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Correlation between Candida spp. and DMFT index in a rural population
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Keywords

Caries. Candida. Age groups

How to Cite

1.
Cortelli SC, Junqueira JC, Faria I da S, Koga Ito CY, Cortelli JR. Correlation between Candida spp. and DMFT index in a rural population. Braz. J. Oral Sci. [Internet]. 2015 Nov. 25 [cited 2024 Feb. 26];5(17):1007-11. Available from: https://periodicos.sbu.unicamp.br/ojs/index.php/bjos/article/view/8641886

Abstract

Oral presence of Candida spp. was correlated with caries experience (dmft/DMFT index) in a rural population. dmft/DMFT index were evaluated in individuals between 6-12 years of age (n=57), 13-18 years of age (n=48) and 19-45 years of age (n=54). For the isolation of Candida spp., saliva samples were collected and spread on Sabouraud dextrose agar plates. The number of colony- forming units per plate (CFU/plate) was calculated and the isolates were identified. Data were analyzed by Chi-square and Spearman’s correlation coefficient (p<0.05). The mean value obtained for dmft/DMFT index were 6.63 (6-12 years of age), 11.44 (13-18 years of age), and 21.16 (19-45 years of age). Candida spp. were isolated from 60% of the individuals between 6-12 years of age, 70% of the individuals between 13-18 years of age and 95% of the individuals between 19-45 years of age. In the 13-18 years of age group a positive correlation between Candida and DMFT was observed. No correlation was observed among Candida and DMFT index in the others age groups. In conclusion, the presence of Candida spp. in the oral cavity seem to be related with past caries experience in young adults from 13 to 18 years of age.
https://doi.org/10.20396/bjos.v5i17.8641886
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References

Raitio M, Pienihäkkinen K, Scheinin A. Assessment of single risk indicators in relation to caries increment in adolescents. Acta Odontol Scand. 1996; 54: 113-7.

Pienihäkkinen K. Caries prediction through combined use of incipient caries lesions, salivary buffering capacity, lactobacilli and yeasts in Finland. Community Dent Oral Epidemiol. 1987; 15: 325-8.

Künzel W, Fisher T, Lorenz R, Brümann S. Decline of caries prevalence after the cessation of water fluoridation in the former East Germany. Community Dent Oral Epidemiol. 2000; 28: 382-9.

Vrbic V. Reasons for the caries decline in Slovenia. Community Dent Oral Epidemiol. 2000; 28: 126-32.

Coulter WA, Murray SD, Kinirons MJ. The use of a concentrated oral rinse culture technique to sample oral Candida and Lactobacilli in children, and the relationship between Candida and Lactobacilli levels and dental caries experience: a pilot study. Int J Paediatr Dent. 1993; 3: 17-21.

Karjalainen S, Soderling E, Sewon L, Lapinleimu H, Simell O. A prospective study on sucrose consumption, visible plaque, caries in children from 3 to 6 years of age. Community Dent Oral Epidemiol. 2001; 29: 136-42.

Mazengo CM, Tenovuo J, Hausen H. Dental caries in relation to diet, saliva and cariogenic microorganisms in Tanzanians of selected age groups. Community Dent Oral Epidemiol. 1996; 24: 169-74.

Höfling JF, Spolidório DMP, Pereira CV, Rosa EAR, Moreira D. Association between Streptococcus mutans/Streptococcus sobrinus in students of different social levels and their relationship with the cariogenic activity in these populations. Rev Odontol Univ São Paulo. 1999; 13: 173-80.

Featherstone JD. The science and practice of caries prevention. J Am Dent Assoc. 2000; 131: 887-99.

Moalic E, Gestalin A, Quinio D, Gest PE, Zerilli A, Le Flohic AM. The extent of oral fungal flora in 353 students and possible relationships with dental caries. Caries Res. 2001; 35: 149-55.

Russel JI, MacFarlane TW, Aitchison TC, Stephen KW, Burchell CK. Caries prevalence and microbiological and salivary caries activity tests in Scottish adolescents. Community Dent Oral Epidemiol. 1990; 18: 120-5.

Radford JR, Ballantyne HM, Nugent Z, Beighton D, Robertson M, Longbottom C et al. Caries-associated micro-organisms in infants from different socio-economic backgrounds in Scotland. J Dent. 2000; 28: 307-12.

Marchant S, Brailsford SR, Twomey AC, Roberts GJ, Beighton D. The predominant microflora of nursing caries lesions. Caries Res. 2001; 35: 397-406.

Radford JR, Ballantyne HM, Nugent Z, Robertson M, Longbottom C, Pitts NB et al. Does social deprivation in 1, 2, 3 and 4-year-old Scottish infants influence the frequency isolation of caries-associated micro-organisms? J Dent. 2001; 29: 325- 32.

Gábris K, Nagy G, Madléna M, Dénes ZS, Márton S, Keszthelyi et al. Associations between microbiological and salivary caries activity tests and caries experience in Hungarian adolescents. Caries Res. 1999; 33: 191-5.

Ollila P, Niemelä M, Uhari M, Larmas M. Risk factors for colonization of salivary lactobacilli and Candida in children. Acta Odontol Scand. 1997; 55: 9-13.

Koga-Ito CY, Unterkircher CS, Watanabe H, Martins CAP, Vidotto V, Jorge AOC. Caries risk tests and salivary levels of immunoglobulins to Streptococcus mutans and Candida albicans in mouthbrething syndrome patients. Caries Res. 2003; 37: 38- 43.

World Health Organization. Oral health surveys: basic methods. 4th ed. Geneva: Swiss; 1997.

Williams DW, Lewis MAO. Isolation and identification of Candida from the oral cavity. Oral Dis. 2000; 6: 3-11.

Burford-Mason AP, Weber JCP, Willoughby JMT. Oral carriage of Candida albicans, ABO blood group and secretor status in healthy subjects. J Med Vet Mycol. 1988; 26: 49-56.

Jabra-Rizk MA, Falkler WA Jr, Enwonwu CO, Onwujekwe DI Jr, Merz WG, Meiller TF. Prevalence of yeast among children in Nigeria and the United States. Oral Microbiol Immunol. 2001; 16: 383-5.

Moreira D, Spolidório DMP, Rodrigues JAO, Boriollo MFG, Pereira CV, Rosa EAR et al. Candida spp. biotypes in the oral cavity of school children from different socioeconomic categories in Piracicaba-SP, Brazil. Pesqui Odontol Bras. 2001; 15: 187-95.

Darwazeh AMG, Al-Dosari A, Al-Bagieh NH. Oral Candida and nasal Aspergillus flora in a group of Saudi healthy dentate subjects. Int Dent J. 2002; 52: 273-7.

Jorge AOC, Koga-Ito CY, Gonçalves CR, Fantinato V, Unterkircher CS. Presence of Candida genus yeasts in the saliva of patients with different predisposing factors and of control individuals. Rev Odontol Univ São Paulo. 1997; 11: 279-85.

Akpan A, Morgan R. 2002. Oral candidiasis. Postgrad Med J. 2002; 78: 455-9.

Vargas SL, Patrick CC, Ayers GD, Hughes WT. Modulating effect of dietary carbohydrate supplementation Candida albicans colonization and invasion in a neutropenic mouse model. Infect Immun. 1993; 61: 619-26.

Souza EM, Lima DMM, Cavalcanti MDG, Santos MJ. Isolation and study of Candida albicans and Actinomycetes in oral cavity. Rev Microbiol. 1980; 11: 89-96.

Samaranayake LP, MacFarlane TW. Oral candidosis. London: Wright; 1990.

Soderling E, Pienihakkinen K, Alanen ML, Hietaoja M, Alanen P. Salivary flow rate, buffer effect, sodium, and amylase in adolescents: a longitudinal study. Scand J Dent Res. 1993; 101: 98-102.

Reynaud AH, Nygaard-Ostby B, Boygard GK, Eribe ER, Olsen I, Gjermo P. Yeasts in periodontal pockets. J Clin Periodontol. 2001; 28: 860-4.

Russel JI, MacFarlane TW, Aitchison TC, Stephen KW, Burchell CK. Caries prevalence and microbiological and salivary caries activity tests in Scottish adolescents. Community Dent Oral Epidemiol 1990; 18: 120-5.

Parvinen T, Larmas M. The relation of stimulated salivary flow rate and pH to Lactobacillus and yeast concentrations in saliva. J Dent Res. 1981; 60: 1929-35.

Williamson JJ. A study of extent of variation in daily counts of Candida albicans in saliva. Aust Dent J. 1972; 17: 106-9.

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