Gera István, Vári Melinda
Semmelweis Egyetem, Fogorvostudományi Kar, Parodontológai Klinika, Budapest.
Fogorv Sz. 2009 Jun;102(3):87-95.
Periodontitis is an infectious disease. It had previously been considered as a diseases caused merely by dental plaque. During the 1990-ies a substantial number of publications indicated the role of other risk factors in its pathogenesis, such as behavioral, systemic and genetic causes. Based on recent research data, genetic and ethnic factors have become the leading susceptibility or severity factors for destructive periodontitis. The family background of early onset aggressive periodontitis has long been known. Hereditary syndromes can very frequently be associated with severe periodontitis. Both facts can support the alleged connection between certain genes' mutation and periodontal manifestation. Periodontal disease associated with systemic hereditary syndromes mainly shows a Mendelian inheritance. The locus and the characteristics of the gene mutations have in many cases been identified. Nevertheless several polygenic gene single nucleotide mutations can also be a predisposing or severity factor for periodontitis. Part I of the literature review is focusing on those syndromes in which major PMN leukocyte deficiency or dysfunction or certain structural protein deficiency occur.
牙周炎是一种感染性疾病。它曾被认为仅仅是由牙菌斑引起的疾病。在20世纪90年代,大量出版物表明其他风险因素在其发病机制中的作用,如行为、全身和遗传因素。基于最近的研究数据,遗传和种族因素已成为破坏性牙周炎的主要易感性或严重程度因素。早发性侵袭性牙周炎的家族背景早已为人所知。遗传综合征常常与严重的牙周炎相关。这两个事实都可以支持某些基因突变与牙周表现之间所谓的联系。与全身遗传综合征相关的牙周疾病主要表现为孟德尔遗传。在许多情况下,基因突变的位点和特征已经确定。然而,一些多基因单核苷酸突变也可能是牙周炎的易感或严重程度因素。文献综述的第一部分重点关注那些出现主要中性粒细胞缺乏或功能障碍或某些结构蛋白缺乏的综合征。