Hartsfield James K, Jacob George Jeryn, Morford Lorri Ann
E. Preston Hicks Professor of Orthodontics and Oral Health Research, University of Kentucky Center for the Biologic Basis of Oral/Systemic Diseases, Hereditary Genetics/Genomics Core.
Craniofacial Genetics Fellow, University of Kentucky Center for the Biologic Basis of Oral/Systemic Diseases, Hereditary Genetics/Genomics Core.
Semin Orthod. 2017 Dec;23(4):336-347. doi: 10.1053/j.sodo.2017.07.003.
Uncovering the genetic factors that correlate with a clinical deviation of previously unknown etiology helps to diminish the unknown variation influencing the phenotype. Clinical studies, particularly those that consider the effects of an appliance or treatment regimen on growth, need to be a part of these types of genetic investigations in the future. While the day-to-day utilization of "testing" for genetic factors is not ready for practice yet, genetic testing for monogenic traits such as Primary Failure of Eruption (PFE) and Class III malocclusion is showing more promise as knowledge and technology advances. Although the heterogeneous complexity of such things as facial and dental development, the physiology of tooth movement, and the occurrence of External Apical Root Resorption (EARR) make their precise prediction untenable, investigations into the genetic factors that influence different phenotypes, and how these factors may relate to or impact environmental factors (including orthodontic treatment) are becoming better understood. The most important "genetic test" the practitioner can do today is to gather the patient's individual and family history. This would greatly benefit the patient, and augment the usefulness of these families in future clinical research in which clinical findings, environmental, and genetic factors can be studied.
揭示与病因不明的临床偏差相关的遗传因素,有助于减少影响表型的未知变异。临床研究,尤其是那些考虑矫治器或治疗方案对生长影响的研究,未来需要成为这类基因研究的一部分。虽然目前针对遗传因素的“检测”日常应用尚未准备好用于实践,但随着知识和技术的进步,对诸如萌出原发性失败(PFE)和Ⅲ类错牙合等单基因性状的基因检测显示出更大的前景。尽管面部和牙齿发育、牙齿移动生理学以及根尖外吸收(EARR)等情况具有异质性复杂性,使其精确预测难以实现,但对影响不同表型的遗传因素以及这些因素如何与环境因素(包括正畸治疗)相关或相互影响的研究正日益明晰。如今从业者所能进行的最重要的“基因检测”是收集患者的个人史和家族史。这将极大地造福患者,并增加这些家族在未来临床研究中的有用性,在这类研究中可以对临床发现、环境因素和遗传因素进行研究。