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Tooth loss represents the most prevalent form of dental agenesis. Anterior tooth loss primarily impacts aesthetics and psychological well-being, whereas posterior tooth loss influences bone growth patterns and masticatory function. Prolonged tooth loss can significantly hinder subsequent restorative procedures. Genetic factors are among the principal contributors to tooth loss, as genes dictate the location, quantity, and morphology of teeth; mutations at specific gene loci may result in underdevelopment or even complete absence of teeth. Investigating the relationship between gene polymorphisms and tooth loss could yield novel insights for future clinical interventions aimed at addressing this issue. Consequently, this study aims to elucidate the correlation between and gene polymorphisms and instances of tooth loss. We searched Cochrane, PubMed, Web of Science, MEDLINE, EMBASES, and CNKI journal databases for articles up to April 1, 2024 to determine the association of and genes with the risk of dental development. Used STATA version 11.2 to calculate the odds ratio (OR) and 95% confidence interval (CI). Analyzed meta-regression, sensitivity, and publication bias. Used Bayesian measures of the false positive reporting probability and false discovery probability to examine the reliability of the calculation. Finally, 12 eligible reports were included in this study, including 7 reports on , with 873 cases of polymorphism and 812 cases of control; 5 reports on , with 668 cases of polymorphism and 668 cases of control; 7 reports on , with 762 cases of polymorphism and 1,544 cases of control. The ORs and 95% CIs showed a statistically significant relationship between or polymorphism and tooth agenesis risk. Moreover, there was no association observed for the polymorphism. In further subgroup analysis of the polymorphisms (, ), we found an increased risk of tooth loss in the Caucasian and Hungarian groups. This article concludes that the and polymorphism might help to increase the risk of tooth agenesis. Understanding the mechanisms of genetic mutations will enable clinical physicians and human geneticists to develop new strategies for future therapeutic research and preventive treatments.
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http://dx.doi.org/10.1515/biol-2022-0987 | DOI Listing |
Front Aging Neurosci
August 2025
Department of Prosthodontics, Beijing Stomatological Hospital, School of Stomatology, Capital Medical University, Beijing, China.
Introduction: Alzheimer's Disease (AD) is a common neurodegenerative disease among the elderly population. It has been posited that the onset and progression of AD are influenced by a combination of various factors. Occlusal support loss due to tooth loss has been reported to be a risk factor triggering cognitive dysfunction.
View Article and Find Full Text PDFInt J Dent
August 2025
Department of Periodontics, Virginia Commonwealth University, Richmond, Virginia, USA.
Periodontal splints offer a noninvasive and inexpensive treatment modality to stabilize mobile teeth. This study evaluated periodontal splints to examine their longevity and long-term stability. A retrospective chart review was performed for patients who received splints on mandibular or maxillary anterior teeth.
View Article and Find Full Text PDFInt Endod J
September 2025
Department of Biochemistry, School of Dentistry, IHBR, Kyungpook National University, Daegu, South Korea.
Aim: Prickle planar cell polarity (PCP) protein 2 (Prickle2) encodes a homologue of Drosophila prickle and is involved in the non-canonical Wnt/PCP signalling pathway. However, its exact role in dentinogenesis remains unclear. Dentinogenesis, a key process in tooth morphogenesis, involves the patterned arrangement of odontoblasts and the formation of dentine matrix along the pulp cavity.
View Article and Find Full Text PDFFront Oncol
August 2025
Department of Medical Oncology, Catalan Institute of Oncology, Dr. Josep Trueta University Hospital, Girona, Spain.
Inflammatory breast cancer (IBC) is a rare and aggressive breast cancer type, accounting for 5-7% of breast cancer-related deaths, and its bilateral involvement is exceedingly uncommon. We report a case of metachronous bilateral IBC in a 50-year-old premenopausal woman with Charcot-Marie-Tooth disease, offering novel insight into the diagnostic, therapeutic, and molecular challenges of this condition. The patient initially presented with acute right breast erythema, skin thickening, and , followed by contralateral breast involvement with similar symptoms.
View Article and Find Full Text PDFSpinal muscular atrophy with respiratory distress type 1 (SMARD1) and Charcot Marie Tooth type 2S (CMT2S) are due to mutations in immunoglobulin mu binding protein two (IGHMBP2). We generated the -R604X mouse (R605X-humans) to understand how alterations in IGHMBP2 function impact disease pathology. The IGHMBP2-R605X mutation is associated with patients with SMARD1 or CMT2S.
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