La Rosa Giusy Rita Maria, Loreto Carla, Pedullà Eugenio, Lombardo Claudia
Department of General Surgery and Surgical-Medical Specialties, University of Catania, Catania, Italy.
Section of Human Anatomy, Department of Biomedical and Biotechnology Sciences, University of Catania, Catania, Italy.
Arch Oral Biol. 2025 Feb;170:106130. doi: 10.1016/j.archoralbio.2024.106130. Epub 2024 Nov 16.
This systematic review aimed to investigate the association between genetic polymorphisms in estrogen receptor alpha (ERα) and beta (ERβ) and the presence and severity of temporomandibular disorders (TMDs).
A comprehensive search was conducted in PubMed, Scopus and Web of Science on October 19, 2024, without language or time restrictions. Studies were included if they were cross-sectional, case-control, or cohort designs and reported data on ER-polymorphisms and TMDs, diagnosed using validated criteria. Two independent reviewers screened the results to identify eligible studies. Data were extracted and synthesized narratively due to high heterogeneity across included studies, with a subgroup analysis performed to evaluate the influence of sex. The risk of bias was assessed using the Joanna Briggs Institute's critical appraisal tools.
The search identified 277 articles, of which 8 studies met the inclusion criteria. Seven were case-control and two cross-sectional studies. The most commonly investigated ER polymorphisms were ESR1 (Pvu II and Xba I) and ESR2 (rs1676303). Some studies identified associations between specific polymorphisms and TMD-related pain or joint conditions, although results varied across different populations and subtypes of TMDs.
The findings suggest potential associations between specific ERα and ERβ polymorphisms and TMD risk, particularly in women. However, inconsistencies across studies underscore the need for prospective and larger studies to confirm these genetic links and clarify their clinical significance.
CRD42024581266.
本系统评价旨在研究雌激素受体α(ERα)和β(ERβ)基因多态性与颞下颌关节紊乱病(TMDs)的存在及严重程度之间的关联。
于2024年10月19日在PubMed、Scopus和Web of Science上进行了全面检索,无语言或时间限制。纳入的研究需为横断面研究、病例对照研究或队列研究,并报告使用经过验证的标准诊断的ER多态性和TMDs的数据。两名独立的评审员筛选结果以确定符合条件的研究。由于纳入研究之间存在高度异质性,因此对数据进行了提取并进行叙述性综合分析,并进行了亚组分析以评估性别的影响。使用乔安娜·布里格斯研究所的批判性评价工具评估偏倚风险。
检索到277篇文章,其中8项研究符合纳入标准。7项为病例对照研究,2项为横断面研究。最常研究的ER多态性是ESR1(Pvu II和Xba I)和ESR2(rs1676303)。一些研究发现特定多态性与TMD相关疼痛或关节状况之间存在关联,尽管不同人群和TMD亚型的结果有所不同。
研究结果表明特定的ERα和ERβ多态性与TMD风险之间可能存在关联,尤其是在女性中。然而,研究之间的不一致性强调需要进行前瞻性和更大规模的研究来证实这些基因联系并阐明其临床意义。
CRD42024581266。