Periodontal Diseases and Dental Caries in Children with Type 1 Diabetes Mellitus

. 2015 ; 2015 () : 379626. [epub] 20150804

Jazyk angličtina Země Spojené státy americké Médium print-electronic

Typ dokumentu časopisecké články, práce podpořená grantem, přehledy

Perzistentní odkaz   https://www.medvik.cz/link/pmid26347009

Type 1 diabetes mellitus is a chronic metabolic disease of an autoimmune origin with early manifestation predominantly in the childhood. Its incidence has been rising in most European countries. Diabetes has been intensively studied by all branches of medicine. There were a number of studies investigating oral consequences of diabetes; however, unambiguous conclusions were drawn only for the relationship between diabetes and periodontal impairment. Many studies confirmed higher plaque levels and higher incidence of chronic gingivitis both in adults and in children with diabetes. Juvenile periodontitis is rare both in healthy subjects and in those with type 1 diabetes. Yet certain findings from well-conducted studies, for example, differences in oral microflora or the impact of metabolic control of diabetes on periodontal health, indicate a higher risk of periodontitis in children with type 1 diabetes. As for the association of diabetes and dental caries, the results of the studies are inconsistent. However, it was found that some risk factors for dental caries are either more or less prevalent in the diabetic population. Despite an extensive research in this area we have to acknowledge that many questions have remained unanswered. There is a need for continued, thorough research in this area.

Zobrazit více v PubMed

American Diabetes Association. Diagnosis and classification of diabetes mellitus. Diabetes Care. 2014;37(supplement 1):S81–S90. PubMed

WHO Study Group. Diabetes mellitus, http://whqlibdoc.who.int/trs/WHO_TRS_727.pdf.

WHO Forty-third World Health Assembly: ICD 10, http://apps.who.int/classifications/icd10/browse/2014/en#/E10.

Gardner D. G., Shoback D. Greenspan's Basic and Clinical Endocrinology. 8th. San Francisco, Calif, USA: McGraw-Hill Medical; 2007.

Oikarinen S., Tauriainen S., Hober D., et al. Virus antibody survey in different european populations indicates risk association between coxsackievirus B1 and type 1 diabetes. Diabetes. 2014;63(2):655–662. doi: 10.2337/db13-0620. PubMed DOI

Hober D., Sane F. Enteroviral pathogenesis of type 1 diabetes. Discovery Medicine. 2010;10(51):151–160. PubMed

Virtanen S. M., Knip M. Nutritional risk predictors of β cell autoimmunity and type 1 diabetes at a young age. The American Journal of Clinical Nutrition. 2003;78(6):1053–1067. PubMed

D'Angeli M. A., Merzon E., Valbuena L. F., Tirschwell D., Paris C. A., Mueller B. A. Environmental factors associated with childhood-onset type 1 diabetes mellitus: an exploration of the hygiene and overload hypotheses. Archives of Pediatrics and Adolescent Medicine. 2010;164(8):732–738. doi: 10.1001/archpediatrics.2010.115. PubMed DOI PMC

Cinek O. Epidemiology of childhood type 1 diabetes mellitus: lessons from central and Eastern European data. Hormone Research in Paediatrics. 2011;76(1):52–56. doi: 10.1159/000329168. PubMed DOI

Cinek O., Lánská V., Koloušková S., et al. Type I diabetes mellitus in Czech children diagnosed in 1990-1997: A significant increase in incidence and male predominance in the age group 0-4 years. Diabetic Medicine. 2000;17(1):64–69. doi: 10.1046/j.1464-5491.2000.00202.x. PubMed DOI

Cinek O., Šumník Z., Vavřinec J. Childhood diabetes in the Czech Republic: a steady increase in incidence. Casopis Lekaru Ceskych. 2005;144(4):266–271. PubMed

Karvonen M., Viik-Kajander M., Moltchanova E., Libman I., LaPorte R., Tuomilehto J. Incidence of childhood type 1 diabetes worldwide. Diabetes Mondiale (DiaMond) Project Group. Diabetes Care. 2000;23(10):1516–1526. doi: 10.2337/diacare.23.10.1516. PubMed DOI

Yusof W. Z. Periodontitis in children, adolescent and young adults. The changing concepts: 2. Aetiology and treatment. Singapore Dental Journal. 1988;13(1):4–9. PubMed

Orbak R., Simsek S., Orbak Z., Kavrut F., Colak M. The influence of type-1 diabetes mellitus on dentition and oral health in children and adolescents. Yonsei Medical Journal. 2008;49(3):357–365. doi: 10.3349/ymj.2008.49.3.357. PubMed DOI PMC

Salvi G. E., Franco L. M., Braun T. M., et al. Pro-inflammatory biomarkers during experimental gingivitis in patients with type 1 diabetes mellitus: a proof-of-concept study. Journal of Clinical Periodontology. 2010;37(1):9–16. doi: 10.1111/j.1600-051x.2009.01500.x. PubMed DOI

Salvi G. E., Kandylaki M., Troendle A., Persson G. R., Lang N. P. Experimental gingivitis in type 1 diabetics: a controlled clinical and microbiological study. Journal of Clinical Periodontology. 2005;32(3):310–316. doi: 10.1111/j.1600-051x.2005.00682.x. PubMed DOI

Xavier A. C. V., Silva I. N., Costa F. D. O., Corrêa D. S. Periodontal status in children and adolescents with type 1 diabetes mellitus. Arquivos Brasileiros de Endocrinologia e Metabologia. 2009;53(3):348–354. doi: 10.1590/s0004-27302009000300009. PubMed DOI

Siudikiene J., Maciulskiene V., Dobrovolskiene R., Nedzelskiene I. Oral hygiene in children with type I diabetes mellitus. Stomatologija. 2005;7(1):24–27. PubMed

Lalla E., Cheng B., Lal S., et al. Periodontal changes in children and adolescents with diabetes: a case-control study. Diabetes Care. 2006;29(2):295–299. doi: 10.2337/diacare.29.02.06.dc05-1355. PubMed DOI

Preshaw P. M., Alba A. L., Herrera D., et al. Periodontitis and diabetes: a two-way relationship. Diabetologia. 2012;55(1):21–31. doi: 10.1007/s00125-011-2342-y. PubMed DOI PMC

Thorstensson H. Periodontal disease in adult insulin-dependent diabetics. Swedish Dental Journal. Supplement. 1995;107:1–68. PubMed

Dusková J., Broukal Z. Compensation criteria of basal disease in the prevention and treatment of periodontal disease in patients with diabetes mellitus. Prakticke Zubni Lekarstvi. 1991;39(2):51–54. PubMed

Iughetti L., Marino R., Bertolani M. F., Bernasconi S. Oral health in children and adolescents with IDDM—a review. Journal of Pediatric Endocrinology and Metabolism. 1999;12(5, supplement 2):603–610. PubMed

Lalla E., Cheng B., Lal S., et al. Diabetes mellitus promotes periodontal destruction in children. Journal of Clinical Periodontology. 2007;34(4):294–298. doi: 10.1111/j.1600-051X.2007.01054.x. PubMed DOI

Salvi G. E., Carollo-Bittel B., Lang N. P. Effects of diabetes mellitus on periodontal and peri-implant conditions: update on associations and risks. Journal of Clinical Periodontology. 2008;35(supplement 8):398–409. doi: 10.1111/j.1600-051x.2008.01282.x. PubMed DOI

Cameron A. C., Widmer R. P. Handbook of Pediatric Dentistry. 3rd. Mosby Elsevier; 2008.

Tervonen T., Lamminsalo S., Hiltunen L., Raunio T., Knuuttila M. Resolution of periodontal inflammation does not guarantee improved glycemic control in type 1 diabetic subjects. Journal of Clinical Periodontology. 2009;36(1):51–57. doi: 10.1111/j.1600-051X.2008.01343.x. PubMed DOI

Llambés F., Silvestre F.-J., Hernández-Mijares A., Guiha R., Caffesse R. The effect of periodontal treatment on metabolic control of type 1 diabetes mellitus. Clinical Oral Investigations. 2008;12(4):337–343. doi: 10.1007/s00784-008-0201-0. PubMed DOI

Calabrese N., D'Aiuto F., Calabrese A., Patel K., Calabrese G., Massi-Benedetti M. Effects of periodontal therapy on glucose management in people with diabetes mellitus. Diabetes and Metabolism. 2011;37(5):456–459. doi: 10.1016/j.diabet.2011.05.004. PubMed DOI

Nishimura F., Takahashi K., Kurihara M., Takashiba S., Murayama Y. Periodontal disease as a complication of diabetes mellitus. Annals of Periodontology. 1998;3(1):20–29. doi: 10.1902/annals.1998.3.1.20. PubMed DOI

Ryan M. E., Ramamurthy N. S., Sorsa T., Golub L. M. MMP-Mediated events in diabetes. Annals of the New York Academy of Sciences. 1999;878:311–334. doi: 10.1111/j.1749-6632.1999.tb07692.x. PubMed DOI

Ryan M. E., Carnu O., Kamer A. The influence of diabetes on the periodontal tissues. Journal of the American Dental Association. 2003;134:34S–40S. PubMed

Ryan M. E., Usman A., Ramamurthy N. S., Golub L. M., Greenwald R. A. Excessive matrix metalloproteinase activity in diabetes: Inhibitions by tetracycline analogues wit zinc reactivity. Current Medicinal Chemistry. 2001;8(3):305–316. doi: 10.2174/0929867013373598. PubMed DOI

Grover H. S., Luthra S. Molecular mechanisms involved in the bidirectional relationship between diabetes mellitus and periodontal disease. Journal of Indian Society of Periodontology. 2013;17(3):292–301. doi: 10.4103/0972-124x.115642. PubMed DOI PMC

Slade G. D., Offenbacher S., Beck J. D., Heiss G., Pankow J. S. Acute-phase inflammatory response to periodontal disease in the US population. Journal of Dental Research. 2000;79(1):49–57. doi: 10.1177/00220345000790010701. PubMed DOI

Molvig J., Baek L., Christensen P., et al. Endotoxin-stimulated human monocyte secretion of interleukin 1, tumour necrosis factor alpha, and prostaglandin E2 shows stable interindividual differences. Scandinavian Journal of Immunology. 1988;27(6):705–716. doi: 10.1111/j.1365-3083.1988.tb02404.x. PubMed DOI

Taylor G. W. The effects of periodontal treatment on diabetes. Journal of the American Dental Association. 2003;134:41S–48S. PubMed

Kornman K. S. Mapping the pathogenesis of periodontitis: a new look. Journal of Periodontology. 2008;79(8, supplement):1560–1568. doi: 10.1902/jop.2008.080213. PubMed DOI

Alonso N., Martínez-Arconada M. J., Granada M. L., et al. Regulatory T cells in type 1 diabetic patients with autoimmune chronic atrophic gastritis. Endocrine. 2009;35(3):420–428. doi: 10.1007/s12020-009-9166-2. PubMed DOI

Matthews D. C. The relationship between diabetes and periodontal disease. Journal of the Canadian Dental Association. 2002;68(3):161–164. PubMed

Mehta S. N., Volkening L. K., Quinn N., Laffel L. M. Intensively managed young children with type 1 diabetes consume high-fat, low-fiber diets similar to age-matched controls. Nutrition Research. 2014;34(5):428–435. doi: 10.1016/j.nutres.2014.04.008. PubMed DOI PMC

Patton S. R. Adherence to diet in youth with type 1 diabetes. Journal of the American Dietetic Association. 2011;111(4):550–555. doi: 10.1016/j.jada.2011.01.016. PubMed DOI PMC

Moreira A. R., Passos I. A., Sampaio F. C., Soares M. S. M., Oliveira R. J. Flow rate, pH and calcium concentration of saliva of children and adolescents with type 1 diabetes mellitus. Brazilian Journal of Medical and Biological Research. 2009;42(8):707–711. doi: 10.1590/s0100-879x2009005000006. PubMed DOI

López M. E., Colloca M. E., Páez R. G., Schallmach J. N., Koss M. A., Chervonagura A. Salivary characteristics of diabetic children. Brazilian Dental Journal. 2003;14(1):26–31. doi: 10.1590/s0103-64402003000100005. PubMed DOI

Siudikiene J., MacHiulskiene V., Nyvad B., Tenovuo J., Nedzelskiene I. Dental caries increments and related factors in children with type 1 diabetes mellitus. Caries Research. 2008;42(5):354–362. doi: 10.1159/000151582. PubMed DOI

Javed F., Sundin U., Altamash M., Klinge B., Engström P.-E. Self-perceived oral health and salivary proteins in children with type 1 diabetes. Journal of Oral Rehabilitation. 2009;36(1):39–44. doi: 10.1111/j.1365-2842.2008.01895.x. PubMed DOI

Tenovuo J., Lehtonen O. P., Viikari J., Larjava H., Vilja P., Tuohimaa P. Immunoglobulins and innate antimicrobial factors in whole saliva of patients with insulin-dependent diabetes mellitus. Journal of Dental Research. 1986;65(1):62–66. doi: 10.1177/00220345860650011101. PubMed DOI

Zalewska A., Knaś M., Kuźmiuk A., et al. Salivary innate defense system in type 1 diabetes mellitus in children with mixed and permanent dentition. Acta Odontologica Scandinavica. 2013;71(6):1493–1500. doi: 10.3109/00016357.2013.773071. PubMed DOI

Alves C., Brandão M., Andion J., Menezes R. Oral health knowledge and habits in children with type 1 diabetes mellitus. Brazilian Dental Journal. 2009;20(1):70–73. PubMed

Lal S., Cheng B., Kaplan S., et al. Accelerated tooth eruption in children with diabetes mellitus. Pediatrics. 2008;121(5):e1139–e1143. doi: 10.1542/peds.2007-1486. PubMed DOI

Alves C., Menezes R., Brandão M. Salivary flow and dental caries in Brazilian youth with type 1 diabetes mellitus. Indian Journal of Dental Research. 2012;23(6):758–762. doi: 10.4103/0970-9290.111254. PubMed DOI

El-Tekeya M., El Tantawi M., Fetouh H., Mowafy E., Khedr N. A. Caries risk indicators in children with type 1 diabetes mellitus in relation to metabolic control. Pediatric Dentistry. 2012;34(7):510–516. PubMed

Tagelsir A., Cauwels R., Kroos S., Vanobbergen J., Martens L. C. Dental caries and dental care level (restorative index) in children with diabetes mellitus type 1. International Journal of Paediatric Dentistry. 2011;21(1):13–22. doi: 10.1111/j.1365-263X.2010.01094.x. PubMed DOI

Akpata E. S., Alomari Q., Mojiminiyi O. A., Al-Sanae H. Caries experience among children with type 1 diabetes in Kuwait. Pediatric Dentistry. 2012;34(7):468–472. PubMed

del Valle L. M. L., Ocasio-López C. Comparing the oral health status of diabetic and non-diabetic children from Puerto Rico: a case-control pilot study. Puerto Rico Health Sciences Journal. 2011;30(3):123–127. PubMed PMC

Rai K., Hegde A., Kamath A., Shetty S. Dental caries and salivary alterations in type i diabetes. The Journal of Clinical Pediatric Dentistry. 2011;36(2):181–184. doi: 10.17796/jcpd.36.2.x436ln878221g364. PubMed DOI

Siudikiene J., Machiulskiene V., Nyvad B., Tenovuo J., Nedzelskiene I. Dental caries and salivary status in children with type 1 diabetes mellitus, related to the metabolic control of the disease. European Journal of Oral Sciences. 2006;114(1):8–14. doi: 10.1111/j.1600-0722.2006.00277.x. PubMed DOI

Twetman S., Petersson G. H., Bratthall D. Caries risk assessment as a predictor of metabolic control in young Type 1 diabetics. Diabetic Medicine. 2005;22(3):312–315. doi: 10.1111/j.1464-5491.2005.01419.x. PubMed DOI

Miko S., Ambrus S. J., Sahafian S., Dinya E., Tamas G., Albrecht M. G. Dental caries and adolescents with type 1 diabetes. British Dental Journal. 2010;208(6):p. E12. doi: 10.1038/sj.bdj.2010.290. PubMed DOI

Moore P. A., Weyant R. J., Etzel K. R., et al. Type 1 diabetes mellitus and oral health: assessment of coronal and root caries. Community Dentistry and Oral Epidemiology. 2001;29(3):183–194. doi: 10.1034/j.1600-0528.2001.290304.x. PubMed DOI

Kneckt M. C., Syrjälä A.-M. H., Knuuttila M. L. E. Attributions to dental and diabetes health outcomes. Journal of Clinical Periodontology. 2000;27(3):205–211. doi: 10.1034/j.1600-051x.2000.027003205.x. PubMed DOI

Syrjälä A.-M. H., Kneckt M. C., Knuuttila M. L. E. Dental self-efficacy as a determinant to oral health behaviour, oral hygiene and HbA1c level among diabetic patients. Journal of Clinical Periodontology. 1999;26(9):616–621. doi: 10.1034/j.1600-051x.1999.260909.x. PubMed DOI

Najít záznam

Citační ukazatele

Pouze přihlášení uživatelé

Možnosti archivace

Nahrávání dat ...