A RETROSPECTIVE REVIEW OF THE SPECTRUM OF HIV-RELATED KIDNEY PATHOLOGY AT A TERTIARY CENTRE IN SOUTH AFRICA

 

Certificate Output Instructions

For best output, select "Paper Size" as "A4" and "Margin" as "0" or "None".

To save or print to PDF, please select Print Destination > Save as PDF, enable Background Graphics under "More Settings", then click "Save".

 


 

Certificate Background

   

Presented the abstract " "
(Abstract co-author(s):  )

 

 

E-Poster Presentation

During the congress, E-Posters will be accessible to all participants on the congress website 24/7, as well as in the E-poster stations in the congress center. 

Preparing your E-Poster

Please review the E-Poster format requirements carefully when preparing your E-Poster. Should your E-Poster not meet the mentioned requirements, it may not be displayed as described above.

​E-Poster Submission Deadline

Please prepare and upload your E-Poster no later than March 14, 2026 11.59PM CET. After this date, you will no longer be able to prepare and upload your E-poster and it will not be displayed and accessible on the congress website.​

E-Poster Format Requirements
  • PDF file
  • Layout: Portrait (vertical orientation)
  • One page only (Dim A4: 210 x 297mm or PPT)
  • E-Poster can be prepared in PowerPoint (one (1) PowerPoint slide) but must be saved and submitted as PDF file.
  • File Size: Maximum file size is 2 Megabytes (2 MB)
  • No hyperlinks, animated images, animations, and slide transitions
  • Language: English
  • Include your abstract number
  • E-posters can include QR codes, tables and photos
https://storage.unitedwebnetwork.com/files/1099/455c33f0cc4e75ff1705d11f7fe39e6c.pdf
A RETROSPECTIVE REVIEW OF THE SPECTRUM OF HIV-RELATED KIDNEY PATHOLOGY AT A TERTIARY CENTRE IN SOUTH AFRICA

Please follow the instructions below to input your abstract title.

Abstract titles should be brief and reflect the content of the abstract.

  • The title will not be accepted if it exceeds 25 words.
  • Type in CAPITAL LETTERS.
  • Lowercase may be used for abbreviations only, for example, mRNA.
Thabiet
Jardine
Anna-liise Kaapangelwa 14602938@sun.ac.za Stellenbosch University and Tygerberg Hospital Division of Nephrology, Department of Medicine, Faculty of Medicine and Health Sciences Cape Town South Africa -
Thabiet Jardine thabietj@gmail.com Stellenbosch University and Tygerberg Hospital Division of Nephrology, Department of Medicine, Faculty of Medicine and Health Sciences Cape Town South Africa *
Liezel Coetzee lc@sun.ac.za National Health Laboratory Service, Stellenbosch University and Tygerberg Hospital Division of Anatomical Pathology, Department of Pathology, Faculty of Medicine and Health Sciences Cape Town South Africa -
Mogamat-Yazied Chothia yaziedc@sun.ac.za Stellenbosch University and Tygerberg Hospital Division of Nephrology, Department of Medicine, Faculty of Medicine and Health Sciences Cape Town South Africa -
-
-
-
-
-
-
-
-
-
-
-

South Africa has one of the highest prevalences of human immunodeficiency virus (HIV) infection worldwide. Kidney disease is a common and important complication of HIV, and a wide spectrum of kidney pathology associated with HIV infection has been described, with human immunodeficiency virus-associated nephropathy (HIVAN) the most well-characterised and historically the most prevalent. However, since the rollout of antiretroviral therapy (ART) in South Africa in 2004, the patterns of HIV-related kidney pathology have changed. This study aims to describe the spectrum of kidney pathology among people living with HIV who underwent kidney biopsy over a 29-year period at a tertiary centre in Cape Town, South Africa, and to describe patterns of kidney pathology before and after the rollout of ART.

This retrospective descriptive study included people living with HIV who underwent native kidney biopsy at Tygerberg Hospital during the period of 1 January 1992 to 31 December 2020. Patients were categorised by biopsy year into a pre-ART rollout period (before 2004) and a post-ART rollout period (2004 or later). We described the frequencies and proportions of histopathological patterns of kidney injury in the overall cohort and compared their distribution before and after the rollout of ART. In addition, clinical, demographic and laboratory characteristics were summarised and compared between the two periods. The most common non-HIVAN histopathological patterns were also identified.

The cohort consisted of 554 people living with HIV who underwent kidney biopsy during the study period. Most biopsies were performed after ART rollout (499/554, 90.1%). The mean age at biopsy was 36.5 years, with a relatively equal distribution by sex. Data on ART use were unavailable for patients in the pre-ART period, but were available for most patients in the post-ART rollout period, of whom 54.8% (232/423) were using ART at the time of biopsy. HIV-associated nephropathy (HIVAN) was diagnosed in 45.7% of all patients (253/554), with one-third of those with HIVAN (84/253, 33.2%) having an additional histopathological pattern of kidney injury. In the pre-ART rollout period, HIVAN was the most prevalent diagnosis (33/55, 60.0%), whereas a lower prevalence was observed post-ART rollout (220/499, 44.1%). During the post-ART rollout period, more than half of the patients (279/499, 55.9%) exhibited only non-HIVAN kidney pathology. The most frequently observed non-HIVAN histopathological patterns were immune complex-mediated glomerulonephritis (206/385, 53.5%) and tubulointerstitial disease (153/385, 39.7%). In an exploratory analysis, ART use was associated with lower odds of isolated HIVAN (aOR=0.39, 95% CI 0.24-0.64) after adjustment for the case mix.

Figure 1. Stacked bar chart showing proportions of HIV-associated kidney pathology by time periodFigure 2. Trends in HIV-associated kidney pathology over time (three-year moving average curves)Figure 3. Clustered bar chart showing spectrum of non-HIVAN kidney pathology

This study describes the spectrum of kidney pathology among patients with HIV at a tertiary centre in Cape Town, South Africa, over nearly three decades, demonstrating a substantial burden of HIVAN overall. Unsurprisingly, we observed a lower proportion of patients with HIVAN in the post-ART rollout period compared to the period before ART rollout. An increase in the proportion of patients with non-HIVAN pathology, most notably immune complex-mediated glomerulonephritis and tubulointerstitial disease, accompanied the decrease in the proportion of patients with HIVAN in the period after ART rollout. 

Kewords