Hepato-renal Regulation of Water Conservation in Heart Failure Patients With SGLT-2 Inhibitor Treatment

Heart Failure Clinical Trial

— DAPA-Shuttle1  

Official title:

Hepato-renal Regulation of Water Conservation in Heart Failure Patients With SGLT-2 Inhibitor Treatment

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04080518
• Other study ID #: 2018/2414
• Status: Completed
• Phase: Phase 4
• Start date: November 11, 2019
• Est. completion date: November 10, 2021

Study information

• Verified date: April 2023
• Source: National Heart Centre Singapore
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to investigate the effects of Dapagliflozin (FORXIGA) 10mg (n=20) and placebo (n=20) on the renal concentration mechanism, mobilization of Na+ from tissue stores, and mobilization of muscle glycogen and fat, in patients heart failure NYHA classes I and II,with or w/o T2DM in a 4-week double-blind, placebo-controlled, randomized study with 2 treatment arms.

Description:

Sodium-glucose co-transporter-2 (SGLT-2) inhibitors are a new class of oral medications used for T2DM, which lower blood glucose levels by increasing renal sodium (Na+) and glucose excretion. However, their applications seem to go beyond glycemic control. Recent studies have shown that treatment with SGLT-2 inhibitors significantly improves cardiovascular outcome, with unprecedented reductions in cardiovascular mortality and heart failure hospitalizations. The underlying mechanism of this surprising effect is unclear.

Our hypothesis is that increased Na+ and glucose excretion induced by SGLT-2 inhibitors predisposes to water loss, to which the body responds by increasing urea production in an effort to prevent dehydration. Urea is accumulated in the renal medulla, where it provides the alternative osmotic driving force for water reabsorption. However, hepatic urea production is an energy-intense process, for which amino acids from skeletal muscle are the ideal fuel because they provide both the nitrogen and the energy needed for urea generation. Alanine is transported from muscle to the liver, where it serves as a substrate for new pyruvate generation, which can then be used for the urea cycle, glucose production or ketone body generation. In the same time, as increasing amounts of alanine are shuttled to the liver, muscle will deplete its glucose reservoirs and reprioritize fuel utilization in favour of fatty acids.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 40
• Est. completion date: November 10, 2021
• Est. primary completion date: November 10, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 21 Years and older

Eligibility

Inclusion Criteria:

1. Diagnosis of heart failure NYHA stage I or II - as shown by their medical records

2. Stable anti-hypertensive treatment (>4 weeks)

3. Male and female patients older than 21 years

4. Willingness to participate and ability to provide informed consent

5. Willingness to use effective birth control if of childbearing potential. Any kind of contraception method will be allowed for the period of the study

Exclusion Criteria:

1. Patients with congestive heart failure NYHA stages I (LVEF >40%) without type 2 diabetes mellitus.

2. Patients with congestive heart failure NYHA stages III and IV

3. Prior serious hypersensitivity reaction to Dapagliflozin (Forxiga®)

4. Treatment with any SGLT-2 inhibitor or combined SGLT-1 and 2 inhibitors within 1 week prior to Visit 1 or during screening period until Visit 1

5. Pregnant and breast-feeding women

6. Diagnosis of type 1 diabetes mellitus

7. Patients with type 2 diabetes mellitus with HbA1C > 10.5% from most recent medical records or antidiabetic therapies other than metformin, sulfonylureas or gliptins at screening.

8. Patients with type 2 diabetes mellitus whose antidiabetic treatment (metformin and/or sulfonylureas and/or gliptins) has been changed or unstable within 6 weeks prior to Visit 1

9. . Unstable or rapidly progressing renal disease

10. Chronic cystitis and recurrent urinary tract infections

11. Impaired renal function with eGFR<45 ml/min/1.73m2 or proteinuria > 0.5 g/24h

12. Severe hepatic impairment (Child-Pugh class C)

13. Any major cardiovascular event/vascular disease within 3 months prior to enrolment, as assessed by the investigator

14. Severe edema (as judged by the investigator)

15. Active cancer, history of bladder cancer

16. HIV infection

17. Patients who have received an organ or bone marrow transplant

18. Patients who have had major surgery in the past 3 months

19. Patients who have severe comorbid conditions likely to compromise survival or study participation

20. Patients who exhibit noticeable anxiety and/or claustrophobia or who exhibit severe vertigo when they are moved into the MRI scanner

21. Patients with exclusion criteria for the MRI, such as:

1. implanted devices (surgical clips, heart pacemakers or defibrillators, cochlear implants)

2. iron-based tattoos

3. any other pieces of metal or devices that are not MR-Safe anywhere in the body

22. Unwillingness or other inability to cooperate

Related Conditions & MeSH terms

• Diabetes Mellitus
• Heart Failure

Intervention

Drug:
• Dapagliflozin 10 MG [Forxiga]
24 Hour Urine Collection, Sodium (23Na) MRI and Magnetic Resonance (MR) spectroscopy scan, Blood collection for metabolomic and osmolyte analysis

Locations

Country	Name	City	State
Singapore	National Heart Centre Singapore	Singapore

Sponsors (2)

Lead Sponsor	Collaborator
National Heart Centre Singapore	Duke-NUS Medical School (Singapore)

Country where clinical trial is conducted

Singapore, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	To demonstrate that SGLT-2 inhibition induces urea-dominated renal water conservation within the renal concentration mechanism. ( Change from baseline in urinary osmolyte concentration	Change from baseline in urinary osmolyte concentration; Change from baseline in Na+; Change from baseline in urea concentration	Baseline, Day 3, and Day 28.
Secondary	To demonstrate that SGLT-2 inhibition increases plasma co-peptin levels in an effort to prevent dehydration	The investigators will study the changes in plasma co-peptin levels shortly after SGLT-2 inhibitor treatment initiation.	Baseline, Day 3 and Day 28
Secondary	Analysis of skin and muscle Na+ content	The investigators will compare the changes in skin and muscle Na+ content shortly after SGLT-2 inhibitor treatment initiation. Tissue Na+ content will be measured non-invasively with 23NaMRI, using a Siemens 3T MRI scanner system.	Baseline, Day 3, and Day 28.
Secondary	Analysis of glycogen and fat content in skeletal muscle and liver	The investigators will compare changes from baseline in muscle and liver lipid content (measured with 1HMRS) and assess glycogen content by metabolomic analysis in patients treated with dapagliflozin versus those receiving placebo	Baseline, Day 3 and Day 28