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Periodontology 2000, Vol. 50, 2009, 1324 Printed in Singapore.

All rights reserved

2009 John Wiley & Sons A/S

PERIODONTOLOGY 2000

Is the prevalence of periodontitis in the USA in decline?


C H A R L E S M. C O B B , K A R E N B. W I L L I A M S & M A R Y M. G E R K O V I T C H

Two recent reports have suggested that the prevalence of periodontitis in the USA is in dramatic decline (13, 69). Prevalence refers to the frequency of a given condition or disease in a designated population at a given point (39). At the very least, this is an interesting observation with signicant public health implications in terms of allocation of nancial resources, personnel, treatment emphasis and public health policy. Additionally, if accurate, this observation certainly has implications for dental education curricula as regards course content emphasis, allocation of instructional time and faculty budget lines in departments of periodontics and dental hygiene, and need for and size of residency programs. Lastly, referral patterns to private practice periodontists may be impacted, which, in turn, may produce changes in the delivery of patient-care services (e.g. less time devoted to treatment of chronic periodontitis and more time devoted to esthetic surgical procedures and dental implant site development and placement). One would think that an objective assessment of the stated decline in prevalence of a major oral disease, such as chronic periodontitis, would be relatively straightforward. However, this is not the case. Accurate assessment of the prevalence of periodontitis is complicated by multiple factors such as different operational denitions of clinical periodontitis (25, 34, 69, 81); characteristics of the study populations, such as age, ethnicity and race, geographic location and risk factors (1, 10, 12, 1418, 43, 52, 62, 76, 80); measurement of clinical parameters (e.g. probing depth, clinical attachment loss, bleeding on probing, radiographic bone loss, presence of dental calculus or plaque, etc.); and choice of partial vs. whole-mouth examination (5, 9, 22, 29, 31, 46, 47, 59, 60, 7375, 87). Moreover, most prevalence data are either estimates obtained from relatively small

observational (cross-sectional) studies, or are derived from larger epidemiological studies that do not permit an in-depth diagnostic assessment of subjects. Consequently, determining whether there is a real decline in the actual prevalence in periodontitis in the USA may not be possible, but analysis of trends may provide insight in this regard.

Caveat
The reader is admonished to not mistake this article as being a systematic or in-depth review of the literature. Over the past decade, several outstanding articles and in-depth reviews of the literature have been published that address the prevalence of periodontitis in the USA and other geographic locations worldwide (2, 4, 5, 11, 21, 25, 35, 67, 69, 70). The science of epidemiology is complex and steeped in design and statistical methodology, and, to some extent, sociologic considerations. Simply put, the intent of this paper is to present an abbreviated and uncomplicated review in a manner that may have relevance to the practicing clinician, educators and policy makers alike.

Evolution of the case denition of periodontitis


Periodontitis has been described as an irreversible, cumulative condition, initiated by bacteria but propagated by host factors (58). Susceptibility to development of periodontitis may increase owing to the interaction of environmental, acquired and genetic risk factors that modify the host response to the putative pathogenic microbes (68). Traditionally, the presence and severity of periodontitis have been determined by pocket

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probing depth, clinical attachment loss and bleeding on probing measurements and by evidence of radiographic alveolar bone loss. These data are collectively interpreted contextually for each patient in order to establish a diagnosis of periodontitis that includes both the extent and severity of disease. A major problem associated with interpreting the meaning of these clinical parameters in epidemiologic studies is the lack of consensus on a standard case denition of periodontitis. For example, how much pocket depth, clinical attachment loss and radiographic bone loss equates to slight, moderate or severe periodontitis? In addition, various studies have used different measures of periodontal disease. Lastly, there is signicant variation in the threshold levels used in dening a periodontitis case, regardless of the clinical parameters used for measurement. Simply put, before prevalence of periodontitis can be accurately assessed there must be agreement on what constitutes a case of periodontitis. The rst national US survey to determine the prevalence of periodontal diseases was conducted in 196062 as part of the National Health Examination Survey. Subsequent surveys were conducted in 1971 74 by the National Health and Nutrition Examination Survey or NHANES I, in 1981 by the Health Resources and Services Administration US Public Health Service, in 198586 by the National Institute of Dental Research (currently known as the National Institute of Dental and Craniofacial Research) and in 198894 (by the National Health and Nutrition Examination Survey III), followed by National Health and Nutrition Examination Survey III data-collection cycles in 19992000 and 20022004 (69). It should be noted that since 2005, surveillance of periodontal status in the USA, as part of the National Health and Nutrition Examination Survey, has ceased. Even amongst these national surveys, inconsistencies in methodology, operational denition of periodontitis and selection of disease parameters for measurement inuence the ndings and severely limit valid comparisons between the different surveys (60). Dye & Thornton-Evans (35) and Page & Eke (69) have recently published in-depth reviews that chronicle the histories of national surveillance efforts for periodontal disease in the USA, the evolution of case denitions for periodontitis and the prevalence estimates from various surveys. As noted by these authors, the early epidemiologic surveys focused on gingival inammation and used the Russell Periodontal Index as the instrument for measurement (74). Russells index employs a weighted, six-category severity ranking scale that requires radiographic

interpretation to assign values associated with the three highest ranked values. Additionally, an inherent problem with this scale is the lack of specicity in category attributes and the lack of mutually exclusive severity categories in interpretation. The Russell Periodontal Index was subsequently modied as the Ramfjord Periodontal Disease Index, and applied the Russell Periodontal Index schema to six index teeth, based on the assumption that the six teeth were representative of the entire dentition (73). Both the Russell Periodontal Index and the Ramfjord Periodontal Disease Index yield scores that represent the severity of periodontal disease, and both methods assume that gingivitis is an early stage of periodontitis (Table 1). However, both indices were developed for the rapid screening of large numbers of subjects and do not utilize specic clinical parameters (pocket depth, clinical attachment loss, bleeding on probing or radiographic bone loss) to assess the extent of disease or conform to standard characteristics for measurement categories that are mutually exclusive and collectively exhaustive. Additionally, partialmouth examinations tend to underestimate the prevalence, extent and severity of disease (6, 36, 37, 49, 59). Notably, the Russell Periodontal Index was used for assessing periodontal prevalence in both the 196062 National Health Examination Survey and the 197174 National Health and Nutrition Examination Survey I. The National Health and Nutrition Examination Survey II, conducted in 197680, did not procure oral health data. Consequently, almost a decade elapsed before the Health Resources and Services Administration US Public Health Service conducted the 1981 national survey on prevalence, severity and extent of periodontal disease (19). This survey used a modied Russell Periodontal Index that assessed gingivitis and periodontal pocket depth separately. Thus, this survey became the rst to incorporate the periodontal pocket depth into the examination methodology. Periodontitis was dened as having one or more pockets 4 mm; moderate disease being one or more pockets of 46 mm; and severe disease being one or more pockets with pocket depth >6 mm. The greatest criticism of this assessment was that pocket depth was measured only on the mesial of each available permanent tooth. Thus, survey results concerning pocket depth were based on what was essentially a biased (by site) partial-mouth examination. A second national survey was conducted by the National Institute of Dental Research (currently the National Institute of Dental and Craniofacial Re-

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Table 1. Chronological evolution of case denitions of periodontitis


Year(s) of survey 19601962 US national survey NHES Case denition of periodontitis Dened by Russell Periodontal Index (74) Scores for individual tooth 0 = periodontally normal 1 = mild gingivitis 2 = gingivitis 6 = gingivitis with periodontal pocket 8 = advanced periodontitis with loss of function Score range for case 00.2 = periodontally normal 0.30.7 = gingivitis 0.71.9 = early periodontitis 1.65.0 = established periodontitis 3.88.0 = terminal periodontitis 19711974 1981 NHANES I HRSA USPHS Dened by Russell Periodontal Index (74) One or more periodontal pockets 4 mm; moderate and severe periodontitis dened as one or more periodontal pockets of 46 mm and >6 mm, respectively (19) Disease measure: clinical attachment loss 1.0, 3.0 and 5 mm; pocket depth 46 and 7 mm; gingival recession degree 1 and 3.0 mm (20) Mild periodontitis: one or more teeth with pocket depth 3.0 mm or one or more posterior teeth with Class I furcation involvement Moderate periodontitis: one or more teeth with pocket depth 5.0 mm or two or more teeth (or 30% of teeth examined) with pocket depth 4 mm, or one or more posterior teeth with a Class I furcation involvement Severe periodontitis: two or more teeth (or 30% of teeth examined) with pocket depth 5 mm, or four or more teeth (or 60% of teeth examined) having pocket depth 4 mm, or one or more posterior teeth with a Class II furcation involvement (5) At least three sites with clinical attachment loss 4 mm and at least two sites with pocket depth 3 mm. These clinical parameters did not have to occur at the same site or involve the same tooth (13) Same as NHANES III 19992000 (13) Moderate periodontitis: two or more interproximal sites with >4 mm clinical attachment loss, not on the same tooth, or two or more interproximal sites with probing depths of 5 mm, not on the same tooth Severe periodontitis: two or more interproximal sites with clinical attachment loss 6 mm, not on the same tooth, and one or more interproximal sites with pocket depth 5 mm (69)

19851986

NIDR

19881994

NHANES III

19992000

NHANES III

20022004 2003

NHANES III CDC & AAP

CDC & AAP, Centers for Disease Control and Prevention & the American Academy of Periodontology; HRSA USPHS, Health Resources and Services Administration US Public Health Service; NHANES, National Health and Nutrition Examination Survey; NHES, National Health Examination Survey; NIDR, National Institute of Dental Research.

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search) in 198586 (20). The survey was the rst to measure gingival recession and clinical attachment loss in addition to pocket depth and gingivitis. The survey was also distinctive in that teeth in two randomly selected quadrants (one maxillary and one mandibular) were evaluated, again representing a partial-mouth examination. Each available tooth (exclusive of third molars) in the selected quadrants was probed at the mid-buccal and mesio-buccal surfaces, again potentially biasing ndings by site. Case denition of periodontitis was not applicable in this study as data were presented based on progressive disease severity (Table 1). The National Health and Nutrition Examination Survey III study of 198894 (5, 22), similar to the National Institute of Dental Research National Institute of Dental and Craniofacial Research survey of 198586, used a partial-mouth examination consisting of measurements obtained from all available teeth (exclusive of third molars) in two randomly selected quadrants. The methodology was similar to the 198586 survey where pocket depth was measured at mid-buccal and mesio-buccal sites. A signicant improvement to the methods was added in that clinical attachment loss was determined at these sites and the extent of furcation involvement was noted. Periodontitis was dened as active destruction of the supporting tissues at one or more sites, characterized by pocket depth 3.0 mm and clinical attachment loss 3.0 mm at the same site. The survey subdivided severity of disease into mild periodontitis (one or more teeth with pocket depth 3.0 mm or one or more posterior teeth with Class I furcation involvement); moderate periodontitis [one or more teeth with pocket depth 5.0 mm or two or more teeth (or 30% of teeth examined) with pocket depth 4 mm, or one or more posterior teeth with a Class I furcation involvement]; and severe periodontitis [two or more teeth (or 30% of teeth examined) with pocket depth 5 mm, or four or more teeth (or 60% of teeth examined) with pocket depth 4 mm, or one or more posterior teeth with a Class II furcation involvement]. Data from the National Health and Nutrition Examination Survey III of 19992000 and the 2002 2004 data-collection cycle were based on the following case denition of periodontitis: at least three sites with clinical attachment loss 4 mm and at least two sites with pocket depth 3 mm. Unlike the previous National Health and Nutrition Examination Survey studies, these clinical parameters did not have to occur at the same site or involve the same tooth (13) and thus probably produced ndings that are not directly comparable.

Lastly, in 2003 a standardized case denition of periodontitis for population-based studies was jointly devised by the Centers for Disease Control and Prevention and the American Academy of Periodontology. Moderate periodontitis was dened as two or more interproximal sites with >4 mm clinical attachment loss, not on the same tooth, or two or more interproximal sites with pocket depth >5 mm, not on the same tooth. Severe periodontitis was dened as two or more interproximal sites with clinical attachment loss 6 mm, not on the same tooth, and one or more interproximal sites with pocket depth 5 mm (69). It is apparent that the operational denition of periodontitis has evolved over time, becoming more rened in keeping both with the progression in knowledge of periodontal disease pathogenesis and the need for accurate surveillance data upon which to base public health policy. Paradoxically, the continued evolution of the case denition compromises meaningful comparisons of the obtained data over time. Despite the challenge presented by the lack of continuity in design and case denition between surveys, one can still identify trends in the prevalence of periodontitis.

Prevalence of periodontitis
In 1950, Neal W. Chilton (27) noted that there was very little information of statistically reliable nature on the epidemiologic characteristics of periodontal disease. His opinion was echoed 5 years later by Marshall-Day et al. (64), who noted that much of the information concerning prevalence and incidence of the periodontal diseases was based on clinical impression that was unsupported by reliable statistical data. The authors proceeded to conduct a crosssectional study of adolescents and adults in the Boston, Massachusetts, area. The sample of 1,279 individuals comprised adults participating in a multiphasic health protection program, and high school and college students, yielding an age range of 1365+ years. The examination consisted of a 20-lm radiographic survey, measurement of pocket depth, determination of the presence of supragingival and or subgingival calculus, evaluation of gingival inammation based on visual parameters (e.g. color, contour, consistency, recession and suppuration) and occlusal analysis using study models. The results showed that 87.4% of the population 1965+ years of age exhibited chronic destructive periodontal disease. Additionally, 98100% of those in the 3565+ years age-group suffered from the disease as mani-

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fested by radiographic bone loss that averaged 2.77 mm with a range of 2.163.32 mm. Destructive periodontitis was rarely noted before age 18 years, but the incidence increased rapidly from 14 to 69% between the ages of 19 and 26 years, with a steady increase thereafter until at age 45 years the incidence was 100%. By age 40 years, the authors noted that 90% of the population exhibited periodontal disease consisting of either overt gingivitis or increased pocket depth with bone loss. The study did not establish a case denition for periodontitis or thresholds for the various clinical parameters. Based on US Bureau of Census data, the US population in the year 1955 was 161,497,000, of which 106,373,000 comprised the age group 1965+ years (84). Thus, a prevalence rate of 87.4% translates to 92,970,000 individuals aficted with chronic destructive periodontal disease (Table 2). Having made such an extrapolation, it must be noted that it is highly questionable that a cross-sectional survey of periodontal disease in a population from greater Boston, Massachusetts, can be generalized to that of the population of the total USA. The 196062 National Health Examination Survey examined a sample of 6653 randomly selected individuals between the ages of 18 and 79 years (54) from the target population of approximately 90 million adults. As noted previously, the National Health Examination Survey was the rst attempt to generate a national estimate of periodontal disease prevalence in the USA. Using the Russell Periodontal Index as the instrument for measuring existence and severity

of chronic periodontitis, it was determined that only 27.8% of those examined were free of periodontal disease, while 25% exhibited periodontitis. Although the sample statistically represented 90 million adults, examination of the US Bureau of Census data for the years 1960, 1961 and 1962 indicate that, in general there were 115,200,000 adults in the 1879 years age-group (77). Thus, given a 25% prevalence rate, one can extrapolate that approximately 28,800,000 individuals were aficted with periodontal disease (Table 2). The National Health and Nutrition Examination Survey I, conducted from 1971 to 1974 on a target population of subjects 1874 years of age, again used the Russell Periodontal Index for assessment of periodontal disease (57). The authors reported disease severity by identifying those with one to three periodontal pockets and those with four or more periodontal pockets. Using this stratication, the authors were able to show a positive correlation between disease severity and age. For example, 39.7% of Americans aged 6574 years had four or more pockets compared with 10.3% of those aged 18 44 years. The overall prevalence of periodontitis for the population aged 1874 years was 25.5%. The average number of individuals in this age group from 1971 to 1974 was approximately 132,387,000 (77). Given the 25.5% prevalence rate, about 34,233,262 individuals could have been aficted with chronic or aggressive periodontitis (Table 2). The National Health and Nutrition Examination Survey II was conducted from 1976 to 1980 but did

Table 2. Estimates of periodontal disease extrapolated from national prevalence data


Year(s) of survey US national survey Prevalence of periodontitis (%) Age group of Estimated population (years) population of age group (US census data) 1965+ 1879 1874 19 1864 3090 18 18 106,373,000 (84) 115,200,000 (77) 132,387,000 (77) 163,088,740 (85) 147,535,500 (78) 139,913,000 (78) 209,770,520 (86) 220,359,620 (86) Calculated population within age group with periodontitis 92,970,000 28,800,000 34,233,262 58,712,000 64,620,550 48,969,550 15,313,247 9,255,104

1955 19601962 19711974 1981 19851986 19881994 19992000 20022004

Marshall-Day et al. (64) NHES (54) NHANES I (57) HRSA USPHS (19) NIDR (20) NHANES III (5) NHANES III (13) NHANES III (12)

87.4* 25.0 25.5 36.0 43.8 35.0 7.3 4.2

* The study did not establish a case denition for periodontitis or thresholds for various clinical parameters. Percentage of population examined who exhibited clinical attachment loss 3 mm. HRSA USPHS, Health Resources and Services Administration US Public Health Service; NHANES, National Health and Nutrition Examination Survey; NHES, National Health Examination Survey; NIDR, National Institute of Dental Research.

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not include oral health data from which to estimate the prevalence of periodontitis. However, during the years 19821984, the National Center for Health Statistics conducted the Hispanic Health and Nutrition Examination Survey that focused on three population subgroups of Hispanics aged 1874 years [i.e. Mexican-Americans (n = 5983), Cuban Americans (n = 1192) and Puerto Ricans (n = 2226)]. Here again, the Russell Periodontal Index was used to assess for periodontal disease. Of the dentate examinees, the authors reported that 40.6% of Puerto Ricans, 36.9% of Mexican-Americans and 22.8% of Cuban-Americans exhibited periodontitis. Paradoxically, although Cuban-Americans had the lowest prevalence of periodontitis, as a group they had the greatest prevalence (6.1%) of total tooth loss (52, 53). A 1981 survey of a US population, 19 years of age, sponsored by the Health Resources and Services Administration US Public Health Service, addressed the prevalence and severity of periodontal disease and its role in tooth loss (19). As pocket depth was measured only at the mesial of all available permanent teeth, this methodology probably underestimated disease prevalence. Pocket depth 4 mm affected 36% of the study population, with 8% exhibiting at least one site 6 mm. Only 15% of the survey population was considered free of periodontal disease. Using the US Bureau of Census estimated population of 230,990,000 for the year 1980, there were 163,088,740 individuals 19 years of age (83). Thus, using a 36% prevalence rate, one can extrapolate that approximately 58,712,000 individuals were affected by periodontitis (Table 2). A 198586 survey, sponsored by the National Institute of Dental Research National Institute of Dental and Craniofacial Research, reported a periodontal disease prevalence of 14% involving those in the 18 64 years age-group, using pocket depth as the determinant of disease. When using clinical attachment loss of 3 mm as the determinant of disease, the prevalence rate is 47.2% for the same age-group (20). Extrapolation of disease severity to the estimated US population for the years 198586, as based on Bureau of Census data, indicates that approximately 64,620,550 individuals between the ages of 18 and 64 years were aficted with periodontitis (Table 2). Comparison of pocket depth and clinical attachment loss data from the 1981 Health Resources and Services Administration US Public Health Service, 198586 National Institute of Dental Research and 198894 National Health and Nutrition Examination Survey III surveys shows the prevalence of periodontitis to vary only slightly between the years of

1981 and 1994 (Table 3). However, the most dramatic ndings regarding periodontitis prevalence are presented in the 198894, 199900 and 200204 National Health and Nutrition Examination Survey III reports, using slightly different case denitions for periodontitis. When viewed collectively, ndings from the three National Health and Nutrition Examination Survey III reports show a progressive decrease in the prevalence of periodontitis between the years 1988 and 2004. For example, the rst of these three datacollecting cycles reported a prevalence rate of 35% for individuals aged 3090 years. Based on US Census data for the years 198894 (78), this translates to approximately 49 million US individuals aficted with periodontitis (Table 2). The second and third data-collecting cycles reported a prevalence of 7.3 and 4.2%, respectively, for individuals 18 years translating to 15,313,247 and 9,255,104 people with periodontitis, respectively (Table 2).

Prevalence of periodontitis in military populations


All large epidemiologic studies of periodontal disease in the US population have employed partial-mouth examinations. As noted previously, the partial-mouth examination is likely to produce biased estimates of disease prevalence (6, 36, 49, 59). Thus, consideration of one relatively small study that used full-mouth circumferential probing combined with radiographic evaluation of alveolar bone levels to determine prevalence of periodontitis makes an interesting comparison. In 1990, Horning et al. (46) examined 1788 active duty and 125 retired military personnel and 25 military dependents for a total survey population of 1984

Table 3. Comparison of reported prevalence (%) of periodontitis by case denition in three US periodontal health surveys*
Case denition PD 4 mm PD 6 mm CAL 3 mm CAL 5 mm HRSA USPHS (1981) 36 8 No Data No Data NIDR (198586) 14 1 44 13 NHANES III (198894) 30 4 40 15

* Data extracted from Table1, Oliver et al. (67). CAL, clinical attachment loss; PD, pocket probing depth; HRSA USPHS, Health Resources and Services Administration US Public Health Service; NHANES, National Health and Nutrition Examination Survey; NIDR, National Institute of Dental Research.

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individuals. The mean age of the population was 30.3 with a range of 1384 years. Periodontitis was dened as: early periodontitis, consisting of bleeding on probing and pocket depth of 35 mm; moderate periodontitis, consisting of bleeding on probing, pocket depth of 57 mm, radiographic bone loss up to one-third of the root length and Class I furcation involvement; and advanced periodontitis, consisting of bleeding on probing, pocket depth >7 mm, radiographic bone loss greater than one-third of the root length and Class II or Class III furcation involvement. Given the disease categories and denitions, the authors reported prevalence rates of 33% for early periodontitis, 14% for moderate periodontitis and 15% for advanced periodontitis. Additionally, 0.5% exhibited aggressive periodontitis (juvenile periodontitis) and 0.5% presented with necrotizing ulcerative gingivitis. The overall prevalence rate for periodontitis for the survey population was 63%. If one considers only moderate and advanced periodontitis (plus aggressive periodontitis) the prevalence rate becomes 29.5%. The results of this survey were similar to those of Marshall-Day et al. (64) who reported on a similar sized population (n = 1279). However, the 63% prevalence rate in the study of Horning et al. (46) is obviously higher than that of the 1981 Health Resources and Services Administration US Public Health Service, the 198586 National Institute of Dental Research and the 198894 National Health and Nutrition Examination Survey III surveys, which reported overall prevalence rates of 36, 43.8 and 35%, respectively (5, 19, 20). These comparative results appear to justify some degree of skepticism concerning the reliability of partial-mouth examination vs. that of full-mouth circumferential probing when combined with radiographic evaluation of bone loss. Indeed, Eaton et al. (36) has reported that the prevalence of clinical attachment loss of 2 and 3 mm when using partialmouth vs. full-mouth examination was underestimated by 22 and 36%, respectively. Querna et al. (72), Covington et al. (29) and Diefenderfer et al. (31) examined smaller groups of active duty military personnel (n = 5001107) using the Periodontal Screening and Recording system or a modication thereof. They reported 47.6, 17.6 and 23.8% prevalence rates of periodontitis, respectively. Again, the prevalence rates reported in these three studies are considerably greater than those reported in the comparable 198894 National Health and Nutrition Examination Survey III and the 199900 and 200304 data-collection cycles which were 35, 7.3 and 4.2%, respectively.

Age of subject and prevalence of periodontitis


Burt (25) made the pertinent observation that Any prevalence data need the reference markers of the relevant case denition and the age group to which they apply. As an example, when periodontitis is operationalized as one or more sites with clinical attachment loss of 2 mm, the conclusion is reached that nearly 80% of adults are affected. Furthermore, given that denition, approximately 90% of those in the 5564-years age-group are aficted with periodontitis (25). However, if one denes periodontitis as one or more sites with clinical attachment loss of 4 mm or clinical attachment loss of 6 mm, the prevalence in individuals 5564 years of age decreases to about 50% or <20%, respectively (25). Clearly, age and case denition impact conclusions made about periodontitis prevalence. Past interpretation of such data led to the assumption that periodontitis was a disease of aging, that is, age of and by itself was a risk factor for developing the disease. However, the relationship between age and periodontitis is deceiving. For example, Albandar (2, 3) notes that the effect of age appears to be different for pocket depth and clinical attachment loss, with the latter increasing with increased age. In the case of pocket depth, age appears to have minimal impact. Indeed, several studies have shown that clinical attachment loss increases with age but without signicant loss of function in affected teeth (33, 38, 40, 50). Furthermore, good oral hygiene and periodontal health equate to long-term tooth retention, regardless of age (1, 26). Lastly, it appears that periodontitis may begin in adolescence and or early adulthood (23, 24). This suggests that susceptibility to periodontal disease may be more important than age (5, 88). Consequently, current paradigms view increasing clinical attachment loss as resulting from a lifetime of disease exposure rather than an age-specic disease (25, 71).

Race ethnicity and prevalence of periodontitis


As noted previously, Hispanic populations 18 74 years of age and living in the USA, were the subject of a 198284 National Center for Health Statistics sponsored periodontal health survey. The population subgroup exhibiting the highest prevalence of periodontitis were the Puerto Ricans (40.6%), followed in

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order by Mexican-Americans (36.9%) and CubanAmericans (22.8%) (52). With the exception of the Puerto Rican subgroup, the prevalence of periodontitis in the Hispanic community, for this time period, was very similar to the prevalence rate of 36% reported for the overall US population in the 1981 Health Resources and Services Administration US Public Health Service survey (19). The National Health and Nutrition Examination Survey III of 198894 reported a higher prevalence of periodontitis in non-Hispanic blacks and MexicanAmericans compared with non-Hispanic whites (5). Comparison of pocket depth, clinical attachment loss and furcation involvement, regardless of age, showed the prevalence of adverse clinical parameters to be consistently greater for non-Hispanic blacks and Mexican-Americans than for non-Hispanic whites (Table 4). The pattern of non-Hispanic blacks (African-Americans) exhibiting a higher prevalence of periodontitis followed by Mexican-Americans and non-Hispanic whites appears consistent, regardless of case denition (7, 17, 29, 51). However, as with age, the relationship of race ethnicity with the prevalence of periodontitis comes with several caveats. As Williams (89, 90) and Borrell & Papapanou (11) have suggested, race and ethnicity are social constructs that can strongly inuence socioeconomic status, access to health care (e.g. geographic location and availability of insurance), educational levels and frequency of dental visits. Furthermore, Kaufman et al. (56) and Borrell et al. (15) maintain the importance of recognizing the interaction of socioeconomic status and health status as a function of social, political and historical consequences. As an example, Borrell et al. (15) reported that high-income African-Americans exhibit a higher prevalence of periodontitis than do low-income African-Americans or high-income Caucasians. Indeed, it may be that periodontal disease status may have little association with the use of dental services among low-income patients because those exhibiting

the greatest incidence of clinical attachment loss may be those least likely to seek dental care (41, 42, 79). Interestingly, using multivariate analyses based on data derived from the 198586 National Institute of Dental Research survey, Oliver et al. (67) determined an odds ratio of 79:1 for development of periodontitis for an individual with a high-risk prole consisting of age >34 years, less than 12 years of education, presence of subgingival calculus and bleeding on probing, and had not seen a dentist for 3 years. It should be noted, however, that the odds ratio was not supported by a condence interval and thus may represent an unreliable estimate.

Disconnect between prevalence, diagnosis and treatment of periodontitis


Hujoel et al. (48) have estimated a 31% decrease in the prevalence of periodontitis between the years 1955 and 2000. Furthermore, these authors estimate an additional 8% decrease by the year 2020. They attributed the decrease to changes in tobacco smoking habits. There is a well-established and documented relationship between smoking and development and or severity of periodontitis (55, 61, 62, 80). In spite of actual and projected decreases in smoking habits (66), a better understanding of the pathogenesis of periodontitis, and more rened and goal-directed therapies, there is still evidence that dentistry is not consistently achieving a timely diagnosis and appropriate and timely treatment of existing periodontitis (28, 32). Although not well researched, there is evidence that the use of a probe for diagnosing and recording periodontal status in treatment records in the general dental practice has yet to achieve the level of a routine and consistent habit (8, 30, 44, 65). In fact, McFall et al. (65), in a study of 36 general dental practices, noted that

Table 4. Prevalence (%) of pocket probing depth (PD), clinical attachment loss (CAL) and Class I & II furcation involvement accordng to race ethnic groups of patients, 3090 years of age*
Non-Hispanic whites Furcation PD 3 mm 5 mm 7 mm 62.2 7.6 1.7 CAL 52.0 19.0 6.6 Class I & II 12.8 PD 68.0 14.5 2.0 Mexican-Americans Furcation CAL 64.5 28.4 9.7 Class I & II 19.5 PD 76.0 18.4 5.2 Non-Hispanic blacks Furcation CAL 61.6 28.0 12.2 Class I & II 23.6

* Data extracted from Tables 2, 5, and 8, Albandar et al. (5).

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except for radiographs, the records of most patients contained insufcient diagnostic information to describe their periodontal status. Tugnait et al. (82) used a self-report questionnaire to determine the rate of periodontal examination by 800 general practitioners. Given the problems of validity inherent to data obtained by self-report, the authors found that 44% of the general practitioners claimed to assess probing depths on all new patients. Obviously, at least 56% evidently did not! In this regard, it is interesting to note that at least one study has reported the existence of a disconnect between dentists perception of treatment rendered and actual treatment as recorded in patient records (45). Somewhat more encouraging is the study by Heins et al. (44), who reported that 62% of practices performed and recorded full-mouth periodontal probing on all new patients. Although recall patients received similar scrutiny in 57% of practices, the mean frequency between periodontal probing was 12.7 months. Cobb et al. (28) compared the pattern of referral of periodontitis patients in 1980 vs. 2000 using patient record data from three geographically diverse private periodontal practices. Results of the record audit revealed the following trends occurring over the 20-year time span: decreased use of tobacco; increase in the percentage of patients exhibiting advanced chronic periodontitis with a concomitant decrease in the percentage of patients with mild-to-moderate disease; increase in the average number of missing teeth per patient; and increase in the average number of teeth scheduled for extraction per patient. Docktor et al. (32) used data from patient records from three private periodontal practices located within a major metropolitan area to determine the level of care delivered in the general practice ofce prior to referral. Conclusions from this study support those reported by Cobb et al. (28). In addition, the authors noted that 74% of the patients referred were considered to have advanced periodontitis, and that of those 74%, 30% were treatment planned for extraction of two or more teeth. In addition, periodontal treatment provided by the general dental ofce did not vary because of disease severity. Lastly, the average number of periodontal maintenance visits patient year in the general dental ofce were lower than the standard of care according to severity of disease, for example, 68% of patients with advanced periodontitis reported between none and two periodontal maintenance visits per year rather than the recommended every 3 months. This latter point is rather poignant as Lanning et al. (63) reported that 86% of general dentists surveyed reported providing

periodontal maintenance in their practices. Viewed in aggregate, the trends reported by Cobb et al. (28) and Docktor et al. (32) support the contention that timely diagnosis and appropriate and timely treatment of chronic periodontitis have not signicantly improved over time.

Summary
The prevalence of periodontitis in a given US population is dependent upon case denition, age and race ethnicity. Even given these variables, comparison of data from various US periodontal health surveys are suggestive of a progressive decrease in the prevalence of moderate-to-advanced periodontitis. Furthermore, one may conclude that epidemiology has demonstrated that the majority of the US adult population exhibits, to some extent, a mild, chronic periodontitis. Indeed, it appears that mild attachment loss of 2 mm is compatible with long-term function of the dentition (25). However, regardless of prevalence, for those individuals aficted with more severe disease (clinical attachment loss 3 mm or pocket depth 5 mm), periodontitis remains a signicant social and economic concern.

References
1. Abdellatif HM, Burt BA. An epidemiological investigation into the relative importance of age and oral hygiene status as determinants of periodontitis. J Dent Res 1987: 66: 1318. 2. Albandar JM. Periodontal diseases in North America. Periodontol 2000 2002: 29: 3169. 3. Albandar JM. Global risk factors and risk indicators for periodontal diseases. Periodontol 2000 2002: 29: 177206. 4. Albandar JM. Epidemiology and risk factors of periodontal disease. Dent Clin North Am 2005: 49: 517532. 5. Albandar JM, Brunelle JA, Kingman A. Destructive periodontal disease in adults 30 years of age and older in the United States, 198894. J Periodontol 1999: 70: 1329. 6. Ainamo J, Ainamo A. Partial indices as indicators of severity and prevalence of periodontal disease. Int Dent J 1985: 35: 322326. 7. Arbes SJ Jr, Agustsdottir H, Slade GD. Environmental tobacco smoke and periodontal disease in the United States. Am J Pub Health 2001: 91: 253257. 8. Bader JD, Rozier G, McFall WT Jr, Sams DH, Graves RC, Slome BA, Ramsey DL. Evaluating and inuencing periodontal diagnostic and treatment behaviors in general practice. J Am Dent Assoc 1990: 121: 720724. 9. Beck JD, Cusmano L, Green-Helms W, Koch GG, Offenbacher S. A 5-year study of attachment loss in communitydwelling older adults: incidence density. J Periodontal Res 1997: 32: 506515.

21

Cobb et al.
10. Boehm TK, Scannapieco FA. The epidemiology, consequences and management of periodontal disease in older adults. J Am Dent Assoc 2007: 138(Suppl. 9): 26S33S. 11. Borrell LN, Papapanou PN. Analytical epidemiology of periodontitis. J Clin Periodontol 2005: 32(Suppl. 6): 132 158. 12. Borrell LN, Crawford ND. Social disparities in periodontitis among United States adults 19992004. Community Dent Oral Epidemiol 2008: 36: 383391. 13. Borrell LN, Burt BA, Taylor GW. Prevalence and trends in periodontitis in the USA: The NHANES, 1988 to 2000. J Dent Res 2005: 84: 924930. 14. Borrell LN, Burt BA, Warren RC, Neighbors HW. The role of individual and neighborhood social factors on periodontitis: The third National Health and Nutrition Examination Survey. J Periodontol 2006: 77: 444453. 15. Borrell LN, Burt BA, Neighbors HW, Taylor GW. Social factors and periodontitis in an older population. Am J Public Health 2004: 94: 748754. 16. Borrell LN, Burt BA, Gillespie BW, Lynch J, Neighbors H. Periodontitis in the United States: beyond black and white. J Public Health Dent 2002: 62: 92101. 17. Borrell LN, Lynch J, Neighbors H, Burt BA, Gillespie BW. Is there homogeneity in periodontal health between African Americans and Mexican Americans? Ethn Dis 2002: 12: 97 110. 18. Borrell LN, Taylor GW, Borgnakke WS, Nyquist LV, Woolfolk MW, Allen DJ, Lang WP. Factors inuencing the effect of race on established periodontitis prevalence. J Public Health Dent 2003: 63: 2029. e H. Periodontal diseases in the 19. Brown LJ, Oliver RC, Lo U. S. in 1981: prevalence, severity, extent, and role in tooth mortality. J Periodontol 1989: 60: 363370. e H. Evaluating periodontal status 20. Brown LJ, Oliver RC, Lo of US employed adults. J Am Dent Assoc 1990: 121: 226 232. e H. Prevalence, extent, severity and progres21. Brown LJ, Lo sion of periodontal disease. Periodontol 2000 1993: 2: 5771. 22. Brown LJ, Brunelle JA, Kingman A. Periodontal status in the United States, 198891: prevalence, extent, and demographic variation. J Dent Res 1996: 75: 672683. 23. Burt BA. Epidemiology of dental diseases in the elderly. Clin Geriatric Med 1992: 8: 447459. 24. Burt BA. Periodontitis and aging: reviewing recent evidence. J Am Dent Assoc 1994: 125: 273279. 25. Burt BA. Position paper: epidemiology of periodontal diseases. J Periodontol 2005: 76: 14061419. 26. Burt BA, Ismail AI, Eklund SA. Periodontal disease, tooth loss, and oral hygiene among older Americans. Community Dent Oral Epidemiol 1985: 13: 9396. 27. Chilton NW. Some public health aspects of periodontal disease. J Am Dent Assoc 1950: 40: 2833. 28. Cobb CM, Carrara A, El-Annan E, Youngblood LA, Becker BE, Becker W, Oxford GE, Williams KB. Periodontal referral patterns, 1980 versus 2000: a preliminary study. J Periodontol 2003: 74: 14701474. 29. Covington LL, Breault LG, Hokett SD. The application of periodontal screening and recording J. (PSR) on a military population. J Contemp Dent Pract 2003: 4: 2439. 30. Cury PR, Martins MT, Bonecker M, De Araujo NS. Incidence of periodontal diagnosis in private dental practice. Am J Dent 2006: 19: 163165. 31. Diefenderfer KE, Ahif RL, Simecek JW, Levine ME. Periodontal health status in a cohort of young U S Naval personnel. J Public Health Dent 2007: 67: 4954. 32. Dockter KM, Williams KB, Bray KS, Cobb CM. Relationship between pre-referral periodontal care and periodontal status at time of referral. J Periodontol 2006: 77: 17081716. 33. Douglass CW, Jette AM, Fox CH, Tennstedt SL, Joshi A, Feldman HA, McGuire SM, McKinlay JB. Oral health status of the elderly in New England. J Gerodontol 1993: 48: 3946. 34. Dye BA, Selwitz RH. The relationship between selected measures of periodontal status and demographic and behavioural risk factors. J Clin Periodontol 2005: 32: 798808. 35. Dye BA, Thornton-Evans G. A brief history of national surveillance efforts for periodontal disease in the United States. J Periodontol 2007: 78: 13731379. 36. Eaton KA, Duffy S, Grifths GS, Gilthorpe MS, Johnson NW. The inuence of partial and full-mouth recordings on estimates of prevalence and extent of lifetime cumulative attachment loss: a study in a population of young male military recruits. J Periodontol 2001: 72: 140145. 37. Fleiss JL, Park MH, Chilton NW, Alman JE, Feldman RS, Chauncey HH. Representativeness of the Ramfjord teeth for epidemiological studies of gingivitis and periodontitis. Community Dent Oral Epidemiol 1987: 15: 221224. 38. Fox CH, Jette AM, McGuire SM, Feldman HA, Douglass CW. Periodontal disease among New England elders. J Periodontol 1994: 65: 676684. 39. Gehlbach SH. Interpretation: sensitivity, specicity and predictive value. In: Gehlbach SH, editor. Interpreting the medical literature, 4th edn. New York: McGraw Hill, 2002: 177201. 40. Gilbert GH, Heft MW. Periodontal status of older Floridians attending senior activity centers. J Clin Periodontol 1992: 19: 249255. 41. Gilbert GH, Shelton BJ, Fisher MA. Forty-eight-month periodontal attachment loss incidence in a populationbased cohort study: role of baseline status, incident tooth loss, and specic behavioral factors. J Periodontol 2005: 76: 11611170. 42. Hanson WL, Persson GR. Periodontal conditions and service utilization behaviors in a low income adult population. Oral Health Prev Dent 2003: 1: 99109. 43. Harrigan RC, Easa D, LeSaux C, Millar L, Kagihara LE, Shomaker TS, Greer MHK, Beck JD, Offenbacher S. Oral health disparities and periodontal disease in Asian and Pacic Island populations. Ethn Dis 2005: 15(Suppl. 5): S539S5-46. 44. Heins PJ, Fuller WW, Fries SE. Periodontal probe use in general practice in Florida. J Am Dent Assoc 1989: 119: 147 150. 45. Helminen SE, Vehkalahti M, Murtomaa H. Dentists perception of their treatment practices versus documented evidence. Int Dent J 2002: 52: 7174. 46. Horning GM, Hatch CL, Lutskus J. The prevalence of periodontitis in a military treatment population. J Am Dent Assoc 1990: 121: 616622. 47. Horning GM, Hatch CL, Cohen ME. Risk indicators for periodontitis in a military treatment population. J Periodontol 1992: 63: 297302. m J, del Aguila MA, DeRouen TA. A 48. Hujoel PP, Bergstro hidden periodontitis epidemic during the 20th century? Community Dent Oral Epidemiol 2003: 31: 16.

22

Decline of periodontitis in the USA


49. Hunt R, Fann S. Effect of examining half teeth in a partial periodontal recording of older adults. J Dent Res 1991: 70: 13801385. 50. Hunt RJ, Levy SM, Beck JD. The prevalence of periodontal attachment loss in an Iowa population aged 70 and older. J Public Health Dent 1990: 50: 251256. 51. Hyman JJ, Reid BC. Epidemiologic risk factors for periodontal attachment loss among adults in the United States. J Clin Periodontol 2003: 30: 230237. 52. Ismail AI, Burt BA, Brunelle JA. Prevalence of total tooth loss, dental caries, and periodontal disease in MexicanAmerican adults: results from the Southwestern HHANES. J Dent Res 1987: 66: 11831188. 53. Ismail AI, Szpunar SM. The prevalence of tooth loss, dental caries, and periodontal disease among Mexican Americans, Cuban Americans, and Puerto Ricans: ndings from HHANES 198284. Am J Public Health 1990: 80: 6670. 54. Johnson ES, Kelly JE, Van Kirk LE. Selected dental ndings in adults by age, race and sex. United States 196062. U.S. Department of Health, Education, and Welfare. National Center for Health Statistics. Vital and Health Stat 1965: 11: 127. 55. Kaldahl WB, Johnson GK, Patil KD, Kalkwarf KL. Levels of cigarette consumption and response to periodontal therapy. J Periodontol 1996: 67: 675681. 56. Kaufman JS, Cooper RS, McGee DL. Socioeconomic status and health in blacks and whites: the problem of residual confounding and the resiliency of race. Epidemiol 1997: 8: 621628. 57. Kelly JE, Harvey CR. Basic data on dental examination ndings of persons 1874 years, United States 19711974. Vital Health Stat 1979: 11: 128. 58. Kinane DF. Causation and pathogenesis of periodontal disease. Periodontol 2000 2001: 25: 820. e H. Systematic errors in esti59. Kingman A, Morrison E, Lo mating prevalence and severity of periodontal disease. J Periodontol 1988: 59: 707713. 60. Kingman A, Albander JM. Methodological aspects of epidemiological studies of periodontal diseases. Periodontol 2000 2002: 29: 1130. 61. Krall EA, Dawson-Hughes B, Garvey AJ, Garcia RI. Smoking, smoking cessation, and tooth loss. J Dent Res 1997: 76: 16531659. 62. Krall EA, Dietrich T, Nunn ME, Garcia RI. Risk of tooth loss after cigarette smoking cessation. Prev Chronic Dis 2006: 3: A115. 63. Lanning SK, Best AM, Hunt RJ. Periodontal services rendered by general practitioners. J Periodontol 2007: 78: 823 832. 64. Marshall-Day C, Stephens R, Quigley L Jr. Periodontal disease: prevalence and incidence. J Periodontol 1955: 26: 185203. 65. McFall WT Jr, Bader JD, Rozier G, Ramsey D. Presence of periodontal data in patient records of general practitioners. J Periodontol 1988: 59: 445449. 66. Mendez D, Warner KE. Adult cigarette smoking prevalence: declining as expected (not as desired). Am J Pub Health 2004: 94: 251252. e H. Periodontal diseases in the 67. Oliver RC, Brown LJ, Lo United States population. J Periodontol 1998: 69: 269 278. 68. Page RC, Kornman KS. The pathogenesis of human periodontitis: an introduction. Periodontol 2000 1997: 14: 911. 69. Page RC, Eke PI. Case denition for use in populationbased surveillance of periodontitis. J Periodontol 2007: 78: 13871399. 70. Papapanou PN. Periodontal diseases: Epidemiology. Ann Periodontol 1996: 1: 136. 71. Papapanou PN, Lindhe J, Sterrett JD, Edneroth L. Considerations on the contribution of ageing to loss of periodontal tissue support. J Clin Periodontol 1991: 18: 611615. 72. Querna JC, Rossman JA, Kerns DG. Prevalence of periodontal disease in an active duty military population as indicated by an experimental periodontal index. Mil Med 1994: 159: 233236. 73. Ramfjord SP. Indices for prevalence and incidence of periodontal disease. J Periodontol 1959: 30: 5159. 74. Russell AL. A system of classication and scoring for prevalence surveys of periodontal disease. J Dent Res 1956: 35: 350359. 75. Ship JA, Beck JD. Ten-year longitudinal study of periodontal attachment loss in healthy adults. Oral Surg Oral Med Oral Pathol Oral Radiol Endod 1996: 81: 281290. 76. Skrepcinski FB, Niendorff WJ. Periodontal disease in American Indians and Alaska Natives. J Public Health Dent 2000: 60(Suppl. 1): 261266. 77. Statistical Abstract of the United States. Population by Age and Sex: 1950, 1960 and 1970. Table 34. 95th annual edition. Washington DC: U.S. Department of Commerce, Social and Economic Statistics Administration, Bureau of the Census, 1974, p. 31. 78. Statistical Abstract of the United States. Population by Age and Sex: 1980 and 1998. Table 14. 119th annual edition. Washington DC: U.S. Department of Commerce, Social and Economic Statistics Administration, Bureau of the Census, 1999, p. 15. 79. Tomar SL. Public health perspectives on surveillance for periodontal disease. J Periodontol 2007: 78: 13801386. 80. Tomar SL, Asma S. Smoking-attributable periodontitis in the United States: ndings from NHANES III. National Health and Nutrition Examination Survey. J Periodontol 2000: 71: 743751. 81. Tonetti MS, Claffey N. Advances in the progression of periodontitis and proposal of denitions of periodontitis case and disease progression for use in risk factor research. J Clin Periodontol 2005: 32(Suppl. 6): 210213. 82. Tugnait A, Clerehugh V, Hirschmann PN. Use of the basic periodontal examination and radiographs in the assessment of periodontal diseases in general dental practice. J Dent 2004: 32: 1725. 83. U.S. Bureau of Census. Population Estimates Program, Population Division. Available at: http://www.census.gov/ population/estimates/nation/intle1-1.txt; last accessed on November 28, 2007. 84. U.S. Bureau of Census. Mobility of the Population of the United States: March 1955 to 1956 (P20-73). Table 3. Available at: http://www.census.gov/population/www/ socdemo/migrate/p20-73.html; last accessed on November 22, 2007. 85. U.S. Bureau of Census. Table 11. Resident Population by Age and Sex: 1980 to 2005. Available at: http://www.

23

Cobb et al.
census.gov/compendia/statab/tables/07s0011.xls; last accessed on November 19, 2007. 86. U.S. Bureau of Census. Table 1. Annual Estimates of the Population by Five-Year Age Groups and Sex for the United States: April 1, 2000 to July 1, 2006. Available at: http:// www.census.gov/popest/national/asrh/NC-EST2006/ NC-EST2006-01.xls; last accessed on November 19, 2007. 87. U.S. Department of Health and Human Services. Oral Health of United States Adults: The National Survey of Oral Health in U.S. Employed Adults and Seniors: 19851986: National Findings Epidemiology and Oral Disease Prevention Program, National Institute of Dental Research. Bethesda, MD, U.S. Department of Health and Human Services, Public Service, National Institutes of Health, 1987. 88. Van der Velden U. Effect of age on the periodontium. J Clin Periodontol 1984: 11: 281294. 89. Williams DR. Race and health: basic questions, emerging directions. Ann Epidemiol 1997: 7: 322333. 90. Williams DR. Race, socioeconomic status, and health. The added effects of racism and discrimination. Ann New York Acad Sci 1999: 896: 173188.

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