - 25536209

VL - 100

SP - E396-406

JO - Journal of Clinical Endocrinology and Metabolism

JF - Journal of Clinical Endocrinology and Metabolism

SN - 0021-972X

IS - 3

ER -

ID: 132046811