One-year follow-up on liraglutide treatment for prediabetes and overweight/obesity in clozapine- or olanzapine-treated patients

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Standard

One-year follow-up on liraglutide treatment for prediabetes and overweight/obesity in clozapine- or olanzapine-treated patients. / Svensson, C. K.; Larsen, J. R.; Vedtofte, L.; Jakobsen, M. S.L.; Jespersen, H. R.; Jakobsen, M. I.; Koyuncu, K.; Schjerning, O.; Nielsen, J.; Ekstrøm, C. T.; Correll, C. U.; Vilsbøll, T.; Fink-Jensen, A.

I: Acta Psychiatrica Scandinavica, Bind 139, Nr. 1, 2019, s. 26-36.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Svensson, CK, Larsen, JR, Vedtofte, L, Jakobsen, MSL, Jespersen, HR, Jakobsen, MI, Koyuncu, K, Schjerning, O, Nielsen, J, Ekstrøm, CT, Correll, CU, Vilsbøll, T & Fink-Jensen, A 2019, 'One-year follow-up on liraglutide treatment for prediabetes and overweight/obesity in clozapine- or olanzapine-treated patients', Acta Psychiatrica Scandinavica, bind 139, nr. 1, s. 26-36. https://doi.org/10.1111/acps.12982

APA

Svensson, C. K., Larsen, J. R., Vedtofte, L., Jakobsen, M. S. L., Jespersen, H. R., Jakobsen, M. I., Koyuncu, K., Schjerning, O., Nielsen, J., Ekstrøm, C. T., Correll, C. U., Vilsbøll, T., & Fink-Jensen, A. (2019). One-year follow-up on liraglutide treatment for prediabetes and overweight/obesity in clozapine- or olanzapine-treated patients. Acta Psychiatrica Scandinavica, 139(1), 26-36. https://doi.org/10.1111/acps.12982

Vancouver

Svensson CK, Larsen JR, Vedtofte L, Jakobsen MSL, Jespersen HR, Jakobsen MI o.a. One-year follow-up on liraglutide treatment for prediabetes and overweight/obesity in clozapine- or olanzapine-treated patients. Acta Psychiatrica Scandinavica. 2019;139(1):26-36. https://doi.org/10.1111/acps.12982

Author

Svensson, C. K. ; Larsen, J. R. ; Vedtofte, L. ; Jakobsen, M. S.L. ; Jespersen, H. R. ; Jakobsen, M. I. ; Koyuncu, K. ; Schjerning, O. ; Nielsen, J. ; Ekstrøm, C. T. ; Correll, C. U. ; Vilsbøll, T. ; Fink-Jensen, A. / One-year follow-up on liraglutide treatment for prediabetes and overweight/obesity in clozapine- or olanzapine-treated patients. I: Acta Psychiatrica Scandinavica. 2019 ; Bind 139, Nr. 1. s. 26-36.

Bibtex

@article{10c250b9483640f1bf390043dcd5f005,
title = "One-year follow-up on liraglutide treatment for prediabetes and overweight/obesity in clozapine- or olanzapine-treated patients",
abstract = "Objective: Treatment with most antipsychotics is associated with an increased risk of weight gain and metabolic disturbances. In a randomized trial, we previously demonstrated that 16 weeks of glucagon-like peptide-1 receptor agonist liraglutide treatment vs. placebo significantly reduced glucometabolic disturbances and body weight in prediabetic, overweight/obese schizophrenia-spectrum disorder patients treated with clozapine or olanzapine. The aim of this study was to investigate whether the beneficial effects of the 16-week intervention were sustained beyond the intervention period. Method: One year after completion of the intervention, we investigated changes in body weight, fasting glucose, glycated hemoglobin, C-peptide, and lipids comparing 1-year follow-up levels to end of treatment (week 16) and baseline (week 0) levels. Results: From end of treatment to the 1-year follow-up, body weight had increased in the liraglutide-treated group. However, compared to baseline levels, the placebo-subtracted body weight loss remained significantly reduced (−3.8 kg, 95% CI: −7.3 to −0.2, P = 0.04). Fasting glucose, glycated hemoglobin, C-peptide, and lipids had each returned to baseline levels 1 year after stopping liraglutide. Conclusion: The body weight reduction during 16 weeks of liraglutide treatment was partially sustained 1 year after the intervention was completed. However, the improvements in other metabolic parameters returned to baseline levels.",
keywords = "clozapine, GLP-1, liraglutide, olanzapine, overweight, prediabetes, schizophrenia",
author = "Svensson, {C. K.} and Larsen, {J. R.} and L. Vedtofte and Jakobsen, {M. S.L.} and Jespersen, {H. R.} and Jakobsen, {M. I.} and K. Koyuncu and O. Schjerning and J. Nielsen and Ekstr{\o}m, {C. T.} and Correll, {C. U.} and T. Vilsb{\o}ll and A. Fink-Jensen",
year = "2019",
doi = "10.1111/acps.12982",
language = "English",
volume = "139",
pages = "26--36",
journal = "Acta Psychiatrica Scandinavica",
issn = "0001-690X",
publisher = "Wiley",
number = "1",

}

RIS

TY - JOUR

T1 - One-year follow-up on liraglutide treatment for prediabetes and overweight/obesity in clozapine- or olanzapine-treated patients

AU - Svensson, C. K.

AU - Larsen, J. R.

AU - Vedtofte, L.

AU - Jakobsen, M. S.L.

AU - Jespersen, H. R.

AU - Jakobsen, M. I.

AU - Koyuncu, K.

AU - Schjerning, O.

AU - Nielsen, J.

AU - Ekstrøm, C. T.

AU - Correll, C. U.

AU - Vilsbøll, T.

AU - Fink-Jensen, A.

PY - 2019

Y1 - 2019

N2 - Objective: Treatment with most antipsychotics is associated with an increased risk of weight gain and metabolic disturbances. In a randomized trial, we previously demonstrated that 16 weeks of glucagon-like peptide-1 receptor agonist liraglutide treatment vs. placebo significantly reduced glucometabolic disturbances and body weight in prediabetic, overweight/obese schizophrenia-spectrum disorder patients treated with clozapine or olanzapine. The aim of this study was to investigate whether the beneficial effects of the 16-week intervention were sustained beyond the intervention period. Method: One year after completion of the intervention, we investigated changes in body weight, fasting glucose, glycated hemoglobin, C-peptide, and lipids comparing 1-year follow-up levels to end of treatment (week 16) and baseline (week 0) levels. Results: From end of treatment to the 1-year follow-up, body weight had increased in the liraglutide-treated group. However, compared to baseline levels, the placebo-subtracted body weight loss remained significantly reduced (−3.8 kg, 95% CI: −7.3 to −0.2, P = 0.04). Fasting glucose, glycated hemoglobin, C-peptide, and lipids had each returned to baseline levels 1 year after stopping liraglutide. Conclusion: The body weight reduction during 16 weeks of liraglutide treatment was partially sustained 1 year after the intervention was completed. However, the improvements in other metabolic parameters returned to baseline levels.

AB - Objective: Treatment with most antipsychotics is associated with an increased risk of weight gain and metabolic disturbances. In a randomized trial, we previously demonstrated that 16 weeks of glucagon-like peptide-1 receptor agonist liraglutide treatment vs. placebo significantly reduced glucometabolic disturbances and body weight in prediabetic, overweight/obese schizophrenia-spectrum disorder patients treated with clozapine or olanzapine. The aim of this study was to investigate whether the beneficial effects of the 16-week intervention were sustained beyond the intervention period. Method: One year after completion of the intervention, we investigated changes in body weight, fasting glucose, glycated hemoglobin, C-peptide, and lipids comparing 1-year follow-up levels to end of treatment (week 16) and baseline (week 0) levels. Results: From end of treatment to the 1-year follow-up, body weight had increased in the liraglutide-treated group. However, compared to baseline levels, the placebo-subtracted body weight loss remained significantly reduced (−3.8 kg, 95% CI: −7.3 to −0.2, P = 0.04). Fasting glucose, glycated hemoglobin, C-peptide, and lipids had each returned to baseline levels 1 year after stopping liraglutide. Conclusion: The body weight reduction during 16 weeks of liraglutide treatment was partially sustained 1 year after the intervention was completed. However, the improvements in other metabolic parameters returned to baseline levels.

KW - clozapine

KW - GLP-1

KW - liraglutide

KW - olanzapine

KW - overweight

KW - prediabetes

KW - schizophrenia

U2 - 10.1111/acps.12982

DO - 10.1111/acps.12982

M3 - Journal article

C2 - 30374965

AN - SCOPUS:85057534658

VL - 139

SP - 26

EP - 36

JO - Acta Psychiatrica Scandinavica

JF - Acta Psychiatrica Scandinavica

SN - 0001-690X

IS - 1

ER -

ID: 210293306