| Literature DB >> 35314925 |
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.Entities:
Keywords: Canakinumab; Muckle-Wells syndrome; NLRP3-associated autoinflammatory disease; Renal amyloidosis; Somatic mosaic mutation
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Year: 2022 PMID: 35314925 DOI: 10.1007/s10067-022-06130-1
Source DB: PubMed Journal: Clin Rheumatol ISSN: 0770-3198 Impact factor: 2.980