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Evaluating The Roles of Novel Inflammatory Markers Compared to MCP-1 in Type 2 Diabetic Nephropathy

A

Assiut University

Status

Begins enrollment this month

Conditions

Diabetic Nephropathy

Study type

Observational

Funder types

Other

Identifiers

NCT07173686
MCP-1 DM 2

Details and patient eligibility

About

Diabetic kidney disease (DKD) is one of the most common microvascular complications of type 2 diabetes mellitus (T2DM), affecting up to 40% of diabetic patients and accounting for the leading cause of end-stage renal disease worldwide [1]. The progression of DKD involves multiple mechanisms, including oxidative stress, endothelial dysfunction, and most importantly, chronic inflammation [2].

Systemic inflammation plays a central role in renal injury by promoting glomerular and tubulointerstitial damage. the neutrophil-to-lymphocyte ratio (NLR) and systemic inflammatory index (SII) has emerged as a readily accessible markers of subclinical inflammation. Elevated NLR and SII levels have been significantly associated with increased urinary albumin excretion and decreased estimated glomerular filtration rate (eGFR) in T2DM patients [3]. It was demonstrated that patients in the highest NLR tertile had a higher prevalence of DKD, independent of confounders [4].

High-sensitivity C-reactive protein (hsCRP), is widely used to evaluate systemic inflammation. Recent studies have shown a strong association between elevated hsCRP levels and DKD development [5].Some studies provided genetic evidence supporting a causal relationship between higher hsCRP and diabetic nephropathy [6].

Monocyte chemoattractant protein-1 (MCP-1) is a chemokine involved in monocyte recruitment to inflamed renal tissues. Elevated serum and urinary MCP-1 levels have been found to predict microalbuminuria and eGFR decline in T2DM patients [7,8].

Identifying these markers may help in early diagnosis, risk stratification, and monitoring progression of DKD.

Enrollment

80 estimated patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Adult aged 18-80 years, both genders.
  • clear history of T2DM

Exclusion criteria

  • Kidney disease caused by any other causes
  • Estimated glomerular filtration rate (eGFR) < 30 mL/min/1.73 - m2
  • Existing obvious infection
  • Acute stage of cardiovascular or cerebrovascular diseases
  • Acute complications of diabetes recently (such as diabetic ketoacidosis, et al.)
  • Associated malignant tumors
  • Hematological system, and autoimmune system diseases

Trial design

80 participants in 3 patient groups

Group 1
Description:
diabetic patients without diabetic nephropathy (albumin/creatinine ratio: \< 30 mg alb/gm creatinine )
Group2
Description:
diabetic patients with first stage diabetic nephropathy ( albumin/creatinine ratio: 30-300 mg alb/gm creatinine)
Group 3
Description:
diabetic patients with second stage diabetic nephropathy (albumin/creatinine ratio \>300 mg alb/gm creatinine)

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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