Literature DB >> 35314925

Efficacy of canakinumab on AA amyloidosis in late-onset NLRP3-associated autoinflammatory disease with an I574F somatic mosaic mutation.

Takahiro Itamiya1, Toshihiko Komai2, Hiroko Kanda1,3, Yasuo Nagafuchi1,4, Hyangri Chang5, Shota Shibata6,7, Hiroyuki Ishiura5,7, Hirofumi Shoda1, Tatsushi Toda5,7, Keishi Fujio1.   

Abstract

There have been hundreds of reports on mutations in the NLRP3 gene related to NLRP3-associated autoinflammatory disease, but few of these mutations have occurred as both germline and somatic mosaic mutations. In this case-based review, we report a 68-year-old man with an NLRP3-associated autoinflammatory disease. He developed secondary amyloidosis, including a renal and colorectal presentation in his 50 s. Sequencing of the NLRP3 gene revealed an I574F somatic mosaic mutation, which has up to now only been reported in germline mutations. The patient was treated with canakinumab, which had great efficacy not only on the NLRP3-mediated inflammation, but also on the chronic renal failure and proteinuria provoked by secondary renal amyloidosis. To evaluate the effectiveness of canakinumab, we conducted a literature research on renal amyloidosis related to NLRP3-associated autoinflammatory disease treated with canakinumab. Although our patient had a relatively long medical history and greater amounts of proteinuria than other reported cases, canakinumab had great efficacy on renal impairment, in similar to other reported cases. Along with the first report of a late-onset I574F somatic mosaic mutation in NLRP3-associated autoinflammatory disease, this report demonstrates the effectiveness of canakinumab on renal amyloidosis, probably through the way that IL-1β blockade minimizes podocyte injury.
© 2022. The Author(s), under exclusive licence to International League of Associations for Rheumatology (ILAR).

Entities:  

Keywords:  Canakinumab; Muckle-Wells syndrome; NLRP3-associated autoinflammatory disease; Renal amyloidosis; Somatic mosaic mutation

Mesh:

Substances:

Year:  2022        PMID: 35314925     DOI: 10.1007/s10067-022-06130-1

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   2.980


  17 in total

1.  Follow-up and quality of life of patients with cryopyrin-associated periodic syndromes treated with Anakinra.

Authors:  Loredana Lepore; Giulia Paloni; Roberta Caorsi; Maria Alessio; Donato Rigante; Nicola Ruperto; Marco Cattalini; Alberto Tommasini; Francesco Zulian; Alessando Ventura; Alberto Martini; Marco Gattorno
Journal:  J Pediatr       Date:  2010-05-15       Impact factor: 4.406

2.  Additional Benefit of Canakinumab on Proteinuria in a Case With Muckle-Wells Syndrome in Remission Under Anakinra.

Authors:  Ufuk İlgen; Orhan KÜÇÜkŞahİn
Journal:  Arch Rheumatol       Date:  2019-11-06       Impact factor: 1.472

3.  Renal and thyroid amyloidosis secondary tocryopyrin-associated periodic syndrome(Muckle-Wells syndrome) (NLRP3 mutation).

Authors:  Luis Bolaños; Juan M Mosquera-Reboredo; Mercedes Cao; Tamara Ferreiro; Beatriz Veleiro; Francisco Valdés; Eduardo Vázquez-Martul
Journal:  Nefrologia       Date:  2013       Impact factor: 2.033

4.  High incidence of NLRP3 somatic mosaicism in patients with chronic infantile neurologic, cutaneous, articular syndrome: results of an International Multicenter Collaborative Study.

Authors:  Naoko Tanaka; Kazushi Izawa; Megumu K Saito; Mio Sakuma; Koichi Oshima; Osamu Ohara; Ryuta Nishikomori; Takeshi Morimoto; Naotomo Kambe; Raphaela Goldbach-Mansky; Ivona Aksentijevich; Geneviève de Saint Basile; Bénédicte Neven; Mariëlle van Gijn; Joost Frenkel; Juan I Aróstegui; Jordi Yagüe; Rosa Merino; Mercedes Ibañez; Alessandra Pontillo; Hidetoshi Takada; Tomoyuki Imagawa; Tomoki Kawai; Takahiro Yasumi; Tatsutoshi Nakahata; Toshio Heike
Journal:  Arthritis Rheum       Date:  2011-11

5.  NLRP3-associated autoinflammatory diseases: Phenotypic and molecular characteristics of germline versus somatic mutations.

Authors:  Camille Louvrier; Eman Assrawi; Elma El Khouri; Isabelle Melki; Bruno Copin; Emmanuelle Bourrat; Noémie Lachaume; Bérengère Cador-Rousseau; Philippe Duquesnoy; William Piterboth; Fawaz Awad; Claire Jumeau; Marie Legendre; Gilles Grateau; Sophie Georgin-Lavialle; Sonia A Karabina; Serge Amselem; Irina Giurgea
Journal:  J Allergy Clin Immunol       Date:  2019-12-06       Impact factor: 10.793

6.  Genetic and clinical features of cryopyrin-associated periodic syndromes in Turkish children.

Authors:  Fehime Kara Eroglu; Ozgür Kasapcopur; Nesrin Beşbaş; Fatih Ozaltin; Yelda Bilginer; Kenan Barut; Anna Mensa-Vilaro; Kenji Nakagawa; Toshio Heike; Ryuta Nishikomori; Juan Arostegui; Seza Ozen
Journal:  Clin Exp Rheumatol       Date:  2016-05-10       Impact factor: 4.473

7.  Renal involvement in secondary amyloidosis of Muckle-Wells syndrome: marked improvement of renal function and reduction of proteinuria after therapy with human anti-interleukin-1β monoclonal antibody canakinumab.

Authors:  Roberto Scarpioni; Donato Rigante; Luca Cantarini; Marco Ricardi; Vittorio Albertazzi; Luigi Melfa; Antonio Lazzaro
Journal:  Clin Rheumatol       Date:  2014-02-09       Impact factor: 2.980

8.  Anti-interleukin 1 treatment in secondary amyloidosis associated with autoinflammatory diseases.

Authors:  Rezan Topaloglu; Ezgi Deniz Batu; Diclehan Orhan; Seza Ozen; Nesrin Besbas
Journal:  Pediatr Nephrol       Date:  2015-11-12       Impact factor: 3.714

Review 9.  Consensus proposal for taxonomy and definition of the autoinflammatory diseases (AIDs): a Delphi study.

Authors:  Eldad Ben-Chetrit; Marco Gattorno; Ahmet Gul; Daniel L Kastner; Helen J Lachmann; Isabelle Touitou; Nicolino Ruperto
Journal:  Ann Rheum Dis       Date:  2018-08-12       Impact factor: 19.103

10.  A web-based collection of genotype-phenotype associations in hereditary recurrent fevers from the Eurofever registry.

Authors:  Riccardo Papa; Matteo Doglio; Helen J Lachmann; Seza Ozen; Joost Frenkel; Anna Simon; Bénédicte Neven; Jasmin Kuemmerle-Deschner; Huri Ozgodan; Roberta Caorsi; Silvia Federici; Martina Finetti; Maria Trachana; Jurgen Brunner; Liliana Bezrodnik; Mari Carmen Pinedo Gago; Maria Cristina Maggio; Elena Tsitsami; Wafaa Al Suwairi; Graciela Espada; Anna Shcherbina; Guzide Aksu; Nicolino Ruperto; Alberto Martini; Isabella Ceccherini; Marco Gattorno
Journal:  Orphanet J Rare Dis       Date:  2017-10-18       Impact factor: 4.123

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