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Towards Genetic Dissection of Skeletal Class III Malocclusion: A Review of Genetic Variations Underlying the Phenotype in Humans and Future Directions
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. Environme...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10179046/ https://www.ncbi.nlm.nih.gov/pubmed/37176653 http://dx.doi.org/10.3390/jcm12093212 |
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author | Zohud, Osayd Lone, Iqbal M. Midlej, Kareem Obaida, Awadi Masarwa, Samir Schröder, Agnes Küchler, Erika C. Nashef, Aysar Kassem, Firas Reiser, Vadim Chaushu, Gavriel Mott, Richard Krohn, Sebastian Kirschneck, Christian Proff, Peter Watted, Nezar Iraqi, Fuad A. |
author_facet | Zohud, Osayd Lone, Iqbal M. Midlej, Kareem Obaida, Awadi Masarwa, Samir Schröder, Agnes Küchler, Erika C. Nashef, Aysar Kassem, Firas Reiser, Vadim Chaushu, Gavriel Mott, Richard Krohn, Sebastian Kirschneck, Christian Proff, Peter Watted, Nezar Iraqi, Fuad A. |
author_sort | Zohud, Osayd |
collection | PubMed |
description | 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. |
format | Online Article Text |
id | pubmed-10179046 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-101790462023-05-13 Towards Genetic Dissection of Skeletal Class III Malocclusion: A Review of Genetic Variations Underlying the Phenotype in Humans and Future Directions Zohud, Osayd Lone, Iqbal M. Midlej, Kareem Obaida, Awadi Masarwa, Samir Schröder, Agnes Küchler, Erika C. Nashef, Aysar Kassem, Firas Reiser, Vadim Chaushu, Gavriel Mott, Richard Krohn, Sebastian Kirschneck, Christian Proff, Peter Watted, Nezar Iraqi, Fuad A. J Clin Med Perspective 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. MDPI 2023-04-29 /pmc/articles/PMC10179046/ /pubmed/37176653 http://dx.doi.org/10.3390/jcm12093212 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Perspective Zohud, Osayd Lone, Iqbal M. Midlej, Kareem Obaida, Awadi Masarwa, Samir Schröder, Agnes Küchler, Erika C. Nashef, Aysar Kassem, Firas Reiser, Vadim Chaushu, Gavriel Mott, Richard Krohn, Sebastian Kirschneck, Christian Proff, Peter Watted, Nezar Iraqi, Fuad A. Towards Genetic Dissection of Skeletal Class III Malocclusion: A Review of Genetic Variations Underlying the Phenotype in Humans and Future Directions |
title | Towards Genetic Dissection of Skeletal Class III Malocclusion: A Review of Genetic Variations Underlying the Phenotype in Humans and Future Directions |
title_full | Towards Genetic Dissection of Skeletal Class III Malocclusion: A Review of Genetic Variations Underlying the Phenotype in Humans and Future Directions |
title_fullStr | Towards Genetic Dissection of Skeletal Class III Malocclusion: A Review of Genetic Variations Underlying the Phenotype in Humans and Future Directions |
title_full_unstemmed | Towards Genetic Dissection of Skeletal Class III Malocclusion: A Review of Genetic Variations Underlying the Phenotype in Humans and Future Directions |
title_short | Towards Genetic Dissection of Skeletal Class III Malocclusion: A Review of Genetic Variations Underlying the Phenotype in Humans and Future Directions |
title_sort | towards genetic dissection of skeletal class iii malocclusion: a review of genetic variations underlying the phenotype in humans and future directions |
topic | Perspective |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10179046/ https://www.ncbi.nlm.nih.gov/pubmed/37176653 http://dx.doi.org/10.3390/jcm12093212 |
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