Towards Genetic Dissection of Skeletal Class III Malocclusion: A Review of Genetic Variations Underlying the Phenotype in Humans and Future Directions

被引:20
|
作者
Zohud, Osayd [1 ]
Lone, Iqbal M. [1 ]
Midlej, Kareem [1 ]
Obaida, Awadi [2 ]
Masarwa, Samir [2 ]
Schroeder, Agnes [3 ,4 ]
Kuechler, Erika C. [3 ]
Nashef, Aysar [5 ]
Kassem, Firas [6 ,7 ]
Reiser, Vadim [8 ]
Chaushu, Gavriel [8 ,9 ]
Mott, Richard [10 ]
Krohn, Sebastian [3 ]
Kirschneck, Christian [3 ]
Proff, Peter [3 ]
Watted, Nezar [2 ,11 ,12 ]
Iraqi, Fuad A. [1 ,3 ,12 ]
机构
[1] Tel Aviv Univ, Sackler Fac Med, Dept Clin Microbiol & Immunol, IL-6997801 Tel Aviv, Israel
[2] Ctr Dent Res & Aesthet, IL-4491800 Jatt, Israel
[3] Univ Regensburg, Univ Hosp Regensburg, Dept Orthodont, D-93047 Regensburg, Germany
[4] Inst Clin Microbiol & Hyg, D-93053 Regensburg, Germany
[5] Baruch Padeh Med Ctr, Dept Oral & Maxillofacial Surg, IL-1520800 Poriya, Israel
[6] Meir Med Ctr, Dept Otorhinolaryngol Head & Neck Surg, IL-4428164 Kefar Sava, Israel
[7] Tel Aviv Univ, Sackler Fac Med, IL-6997801 Tel Aviv, Israel
[8] Rabin Med Ctr, Dept Oral & Maxillofacial Surg, Beilinson Campus, IL-4941492 Petah Tiqwa, Israel
[9] Tel Aviv Univ, Sch Dent Med, IL-69978 Tel Aviv, Israel
[10] UCL, Dept Genet, London SE1 7EH, England
[11] Arab Amer Univ, Fac Dent, Dept Orthodont, Jenin 34567, Palestine
[12] Gathering Prosper Initiat, IL-4491800 Jatt, Israel
关键词
quantitative trait loci (QTL) mapping; genome-wide association study (GWAS); epigenetics-wide association study (EWAS); RNAseq analysis; expression quantitative trait loci (eQTL); micro and small RNA analysis; MYOSIN HEAVY-CHAIN; GENOME-WIDE ASSOCIATION; MASSETER MUSCLE; MANDIBULAR PROGNATHISM; MESSENGER-RNA; ORTHOGNATHIC SURGERY; PREVALENCE; LINKAGE; MICROSATELLITE; CONTRIBUTES;
D O I
10.3390/jcm12093212
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Introduction: Skeletal abnormalities and malocclusions have varied features that impact populations globally, impairing aesthetics and lowering life quality. The prevalence of the Skeletal Class III disease is the lowest among all angle malocclusions, with varied prevalence across nations. Environmental, genetic, and societal factors play a role in its numerous etiologies. In this study, we conducted a thorough search across the published data relating to quantitative trait loci (QTL) and the genes associated with Class III progression in humans, discussed these findings and their limitations, and proposed future directions and strategies for studying this phenotype. Methods: An inclusive search of published papers in the PubMed and Google Scholar search engines using the following terms: 1. Human skeletal Class III; 2. Genetics of Human skeletal Class III; 3. QTL mapping and gene associated with human skeletal Class III; 4. enriched skeletal Class-III-malocclusion-associated pathways. Results: Our search has found 53 genes linked with skeletal Class III malocclusion reported in humans, genes associated with epigenetics and phenomena, and the top 20 enriched pathways associated with skeletal Class III malocclusion. Conclusions: The human investigations yielded some contentious conclusions. We conducted a genome-wide association study (GWAS), an epigenetics-wide association study (EWAS), RNA-seq analysis, integrating GWAS and expression quantitative trait loci (eQTL), micro- and small-RNA, and long non-coding RNA analysis in tissues connected to skeletal Class III malocclusion phenotype in tissues connected with the skeletal phenotype. Finally, we invite regional, national, and international orthodontists and surgeons to join this effort by contributing human samples with skeletal Class III malocclusion following the accepted Helsinki ethical protocol to challenge these phenomena jointly.
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页数:17
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