Effect of zinc supplements on the incidence of caries and on the concentration of salivary A immunoglobulins in short stature school children

Authors

  • Janeth Parra Facultad de Odontología, Universidad de Cuenca, Cuenca, Ecuador.
  • Diana Astudillo Facultad de Ciencias Químicas, Universidad de Cuenca, Cuenca, Ecuador
  • Pablo Parra Médico Internista-Neumólogo, Hospital José Carrasco Arteaga, Cuenca, Ecuador.
  • Fernando Sempértegui Facultad de Ciencias Médicas, Universidad Central del Ecuador, Quito, Ecuador.

DOI:

https://doi.org/10.18537/mskn.04.01.03

Keywords:

DMFT, DMFS, zinc, IgA salival, oral hygiene

Abstract

Young children in Ecuador show high prevalence of chronic zinc deficiency, associated with a decline in cellular and humoral immunity, and increased risk of tooth decay. The research reported in this paper presents the effect of the daily consumption of 10 mg zinc sulfate versus the control group receiving a solution with an inactive substance during 42 weeks, on respectively the children’s weight, height, the immunoglobulin A (IgA) concentration in saliva, the plasma concentrations of zinc, and the indices of Klein and Palmer (DMFT and DMFS). In the survey special attention was given to the detection of early stage tooth decay, also called incipient decay. Parallel, information about the children’s hygiene and living condition was collected using structured questionnaires. Statistical analysis of the collected data revealed that DMFS is less and the final concentration of plasma zinc higher in the experimental group of children receiving daily a zinc supplement (17,30 ± 9,55 vs. 20,03 ± 10,74; p = 0,032; 123 ± 24,29 μg dl-1 vs. 105,57 ± 15,75 μg dl-1; p < 0,001). Multiple linear regression showed that zinc supplements are associated with reduced DMFS (beta = -3,9; p = 0,033) and DMFT (beta = -1,33; p = 0,05), and that the basal state of zinc allies with a lower final concentration of IgA in saliva (beta = - 0,043; p = 0,011). More intensive toothbrush with the use of toothpaste was associated with a reduction of DMFS (beta = -7,14; p = 0,033). Rinsing the mouth with potable water resulted in a decline of DMFT (beta = -1,42; p = 0,035). The study revealed that zinc supplements and oral hygiene positively affect oral health, likely through an improvement of oral mucosal immunity, which when applied will reduce the magnitude of this public health problem.

 

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References

Ariede Petinuci, P., K. Polido Kaneshiro, M.A. Rabelo, 2005. Dental caries and dental fluorosis in 7-12-yearold schoolchildren in Catalão, Goiás, Brazil. J. Appl. Oral. Sci., 13(1), 35-40.

Atasoy, H.B., Z.I. Ulusoy, 2012. The relationship between zinc deficiency and children's oral health. Pediatr. Dent., 34(5), 383-6.

Beck, F.W., A.S. Prasad, J. Kaplan, J.T. Fitzgerald, G.J. Brewer, 1997. Changes in cytokine production and T cell subpopulations in experimentally induced zinc-deficient humans. Am. J. Physiol., 272(6 Pt 1), E1002-7.

Aydin Sevinç, B., L. Hanley, 2010. Antibacterial activity of dental composites containing zinc oxide nanoparticles. J. Biomed. Mater. Res. B Appl. Biomater., 94, 22-31.

Bhutta, Z.A., R.E. Black, K.H. Brown, J.M. Gardner, S. Gore, A. Hidayat, F. Khatun, R. Martorell, N.X. Ninh, M.E. Penny, J.L. Rosado, S.K. Roy, M. Ruel, S. Sazawal, A. Shankar, 1999. Prevention of diarrhea and pneumonia by zinc supplementation in children in developing countries: pooled analysis of randomized controlled trials. J. Pediatr., 135(6), 689-97.

Brown, K.H., J.M. Peerson, J. Rivera, L.H. Allen, 2002. Effect of supplemental zinc on the growth and serum zinc concentrations of prepubertal children a meta-analysis of randomized controlled trials. Am. J. Clin. Nutr., 75(6), 1062-1071.

Cerklewski, F.L., 1981. Effect of suboptimal zinc nutrition during gestation and lactation on rat molar tooth composition and dental caries. J. Nutr., 111(10), 1780-3.

Fraker, P.J., L.E. King, T. Laakko, T.L. Vollmer, 2000. The dynamic link between the integrity of the immune system and zinc status. J. Nutr., 130, 1399S-406S.

Freire, W., 1988. Diagnostico de la situación alimentaria, nutricional y de salud de la población ecuatoriana menor de 5 años: Resumen. CONADE-M.S.P., Ecuador. Descargado de http://www.repositorio.iaen.edu.ec .../DIAGNOSTICO%20DE%20... en 2012, 62 págs.

Hau, J., E. Andersson, H.E. Carlsson, 2001. Development and validation of a sensitive ELISA for quantification of secretory IgA in rat saliva and faeces. Lab. Animal., 35(4), 301-6.

Hu, D., P.K. Sreenivasan, Y.P. Zhang, W. De Vizio, 2010. The effects of a zinc citrate dentifrice on bacteria found on oral surfaces. Oral Health Prev. Dent., 8(1),:47-53.

International Zinc Nutrition Consultative Group (IZiNCG), K.H. Brown, J.A. Rivera, Z. Bhutta, R.S. Gibson, J.C. King, B. Lönnerdal, M.T. Ruel, B. Sandtröm, E. Wasantwisut, C. Hotz, 2004. International Zinc Nutrition Consultative Group (IZiNCG) Technical Document #1. Assessment of the risk of zinc deficiency in populations and options for its control. Food. Nutr. Bull., 25(1 Suppl 2), S99-203.

Johnson, D.A., O.F. Alvares, 1984. Zinc deficiency-induced changes in rat parotid salivary proteins. J. Nutr.,114(10), 1955-64.

Larrea, C., W. Freire, Ch. Lutter, 2001. Equidad desde el principio: Situación nutricional de los niños ecuatorianos. Organización Panamericana de la Salud, Washington D.C., EE.UU., 41 págs.

Lee, S.R., H.K. Kwon, K.B. Song, Y.H. Choi, 2004. Dental caries and salivary immunoglobulin A in Down syndrome children. J. Paediatr. Child Health., 40(9-10), 530-3.

Lynch, R.J., 2011. Zinc in the mouth, its interactions with dental enamel and possible effects on caries; a review of the literature. Int. Dent. J., 61 Suppl 3, 46-54.

Nicolau, B., W. Marcenes, P. Allison, A. Sheiham, 2005. The life course approach: explaining the association between height and dental caries in Brazilian adolescents. Community Dent. Oral Epidemiol., 33(2), 93-8.

Peres, K.G., R. Latorre Mdo, M.A. Peres, J. Traebert, M. Panizzi, 2003. Impact of dental caries and dental fluorosis on 12-year-old school children's self-perception of appearance and chewing. Cad. Saude Publica, 19(1), 323-30.

Prasad, A.S., S. Meftah, J. Abdallah, J. Kaplan, G.J. Brewer, J.F. Bach, M. Dardenne, 1988. Serum thymulin in human zinc deficiency. J. Clin. Invest., 82(4), 1002-10.

PRECONC,1992. Odontología Preventiva (Curso 1). Programa de Educación Continua Odontológica No Convencional, Organización Panamericana de la Salud. Buenos Aires, págs. 28-32.

Proctor, G.B., G.H. Carpenter, 2001. Chewing stimulates secretion of human salivary secretory immunoglobulin A. J. Dent. Res., 80(3), 909-13.

Sazawal, S., R.E. Black, M.K. Bhan, S. Jalla, A. Sinha, N. Bhandari, 1997. Efficay of zinc supplementation in reducing the incidence and prevalence of acute diarrhea- a community-based, double-blind, controlled trial. Am. J. Clin. Nutr., 66(2), 413-418.

Secretaria de Salud de Bogotá, Grupo Salud Oral, 2007. Proyecto de Desarrollo de Autonomía de salud Oral. Bogotá DC, Colombia. Descargado de http://saludpublicabogota.org/wiki/images/3/34/Salud_oral.pdf en noviembre 2012.

Sempértegui, F., B. Estrella, E. Correa, L. Aguirre, B. Saa, M. Torres, F. Navarrete, C. Alarcón, J. Carrión, Rodríguez, J.K. Griffiths, 1996. Effects of short-term zinc supplementation on cellular immunity, respiratory symptoms, and growth of malnourished Equadorian children. Eur. J. Clin. Nutr., 50(1), 42-46.

Shankar, A.H., A.S. Prasad, 1998. Zinc and immune function : the biological basis of altered resistance to infection. Am. J. Clin. Nutr., 68(2 Suppl), 447S-463S.

Smith, P.G., R.H. Morrow, 1991. Methods for field trials of intervention against tropical diseases: a toolbox. Oxford University Press, New York, 352 págs.

Struska, A., M. Mielnik-Blaszczak, 2003. Correlation between frequency of caries in deciduous dentition and physical development of children in the first six months of life. Ann. Univ. Mariae Curie Sklodowska Med., 58(1),179-84.

Tar, I., E. Nemes, J. Nemes, M. Alberth, G. Keszthelyi, 1999. The role of salivary immunoglobulins (secretory IgA, IgM, IgG) in caries prevalence and primary B-cell deficiency. Fogorv Sz., 92(11), 331-8.

Talukder, P., T. Satho, K. Irie, T. Sharmin, D. Hamady, Y. Nakashima, N. Kashige, F. Miake, 2011. Trace metal zinc stimulates secretion of antimicrobial peptide LL-37 from Caco-2 cells through ERK and p38 MAP kinase. Int. Immunopharmacol., 11(1), 141-4.

Toledano, M., M. Yamauti, E. Osorio, R. Osorio, 2012. Zinc-inhibited MMP-mediated collagen degradation after different dentine demineralization procedures. Caries Res., 46, 201-7.

WHO, 2000. Global Oral Health Data Bank and WHO Oral Health Country/Area Profile Programme. En: Petersen, P.E., Challenges to improvement of oral health in the 21st century - the approach of the WHO Global Oral Health Programme. Int. Dent. J., 54, 329-343.

WHO, 1987. Oral health surveys. Basic Methods (3rd Ed.). World Health Organization, Geneve, Suiza.

Wuehler, S.E., F. Sempértegui, K.H. Brown, 2008. Dose-response trial of prophylactic zinc supplements, with or without copper, in young Ecuadorian children at risk of zinc deficiency. Am. J. Clin. Nutr., 87, 723–33.

Zahir, S., S. Sarkar, 2006. Study of trace elements in mixed saliva of caries free and caries active children. J. Indian Soc. Pedod. Prev. Dent., 24(1), 27-9.

Zhou, J.R., N.M. Cnara, J.W. Erdman Jr., 1993. Bone zinc is poorly released in young, growing rats fed marginally zinc-restricted diet. J. Nutr., 123(8), 1383-8.

Published

2013-06-25

How to Cite

Parra, J., Astudillo, D., Parra, P., & Sempértegui, F. (2013). Effect of zinc supplements on the incidence of caries and on the concentration of salivary A immunoglobulins in short stature school children. Maskana, 4(1), 29–39. https://doi.org/10.18537/mskn.04.01.03

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Research articles

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