Weight-dependent and weight-independent effects of dulaglutide on blood pressure in patients with type 2 diabetes

被引:9
作者
Ferdinand, Keith C. [1 ]
Dunn, Julia [2 ]
Nicolay, Claudia [2 ]
Sam, Flora [2 ]
Blue, Emily K. [2 ]
Wang, Hui [3 ]
机构
[1] Tulane Univ, Sch Med, New Orleans, LA 70118 USA
[2] Eli Lilly & Co, Indianapolis, IN USA
[3] TechData Serv Co, King Of Prussia, PA USA
关键词
Blood pressure; Diabetes; Dulaglutide; Glucagon-like peptide-1; Hypertension; Weight; GLUCAGON-LIKE PEPTIDE-1; PULSE PRESSURE; CATECHOLAMINE NEURONS; RECEPTOR AGONISTS; HYPERTENSION; EFFICACY; COMPLICATIONS; METAANALYSIS; LIRAGLUTIDE; ASSOCIATION;
D O I
10.1186/s12933-023-01775-x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Patients with type 2 diabetes (T2D) treated with glucagon-like peptide-1 receptor agonists may experience reductions in weight and blood pressure. The primary objective of the current study was to determine the weight-dependent and weight-independent effects of similar to 6 months treatment with dulaglutide 1.5 mg treatment in participants with T2D. Methods Mediation analysis was conducted for five randomized, placebo-controlled trials of dulaglutide 1.5 mg to estimate the weight-dependent (i.e., mediated by weight) and weight-independent effects from dulaglutide vs. placebo on change from baseline for systolic blood pressure (SBP), diastolic blood pressure (DBP), and pulse pressure. A random-effects meta-analysis combined these results. To investigate a dose response between dulaglutide 4.5 mg and placebo, mediation analysis was first conducted in AWARD-11 to estimate the weight-dependent and weight-independent effects of dulaglutide 4.5 mg vs. 1.5 mg, followed by an indirect comparison with the mediation result for dulaglutide 1.5 mg vs. placebo. Results Baseline characteristics were largely similar across the trials. In the mediation meta-analysis of placebo-controlled trials, the total treatment effect of dulaglutide 1.5 mg after placebo-adjustment on SBP was - 2.6 mmHg (95% CI - 3.8, - 1.5; p < 0.001) and was attributed to both a weight-dependent effect (- 0.9 mmHg; 95% CI: - 1.4, - 0.5; p < 0.001) and a weight-independent effect (- 1.5 mmHg; 95% CI: - 2.6, - 0.3; p = 0.01), accounting for 36% and 64% of the total effect, respectively. For pulse pressure, the total treatment effect of dulaglutide (- 2.5 mmHg; 95% CI: - 3.5, - 1.5; p < 0.001) was 14% weight-dependent and 86% weight-independent. For DBP there was limited impact of dulaglutide treatment, with only a small weight-mediated effect. Dulaglutide 4.5 mg demonstrated an effect on reduction in SBP and pulse pressure beyond that of dulaglutide 1.5 mg which was primarily weight mediated. Conclusions Dulaglutide 1.5 mg reduced SBP and pulse pressure in people with T2D across the placebo-controlled trials in the AWARD program. While up to one third of the effect of dulaglutide 1.5 mg on SBP and pulse pressure was due to weight reduction, the majority was independent of weight. A greater understanding of the pleotropic effects of GLP-1 RA that contribute to reduction in blood pressure could support developing future approaches for treating hypertension.
引用
收藏
页数:11
相关论文
共 46 条
[1]   Association of systolic blood pressure with macrovascular and microvascular complications of type 2 diabetes (UKPDS 36): prospective observational study [J].
Adler, AI ;
Stratton, IM ;
Neil, HAW ;
Yudkin, JS ;
Matthews, DR ;
Cull, CA ;
Wright, AD ;
Turner, RC ;
Holman, RR .
BMJ-BRITISH MEDICAL JOURNAL, 2000, 321 (7258) :412-419
[2]   Achievement of Goals in U.S. Diabetes Care, 1999-2010 [J].
Ali, Mohammed K. ;
Bullard, Kai McKeever ;
Saaddine, Jinan B. ;
Cowie, Catherine C. ;
Imperatore, Giuseppina ;
Gregg, Edward W. .
NEW ENGLAND JOURNAL OF MEDICINE, 2013, 368 (17) :1613-1624
[3]   Prevalence and incidence of microvascular and macrovascular complications over 15 years among patients with incident type 2 diabetes [J].
An, Jaejin ;
Nichols, Gregory A. ;
Qian, Lei ;
Munis, Mercedes A. ;
Harrison, Teresa N. ;
Li, Zhuoxin ;
Wei, Rong ;
Weiss, Tracey ;
Rajpathak, Swapnil ;
Reynolds, Kristi .
BMJ OPEN DIABETES RESEARCH & CARE, 2021, 9 (01)
[4]   = METFORMIN:NONGLYCEMIC EFFECTS AND POTENTIAL NOVEL INDICATIONS [J].
Anabtawi, Abeer ;
Miles, John M. .
ENDOCRINE PRACTICE, 2016, 22 (08) :999-1007
[5]   Blood pressure control in type 2 diabetes mellitus with arterial hypertension. The important ancillary role of SGLT2-inhibitors and GLP1-receptor agonists [J].
Berraa, C. ;
Manfrini, R. ;
Regazzolic, D. ;
Radaellia, M. G. ;
Disoteod, O. ;
Sommesee, C. ;
Fiorina, P. ;
Ambrosioi, G. ;
Folli, F. .
PHARMACOLOGICAL RESEARCH, 2020, 160
[6]   Effects of glucagon-like peptide-1, yohimbine, and nitrergic modulation on sympathetic and parasympathetic activity in humans [J].
Bharucha, Adil E. ;
Charkoudian, Nisha ;
Andrews, Christopher N. ;
Camilleri, Michael ;
Sletten, David ;
Zinsmeister, Alan R. ;
Low, Phillip A. .
AMERICAN JOURNAL OF PHYSIOLOGY-REGULATORY INTEGRATIVE AND COMPARATIVE PHYSIOLOGY, 2008, 295 (03) :R874-R880
[7]   Effect of dulaglutide 3.0 and 4.5 mg on weight in patients with type 2 diabetes: Exploratory analyses of AWARD-11 [J].
Bonora, Enzo ;
Frias, Juan P. ;
Tinahones, Francisco J. ;
Van, Joanna ;
Malik, Raleigh E. ;
Yu, Zhuoxin ;
Mody, Reema ;
Bethel, Angelyn ;
Kwan, Anita Y. M. ;
Cox, David A. .
DIABETES OBESITY & METABOLISM, 2021, 23 (10) :2242-2250
[8]   The results of direct and indirect treatment comparisons in meta-analysis of randomized controlled trials [J].
Bucher, HC ;
Guyatt, GH ;
Griffith, LE ;
Walter, SD .
JOURNAL OF CLINICAL EPIDEMIOLOGY, 1997, 50 (06) :683-691
[9]   Cardiovascular Risk Reduction With Liraglutide: An Exploratory Mediation Analysis of the LEADER Trial [J].
Buse, John B. ;
Bain, Stephen C. ;
Mann, Johannes F. E. ;
Nauck, Michael A. ;
Nissen, Steven E. ;
Pocock, Stuart ;
Poulter, Neil R. ;
Pratley, Richard E. ;
Linder, Martin ;
Monk Fries, Tea ;
Orsted, David D. ;
Zinman, Bernard .
DIABETES CARE, 2020, 43 (07) :1546-1552
[10]   2020 Expert Consensus Decision Pathway on Novel Therapies for Cardiovascular Risk Reduction in Patients With Type 2 Diabetes [J].
Das, Sandeep R. ;
Everett, Brendan M. ;
Birtcher, Kim K. ;
Brown, Jenifer M. ;
Januzzi, James L., Jr. ;
Kalyani, Rita R. ;
Kosiborod, Mikhail ;
Magwire, Melissa ;
Morris, Pamela B. ;
Neumiller, Joshua J. ;
Sperling, Laurence S. .
JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY, 2020, 76 (09) :1117-1145