Edinburgh Dental Institute, University of Edinburgh, Edinburgh, UK.
Department of Paediatric Dentistry, NHS Lothian, Edinburgh, UK.
J Orthod. 2021 Sep;48(3):221-230. doi: 10.1177/1465312520984166. Epub 2021 Jan 18.
Different genes and loci that are associated with non-syndromic developmental tooth agenesis (TA) have the same causation pathway in the development of tumours including breast cancer (BC), epithelial ovarian cancer (EOC), colorectal cancer (CRC) and lung cancer (LC).
To assess the link between TA and the development of cancer.
This registered review included a comprehensive search of electronic databases (Cochrane Central Register of Controlled Trials [CENTRAL], LILACS, Scopus, Web of Science and Medline via Ovid) until 1 April 2020, supplemented by manual, grey literature and reference lists search. There was no restriction in term of date of publication, gender, race or type of hypodontia.
The primary outcome was the relationship between TA and cancer. The secondary outcome was to identify the genetic correlation between TA and cancer.
Study selection, data extraction and risk of bias assessment were performed independently and induplicate by two reviewers, with disputes resolved by a third reviewer.
Eight studies with a moderate-high risk of bias were included in the final review, with a total of 5821 participants. Due to the heterogeneity among the included studies, the data were presented narratively. Limited studies reported a high prevalence of EOC (19.2%-20%) and CRC (82%-100%) in individuals with TA (depending on the study) compared to those without TA (3% for EOC and 0% for CRC). While others reported a weak correlation between EOC and CRC and TA ( > 0.05). Weak evidence suggested a strong correlation between breast, cervical uterine and prostate cancers and TA ( < 0.05).
Though low-quality evidence suggests a link between TA and cancer, it was not possible to verify that TA can hold a predictive value as a marker for cancers. Further research is needed to confirm the association.
PROSPERO (CRD42020139751).
与非综合征性发育性牙齿缺失(TA)相关的不同基因和基因座在肿瘤的发生中具有相同的发病途径,包括乳腺癌(BC)、上皮性卵巢癌(EOC)、结直肠癌(CRC)和肺癌(LC)。
评估 TA 与癌症发生之间的联系。
本注册综述包括对电子数据库(Cochrane 对照试验中心注册库[CENTRAL]、LILACS、Scopus、Web of Science 和 Ovid 中的 Medline)的全面检索,截至 2020 年 4 月 1 日,还补充了手动检索、灰色文献和参考文献检索。检索时没有对出版日期、性别、种族或类型的缺牙进行限制。
主要结局是 TA 与癌症之间的关系。次要结局是确定 TA 与癌症之间的遗传相关性。
研究选择、数据提取和偏倚风险评估由两名评审员独立进行,有争议的问题由第三名评审员解决。
最终综述纳入了 8 项偏倚风险较高的研究,共纳入 5821 名参与者。由于纳入研究之间存在异质性,数据以叙述的方式呈现。有限的研究报告称,TA 患者(取决于研究)中 EOC(19.2%-20%)和 CRC(82%-100%)的患病率较高,而 TA 患者(EOC 为 3%,CRC 为 0%)。而其他研究则报告 EOC 和 CRC 与 TA 之间存在弱相关性(>0.05)。证据表明,TA 与乳腺癌、宫颈癌、子宫内膜癌和前列腺癌之间存在很强的相关性(<0.05)。
尽管低质量证据表明 TA 与癌症之间存在关联,但尚无法证实 TA 可作为癌症的预测标志物。需要进一步研究来证实这种关联。
PROSPERO(CRD42020139751)。