Mohammad Zakir Hossain1, Sulinda Daud2, Phrabhakaran Nambiar3, Fathilah Abdul Razak4, Norintan Ab-Murat5, Roslan Saub5, Marina M Bakri4. 1. Department of Oral and Craniofacial Sciences, Faculty of Dentistry, University of Malaya, Kuala Lumpur, Malaysia; Department of Oral Physiology, Faculty of Dentistry, Matsumoto Dental University, Nagano, Japan. Electronic address: zakir@po.mdu.ac.jp. 2. Dental Faculty, Segi University College, Petaling Jaya, Malaysia. 3. Department of Oro-maxillofacial Surgical & Medical Sciences, Faculty of Dentistry, University of Malaya, Kuala Lumpur, Malaysia. 4. Department of Oral and Craniofacial Sciences, Faculty of Dentistry, University of Malaya, Kuala Lumpur, Malaysia. 5. Department of Community Oral Health and Clinical Prevention, University of Malaya, Kuala Lumpur, Malaysia.
Abstract
OBJECTIVE: The aim of this study was to investigate correlations between dental pulp cell count of odontoblasts, subodontoblasts and fibroblasts and age, within different age groups. Formulation of regression equations using the dental pulp cell count for predicting age was attempted. DESIGN: Eighty-one extracted teeth were grouped into two age groups (6-25 years, 26-80 years). The teeth were demineralized and histological sections were prepared for cell count. Regression equations were generated from regression analysis of cell count and tested for age estimation. RESULTS: The number of dental pulp cells were found to increase until around the third decade of life and following this, the odontoblasts and subodontoblasts cell numbers began to decline while the fibroblasts seemed to remain almost stationary. The Pearson correlation test revealed a significant positive correlation between the cell number for all type of cells and age in the 6-25 years group (r=+0.791 for odontoblasts, r=+0.600 for subodontoblasts and r=+0.680 for fibroblasts). In the 26-80 years age group, a significant negative correlation of the odontoblasts (r=-0.777) and subodontoblasts (r=-0.715) with age was observed but for fibroblasts, the correlation value was negligible (r=-0.165). Regression equations generated using odontoblasts and subodontoblasts cell number were applicable for age estimation. The standard error of estimates (SEEs) were around±5years for 6-25 years and±8years for 26-80 years age groups. The mean values of the estimated and chronological ages were not significantly different. CONCLUSIONS: A significant correlation between the cell count of odontoblasts and subodontoblasts with age was demonstrated. Regression equations using odontoblasts and subodontoblasts cell number can be used to predict age with some limitations.
OBJECTIVE: The aim of this study was to investigate correlations between dental pulp cell count of odontoblasts, subodontoblasts and fibroblasts and age, within different age groups. Formulation of regression equations using the dental pulp cell count for predicting age was attempted. DESIGN: Eighty-one extracted teeth were grouped into two age groups (6-25 years, 26-80 years). The teeth were demineralized and histological sections were prepared for cell count. Regression equations were generated from regression analysis of cell count and tested for age estimation. RESULTS: The number of dental pulp cells were found to increase until around the third decade of life and following this, the odontoblasts and subodontoblasts cell numbers began to decline while the fibroblasts seemed to remain almost stationary. The Pearson correlation test revealed a significant positive correlation between the cell number for all type of cells and age in the 6-25 years group (r=+0.791 for odontoblasts, r=+0.600 for subodontoblasts and r=+0.680 for fibroblasts). In the 26-80 years age group, a significant negative correlation of the odontoblasts (r=-0.777) and subodontoblasts (r=-0.715) with age was observed but for fibroblasts, the correlation value was negligible (r=-0.165). Regression equations generated using odontoblasts and subodontoblasts cell number were applicable for age estimation. The standard error of estimates (SEEs) were around±5years for 6-25 years and±8years for 26-80 years age groups. The mean values of the estimated and chronological ages were not significantly different. CONCLUSIONS: A significant correlation between the cell count of odontoblasts and subodontoblasts with age was demonstrated. Regression equations using odontoblasts and subodontoblasts cell number can be used to predict age with some limitations.
Authors: Marytere Guerrero-Jiménez; Geovanny I Nic-Can; Nelly Castro-Linares; Fernando Javier Aguilar-Ayala; Michel Canul-Chan; Rafael A Rojas-Herrera; Ricardo Peñaloza-Cuevas; Beatriz A Rodas-Junco Journal: PeerJ Date: 2019-12-06 Impact factor: 2.984
Authors: Shilpa Bhandi; Ahmed Al Khatani; Hassan Abdulaziz Sumayli; Mushyirah Yahya Sabyei; Abdulaziz Mohammed Al Zailai; Mohammed Ali Sumayli; Hanan Ibrahim Hakami; Mohammed Abdurabu Jafer; Nishant Vyas; Hosam Ali Baeshen; Luca Testarelli; Shankargouda Patil Journal: Saudi J Biol Sci Date: 2021-03-17 Impact factor: 4.219