Kurmi Pooja, Nalabothu Prasad, Sahoo Shubhasmita, Verma Henu Kumar, Reddy Srinivas Gosla, Bhaskar L V K S
Department of Zoology, Guru Ghasidas Vishwavidyalaya, Bilaspur, India.
Department of Paediatric Oral Health and Orthodontics, University Center for Dental Medicine Basel UZB, Basel, Switzerland.
J Oral Biol Craniofac Res. 2025 Jul-Aug;15(4):691-695. doi: 10.1016/j.jobcr.2025.03.019. Epub 2025 Apr 18.
Matrilin-1 was shown to regulate the formation of cartilage matrix and to promote chondrocyte differentiation. This meta-analysis aims to synthesize evidence regarding the link between mandibular prognathism (MP) risk and the polymorphisms in the MATN1 gene.
Relevant publications were retrieved by searching the PubMed, Web of Science, and Google Scholar databases. The association between MP and the MATN1 gene polymorphisms (rs20566, rs1065755 was assessed by calculating odds ratios (ORs) and 95 % CIs. Between studies, heterogeneity was identified using the Cochrane Q test and I statistics. To assess the robustness of the meta-analysis sensitivity analysis was performed. The web tool MetaGenyo was used to conduct a meta-analysis.
A total of four Asian and one Caucasian study were eventually taken for meta-analysis. Overall, the MATN1 rs20566 and rs1065755 polymorphisms are not associated with elevated risk of MP (rs20566 AA + AG versus GG OR = 1.35, 95 % CI = 0.32-5.67; rs1065755 TT + CT versus CC OR = 2.02, 95 % CI = 0.87-4.68). The degree of heterogeneity is found to be large for the MATN1 polymorphisms (for rs20566, I89 %, and for rs1065755, I60 %).
In conclusion, this meta-analysis did not provide evidence for the link between MATN1 polymorphisms and MP. However, the results conflict with the biological plausibility that matrilin-1 levels modulate cartilage development. Therefore, careful interpretation is needed, and further research is recommended.
Matrilin-1被证明可调节软骨基质的形成并促进软骨细胞分化。本荟萃分析旨在综合有关下颌前突(MP)风险与MATN1基因多态性之间联系的证据。
通过检索PubMed、科学网和谷歌学术数据库获取相关出版物。通过计算比值比(OR)和95%置信区间(CI)评估MP与MATN1基因多态性(rs20566、rs1065755)之间的关联。在各研究之间,使用Cochrane Q检验和I统计量识别异质性。为评估荟萃分析的稳健性,进行了敏感性分析。使用网络工具MetaGenyo进行荟萃分析。
最终纳入荟萃分析的共有四项亚洲研究和一项高加索研究。总体而言,MATN1 rs20566和rs1065755多态性与MP风险升高无关(rs20566 AA + AG与GG相比,OR = 1.35,95% CI = 0.32 - 5.67;rs1065755 TT + CT与CC相比,OR = 2.02,95% CI = 0.87 - 4.68)。发现MATN1多态性的异质性程度较大(rs20566为I = 89%,rs1065755为I = 60%)。
总之,本荟萃分析未提供MATN1多态性与MP之间存在联系的证据。然而,这些结果与Matrilin-1水平调节软骨发育的生物学合理性相矛盾。因此,需要谨慎解读,并建议进一步研究。