Department of Periodontics, University of Maryland Dental School, Baltimore, MD 21201, USA.
J Periodontol. 2010 Nov;81(11):1505-17. doi: 10.1902/jop.2010.100045. Epub 2010 Jul 1.
Epidemiologic studies provide broad-based evidence that men are at greater risk for developing destructive periodontal disease than women, even after adjusting for behavioral and environmental factors, such as oral hygiene practice and smoking. What requires clarification, however, is whether sex-specific differences in immune function provide a plausible biologic basis for a sexual dimorphism in susceptibility to destructive periodontal disease. This review examines evidence that might provide an underlying biologic basis for a sexual dimorphism in the prevalence and severity of destructive periodontal disease.
A narrative review of the literature related to sexual dimorphism in pathogen-mediated inflammatory diseases and immune response was retrieved from searches of computerized databases (MEDLINE, PubMed, and SCOPUS).
Sex steroids exert profound effects on multiple immunologic parameters regulating both the amplification and resolution of inflammation. Strong evidence exists for sexual dimorphisms in immune function, involving both innate and acquired immunity. Injury and infection have been associated with higher levels of inflammatory cytokines, including interleukin-1β and tumor necrosis factor-α, in men than women, paralleling observed sex-specific differences in periodontitis.
Differential gene regulation, particularly in sex steroid-responsive genes, may contribute to a sexual dimorphism in susceptibility to destructive periodontal disease.
流行病学研究提供了广泛的证据表明,男性比女性更容易患破坏性牙周病,即使在调整了行为和环境因素(如口腔卫生习惯和吸烟)之后。然而,需要澄清的是,免疫功能的性别特异性差异是否为破坏性牙周病易感性的性别二态性提供了合理的生物学基础。这篇综述探讨了可能为破坏性牙周病的患病率和严重程度的性别二态性提供潜在生物学基础的证据。
从计算机数据库(MEDLINE、PubMed 和 SCOPUS)中检索了与病原体介导的炎症性疾病和免疫反应的性别二态性相关的文献的叙述性综述。
性激素对调节炎症放大和消退的多种免疫参数产生深远影响。在免疫功能方面存在强烈的性别二态性,涉及先天免疫和获得性免疫。损伤和感染与男性比女性更高水平的炎症细胞因子有关,包括白细胞介素-1β和肿瘤坏死因子-α,这与牙周炎中观察到的性别特异性差异相平行。
差异基因调控,特别是在性激素反应基因中,可能导致对破坏性牙周病易感性的性别二态性。