Clinical Trial Details
— Status: Completed
Administrative data
NCT number |
NCT05695573 |
Other study ID # |
DN UMOD |
Secondary ID |
|
Status |
Completed |
Phase |
|
First received |
|
Last updated |
|
Start date |
July 5, 2019 |
Est. completion date |
June 1, 2022 |
Study information
Verified date |
December 2023 |
Source |
Tanta University |
Contact |
n/a |
Is FDA regulated |
No |
Health authority |
|
Study type |
Observational
|
Clinical Trial Summary
Detecting diabetes-related kidney diseases early is crucial to prevent end-stage renal
disease (ESRD). Existing biomarkers' specificity and sensitivity vary, emphasizing the need
for novel markers. This research assesses urinary uromodulin levels and its gene expression,
aiming to identify a potential marker for early diabetic nephropathy (DN) detection in type 2
diabetes patients. Uromodulin, encoded by the UMOD gene, is expressed mainly in the thick
ascending limb of Henle's loop epithelial cells, making it a promising candidate for early DN
detection and progression towards ESRD, potentially reducing chronic kidney disease
prevalence.
Description:
Introduction:
Diabetes mellitus (DM) is a metabolic disorder characterized by elevated blood glucose levels
resulting from deficiencies in insulin secretion, insulin action, or both. Prolonged
hyperglycemia associated with diabetes can lead to lasting damage and dysfunction in various
organs, including the eyes, kidneys, nerves, heart, and blood vessels (American Diabetes
Association, 2008).
Among the complications of diabetes, diabetic nephropathy (DN) stands out as a significant
contributor to chronic kidney disease (CKD) (Macisaac et al., 2014). Pathophysiologically, DN
progresses from an early phase featuring glomerular hypertrophy, hyperfiltration, and
microalbuminuria to an advanced phase marked by progressive glomerulosclerosis, increased
urinary albumin excretion (UAE), and impaired renal function (Schrijvers et al., 2004).
Traditionally, DN severity is assessed by measuring urine albumin levels, with persistent
microalbuminuria (30-300 mg/24 hr) or macroalbuminuria (>300 mg/24 hr) serving as markers and
predictors of DN and its progression to end-stage renal disease (Adler et al., 2003).
Current practices in biomarker use for DN diagnosis show conflicting results regarding
sensitivity and specificity in recent studies. Therefore, it is imperative to identify novel
biomarkers for early DN detection and progression to reduce the prevalence of chronic kidney
diseases in the population (Carole et al., 2017).
Uromodulin, also known as Tamm-Horsfall protein, is an 85 kDa glycoprotein normally secreted
by epithelial cells lining the thick ascending limb (TAL) of Henle's loop and early distal
tubule. It is released through proteolytic cleavage of glycosylphosphatidylinositol
(GPI)-anchored protein, primarily localized to the apical plasma membrane. Uromodulin levels
undergo significant changes in urinary excretion during pathological conditions, making it a
valuable marker for renal disease