NORTHWEST AIDS EDUCATION AND TRAINING CENTER. HIV and the Kidney. Leah Haseley, MD. Presentation prepared by: LH NW AETC ECHO June 2012

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NORTHWEST AIDS EDUCATION AND TRAINING CENTER HIV and the Kidney Leah Haseley, MD Presentation prepared by: LH NW AETC ECHO June 2012

Etiology of renal disease in HIV 1985- The virus 1995- The antivirals 2005- The usual (diabetes and HTN)

Renal Disease in the HIV positive patient Pre-renal Diarrhea Sepsis Cachexia! Vascular TTP Infiltrative KS Lymphoma Amyloid! GN HIVAN HIVIKD KD! Tubular Pentamidine Foscarnet Tenofovir AmphoB AZT (Rhabdo) HIV (Rhabdo) Ischemic!!! Interstitium TMP-SMX Rifampin MAI Plasmocytic IN DILS Post-Renal Crystalline Indinavir Tumors Fungus balls Mycobacteria Retro. Fibrosis

Renal disease in HIV Up to 10% have impaired GFR Risks HepC HTN Diabetes Black race Low CD4 count/high viral load HAART (TDF, Indinivir, atazanivir?) Age Low muscle mass Pre-existing CKD Consequences Vascular disease Increased Mortality

HIV -associated Nephropathy HIVAN Initially described in 1984 (New York, Miami) To date: 90% cases reported in blacks HIV infects glomerular and tubular cells Collapsing FSGS and cystic tubules Courtesy of Charles Alpers, MD UWMC

HIV Nephropathy

HIV associated Nephropathy

HIVAN: Significance HIVAN is the most common finding at renal biopsy among HIV- infected patients HIVAN occurs almost exclusively in Black patients and is the 4th most common cause of ESRD among African American men age 20-64 HIVAN is an indication to start HAART regardless of viral load

HIVAN: Treatment FIRST BIOPSY!! Diagnosis of HIVAN is an indication for ART: Dramatic reduction in incidence of HIVAN and some reversibility of CKD with HAART ACE inhibitors Nephrotic hygiene watch for hypercoaguable events, encapsulated organisms, hyperlipidemia Treat HTN to < 130/80 Optimize co-existent conditions- e.g. diabetes Discourage smoking, cocaine use

HIVIKD HIV immune kidney disease IgA Nephropathy Postinfectious glomerulonephritis Lupus-like glomerulonephritis MPGN (Hep C with cryoglobulins) Membranous GN (HepB) Immunotactoid GN

IgA Nephropathy in HIV IgA levels commonly elevated in HIV Autopsy studies among Caucasian Europeans with HIV show 8% have mesangial IgA deposits IgA-p24 HIV containing immune complexes eluted from glomeruli of HIV patients Idiotypic IgA antibodies also described: IgA-IgG-gp120 Mesangial deposits of IgA Courtesy of Gerald Appel, MD

Nephritic syndrome Hematuria HIV immune kidney disease presentation/diagnosis Proteinuria Acute or chronic kidney disease HTN Fluid overload Suggested labs: ANA, RF, cryoglobulins, C3, C4, hepatitis serologies

HIVIKD: Management Biopsy first (60% of pts thought to have HIVAN actually have an HIVIKD) Efficacy of HAART not clear Consider immunosuppressives depending on pt safety Examples: MPGN with cryoglobulins: rituximab, treat HepC IgA nephropathy: steroids, cyclophosphamide

HAART Nephrotoxicity Tenofovir: Fanconi Syndrome, AKI, CKD Indinivir: Stones, interstitial nephritis Atazanivir: Stones

HAART Is tenofovir nephrotoxic? ü Subclinical tubular defects ü Fanconi Sydrome: glycosuria, phosphaturia, aminoaciduria, RTA ü ATN (reversible) CKD: Ø Randomized control trials Ø Industry sponsored ü Observational

Rates of Discontinuation Due to Renal Impairment in early TDF Studies Study TDF Pts (N)! Percent (%) Discontinuation TDF Control Follow-up (weeks) Reference Overall Discontinuation Due to TDF Renal Events (0-1%) Courtesy of Gilead Pharmaceuticals

Department of Veteran Affairs TDF study Subjects 10,842 HAART naïve veterans 1997-2007 Exclude: advanced CKD 4303 exposed to TDF for mean of 1.3 years (max 6.3 years) Results 30% increased risk of proteinuria per year of exposure 11% increase risk of rapid decline in renal function 10% increased risk of creatinine doubling 33% increased risk of GFR < 60. NO increased risk of GFR < 30 Scherzer, AIDS, 2012

Vulnerability to TDF nephrotoxicity Basolateral Blood Apical Urinary Tenofovir Didanosine OAT MRP Tenofovir Ritonovir Genetics

Recommended monitoring protocol for TDF nephrotoxicity Hall et al AJKD 2011

HAART in ESRD HAART medications can be used safely in dialysis patients, and are probably underutilized PIs do not require dose adjustments NNRTIs do not require dose adjustments NRTIs require 3-7 fold reduction in dose EXCEPT abacavir Tenofovir is given only once weekly after hemodialysis