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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...

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Autores principales: 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.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
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.
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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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