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Periodontal disease

Periodontal disease is the name for bacterial infections of the gums in the mouth. In most cases this disease is linked to poor oral hygiene. Some people however can have a genetic pre-disposition to the disease. The disease once initiated can progress more rapidly in people who have diabetes, especially if the diabetes is poorly controlled. Smoking is a strong risk factor for periodontal disease. more...

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Symptoms

  • occasional redness or bleeding of gums while brushing or using dental floss teeth or biting into hard food (e.g. apples)
  • occasional swellings that recur
  • halitosis or bad breath
  • persistent bad taste in the mouth
  • shaky teeth in later stages
  • recession of gums resulting in apparent lengthening of teeth (also caused by heavy handed brushing using a hard tooth brush)
  • pockets between the teeth and the gums (Pockets are sites where the jaw bone has been destroyed gradually or by repeated swellings. Teeth become loose or shaky when sufficient jaw bone has been destroyed. The unfortunate thing is that the bone destruction is largely painless.)
  • lack of pain when bleeding happens after cleaning is NOT a sign of health.

Treatment

  • regular brushing and flossing and using an interdental brush at least daily.
  • treatment by a Periodontist, which includes professional cleaning to remove calculus (tartar, tooth stone)and may include drugs (infrequently), and/or surgery occasionally.

Prevention

  • brushing properly on a regular basis (2 times a day)
  • flossing daily and using interdental brushes if there is sufficient space between teeth and behind the last tooth in each quarter.
  • regular dental checkups and professional teeth cleaning as required. This serves to monitor the person's oral hygiene methods and how the condition has responded to treatment. Professional tooth cleaning will not prevent or control the disease because the bacterial plaque (biofilm) returns on the tooth surfaces every 24 hours.

See also

  • Actinomyces naeslundii (a kind of bacteria)
  • dental plaque

Disease progression and predisposition

  • According to the Sri Lanka Tea Labourer study, on the absence of any oral hygiene activity, approximately 10% will suffer from severe periodontal disease with rapid loss of attachment(>2mm/yr). 80% will suffer from moderate loss (1-2 mm/year) and the remaining 10% will not suffer any loss.

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Phytotherapy for periodontal disease and improved oral hygiene
From Townsend Letter for Doctors and Patients, 6/1/05 by Kerry Bone

Historical Context

There is a long and venerable history of the use of plants to improve dental health and promote oral hygiene. This was highlighted in an excellent, but now dated, review by Lewis and Elvin-Lewis, the former being a botanist and the latter a dentist. (1) In their review they note a quotation attributed to the prophet Muhammed: "the Siwak (chewing stick) is an implement for the cleansing of teeth and a pleasure to God."

[ILLUSTRATION OMITTED]

They go on to write: "In vast parts of the world where toothbrushing is uncommon, the practice of tooth cleaning by chewing sticks has been known since antiquity. The precise method for use of these implements was recorded by the Babylonians in 5000 BC.... The use of chewing sticks persists today among many African and southern Asian communities as well as in isolated areas of tropical America and the southern United States.... Users who often prefer chewing sticks to modern toothbrushing techniques attribute their dental health to the traditional practice. It is noteworthy that caries rates are often very low among such users in spite of the high carbohydrate diets they normally consume.... The plants used are very carefully selected for such properties as foaminess, hardness, or bitterness, and certain species are more popular than others. A great number have related medicinal properties that may be antibacterial ... etc."

Popular plants which are fashioned into chewing sticks include Salvadora persica (arak) and neem. In fact Salvadora is so popular that the generic term miswak is often applied exclusively to this species by some writers.

Plants have also been incorporated into dentifrices and there are several modern examples of this practice. They were also used to provide natural chewing gums for oral hygiene, to treat toothache, gingivitis and periodontal disease.

Oral Infections and Systemic Diseases

Modern research is suggesting that systemic health may be more affected by oral hygiene than previously recognized. A recent review discussed possible etiological associations between periodontitis (the progressive destruction of the supporting structures of the teeth which is triggered by bacterial plaque) and cardiovascular disease in general, and in infective endocarditis specifically, as well as rheumatoid arthritis, pneumonia and preterm birth and low birth weight. (2) For example, a number of epidemiological studies have associated periodontitis with cardiovascular disease. These include follow-up investigations, case-control studies and cross-sectional studies. (2) Periodontal inflammation facilitates the entrance of bacteria into the bloodstream, especially after chewing food or cleaning teeth. Either direct effects from the bacteremia or secondary effects from the inflammation which their presence may trigger could lead to thrombus formation and/or the development of atherosclerotic lesions.

Be that as it may, the greatest loss of teeth in adults is caused by periodontal disease, which can be very difficult to treat. This suggests a potentially valuable role for phytotherapy in assisting with the management of this difficult and serious disease. The evidence and research which supports such a role for a few key plants (or plant products) is reviewed below.

Chewing Sticks or Miswak

The periodontal status of more than 200 adult Sudanese who habitually used either miswak or a toothbrush were compared. (3) Although gingival bleeding and dental calculus were highly prevalent in the test population, miswak users had significantly (p < 0.05) lower dental calculus and signs of periodontal disease and a tendency to lower gingival bleeding (p = 0.09). A Saudi Arabian study compared the effect of miswak or toothbrushing on plaque removal and dental health using a single blind, randomized, crossover design. (4) Compared to the use of a toothbrush, the miswak resulted in significant reductions in plaque (p < 0.001) and gingival (p < 0.01) indices. Furthermore, image analysis of the plaque distribution showed a significantly greater reduction in plaque for the miswak use. Another Sudanese study compared the levels of 25 oral bacteria in miswak and toothbrush users. (5) Certain bacteria, particularly several oral streptococci species, were lower in the miswak users. However, miswak use was associated with greater gum recession in one study, which was attributed to their abrasive properties. (6)

The antimicrobial effects of neem (Azadirachta indica) and arak (Salvadora persica) were compared in vitro against plaque-forming bacteria. (7) The extract of arak was slightly superior to neem at inhibiting their growth. A mouthwash made from arak was found to significantly reduce gingival bleeding (p < 0.01) in an open clinical study. (8) Although plaque scores were not significantly reduced in the three-week study, the use of arak resulted in lower rates of Streptococcus mutans, a bacterium associated with dental plaque. A six-week clinical trial found that a neem leaf gel significantly (p < 0.05) reduced the plaque index and oral bacterial count when compared with a conventional antibacterial mouthrinse. (9)

Propolis

Propolis is a resin rich in flavonoids which is manufactured by bees from plants. The in vitro antimicrobial activity of flavonoids and propolis is well documented. In the context of cariogenic bacteria, flavonoids have been shown to be active (10) and especially the well known antimicrobial and flavonoid-rich herb Scutellaria baicalensis (Baical skullcap). (11)

The effect of irrigation with propolis extract as an adjuvant treatment after scaling and root planing for chronic periodontitis was evaluated in a placebo-controlled clinical trial. (12) It was observed that subgingival irrigation with propolis extract in conjunction with conventional treatment was more effective than conventional treatment alone in terms of both clinical and microbiological assessments. A Russian study found that a 4% alcoholic solution of propolis added to root canal filling demonstrated good efficacy in periodontitis. (13)

A silicate toothpaste containing propolis demonstrated good plaque-cleaning, plaque-inhibiting and anti-inflammatory activities in an open clinical study over 4 weeks. (14) The effect of a propolis mouthrinse on 3-day dental plaque accumulation was assessed in a double-blind, crossover study which enrolled six healthy volunteers. (15) During each 3-day study period the volunteers refrained from all oral hygiene and rinsed with a 20% sucrose solution five times a day to enhance plaque formation. The mouthrinse was used twice a day. The plaque index for the propolis treatment was significantly lower than placebo (0.78 [+ or -] 0.17 vs 1.41 [+ or -] 0.14). The insoluble polysaccharide content of plaque was also reduced by 61.7% compared to placebo (p < 0.05). However, another study found only a marginally positive effect on dental plaque formation, which could reflect on the wide variation in the chemical composition of propolis. (16) The antibacterial action of propolis against oral bacteria has been demonstrated both in vitro and in vivo. (17,18)

Tea Tree Oil

The in vitro antibacterial effects of several essential oils were tested on oral bacteria. (19) Periodontopathic bacterial strains were killed completely by exposure for 30 seconds to 0.2% Manuka oil, tea tree oil or eucalyptus oil. Tea tree and Manuka oils also showed significant adhesion-inhibiting activity against Porphyromonas gingivalis. All the essential oils tested inhibited the adhesion of S. mutans. Another in vitro study confirmed that P. gingivalis was highly susceptible to tea tree oil. (20)

The effects of a topically applied tea tree oil gel on dental plaque and chronic gingivitis were assessed in a double-blind study. (21) Volunteers (n=49) received treatment with either the tea tree oil gel, a chlorhexidine gel or a placebo gel. The group receiving tea tree oil experienced a significant reduction in papillary bleeding and gingivitis, but the plaque score was not reduced. Similarly a pilot clinical study found that tea tree oil mouthrinse did not favorably affect supragingival plaque. (22)

Tea (especially Green Tea)

Tannins are defined as vegetable substances capable of tanning animal hides to produce leather. This is used as a method to preserve the hide and at a molecular level is effected via the crosslinking by the tannins of hide proteins. This definition is prescriptive and powdered hide is still used as a phytochemical test for tannins. Like flavonoids, tannins are polyphenolic compounds which have an affinity for proteins. However, the higher number of phenolic groups and the larger molecular size of tannins mean that they are capable of binding strongly to proteins at several sites and can precipitate them from solution.

One of the most notable effects of tannins in the gut is their dramatic effect on diarrhea. It can be proposed that the effect of tannins is to produce a protective (if temporary) layer of coagulated protein on the mucosa along the upper levels of the gut wall, so numbing the sensory nerve endings and reducing provocative stimuli to additional peristaltic activity. Supporting this central astringent activity, tannins will also inhibit the viability of infecting micro-organisms, check fluid hypersecretion and neutralize inflammatory proteins. Because of their affinity for free protein, they will concentrate in damaged areas. Condensed tannins were able to bind to and inactivate the hypersecretory activity of cholera toxin. (23)

Green tea (Camellia sinensis, a rich source of tannins) appears to be much more potent as an antimicrobial agent than black tea. (24) Bacillus subtilis, Escherichia coli, Proteus vulgaris, Pseudomonas fluorescens, Salmonella sp. and Staphylococcus aureus were used to test the antimicrobial activity of extracts of various tea products. Among the six test organisms, P. fluorescens was the most sensitive to the extracts, while B. subtilis was the least sensitive. In general, antimicrobial activity decreased when the extent of tea fermentation increased. The antimicrobial activities of extracts of tea products with different extents of fermentation also varied with test organisms. Green tea, the unfermented tea, exerted the strongest antimicrobial activity followed by the partially fermented tea products such as Longjing, Tieh-Kuan-Ying, Paochung, and Oolong teas. On the other hand, black tea, the completely fermented tea, showed the least antimicrobial activity. It was also noted that extracts of Oolong tea prepared in summer exhibited the strongest antimicrobial activity, followed by those prepared in spring, winter and fall.

Not surprisingly, the antimicrobial activity of tea has been attributed to its tannin (polyphenolic) phytochemicals. (25) Aqueous extracts of teas of different types and from various sources were found to inhibit a wide range of pathogenic bacteria, including methicillin-resistant Staphylococcus aureus. Tea extracts were bactericidal to staphylococci and Yersinia enterocolitica at well below 'cup of tea' concentrations. Activity was confined to one of four fractions obtained from a green tea extract by partition chromatography. Testing of pure tea compounds and closely related chemicals suggested that the antibacterial activity of extracts of green tea can be explained by its content of epigallocatechin, epigallocatechin gallate and epicatechin gallate (tannin-like molecules). In black tea extracts, theaflavin and its gallates are additional antibacterially active components.

A recent review proposed that various components in green and black tea have properties in vitro that suggest an anticariogenic activity. (26) These include a direct bactericidal effect against S. mutans and S. sobrinus, prevention of bacterial adherence to teeth, inhibition of the enzyme glucosyltransferase, thereby limiting the biosynthesis of an adherence factor, and inhibition of human and bacterial amylases. Studies in animal models have confirmed that these in vitro effects can translate into caries prevention. The review also noted that a limited number of clinical trials suggest that regular tea drinking may reduce the incidence and severity of caries.

The usefulness of application of green tea catechins (tannins) for periodontal disease was investigated in a placebo-controlled trial. (27) Strips containing the catechins as a slow release local delivery system were applied to gum pockets in patients once a week for 8 weeks. The pocket depth and amount of bacteria were markedly decreased in the catechin group, whereas there was no change for the placebo group.

A double-blind study investigated the effect of chewing green tea candy on gingival inflammation. (28) A total of 47 volunteers (23 male, 24 female) were randomly assigned to chew either eight green tea or placebo candies per day for 21 days. While there was an improvement in the green tea group, the placebo group deteriorated slightly. Oolong tea extract was found to significantly inhibit plaque formation in a controlled clinical trial. (29)

A study was undertaken to determine the usefulness of green or black tea for delivering polyphenols into the oral cavity. (30) Volunteers were instructed to hold either green tea leaves or brewed black tea in the mouth for 2 to 5 minutes and then rinse thoroughly. High concentrations of tea polyphenols were observed in saliva in the first hour thereafter.

Sanguinarine and Blood Root

Blood root (Sanguinaria canadensis) contains a mixture of benzophenanthridine alkaloids, mainly sanguinarine. (31) The value of blood root, and particularly sanguinarine, in dentifrices and mouthrinses has been extensively explored. A conservative review published in 1995 conceded that sanguinarine has some value in curbing supragingival plaque and is more effective as a mouthrinse than in a toothpaste. (32) However, like other mouthrinses it does not affect subgingival plaque. (32)

Clinical trials subsequent to this review have yielded conflicting results. Results from one trial supported the combined use of a chlorhexidine mouthrinse for a short term (2 weeks), followed by Sanguinaria mouthrinse and toothpaste up to 3 months, to optimize the effectiveness of the chlorhexidine following scaling and root planing treatment for periodontitis. (33) However, another trial found no significant advantage from using Sanguinaria treatment following such procedures. (34)

Long-term use of Sanguinaria has been associated with oral leukoplakia, which may be precancerous. This has led to one research group recommending the avoidance of Sanguinaria oral products until the risk of malignant transformation is determined. (35) If Sanguinaria is being used, it should not be at the same time as green tea preparations, since tannins bind to and inactivate alkaloids.

Miscellaneous Herbs

Other herbs which have shown antibacterial activity against oral bacteria, or more specifically cariogenic bacteria, include Coptis chinensis and its component berberine, (36,37) cocoa (38) and onions. (39) Dental plaque depends in part on interspecies bacterial adhesion (or coaggregation). A cranberry constituent reversed the coaggregation of 58% of oral bacterial strains tested. (40)

Echinacea has been used in the topical treatment of periodontitis. (41) My clinical experience with the use of both an Echinacea mouthrinse and internal doses of Echinacea for gingivitis and periodontitis suggests it can offer substantial clinical benefit. In particular, the use of a mouthrinse containing an Echinacea extract rich in alkylamides would be preferred, since the alkylamides promote saliva flow, which is a natural defense against plaque-forming bacteria.

Conclusions

Plants contain phytochemicals such as alkaloids, tannins, essential oils and flavonoids which have pronounced antimicrobial activity. This underlies the use since antiquity of herbs to improve oral hygiene and prevent tooth decay, gum disease and periodontitis. The miswak or chewing stick is an underestimated tool for dental hygiene which is only beginning to be explored in controlled clinical studies. Herbs or herbal products which should play a key role in the future of dental hygiene include propolis, tea tree oil, green tea and Echinacea. There is now a question mark over the role of blood root, although oral preparations containing this herb still enjoy relatively widespread use.

References

1. Lewis WH, Elvin-Lewis MPF. Medical Botany: Plants Affecting Man's Health. John Wiley and Sons, New York, 1977, pp 226-270.

2. Holmstrup P, Poulsen AH, Andersen L et al. Oral infections and systemic diseases. Dent Clin N Am 2003, 47: 575-598

3. Darout IA, Albandar JM, Skaug N. Periodontal status of adult Sudanese habitual users of miswak chewing sticks or toothbrushes. Acta Odontol Scand 2000, 58(1): 25-30

4. Al-Otaibi M, Al-Harthy M, Soder B et al. Comparative effect of chewing sticks and toothbrushing on plaque removal and gingival health. Oral Health Prev Dent 2003; 1(4): 301-307

5. Darout IA, Albandar JM, Skaug N et al. Salivary microbiota levels in relation to periodontal status, experience of caries and miswak use in Sudanese adults. J Clin Periodontal 2002; 29(5): 411-420

6. Eid MA, Selim HA, al-Shammery AR. The relationship between chewing sticks (Miswak) and periodontal health 3. Relationship to gingival recession. Quintessence Int 1991; 22(1): 61-64

7. Almas K. The antimicrobial effects of extracts of Azadirachta indica (neem) and Salvadora persica (Arak) chewing sticks. Indian J Dent Res 1999; 10(1): 23-26

8. Khalessi AM, Pack AR, Thomson WM et al. An in vivo study of the plaque control efficacy of Persica: a commercially available herbal mouthwash containing extracts of Salvadora persica. Int Dent J 2004; 54(5): 279-283

9. Pai MR, Acharya LD, Udupa N. Evaluation of antiplaque activity of Azadirachta indica leaf extract gel--a 6-week clinical study. J Ethnopharmacol 2004; 90(1): 99-103

10. Sato M, Fujiwara S, Tsuchiya H et al. Flavones with antibacterial activity against cariogenic bacteria. J Ethnopharmacol 1996; 54(2-3): 171-176

11. Tsao TF, Newman MG, Kwok YY et al. Effect of Chinese and western antimicrobial agents on selected oral bacteria. J Dent Res 1982; 61(9): 1103-1106

12. Gebaraa EC, Pustiglioni AN, de Lima LA et al. Propolis extract as an adjuvant to periodontal treatment. Oral Health Prev Dent 2003; 1(1): 29-35

13. Kosenko SV, Kosovich Tiu. [The treatment of periodontitis with prolonged-action propolis preparations (clinical x-ray research)]. Stomatologiia (Mosk) 1990; 69(2): 27-29

14. Botushanov PI, Grigorov GI, Aleksandrov GA. A clinical study of a silicate toothpaste with extract from propolis. Folia Med (Plovdiv) 2001; 43(1-2): 28-30

15. Koo H, Cury JA, Rosalen PL et al. Effect of a mouthrinse containing selected propolis on 3-day dental plaque accumulation and polysaccharide formation. Caries Res 2002; 36(6): 445-448

16. Murray MC, Worthington HV, Blinkhorn AS. A study to investigate the effect of a propolis-containing mouthrinse on the inhibition of de novo plaque formation. J Clin Periodontol 1997; 24(11): 796-798

17. Steinberg D, Kaine G, Gadalia I. Antibacterial effect of propolis and honey on oral bacteria. Am J Dent 1996; 9(6): 236-239

18. Park YK, Koo MH, Abreu JA et al. Antimicrobial activity of propolis on oral microorganisms. Curr Microbiol 1998; 36(1): 24-28

19. Takarada K, Kimizuka R, Takahashi N et al. A comparison of the antibacterial efficacies of essential oils against oral pathogens. Oral Microbiol Immunol 2004; 19(1): 61-64

20. Kulik E, Lenkeit K, Meyer J. [Antimicrobial effects of tea tree oil (Melaleuca alternifolia) on oral microorganisms)]. Schweiz Monatsschr Zahnmed 2000; 110(11): 125-130

21. Soukoulis S, Hirsch R. The effects of a tea tree oil-containing gel on plaque and chronic gingivitis. Aust Dent J 2004; 49(2): 78-83

22. Arweiler NB, Donos N, Netuschil L et al. Clinical and antibacterial effect of tea tree oil--a pilot study. Clin Oral Investig 2000; 4(2): 70-73

23. H[TEXT UNREADABLE IN ORIGINAL SOURCE]r M, Rimpler H, Heinrich. M. Inhibition of intestinal chloride secretion by proanthocyanidins from Guazuma ulmifolia Planta Med 1995; 61: 208-212

24. Chou CC, Lin LL, Chung KT. Antimicrobial activity of tea as affected by the degree of fermentation and manufacturing season. Int J Food Microbiol 1999; 48: 125-130

25. Yam TS, Shah S, Hamilton-Miller JM. Microbiological activity of whole and fractionated crude extracts of tea (Camellia sinensis), and of tea components. FEMS Microbiol Lett 1997: 152(1): 169-174

26. Hamilton-Miller JM. Anti-cariogenic properties of tea (Camellia sinensis). J Med Microbiol 2001; 50(4): 299-302

27. Hirasawa M, Takada K, Makimura M et al. Improvement of periodontal status by green tea catechin using a local delivery system: a clinical pilot study. J Periodontal Res 2002; 37(6): 433-438

28. Krahwinkel T, Willershausen B. The effect of sugar-free green tea chew candies on the degree of inflammation of the gingiva. Eur J Med Res 2000; 5(11): 463-467

29. Ooshima T, Minami T, Aono W et al. Reduction of dental plaque deposition in humans by oolong tea extract. Caries Res 1994; 28(3): 146-149

30. Lee MJ, Lambert JD, Prabhu S et al. Delivery of tea polyphenols to the oral cavity by green tea leaves and black tea extract. Cancer Epidemiol Biomarkers Prev 2004; 13(1): 132-137

31. Harkrader RJ, Reinhart PC, Rogers JA et al. The history, chemistry and pharmacokinetics of Sanguinaria extract. J Can Dent Assoc 1990; 56(7 Suppl): 7-12

32. Grenby TH. The use of sanguinarine in mouthwashes and toothpaste compared with some other antimicrobial agents. Br Dent J 1995; 178(7): 254-258

33. Tenenbaum H, Dahan M, Soell M. Effectiveness of a sanguinarine regimen after scaling and root planing. J Periodontol 1999; 70(3): 307-311

34. Cullinan MP, Powell RN, Faddy MJ et al. Efficacy of a dentifrice and oral rinse containing sanguinaria extract in conjunction with initial periodontal therapy. Aust Dent J 1997; 42(1): 47-51

35. Eversole LR, Eversole GM, Kopcik J. Sanguinaria-associated oral leukoplakia: comparison with other benign and dysplastic leukoplakic lesions. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 2000; 89(4): 455-464

36. Wang S, Fan M, Bian Z. [Experimental study of bacteriostatic activity of Chinese herbal medicines on primary cariogenic bacteria in vitro]. Zhonghua Kou Qiang Yi Xue Za Zhi 2001; 36(5): 385-387

37. Hu JP, Takahashi N, Yamada T. Coptidis rhizoma inhibits growth and proteases of oral bacteria. Oral Dis 2000; 6(5): 297-302

38. Ooshima T, Osaka Y, Sasaki H et al. Cariostatic activity of cacao mass extract. Arch Oral Biol 2000; 45(9): 805-808

39. Kim JH. Anti-bacterial action of onion (Allium cepa L.) extracts against oral pathogenic bacteria. J Nihon Univ Sch Dent 1997; 39(3): 136-141

40. Weiss EI, Lev-Dor R, Kashamn Y et al. Inhibiting interspecies coaggregation of plaque bacteria with a cranberry juice constituent [published erratam appear in J Am Dent Assoc 1999 Jan; 130(11): 36 and 1999 Mar; 130(3): 332]. J Am Dent Assoc 1998; 129(12): 1719-1723

41. Gasiorowska I, Patalas B, Wiktorowska B. [Echinacin externa use in the treatment of periodontopathies]. Czas Stomatol 1981; 34(7): 677-679

by Kerry Bone, FNIMH, FNHAA

P.O. Box 713 * Warwick QLD 4370, Australia

+61 7 4661 0700 * Fax +61 7 46610788 * www.mediherb.com

FNIMH = Fellow, National Institute of Medical Herbalists (UK)

FNHAA = Fellow, National Herbalists Association of Australia

COPYRIGHT 2005 The Townsend Letter Group
COPYRIGHT 2005 Gale Group

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