Pleiotropic effects of liraglutide in patients with type 2 diabetes and moderate renal impairment: Individual effects of treatment

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Pleiotropic effects of liraglutide in patients with type 2 diabetes and moderate renal impairment : Individual effects of treatment. / Zobel, Emilie H.; von Scholten, Bernt J.; Goldman, Bryan; Persson, Frederik; Hansen, Tine W.; Rossing, Peter.

In: Diabetes, Obesity and Metabolism, Vol. 21, No. 5, 2019, p. 1261-1265.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Zobel, EH, von Scholten, BJ, Goldman, B, Persson, F, Hansen, TW & Rossing, P 2019, 'Pleiotropic effects of liraglutide in patients with type 2 diabetes and moderate renal impairment: Individual effects of treatment', Diabetes, Obesity and Metabolism, vol. 21, no. 5, pp. 1261-1265. https://doi.org/10.1111/dom.13638

APA

Zobel, E. H., von Scholten, B. J., Goldman, B., Persson, F., Hansen, T. W., & Rossing, P. (2019). Pleiotropic effects of liraglutide in patients with type 2 diabetes and moderate renal impairment: Individual effects of treatment. Diabetes, Obesity and Metabolism, 21(5), 1261-1265. https://doi.org/10.1111/dom.13638

Vancouver

Zobel EH, von Scholten BJ, Goldman B, Persson F, Hansen TW, Rossing P. Pleiotropic effects of liraglutide in patients with type 2 diabetes and moderate renal impairment: Individual effects of treatment. Diabetes, Obesity and Metabolism. 2019;21(5):1261-1265. https://doi.org/10.1111/dom.13638

Author

Zobel, Emilie H. ; von Scholten, Bernt J. ; Goldman, Bryan ; Persson, Frederik ; Hansen, Tine W. ; Rossing, Peter. / Pleiotropic effects of liraglutide in patients with type 2 diabetes and moderate renal impairment : Individual effects of treatment. In: Diabetes, Obesity and Metabolism. 2019 ; Vol. 21, No. 5. pp. 1261-1265.

Bibtex

@article{4ed9072ef6634623863adc9e10c5264f,
title = "Pleiotropic effects of liraglutide in patients with type 2 diabetes and moderate renal impairment: Individual effects of treatment",
abstract = " Liraglutide has pleiotropic effects favouring cardiovascular and renal risks. We investigated individual responses to liraglutide in six cardio-renal risk factors to examine whether responses in one risk factor are associated with changes in other risk factors (cross-dependency). We performed secondary analysis of the LIRA-RENAL trial (n = 279) in type 2 diabetes. HbA1c, body weight, systolic blood pressure (SBP) , low density lipoprotein (LDL)-cholesterol, urine albumin-to-creatinine ratio (UACR) and estimated glomerular filtration rate (eGFR) were measured at baseline and after 26 weeks of liraglutide/placebo treatment: “Good responders” had a change within the best quartile. In the liraglutide-treated group, good HbA1c responders showed similar changes in other risk factors analysed to low responders (P ≥ 0.17). Good body weight responders had a larger reduction in HbA1c than low body weight responders (−1.6 ± 0.94 vs. –1.0 ± 0.82%; P = 0.003), but similar changes in the other risk factors (P ≥ 0.11). Good and low responders in SBP, UACR, LDL-cholesterol or eGFR showed similar changes in other risk factors (P ≥ 0.07). Treatment response to liraglutide is largely individual; aside from an association between body weight and HbA1c reduction, there are no obvious cross-dependencies in risk factor response. ",
keywords = "diabetic nephropathy, liraglutide, type 2 diabetes",
author = "Zobel, {Emilie H.} and {von Scholten}, {Bernt J.} and Bryan Goldman and Frederik Persson and Hansen, {Tine W.} and Peter Rossing",
year = "2019",
doi = "10.1111/dom.13638",
language = "English",
volume = "21",
pages = "1261--1265",
journal = "Diabetes, Obesity and Metabolism",
issn = "1462-8902",
publisher = "Wiley-Blackwell",
number = "5",

}

RIS

TY - JOUR

T1 - Pleiotropic effects of liraglutide in patients with type 2 diabetes and moderate renal impairment

T2 - Individual effects of treatment

AU - Zobel, Emilie H.

AU - von Scholten, Bernt J.

AU - Goldman, Bryan

AU - Persson, Frederik

AU - Hansen, Tine W.

AU - Rossing, Peter

PY - 2019

Y1 - 2019

N2 - Liraglutide has pleiotropic effects favouring cardiovascular and renal risks. We investigated individual responses to liraglutide in six cardio-renal risk factors to examine whether responses in one risk factor are associated with changes in other risk factors (cross-dependency). We performed secondary analysis of the LIRA-RENAL trial (n = 279) in type 2 diabetes. HbA1c, body weight, systolic blood pressure (SBP) , low density lipoprotein (LDL)-cholesterol, urine albumin-to-creatinine ratio (UACR) and estimated glomerular filtration rate (eGFR) were measured at baseline and after 26 weeks of liraglutide/placebo treatment: “Good responders” had a change within the best quartile. In the liraglutide-treated group, good HbA1c responders showed similar changes in other risk factors analysed to low responders (P ≥ 0.17). Good body weight responders had a larger reduction in HbA1c than low body weight responders (−1.6 ± 0.94 vs. –1.0 ± 0.82%; P = 0.003), but similar changes in the other risk factors (P ≥ 0.11). Good and low responders in SBP, UACR, LDL-cholesterol or eGFR showed similar changes in other risk factors (P ≥ 0.07). Treatment response to liraglutide is largely individual; aside from an association between body weight and HbA1c reduction, there are no obvious cross-dependencies in risk factor response.

AB - Liraglutide has pleiotropic effects favouring cardiovascular and renal risks. We investigated individual responses to liraglutide in six cardio-renal risk factors to examine whether responses in one risk factor are associated with changes in other risk factors (cross-dependency). We performed secondary analysis of the LIRA-RENAL trial (n = 279) in type 2 diabetes. HbA1c, body weight, systolic blood pressure (SBP) , low density lipoprotein (LDL)-cholesterol, urine albumin-to-creatinine ratio (UACR) and estimated glomerular filtration rate (eGFR) were measured at baseline and after 26 weeks of liraglutide/placebo treatment: “Good responders” had a change within the best quartile. In the liraglutide-treated group, good HbA1c responders showed similar changes in other risk factors analysed to low responders (P ≥ 0.17). Good body weight responders had a larger reduction in HbA1c than low body weight responders (−1.6 ± 0.94 vs. –1.0 ± 0.82%; P = 0.003), but similar changes in the other risk factors (P ≥ 0.11). Good and low responders in SBP, UACR, LDL-cholesterol or eGFR showed similar changes in other risk factors (P ≥ 0.07). Treatment response to liraglutide is largely individual; aside from an association between body weight and HbA1c reduction, there are no obvious cross-dependencies in risk factor response.

KW - diabetic nephropathy

KW - liraglutide

KW - type 2 diabetes

U2 - 10.1111/dom.13638

DO - 10.1111/dom.13638

M3 - Journal article

C2 - 30663196

AN - SCOPUS:85064196441

VL - 21

SP - 1261

EP - 1265

JO - Diabetes, Obesity and Metabolism

JF - Diabetes, Obesity and Metabolism

SN - 1462-8902

IS - 5

ER -

ID: 223516578