The Effect of SGLT2 Inhibitors on Heart Rate Variability and BDNF Levels in Patients With Type 2 Diabetes

Sponsor
Goztepe Training and Research Hospital (Other)
Overall Status
Recruiting
CT.gov ID
NCT05164523
Collaborator
(none)
60
1
19
3.2

Study Details

Study Description

Brief Summary

Cardiac autonomic neuropathy (CAN) in diabetic patients is an indicator of autonomic nervous system dysfunction and is an important marker for cardiovascular events. Very promising results have been obtained with SGLT2 inhibitors in both cardiac and renal outcomes. The aim is to examine the effects of SGLT2 inhibitor use on cardiac autonomic neuropathy, heart rate variability, sympathetic and parasympathetic nervous system parameters, and their relationship with BDNF levels, one of the neuroinflammatory markers.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: 24-hour rhythm Holter
  • Diagnostic Test: 36 item Short Form Survey (SF-36)

Detailed Description

Cardiac autonomic neuropathy (CAN) in diabetic patients is an indicator of autonomic nervous system dysfunction and is an important marker for cardiovascular events. Five-year mortality rates of diabetic patients with CAN are significantly higher than those without. Although there are various methods, primarily scintigraphic and pharmacological tests, to evaluate CAN, the practical use of these methods remains limited. In recent years, heart rate recovery (HRR) and heart rate variability (HRV) have been increasingly used as simple, inexpensive, and non-invasive methods to evaluate the status of heart sympathetic and vagus nerve functions. Values obtained as a result of 24-hour rhythm Holter provide the measurement of sympathetic and parasympathetic activity. While a significant relationship was observed between blood glucose levels and HRV in previous studies, no relationship was found between HbA1c levels and HRV.

Brain-derived neurotrophic factor (BDNF) is a member of the neurotrophin family with growth factor properties. Studies with SGLT2 inhibitors have shown a decrease in HbA1c values, weight loss, and a decrease in both systolic and diastolic blood pressure. Very promising results have been obtained with SGLT2 inhibitors in both cardiac and renal outcomes. As a result of these data, these medications are recommended as drugs that should be used in the foreground following metformin, especially in diabetic patients with cardiac and renal diseases. In the study of Shimuz et al. in which the effects of empagliflozin and placebo on heart rate variability were compared in patients with acute myocardial infarction, HRV improved significantly with the use of empagliflozin in the early period. A study examining the effects of empagliflozin use on HRV in patients with type 2 diabetes is still ongoing. Apart from these 2 studies, no study was found in the literature.

The aim of this study is to examine the effects of SGLT2 inhibitor use on cardiac autonomic neuropathy, heart rate variability, sympathetic and parasympathetic nervous system parameters, and their relationship with BDNF levels, one of the neuroinflammatory markers.

Study Design

Study Type:
Observational
Anticipated Enrollment :
60 participants
Observational Model:
Case-Control
Time Perspective:
Prospective
Official Title:
The Effect of SGLT2 Inhibitors on Heart Rate Variability, Sympathetic and Parasympathetic Activity and a Neuroinflammatory Biomarker, Brain-Derived Neurotrophic Factor Levels in Patients With Type 2 Diabetes
Actual Study Start Date :
Mar 1, 2021
Anticipated Primary Completion Date :
Sep 1, 2022
Anticipated Study Completion Date :
Sep 30, 2022

Arms and Interventions

Arm Intervention/Treatment
Patients with type 2 diabetes treated with SGLT2 inhibitors

metformin using patients with type 2 diabetes who were recently prescribed an SGLT2 inhibitor

Diagnostic Test: 24-hour rhythm Holter
Before starting their newly prescribed medication, the investigators will apply 24-hour rhythm Holter and repeat it at the end of the trial.

Diagnostic Test: 36 item Short Form Survey (SF-36)
Before starting their newly prescribed medication, the investigators will apply SF-36 survey and repeat it at the end of the trial.
Other Names:
  • SF-36
  • Patients with type 2 diabetes treated with other oral agents

    metformin using patients with type 2 diabetes who were recently prescribed a pre-defined antidiabetic medication other than SGLT2 inhibitors

    Diagnostic Test: 24-hour rhythm Holter
    Before starting their newly prescribed medication, the investigators will apply 24-hour rhythm Holter and repeat it at the end of the trial.

    Diagnostic Test: 36 item Short Form Survey (SF-36)
    Before starting their newly prescribed medication, the investigators will apply SF-36 survey and repeat it at the end of the trial.
    Other Names:
  • SF-36
  • Outcome Measures

    Primary Outcome Measures

    1. Heart rate variability parameters [Six months]

      The investigators will evaluate the effects of SGLT2 inhibitor use on heart rate variability derived from 24-hour rhythm Holter compared with other antidiabetic medications.

    2. BDNF concentrations [Six months]

      The investigators will observe the effects of SGLT2 inhibitors and other oral antidiabetic agents on BDNF levels in type 2 diabetic patients.

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    30 Years to 80 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • giving consent

    • being 30 years old or older

    • HbA1c concentrations between 6.5% and 8%

    • using metformin as a single agent for at least 3 months

    • diabetes age <10 years

    Exclusion Criteria: existence of one of the listed conditions:
    • having uncontrolled hypothyroidism, hyperthyroidism, or other diseases that may affect cognitive functions

    • ketoacidosis or coma

    • cerebrovascular disease or psychiatric disorder

    • mental retardation, psychosis, dementia, brain trauma, epilepsy and other cerebral diseases

    • alcohol or other substance abuse

    • hearing loss

    • Presence of diseases that will affect cognitive function such as chronic inflammatory diseases and respiratory system diseases

    • chronic kidney failure (GFR <45)

    • sleep apnea syndrome

    • malignancy

    • using a sulfonylurea or glinide

    • using beta blocker or non-dihydropyridine group calcium antagonists

    • diabetic autonomous neuropathy

    • atrial fibrillation

    • an acute coronary event within the last 3 months

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Istanbul Medeniyet University Goztepe Research and Training Hospital Istanbul Turkey

    Sponsors and Collaborators

    • Goztepe Training and Research Hospital

    Investigators

    • Principal Investigator: Ayse N Erbakan, MD, Istanbul Medeniyet University Goztepe Research and TRaining Hospital

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Ayse N Erbakan, Principal Investigator, Goztepe Training and Research Hospital
    ClinicalTrials.gov Identifier:
    NCT05164523
    Other Study ID Numbers:
    • Heart Rate Variability-BDNF
    First Posted:
    Dec 20, 2021
    Last Update Posted:
    Dec 20, 2021
    Last Verified:
    Dec 1, 2021
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Ayse N Erbakan, Principal Investigator, Goztepe Training and Research Hospital
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 20, 2021