| Literature DB >> 32424308 |
Noriyoshi Mizuno1, Kodai Kume2, Yukiko Nagatani3, Shinji Matsuda4, Tomoyuki Iwata4, Kazuhisa Ouhara4, Mikihito Kajiya4, Katsuhiro Takeda5, Yukiko Matsuda2, Yui Tada2, Ryosuke Ohsawa2, Hiroyuki Morino2, Keichiro Mihara6, Tsuyoshi Fujita4, Hiroyuki Kawaguchi7, Hideki Shiba5, Hideshi Kawakami2, Hidemi Kurihara4.
Abstract
Aggressive periodontitis (AgP) occurs at an early age and causes rapid periodontal tissue destruction. Nucleotide-binding oligomerization domain-containing protein 2 (NOD2) encodes a protein with two caspase recruitment domains and eleven leucine-rich repeats. This protein is expressed mainly in peripheral blood leukocytes and is involved in immune response. NOD2 variants have been associated with increased susceptibility to Crohn's disease, and recently, NOD2 was reported as a causative gene in AgP. The present study aimed to identify potential NOD2 variants in an AgP cohort (a total of 101 patiens: 37 patients with positive family histories and 64 sporadic patients). In the familial group, six patients from two families had a reported heterozygous missense variant (c.C931T, p.R311W). Four patients in the sporadic group had a heterozygous missense variant (c.C1411T, p.R471C), with no reported association to the disease. Overall, two NOD2 variants, were identified in 10% of our AgP cohort. These variants were different from the major variants reported in Crohn's disease. More cases need to be investigated to elucidate the role of NOD2 variants in AgP pathology.Entities:
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Year: 2020 PMID: 32424308 DOI: 10.1038/s10038-020-0777-z
Source DB: PubMed Journal: J Hum Genet ISSN: 1434-5161 Impact factor: 3.172