Article

HIV-associated kidney glomerular diseases: changes with time and HAART.

Department of Infectious and Tropical Diseases, Tenon Hospital, AP-HP, Paris, France.
Nephrology Dialysis Transplantation (impact factor: 3.4). 01/2012; 27(6):2349-55. DOI:10.1093/ndt/gfr676
Source: PubMed

ABSTRACT Treatment and co-morbidities of human immunodeficiency virus (HIV)-infected individuals have changed dramatically in the last 20 years with a potential impact on renal complications. Our objective was to assess the change in distribution of the glomerular diseases in HIV patients.
We retrospectively analysed demographic, clinical, laboratory and renal histopathological data of 88 HIV-infected patients presenting with a biopsy-proven glomerular disease between 1995 and 2007.
In our study including 66% Black patients, HIV-associated nephropathy (HIVAN) was observed in 26 cases, classic focal segmental glomerulosclerosis (FSGS) in 23 cases, immune complex glomerulonephritis in 20 cases and other glomerulopathies in 19 patients. HIVAN decreased over time, while FSGS emerged as the most common cause of glomerular diseases (46.9%) in HIV-infected individuals undergoing kidney biopsy in the last 2004-07 period. Patients with HIVAN were usually Black (97%), with CD4 <200/mL (P = 0.01) and glomerular filtration rate <30 mL/min/1.73 m(2) (P < 0.01). Compared to HIVAN, patients with classic FSGS were less often Black (P < 0.01), have been infected for longer (P = 0.03), were more often co-infected with hepatitis C virus (P = 0.05), showed more often cardiovascular (CV) risk factors (P < 0.01), had less often CD4 <200/mL (P = 0.01), lower HIV viral load (P = 0.01) and tended to be older (P = 0.06).
Classic FSGS associated with metabolic and CV risk factors has overcome HIVAN in HIV-infected patients. Compared with other glomerulopathies, HIVAN remains strongly associated with severe renal failure, Black origin and CD4 lower than 200/mL at presentation.

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Keywords

19 patients
 
66% Black patients
 
88 HIV-infected patients
 
biopsy-proven glomerular disease
 
Black origin
 
CD4 lower
 
classic focal segmental glomerulosclerosis
 
classic FSGS
 
CV risk factors
 
glomerular diseases
 
HIV patients
 
HIV)-infected individuals
 
HIV-infected individuals undergoing kidney biopsy
 
HIV-infected patients
 
last 20 years
 
lower HIV viral load
 
potential impact
 
renal complications
 
renal histopathological data
 
severe renal failure
 

François-Xavier Lescure