AKI in an HIV-Positive Patient Following Amphetamine Use: A Biopsy-Proven Case of Immune Complex Glomerulonephritis and Acute Interstitial Nephritis

Introduction: HIV patients face renal risks from viral effects, ART toxicity, and drug use. Amphetamines can cause AKI via rhabdomyolysis or AIN, but their link to immune complex GN is unclear. We present a rare biopsy-proven case of both GN and AIN in an HIV-positive patient post-amphetamine use. Case Description: A 34-year-old Filipino male with HIV (CD4 283; viral load 60), on lamivudine/tenofovir/dolutegravir, presented with AKI after recent amphetamine use, with severe low back pain, tea-colored urine, and oliguria. Labs showed creatinine 6.4 mg/dL, eGFR 11 mL/min, proteinuria, and hematuria. Ultrasound showed increased renal echogenicity without obstruction. Biopsy revealed immune complex-mediated glomerulonephritis (IgG, IgM, C3, C1q) and acute interstitial nephritis. EM showed podocyte foot process effacement without dense deposits. This case illustrates multifactorial AKI in HIV and the value of early biopsy. Discussion: This case illustrates a complex, multifactorial renal insult in an HIV-positive patient. While amphetamines are associated with AIN, the concurrent immune complex GN raises the possibility of drug-induced immune activation in the setting of HIV-mediated immune dysregulation. The absence of classical lupus-like features and lack of significant electron-dense deposits argue against HIVAN or lupus nephritis.18 glomeruli (2 sclerosed), IgG/IgM/fibrinogen (trace), IgA/C1q (1-2+), C3 (2-3+), vascular (2+).EM showed diffuse podocyte foot process effacement, with no definite electron-dense deposits or tubuloreticular inclusions

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Journal
Journal of the American Society of Nephrology
Published
2025-10-01
DOI
https://doi.org/10.1681/asn.20256h775j72
Primary Topic
Muscle and Compartmental Disorders
Type
article
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article

AKI in an HIV-Positive Patient Following Amphetamine Use: A Biopsy-Proven Case of Immune Complex Glomerulonephritis and Acute Interstitial Nephritis

Jim Anson, Genecarlo Liwanag
Journal of the American Society of Nephrology
Muscle and Compartmental Disorders
article

AKI in an HIV-Positive Patient Following Amphetamine Use: A Biopsy-Proven Case of Immune Complex Glomerulonephritis and Acute Interstitial Nephritis

Jim Anson, Genecarlo Liwanag
article en

Abstract

Introduction: HIV patients face renal risks from viral effects, ART toxicity, and drug use. Amphetamines can cause AKI via rhabdomyolysis or AIN, but their link to immune complex GN is unclear. We present a rare biopsy-proven case of both GN and AIN in an HIV-positive patient post-amphetamine use. Case Description: A 34-year-old Filipino male with HIV (CD4 283; viral load 60), on lamivudine/tenofovir/dolutegravir, presented with AKI after recent amphetamine use, with severe low back pain, tea-colored urine, and oliguria. Labs showed creatinine 6.4 mg/dL, eGFR 11 mL/min, proteinuria, and hematuria. Ultrasound showed increased renal echogenicity without obstruction. Biopsy revealed immune complex-mediated glomerulonephritis (IgG, IgM, C3, C1q) and acute interstitial nephritis. EM showed podocyte foot process effacement without dense deposits. This case illustrates multifactorial AKI in HIV and the value of early biopsy. Discussion: This case illustrates a complex, multifactorial renal insult in an HIV-positive patient. While amphetamines are associated with AIN, the concurrent immune complex GN raises the possibility of drug-induced immune activation in the setting of HIV-mediated immune dysregulation. The absence of classical lupus-like features and lack of significant electron-dense deposits argue against HIVAN or lupus nephritis.18 glomeruli (2 sclerosed), IgG/IgM/fibrinogen (trace), IgA/C1q (1-2+), C3 (2-3+), vascular (2+).EM showed diffuse podocyte foot process effacement, with no definite electron-dense deposits or tubuloreticular inclusions

Journal of the American Society of NephrologyVol. 36(10S)
St. Luke's Medical Center (PH)
Openalex Percentile: Top 43%
Muscle and Compartmental Disorders
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