- Correlation between dental fluorosis risk and bone specific alkaline phosphatase, osteocalcin, matrix metalloproteinase and parathyroid hormone in children
Bone-specific Alkaline Phosphatase, Osteocalcin, Matrix Metalloproteinase, and Parathyroid Hormone Levels and the Risk of Dental Fluorosis
Abstract
Objective Investigating the association between dental fluorosis occurrence in children and bone metabolism-related indicators including bone-specific alkaline phosphatase (BALP), osteocalcin (OC), matrix metalloproteinase (MMP-2, MMP-9, MMP-20), and parathyroid hormone (PTH).Methods A total of 189 cases of school-age children underwent health examinations in our hospital were enrolled, according to the presence or absence of dental fluorosis, they were divided into fluorosis group (n=97) and fluoride-free group (n=92), and the serum BALP, OC, MMP-2, MMP-9, MMP-20, and PTH levels of the two groups were compared, relevant clinical data were collected.In this study, multivariate logistic regression was employed to examine the factors associated with the development of dental fluorosis in children. Results The urine fluoride levels, BALP, MMP-2, and MMP-9 of the children influorosis group were higher thanfluoride-free group, and the mother's educational level, per capita annual household income, OC, and PTH were lower thanfluoride-free group (P<0.05).Based on Spearman correlation analysis, a positive correlation was identified between the urinary fluoride level, the extent of dental fluorosis, and indicators such as BALP, MMP-2, and MMP-9. (r=0.618, 0.558, 0.567, 0.597, 0.602, 0.571, P<0.001), and negatively correlated with OC and PTH (r=-0.580, -0.603, -0.549, -0.515, P<0.001).As the urinary fluoride level and the extent of dental fluorosis increased, there was a gradual elevation in serum BALP, MMP-2, and MMP-9 levels in children, while OC and PTH levels gradually decreased (P<0.05).After adjusting for confounding factors including urinary fluoride,maternal education level, and per capita annual household income, multivariate Logistic regression analysis showed that BALP, OC, MMP-2, MMP-9, PTH were independently associated with the risk of dental fluorosis (P<0.05). Conclusion High BALP, MMP-2, MMP-9, low OC, and PTH are independent factors affecting the occurrence of dental fluorosis and are related tothe extent of dental fluorosis.
References
[2] NI Na, WU Chunfeng, LI Changhua, et al. Analysis of Dental fluorosis in 2393 school-age children[J]. Chinese Journal of Endemic Disease Prevention and Control, 2020, 35(5): 568-569.
[3] Chakraborty A, Pramanik S, Datta K, et al. Possible Association Between Polymorphisms in ESR1, COL1A2, BGLAP, SPARC, VDR, and MMP2 Genes and Dental Fluorosis in a Population from an Endemic Region of West Bengal[J]. Biol Trace Elem Res, 2022,23(9):224-229.
[4] ZHANG Yu, XU Guoxuan, GUO Hui. Investigation and analysis of dental caries and fluoride content in drinking water in children in Nanyang City[J]. Chinese Journal of Endemic Disease Prevention and Control, 2021, 36(2):164-165.
[5] WANG Lihua, AN Dong, BIAN Jianchao, et al. Instructions and illustrations for the preparation of newly revised Dean method diagnostic criteria for dental fluorosis[J]. Chinese Journal of Endemics, 2013, 32(2):213-216.
[6] General Administration of Quality Supervision, Inspection and Quarantine of the People's Republic of China, Standardization Administration of the People's Republic of China. WS/T208-2011 Dental fluorosis diagnosis[S].Beijing: China Standards Press,2011.
[7] Nagendra AH, Bose B, Shenoy P S. Recent advances in cellular effects of fluoride: an update on its signalling pathway and targeted therapeutic approaches[J]. Mol Biol Rep,2021 ,48(7):5661-5673.
[8] Rojanaworarit C, Claudio L, Howteerakul N, et al. Hydrogeogenic fluoride in groundwater and dental fluorosis in Thai agrarian communities: a prevalence survey and case-control study[J]. BMC Oral Health, 2021,21(1):545-560.
[9] JIN Xiang, WANG Yang, CAO Lichun. Analysis of influencing factors of dental fluorosis and caries in children with different hydrofluoride areas in Tianjin[J]. Journal of Environment and Health, 2020,37(8):717-721.
[10] Garcia ALH, Picinini J, Silveira MD, et al. Fluorosilicic acid induces DNA damage and oxidative stress in bone marrow mesenchymal stem cells[J]. Mutat Res Genet Toxicol Environ Mutagen, 2021,861(862):5032-5036.
[11] Collins MT, Marcucci G, Anders HJ, et al. Skeletal and extraskeletal disorders of biomineralization. Nat Rev Endocrinol, 2022,16(4):164-169.
[12] ZHANG Pan-H, LI X X, ZHOU C, et al. Correlation between prevalence of dental fluorosis and dietary nutrient intake in children[J]. Public Health and Preventive Medicine, 2022, 33(3):101-103.
[13] Meena L, Gupta R. Skeletal Fluorosis[J]. N Engl J Med, 2021,385(16):1510-1524.
[14] Srivastava S, Flora SJS. Fluoride in Drinking Water and Skeletal Fluorosis: a Review of the Global Impact[J]. Curr Environ Health Rep, 2020,7(2):140-146.
[15] Fan Zhongxue, Li Xiaoqian, Li Yue, et al. Relationship between drinking water fluoride content and dental fluoride and caries in children in Shaanxi Province[J]. Chinese Journal of Endemics, 2020, 39(5):344-346.
[16] Siddiq H, Pentapati KC, Acharya S. Children's perception of other children with dental fluorosis - A cross-sectional study[J]. J Oral Biol Craniofac Res,2020,10(2):72-77.
[17] Wang S, Zhao Q, Li G, et al. The cholinergic system, intelligence, and dental fluorosis in school-aged children with low-to-moderate fluoride exposure[J]. Ecotoxicol Environ Saf. 2021,20(228):1129-1134.
[18] DONG Lu, YAO Peijie, LI Ping, et al. Status of dental fluorosis in children aged 8-12 years in Xi'an, 2014-2018[J]. School hygiene in China, 2021, 42(1):120-123.
[19] García-Pérez A, Pérez-Pérez NG, Flores-Rojas AI, et al. Marginalization and fluorosis its relationship with dental caries in rural children in Mexico: A cross-sectional study[J]. Community Dent Health, 2020,37(3):216-222.
[20] Saldarriaga A, Rojas-Gualdrón DF, Restrepo M, et al. Clinical changes in the severity of dental fluorosis: a longitudinal evaluation[J]. BMC Oral Health, 2021,21(1):366-366.
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