Diabetes Mellitus Clinical Trial
Official title:
Effect of Sodium Glucose co Transporter 2 (SGLT2) Inhibition on Optical Coherence Tomography Angiography (OCT-A) Parameters in Diabetic Chronic Kidney Disease (CKD)
Diabetes mellitus is a major and growing problem worldwide with many known micro and macrovascular complications. According to International Diabetes Federation, there were 285 million adults diagnosed with diabetes in 2010 and expected to increase to 439 million adult in 2030. It is a leading cause of chronic kidney disease (CKD) followed by hypertension, glomerulonephritis, and cystic kidney disease. Renal impairment patients metabolize and excrete drugs differently from patients with normal renal function and hence only limited number of oral hypoglycemic agent (OHA) available for them. One of the choices is sodium glucose co-transporter-2 inhibitor (SGLT2i) which is now widely used. Apart from its nephroprotective advantage, it also has additional benefit on cardiovascular and renal function based on EMPA-REG OUTCOME trial. One of the examples of SGLT2i is Empagliflozin (JARDIANCE) tablet, which has FDA U.S. Approval in 2014. It acts by reduces renal reabsorption of filtered glucose and lowers the renal threshold for glucose, thus increases urinary glucose excretion. It can cause osmotic diuresis, which may lead to intravascular volume contraction. Apart from its additional cardiovascular and nephroprotective effect, SGLT2 inhibitor might have additional protective effect to the eye. Nowadays, optical coherence tomography angiography (OCT-A) has emerged as one of a non-invasive methods to study the microvasculature of the retina and choroid. Many studies had discussed regarding-pre clinical changes present on OCT-A in patients without clinical diabetic retinopathy. These pre-clinical changes includes capillary dropout, microaneurysm, neovascularization, venous beading and enlargement of fovea avascular zone. However, there are minimal data and publications on different type of diabetic CKD with OCT-A parameters in diabetic patients. The purpose of this study is to determine the effect of short term SGLT2 inhibition on OCT-A parameters (fovea avascular zone (FAZ) size, vessel density and perfusion density) in diabetic CKD.
This is a prospective, single-centred, open-labeled, randomized clinical trial conducted in
,University Kebangsaan Malaysia Medical Centre (UKMMC). This is also a Quasi-experimental
study and all patients from Endocrine, Nephrology and Ophthalmology Clinic in UKM Medical
Centre from November 2019 till November 2021 will be involved in this study. Patients who
fulfill the inclusion criteria will be included in this study. All eligible subjects will be
asked to sign an informed consent.
Participants will be randomized into two groups, diabetic patient with proteinuria and
diabetic patient without proteinuria. Participants will be interviewed on demographic data
(age, gender, race, blood pressure, Body Mass Index) will be taken. Urine sample and
peripheral blood (2-3ml) is collected from patients in sterile container (EDTA tube) and will
be sent for urine albumin creatinine ratio (ACR) and HbA1c test. The eye with best fundal and
signal view on OCT-A will be chosen or if both eyes similar, right eye will be chosen.
Pre-treatment tests fundus photo and OCT-A measurement will be taken at eye clinic after
dilating the pupils with 1% tropicamide and 2.5% phenylephrine hydrochloride. Fundus
examination is taken using a digital mydriatic retinal camera (Topcon Retinal Camera TRC-50DX
(type 1A), Tokyo Japan. OCT-A measurement is taken by using Cirrus HD-OCT, 2016 Carl Zeiss
Meditec.
Then Tab.empagliflozin 25mg once daily for 28 days will be given to both group of patients
proteinuric and non proteinuric diabetic CKD. After 28 days, post-treatment tests of fundus
examination and OCT-A measurement will be taken at eye clinic.
The statistical data analysis will be performed using statistical package for Social Science,
version 22.0 (SPSS, Inc. Chicago III USA) for IOS. The OCT-A parameters studied (FAZ size,
vessel density and perfusion density) will be used as main response variables. All variables
will be defined by method of descriptive statistics. The analysis of quantitative variables
includes a calculation of mean and standard deviation. T test will be performed to test the
significant between the 2 groups. Correlation will be measured with Pearson correlation
coefficient. A p <0.05 will be considered as statistically significant.
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