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Urinary Transforming Growth Factor-Beta 1 (uTGF-β1) and Prevalent CKD Risk in HIV-Positive Patients in West Africa
Udeme E Ekrikpo1,2, Cecilia N Okuku3, Samuel O Ajayi4
1Division of Nephrology and Hypertension, Department of Medicine, University of Cape Town, Cape Town, South Africa.
Insights
Urinary transforming growth factor-β1 (uTGF-β1) is elevated in HIV-positive individuals with chronic kidney disease (CKD). Higher uTGF-β1 levels correlate with CKD severity and proteinuria, particularly in early stages.
Area of Science:
- Nephrology
- Infectious Diseases
- Biochemistry
Background:
- Chronic kidney disease (CKD) is a significant concern in the HIV-infected population.
- Understanding biomarkers for CKD in HIV is crucial for early detection and management.
Purpose of the Study:
- To investigate the association between urinary transforming growth factor-β1 (uTGF-β1) and prevalent CKD in HIV-positive individuals.
- To explore the relationship between uTGF-β1 and CKD severity, proteinuria, and estimated glomerular filtration rate (eGFR).
Main Methods:
- Cross-sectional study comparing HIV-positive patients with and without CKD, excluding those with hypertension, diabetes, or hepatitis.
- Measurements included urinary protein-creatinine ratio (uPCR), serum TGF-β1, and uTGF-β1.
- Statistical analyses involved Spearman correlation, Cuzick trend test, and multivariable robust linear regression.
Main Results:
- Median urinary TGF-β1-creatinine ratio (uTGF-β1Cr) was significantly higher in HIV-positive patients with CKD (HIV+CKD+) compared to those without (HIV+CKD-).
- uTGF-β1Cr correlated positively with age, uPCR, and negatively with eGFR in the HIV+CKD+ group.
- A gradual reduction in median uTGF-β1Cr was observed with increasing CKD severity, and proteinuria explained changes in eGFR associated with uTGF-β1Cr.
Conclusions:
- HIV-positive patients with CKD exhibit elevated uTGF-β1 levels, particularly in the earlier stages of the disease.
- Proteinuria appears to be a key factor linking uTGF-β1 levels to kidney function decline in this population.
Introduction:
This study investigated the association of urinary transforming growth factor-β1 (uTGF-β1) with prevalent chronic kidney disease (CKD) in the HIV-infected population.
Methods:
HIV-positive patients without CKD (HIV+CKD-, n = 194) and 114 with CKD (HIV+CKD+) who did not have hypertension, diabetes mellitus, or hepatitis B or C, had their urinary protein-creatinine ratio (uPCR), serum transforming growth factor (TGF)-β1, and uTGF-β1 measured. uTGF-β1-creatinine ratios (uTGF-β1Cr) were calculated. Spearman correlation was used to determine the association between uTGF-β1Cr and various attributes, and the Cuzick trend test was used to assess the presence of a linear trend in median uTGF-β1Cr levels across the stages of CKD. Multivariable robust linear regression models were used to assess independent association with variability in uTGF-β1Cr and estimated glomerular filtration rate (eGFR) levels.
Results:
The age of the participants was 38.3 ± 10.3 years with 73.4% women. The median uTGF-β1Cr was higher among HIV+CKD+ (4.85 ng/mmol [25th-75th percentile 1.96-12.35] vs. 2.95 [1.02-5.84]; P = 0.001]). There was significant correlation between uTGF-β1Cr and age (P = 0.02), eGFR (P = 0.001), and uPCR (P < 0.001) in the HIV+CKD+ group. Among the HIV+CKD+ patients, there was gradual reduction in the median level of uTGF-β1Cr with CKD severity (P = 0.04). HIV+CKD+ patients had significantly higher levels of uTGF-β1Cr after controlling for potential confounders. Using eGFR as dependent variable, proteinuria explained the changes associated with uTGF-β1Cr levels.
Conclusion:
HIV+CKD+ patients express higher levels of uTGF-β1 especially in the early stages of CKD apparently related to proteinuria levels.
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