Literature DB >> 25984115

Renal thrombotic microangiopathy induced by β-interferon.

Gioacchino Li Cavoli1, Luisa Bono2, Calogera Tortorici2, Carlo Giammarresi1, Ugo Rotolo1.   

Abstract

Entities:  

Year:  2010        PMID: 25984115      PMCID: PMC4421625          DOI: 10.1093/ndtplus/sfq190

Source DB:  PubMed          Journal:  NDT Plus        ISSN: 1753-0784


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Sir, We read with interest the recent case report ‘Minimal change disease with interferon-β therapy for relapsing remitting multiple sclerosis’ [1]. In this paper, the authors include renal thrombotic microangiopathy (TMA) among rare side effects of interferon (IFN) therapy, more frequently described with IFN-α [2]. We report here our experience about this topic. A 36-year-old white female with a 3-year history of multiple sclerosis and normal blood pressure and renal function was admitted for acute renal failure and pulmonary oedema. Three months previously, she started subcutaneous IFN-β-1a treatment of 22 μg thrice weekly. On admission, physical examination showed high blood pressure and severe pleuropericarditis without neurological or dermatological findings. Laboratory tests revealed microangiopathic haemolytic anaemia. Other immunological and microbiological laboratory tests were unremarkable. A renal biopsy disclosed signs of TMA; among 43 glomeruli, light microscopy revealed focal ischaemic signs and mild mesangial cell proliferation; vessel narrowing with thrombi and thickening of arteriolar walls and intimal onion skin-like swelling; light interstitial lymphomonocytic infiltration and focal tubular atrophy. Immunofluorescence showed mesangial IgM, C1q and fibrinogen staining. A diagnosis of haemolytic–uraemic syndrome was made. She was treated with transfusions, haemodialysis, plasma exchange and methylprednisolone i.v. followed by oral prednisone. Her cardiac function improved, and haematological signs progressively disappeared, but renal function did not recover. IFN-β treatment was discontinued. She is now receiving peritoneal dialysis treatment. IFN-α is known to cause a variety of renal lesions, including TMA [3,4], but to our knowledge, our observation is the first report of TMA induced by INF-β. Editorial note: This letter had been sent to Aravindan A. et al., but we did not receive a response. Conflict of interest statement. None declared.
  3 in total

1.  Thrombotic microangiopathy in a patient with chronic myelocytic leukaemia treated with alpha-interferon.

Authors:  H Vacher-Coponat; A Opris; L Daniel; J R Harle; V Veit; M Olmer
Journal:  Nephrol Dial Transplant       Date:  1999-10       Impact factor: 5.992

2.  Renal thrombotic microangiopathy induced by interferon-alpha.

Authors:  C Badid; B McGregor; J M Faivre; A Guerard; L Juillard; D Fouque; M Laville
Journal:  Nephrol Dial Transplant       Date:  2001-04       Impact factor: 5.992

3.  Renal thrombotic microangiopathy induced by interferon-alpha.

Authors:  C C Magee
Journal:  Nephrol Dial Transplant       Date:  2001-10       Impact factor: 5.992

  3 in total
  2 in total

1.  Malignant hypertension and interferon-beta: a case report.

Authors:  S Rubin; A Lacraz; V Galantine; P Gosse
Journal:  J Hum Hypertens       Date:  2013-09-26       Impact factor: 3.012

2.  Renal diseases secondary to interferon-β treatment: a multicentre clinico-pathological study and systematic literature review.

Authors:  Maxime Dauvergne; David Buob; Cédric Rafat; Marie-Flore Hennino; Mathilde Lemoine; Vincent Audard; Dominique Chauveau; David Ribes; Emilie Cornec-Le Gall; Eric Daugas; Evangéline Pillebout; Vincent Vuiblet; Jean-Jacques Boffa
Journal:  Clin Kidney J       Date:  2021-07-06
  2 in total

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