Abstract:Mild proteinuria affected approximately one fifth of patients in our cohort. The determination of albuminuria allowed the differentiation between glomerular and tubular proteinuria, although no relationship with metabolic comorbidities was observed.
“…GFR was also normal with no difference between those with or without HIV. Other cohorts have reported similar findings [13,14,26].…”
Section: Discussionsupporting
confidence: 74%
“…Other studies have reported a prevalence of microalbuminuria between 10 and 30% in African HIV+ children [12,13,17]. The lower prevalence found in this cohort could be due to children starting ART relatively earlier than in other African cohorts, or fewer children receiving a TDF-based regimen.…”
Section: Discussioncontrasting
confidence: 56%
“…Previous studies in HIV+ adults have shown that decreased CD4 counts, higher HIV-RNA levels and non-nucleoside reverse transcriptase inhibitors are associated with increased prevalence of microalbuminuria [10]. Studies have reported that microalbuminuria is present in 11-15% of HIV-infected children on ART in the USA, Spain and Brazil [12][13][14]. However, an Indian study reported that in a cohort of HIV+ children on ART with a mean age of 11.5 years, 20% had microalbuminuria [15].…”
Proteinuria and microalbuminuria appear to be uncommon in this population. Follow up of those with microalbuminuria may inform long-term outcomes and management of this growing population of HIV+ youth.
“…GFR was also normal with no difference between those with or without HIV. Other cohorts have reported similar findings [13,14,26].…”
Section: Discussionsupporting
confidence: 74%
“…Other studies have reported a prevalence of microalbuminuria between 10 and 30% in African HIV+ children [12,13,17]. The lower prevalence found in this cohort could be due to children starting ART relatively earlier than in other African cohorts, or fewer children receiving a TDF-based regimen.…”
Section: Discussioncontrasting
confidence: 56%
“…Previous studies in HIV+ adults have shown that decreased CD4 counts, higher HIV-RNA levels and non-nucleoside reverse transcriptase inhibitors are associated with increased prevalence of microalbuminuria [10]. Studies have reported that microalbuminuria is present in 11-15% of HIV-infected children on ART in the USA, Spain and Brazil [12][13][14]. However, an Indian study reported that in a cohort of HIV+ children on ART with a mean age of 11.5 years, 20% had microalbuminuria [15].…”
Proteinuria and microalbuminuria appear to be uncommon in this population. Follow up of those with microalbuminuria may inform long-term outcomes and management of this growing population of HIV+ youth.
“…5,6 However, persistent renal function abnormalities occur in one fifth of HIV-infected children and are associated with improved survival, black race and Hispanic ethnicity and exposure to nephrotoxic drugs. 7,8 Current recommendations in children and adolescents with HIV and no previous evidence of kidney disease suggest screening for renal dysfunction with estimated glomerular filtration rate (GFR) at HAART initiation or change and at least twice yearly, and for kidney damage (urinalysis or quantitative proteinuria) at HAART initiation or change and at least yearly 5,9 or, if the patient is receiving tenofovir, at shorter intervals (3-6 months). 6 The best method for estimating GFR in children remains uncertain.…”
Cystatin C values were associated with GFR and β-2-microglobulin. Cystatin C may be useful as a marker of renal function in HIV-infected pediatric patients, independently of ongoing inflammation or viremia.
Human immunodeficiency virus (HIV) infection continues to be a leading cause of morbidity and mortality. HIV-infected individuals are now surviving for a relatively longer period and this is because of easy accessibility to antiretroviral therapy these days. As a result, chronic disease-related complications are now being recognized more often. Kidney disease in HIV-infected children can vary from glomerular to tubular-interstitial involvement. We searched the database to identify various kidney diseases seen in HIV-infected children. We describe the epidemiology, pathogenesis, pathology, clinical and laboratory manifestations, management and outcome of commonly seen kidney disease in HIV-infected children. We also provide a brief overview of toxicity of antiretroviral drugs seen in HIV-infected children. Kidney involvement in HIV-infected children may arise because of HIV infection per se, opportunistic infections, immune mediated injury and drug toxicity. HIV-associated nephropathy is perhaps the most common and most severe form of kidney disease. Proteinuria may be a cost-effective screening test in the long-term management of HIV-infected children, however, there are no definite recommendations for the same. Other important renal diseases are HIV immune complex kidney disease, thrombotic microangiopathy, interstitial nephritis and vasculitis.
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