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Focal Segmental Glomerulosclerosis Complicating Therapy With Inotersen, an Antisense Oligonucleotide Inhibitor: A Case Report.
Law, Steven; Arnold, Julia; Rauf, Muhammad U; Heptinstall, Lauren; Gilbertson, Janet; Rowczenio, Dorota; Baharani, Jyoti; Langman, Gerald; Fontana, Marianna; Gillmore, Julian D.
Affiliation
  • Law S; National Amyloidosis Centre, Division of Medicine, University College London, United Kingdom. Electronic address: stevenlaw@nhs.net.
  • Arnold J; Department of Renal Medicine, Heartlands Hospital, University Hospitals Birmingham Foundation Trust, Birmingham, United Kingdom.
  • Rauf MU; National Amyloidosis Centre, Division of Medicine, University College London, United Kingdom.
  • Heptinstall L; Department of Pathology, Royal Free Hospital, London, United Kingdom.
  • Gilbertson J; National Amyloidosis Centre, Division of Medicine, University College London, United Kingdom.
  • Rowczenio D; National Amyloidosis Centre, Division of Medicine, University College London, United Kingdom.
  • Baharani J; Department of Renal Medicine, Heartlands Hospital, University Hospitals Birmingham Foundation Trust, Birmingham, United Kingdom.
  • Langman G; Department of Cellular Pathology, Heartlands Hospital, University Hospitals Birmingham Foundation Trust, Birmingham, United Kingdom.
  • Fontana M; National Amyloidosis Centre, Division of Medicine, University College London, United Kingdom.
  • Gillmore JD; National Amyloidosis Centre, Division of Medicine, University College London, United Kingdom.
Am J Kidney Dis ; 81(5): 606-610, 2023 05.
Article in En | MEDLINE | ID: mdl-36228827
Inotersen is an antisense oligonucleotide inhibitor licensed for the treatment of polyneuropathy complicating hereditary transthyretin amyloidosis (ATTRv). Nephrotoxicity has been reported with inotersen, including progression to kidney failure. We describe what is to our knowledge the first reported case of inotersen-associated nephrotic syndrome secondary to focal segmental glomerulosclerosis (FSGS) and review the literature concerning inotersen-induced nephrotoxicity. We report a woman in her early 30s with ATTRv associated with the V50M transthyretin (TTR) variant, who presented with nephrotic syndrome 7 months after commencement of inotersen. Renal histology demonstrated FSGS and scanty glomerular amyloid deposition. Discontinuation of inotersen alone resulted in complete clinical and biochemical resolution of nephrotic syndrome. Inotersen is associated with significant nephrotoxicity. In the phase 3 NEURO-TTR clinical trial, 3% of patients in the treatment arm developed a crescentic glomerulonephritis. All affected patients carried the V50M TTR variant, which is known to be associated with renal amyloid deposition. This case adds to the spectrum of kidney disease associated with inotersen and indicates that discontinuation of the drug alone may result in resolution of renal complications without additional immunosuppression. Monitoring of kidney function is essential in patients with ATTRv receiving inotersen, particularly if there is evidence of existing renal amyloid.
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Full text: 1 Database: MEDLINE Main subject: Glomerulosclerosis, Focal Segmental / Renal Insufficiency / Nephrotic Syndrome Limits: Female / Humans Language: En Year: 2023 Type: Article

Full text: 1 Database: MEDLINE Main subject: Glomerulosclerosis, Focal Segmental / Renal Insufficiency / Nephrotic Syndrome Limits: Female / Humans Language: En Year: 2023 Type: Article