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ABO/Rh Blood Group Phenotypes as Predictor of Treatment Outcomes in Diabetic Kidney Disease

ABO/Rh Blood Group Phenotypes as Independent Predictor of Treatment Outcomes in Diabetic Kidney Disease: A 1-Year Prospective Cohort Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07757269
Enrollment
161
Registered
2026-08-11
Start date
2024-05-01
Completion date
2026-02-28
Last updated
2026-08-11

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Kidney Disease

Brief summary

Background and aim: ABO blood groups are biologically plausible modulators of endothelial function, coagulation, and inflammation - pathways central to diabetic kidney disease (DKD). This study evaluates whether ABO/Rh phenotypes associate with differential treatment outcomes in DKD. Methods: This 1-year prospective cohort study enrolled 161 adults with type 2 diabetes and established DKD (all receiving ACE-I/ARB plus SGLT2 inhibitors) from Cairo University outpatient clinics. eGFR, ACR, HbA1c, lipids, electrolytes, and blood pressure were assessed at baseline and one year. Percent changes in eGFR and ACR were calculated and the Kidney Failure Risk Equation estimated 2- and 5-year risk of progressing to end stage kidney disease. Multivariable linear regression identified independent predictors of renal outcome changes.

Interventions

DIAGNOSTIC_TESTLaboratory measurements: eGFR, ACR, HbA1c, total cholesterol, triglycerides, sodium, potassium

Random mid stream spot urine samples were collected in sterile containers, and albumin to creatinine ratio (ACR) was measured using the Roche Cobas chemistry analyzer. Albuminuria was categorized according to Kidney Disease Improving Global Outcomes (KDIGO) criteria as A1 (\<30 mg/g), A2 (30-300 mg/g), and A3 (\>300 mg/g) . The Kidney Failure Risk Equation (KFRE) was applied to estimate the predicted 2 year and 5 year risk of progression to end stage renal disease using baseline eGFR and ACR values . Percent change in both eGFR and ACR was calculated using the formula: ((Post - Pre) / Pre) × 100 . Significant (accelerated) DKD progression was defined as a ≥25% sustained decline in eGFR over 12 months or an annual loss of ≥15 mL/min/1.73 m² , while rapid eGFR decline was defined as a reduction \>5 mL/min/1.73 m² per year; end stage renal disease was defined as eGFR \<15 mL/min/1.73 m² or initiation of dialysis therapy . Albumin to creatinine ratio (ACR) response was c

Sponsors

Cairo University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Adults aged ≥18 years with type 2 DM * Evident diabetic kidney disease * Recorded ABO blood group phenotypes * Receiving Angiotensin converting enzyme inhibitor (ACEI) or angiotensin receptor blockers (ARBs) in addition Sodium-glucose cotransporter 2 inhibitor (SGLT2i) as part of their ongoing therapy prior to enrolment.

Exclusion criteria

* Pre-existed glomerular diseases or any other primary kidney disorder, * Active urinary sediment * Type 1 diabetes mellitus * Gestational diabetes * History of kidney transplantation * Documented episode of acute kidney injury, * Family history of non-diabetic forms of kidney disease * \>30% declines in eGFR after initiation of RAAS inhibitors

Design outcomes

Primary

MeasureTime frameDescription
the progression or therapeutic response of diabetic kidney disease12 monthsassessed by the magnitude of percentage change in ACR and percentage change in eGFR across ABO blood groups

Countries

Egypt

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 12, 2026