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Supplementary Table 1. Baseline Patient Characteristics Normally distributed data are presented as mean (±SD), data that were not of a normal distribution are presented as median (ICR). The baseline characteristics were assessed at the screening visit, and 24-Hr urine and blood pressure data during the Baseline Test Period, n=18 (except for 24-Hr blood pressure measurements where n=17)). Abbreviations: ACE, angiotensin converting enzyme; ARBs, angiotensin II receptor blockers; bpm, beats/min; cm, centimeters; egfr, estimated glomerular filtration rate; ICR, interquartile range; Kg, kilograms; m, meters; mg, milligrams; mmhg, millimeters of mercury; MI, myocardial infarction; ml, millilitres; mmol, millimoles; OHA, oral hypoglycemic agent; μmol, micromoles; yrs, years.

Supplementary Table 2. The effect of 21 day liraglutide treatment on metabolic parameters and serum biochemistry compared to cross-over treatment with placebo Treatment group means are presented as mean ± SD, and the within-subject difference (change from Day 21-Day1) compared to cross-over treatment with placebo is presented as the LSMD ± SE. Abbreviations: ANG II, angiotensin II; CRP, c-reactive protein, egfr, estimated glomerular filtration ratehba1c, glycosylated haemoglobin A1c; HDL, high-density lipoprotein, IU, international units; LDL, low-density lipoprotein, and LSMD, least squares mean difference; mg/l, milligrams per litre; mmol/l, millimoles per litre; SE, standard error, SD, standard deviation; TSH, thyroid stimulating hormone.

Supplementary Table 3. The effect of 21 day liraglutide treatment on anthropometric and hemodynamic parameters measured in the office at clinic visits compared to cross-over treatment with placebo Treatment group means are presented as mean ± SD, and the within-subject difference (change from Day 21-Day1) compared to cross-over treatment with placebo is presented as the LSMD ± SE. Abbreviations: BMI, body mass index; bpm, beats per minute; cm, centimeters; DBP, diastolic blood pressure; HR, heart rate; Hr, hour, Kg, kilograms; MAP, mean arterial pressure; mmhg, millimeters of mercury; SBP, systolic blood pressure, SD, standard deviation; SE, standard error.

Supplementary Table 4. Adverse Events Data presented as absolute numbers and percentages are provided in brackets. Included are each type of AE reported during treatment with either placebo group or with liraglutide for all 20 subjects who participated in the research study. Abbreviations: AE, Adverse Event; GI, gastrointestinal.

Supplementary Figure 1A. Study Design and Timeline 1A) Patients entered the study during the Baseline Test Period, which occurred -7 to -1 days prior to Treatment Period 1. During the Baseline Test Period, patients completed a 24-Hr ABPM and a 24-Hr urine collection. Patients then entered Treatment Period 1 on Day 1 and presented to clinic for Clinic Visit #1. At Clinic Visit #1, office BP and HR was measured (Time = 0hrs) by an automated oscillometric device, and a venous canula was placed to allow access for blood sampling. Patients received their first dose of study drug at a dose of 0.6 mg sc which they continued daily (denoted by the dashed lines). On Day 8, the daily dose of study drug was increased, and was titrated weekly (Day 8 and Day 15) to a final dose of 1.8 mg as indicated. After study drug administration, blood was sampled hourly for 4 hours (2b). After 21 days of treatment, patients returned for Clinic Visit #2 (all clinic visits identical), and then entered the 21 day Treatment Washout Period. On Day 42, patients entered Treatment Period 2, where they crossed over to receive reciprocal treatment to Treatment Period 1. Patients received their first dose of study drug at Clinic Visit #3 and continued daily administration and weekly dose titration (occurring on Day 49, and Day 56) for 21 days until Clinic Visit#4 which marked the end of Treatment Period 2 and the end of the study. Abbreviations: ABPM, ambulatory blood pressure monitoring; ANP, atrial natriuretic peptide; BP, blood pressure; hrs, hours; Hr, hour, HR, heart rate, mg, milligrams; sc, sub-cutaneous.

Supplementary Figure 1B. Experimental Study Protocol 1B) At all Clinic Visits, patients underwent blood sampling before (-5 minutes, 0) and hourly (1, 2, 3, 4 hours) after administration of study drug for measurement of baseline and dynamic changes in plasma ANP/Nt-proBNP, serum biochemistry and vasoactive hormone concentrations in response to study drug administration. Abbreviations: ANP, atrial natriuretic peptide; BP, blood pressure; HR, heart rate; Nt-proBNP, N- terminal pro-b-type natriuretic peptide.

Supplementary Figure 2. Patient Flow Diagram

Supplementary Figure 3. Effect of 1 day or 21 day treatment with liraglutide on cardiac natriuretic peptide concentrations compared to cross-over treatment with placebo. Blood was collected from subjects and plasma ANP levels were measured hourly following 1 day (3A) and following 21 days (3B) of treatment with liraglutide and with placebo. Presented are the mean plasma ANP (pg/ml) concentrations with 95% CI. Mean serum Nt-ProBNP concentrations were also measured following 1 day (3C) and following 21 days (3D) of treatment with liraglutide and with placebo. Presented are the mean serum Nt-ProBNP (pmol/l) concentrations with 95% CI. Treatment Doses: 1 day (0.6 mg), 21 day (1.8 mg). Abbreviations: ANP, atrial natriuretic peptide; BNP, b-type natriuretic peptide; CI, confidence interval; Nt-ProBNP, N-terminal probnp.

Supplementary Figure 4. The effect of 21 day liraglutide treatment on 24-Hr, daytime, and nighttime urinary albumin-tocreatinine ratio compared to cross-over treatment with placebo The effect of 21 day liraglutide treatment on 24-Hr, daytime, and nighttime urinary sodium excretion compared to cross-over treatment with placebo The mean (95% CI) 24-Hr, daytime, nighttime urinary albumin-to-creatinine ratio for the treatment groups (liraglutide, placebo) is presented in 4A. The within-subject change (LSMD) in the 24-Hr, daytime, nighttime urinary albumin-to-creatinine ratio from baseline for liraglutide compared to placebo (from baseline) are presented in 4B. For the Box plots and whiskers graph, horizontal line indicates the median change, and the box represents interquartile range for the change, and outliers are presented as single points. Nonparametric tests were used for comparison (Wilcoxon rank-sum); *, denotes the normal approximation for 2-sided p-value <0.05; ** denotes the normal approximation for 2-sided p-value <0.005 for liraglutide compared to placebo (baseline-subtracted). Abbreviations: ACR, albumin-to-creatinine ratio; CI, confidence interval, Hr, hour, LSMD, Least squares mean difference; mg, milligrams; mmol, millimoles.