Up to 40% of HIV-positive people develop variable degrees of lentivirus-associated nephropathy, which may be associated with
glomerular damage, proteinuria, and progressive decreases in renal function. The abnormal histologic findings that have been
associated with HIV infection are the collapsing form of focal segmental glomerulosclerosis with secondary microcystic tubular
Cats infected with FIV are known to be more likely to be proteinuric and azotemic than uninfected cats, and glomerulosclerosis,
microcystic tubular dilation, a thickened Bowman's membrane, mononuclear interstitial infiltrates, and fibrosis have been
reported, suggesting a possibly similar pathogenesis as that seen in people.1,2 Viral replication has been demonstrated in feline renal tubular cells in cats naturally infected with FIV by use of immunohistochemistry
for the p24 viral antigen and polymerase chain reaction analysis for viral gag DNA and RNA sequences.3 Collectively, these findings support the authors' hypothesis of an association between FIV and the initiation and evolution
of renal disease in cats.
Nevertheless, a direct pathogenic effect of FIV infection has been difficult to determine because of the many factors that
alter the course of disease. For example, ethnicity (i.e. genetic background) significantly affects the risk of HIV-associated nephropathy in people, and coinfection with other viruses.
In cats, coinfection with calicivirus is usually required for development of FIV-associated stomatitis and may be indirect
evidence that uncharacterized environmental or genetic factors may be critical for the development of FIV-induced kidney disease,
if such causal relationship exists. As demonstrated in this study, age may play an unclear role in whether FIV is associated
with CKD. Concurrent diseases, the cat's overall health, and the viral strain or viral load may also be important factors
that were not evaluated by these authors.
This study suggests that testing for FIV infection should be part of the diagnostic evaluation in young or middle-aged cats
with CKD. It is still premature to conclude that the demonstrated association implies causality. For example, the presence
of both diseases in younger animals may be due to these animals being more likely to lead indoor-outdoor lives and, therefore,
exposed to risk factors that increase the likelihood of each disease separately. If the association between these two diseases
in younger animals does hold true in the future, it may be that FIV is not found as commonly in the older CKD population because
of a more rapid progression of disease in FIV-infected cats and, therefore, decreased survival. Regardless, this study establishes
that additional studies are merited to investigate a causal association between lentiviral infection and kidney damage in
cats and to determine whether survival time in young cats with CKD is affected by concurrent FIV infection.
White JD, Malik R, Norris JM, et al. Association between naturally occurring chronic kidney disease and feline immunodeficiency
virus infection status in cats. J Am Vet Med Assoc 2010;236(4):424-429.
The information in "Research Updates" was provided by Erika Meler, DVM, MS, and Barrak Pressler, DVM, PhD, DACVIM, Department
of Veterinary Clinical Sciences, School of Veterinary Medicine, Purdue University, West Lafayette, IN 47907.
1. Levy JK. CVT Update: feline immunodeficiency virus. In: Bonagura JD, ed. Kirk's current veterinary therapy XIII: small animal practice. Philadelphia, Pa: WB Saunders Co, 2000;284-291.
2. Baxter KG, Levy JK, Edinboro CH, et al. Renal disease in cats infected with feline immunodeficiency virus (abstr). J Vet Intern Med 2010;24:677.
3. Poli A, Abramo F, Matteucci D, et al. Renal involvement in feline immunodeficiency virus infection: p24 antigen detection,
virus isolation and PCR analysis. Vet Immunol Immunopathol 1995;46(1-2):13-20.