The Effect of SGLT2 Inhibitors on Cognitive Functions and BDNF Levels in Patients With Type 2 Diabetes

April 16, 2022 updated by: Ayse N Erbakan, Goztepe Training and Research Hospital

The Effect of SGLT2 Inhibitors on Cognitive Functions and a Neuroinflammatory Biomarker, Brain-Derived Neurotrophic Factor Levels in Patients With Type 2 Diabetes

Cognitive impairment is a common complication in diabetes for various reasons. Although glycemic control improves cognitive impairment, different antidiabetic medications' effects on cognitive functions are still being investigated. Brain-derived neurotrophic factor (BDNF) is a neuroinflammatory marker and a member of the neurotrophin family with growth factor properties. BDNF levels have been shown to decrease in mild cognitive dysfunction or in late-onset Alzheimer's disease. Our aim is to examine the effect of SGLT2 inhibitor use on cognitive functions and BDNF levels.

Study Overview

Detailed Description

Type 2 diabetes is a complex metabolic disorder that can cause serious damage to various organs. Impairment in cognitive functions is one of the common complications in patients with diabetes. Impairment in cognitive functions and significant dementia were found to be approximately 1.5 times more common in individuals with diabetes than individuals without diabetes. In particular, inadequate glycemic control, the frequency of hypoglycemia, vascular diseases, insulin resistance, inflammatory cytokines and oxidative stress stand out as possible causes. Brain-derived neurotrophic factor (BDNF) is a member of the neurotrophin family with growth factor properties. BDNF plays a critical role in cell differentiation, migration, and survivable synaptic plasticity of neurons. BDNF also has an important role in learning and memory processes through synapses in the hippocampus. BDNF levels have been shown to decrease in mild cognitive dysfunction or in late-onset Alzheimer's disease. In animal experiments, it has been observed that BDNF values increase with the use of metformin in Parkinson's disease. Similar results were obtained with vildagliptin, alogliptin, rosiglitazone, and exendin-4 in animal experiments.

The effects of drugs used in the treatment of diabetes on protecting or improving cognitive functions have been studied for a long time. Most of these studies are at the preclinical level. In previous studies with Glucagon-Like Peptide 1 (GLP-1) agonists and dipeptidyl peptidase 4 (DPP-4) inhibitors, there are data that both glycemia and incretins improve cognitive functions with their effects on brain structure. Similar positive results are seen for thiazolidinediones. While hyperglycemia control leads to positive results in insulin and sulfonylurea group drugs, the frequency of hypoglycemia can have a negative effect. There is not enough data on SGLT2 inhibitors.

Studies with SGLT2 inhibitors have shown a decrease in HbA1c values, weight loss, and a decrease in both systolic and diastolic blood pressure. Encouraging results have been obtained with SGLT2 inhibitors in both cardiac and renal outcomes, with heart failure in the foreground. As a result of these data, they are recommended as drugs that should be used in the foreground following metformin, especially in diabetic patients with cardiac and renal diseases. Animal studies with empagliflozin and canagliflozin show that both agents reduce cognitive impairment.

Our aim is to examine the effect of SGLT2 inhibitor use on cognitive functions and BDNF, one of the neuroinflammatory markers.

Study Type

Observational

Enrollment (Actual)

25

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

      • Istanbul, Turkey
        • Istanbul Medeniyet University Goztepe Research and TRaining Hospital

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

60 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

patients who refer to a diabetes outpatients clinics to an university hospital

Description

Inclusion Criteria:

  • giving consent
  • being 60 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:

  • 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

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
Patients with type 2 diabetes-SGLT2 inh
patients with type 2 diabetes who were recently prescribed an SGLT2 inhibitor
Before starting their newly prescribed medication, we will apply MOCA and repeat it at the end of the trial.
Before starting their newly prescribed medication, we will apply MOCA and repeat it at the end of the trial.
Before starting their newly prescribed medication, we will apply MOCA and repeat it at the end of the trial.
Before starting their newly prescribed medication, we will apply MOCA and repeat it at the end of the trial.
Patients with type 2 diabetes-control
patients with type 2 diabetes who were recently prescribed a pre-defined antidiabetic medication other than SGLT2 inhibitors
Before starting their newly prescribed medication, we will apply MOCA and repeat it at the end of the trial.
Before starting their newly prescribed medication, we will apply MOCA and repeat it at the end of the trial.
Before starting their newly prescribed medication, we will apply MOCA and repeat it at the end of the trial.
Before starting their newly prescribed medication, we will apply MOCA and repeat it at the end of the trial.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Cognitive functions
Time Frame: Six months
We will observe the effects of SGLT2 inhibitors and other oral antidiabetic agents on cognitive functions in type 2 diabetic patients using Montreal Cognitive Assessment (MOCA) test
Six months
BDNF concentrations
Time Frame: Six months
We will observe the effects of SGLT2 inhibitors and other oral antidiabetic agents on BDNF levels in type 2 diabetic patients. We will also assess whether there is an association between cognitive functions and BDNF concentrations in these prespecified groups of patients.
Six months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
36 item Short Form Survey (SF-36)
Time Frame: Six months
We will observe the effects of SGLT2 inhibitors and other oral antidiabetic agents on quality of life of life in type 2 diabetic patients using SF-36 survey.
Six months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Ayşe N Erbakan, MD, Istanbul Medeniyet University Goztepe Research and TRaining Hospital
  • Study Chair: Mehmet Sargın, Prof, Istanbul Medeniyet University
  • Study Chair: Nazmiye Özbilgin, Prof, University of Health Sciences Siyami Ersek TCS Training and Research Hospital
  • Study Chair: Aytekin Oğuz, Prof, Istanbul Medeniyet University

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 1, 2021

Primary Completion (Actual)

November 30, 2021

Study Completion (Actual)

November 30, 2021

Study Registration Dates

First Submitted

October 17, 2021

First Submitted That Met QC Criteria

April 16, 2022

First Posted (Actual)

April 22, 2022

Study Record Updates

Last Update Posted (Actual)

April 22, 2022

Last Update Submitted That Met QC Criteria

April 16, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Drug and device information, study documents

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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