Clinical Trial Details
— Status: Terminated
Administrative data
NCT number |
NCT05341388 |
Other study ID # |
Cognitive-BDNF |
Secondary ID |
|
Status |
Terminated |
Phase |
|
First received |
|
Last updated |
|
Start date |
March 1, 2021 |
Est. completion date |
November 30, 2021 |
Study information
Verified date |
April 2022 |
Source |
Goztepe Training and Research Hospital |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
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.
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.