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© 2002 International and American Associations for Dental Research NUTRITION AS A MEDIATOR IN THE RELATION BETWEEN ORAL AND SYSTEMIC DISEASE: ASSOCIATIONS BETWEEN SPECIFIC MEASURES OF ADULT ORAL HEALTH AND NUTRITION OUTCOMES
1 Division of General Internal Medicine, Geriatrics and Health Policy, University of Louisville, and Louisville VA Medical Center, 501 East Broadway, Suite 320-06, Louisville, KY 40202; Correspondence: * corresponding author, csritchie{at}louisville.edu
Recent associations between oral health and systemic disease have led to renewed interest in the mouth and its contribution to health outcomes. Many pathways for this relationship have been postulated, among them the potential mediating role of nutrition. The link between various nutrients and systemic disease has been established, but relatively little work has been done in relating oral conditions with nutrition. We searched MEDLINE, from 1966 to July, 2001, to identify articles relating specific oral measures to nutrition outcomes. We included original articles written in English with a sample size greater than 30 that used objective oral health measures. We reviewed a total of 56 articles. Only a small proportion of these studies were methodologically sound. Although many studies were small and cross-sectional, the literature suggests that tooth loss affects dietary quality and nutrient intake in a manner that may increase the risk for several systemic diseases. The impact of tooth loss on diet may be only partially compensated for by prostheses. To date, there is little information relating periodontal disease and oral pain and nutrition. A few studies suggest poorer nutrition among individuals with xerostomia and altered taste. Further, impaired dentition may contribute to weight change, depending on age and other population characteristics. There is a paucity of well-designed studies addressing oral health and nutrition. Before we can acquire a better understanding of how nutrition and oral health interrelate, however, more studies will be required to confirm these associations—preferably longitudinal studies with larger sample sizes and better control of important confounders.
Key Words: Oral health periodontal disease tooth loss prostheses nutrition systemic disease
The scientific community has become increasingly interested in the possible relationship between oral conditions and systemic outcomes such as coronary heart disease, stroke, and mortality (Joshipura et al., 2000). Commonly postulated mediators of this relationship include infection, chronic inflammation, and genetic predisposition to both oral and systemic disease. Nutrition has been postulated as an alternative mediator (Joshipura et al., 1996, 1998). The impact of various oral conditions on nutritional status may relate importantly to nutrient intake and nutritional status. Several studies have established associations among nutrient intake, nutritional status, and various systemic diseases (Willett, 1994). Recent studies have clearly demonstrated the inverse association between fruit and vegetable intake and the development of cardiovascular disease (Cox et al., 2000; Joshipura et al., 2001). Increased fruit and vegetable intake has also been associated with a lower stroke risk (Joshipura et al., 1999). Multiple studies have also suggested the protective role of fruits and vegetables in cancer (Willett, 1994; Terry et al., 2001); however, studies showing no association with specific cancers have also been reported (Michels et al., 2000). Saturated fat intake has been implicated in cardiovascular disease and may play a role in increasing risk for breast and colo-rectal cancer (Lee and Lin, 2000; Zhang et al., 2000; Smith-Warner et al., 2001). Dietary anti-oxidants or fiber has been shown, in epidemiologic and intervention trials, to reduce cardiovascular disease risk; the results, however, have not been as clear-cut as those obtained for fruits and vegetables (Eastwood, 1999). With both fruits and vegetables and individual vitamins and minerals, reduction in disease outcomes occurs through several mechanisms, including protection against free radical damage, modulation of cytokine production, enhancement of endothelial function, and alteration of coagulation parameters (Grimble, 1998; Nappo et al., 1999; Nuttall et al., 1999). This potential mediating role of nutrition in the oral-health/systemic-disease relationship has triggered our interest in reviewing the literature relating common oral conditions to nutritional outcomes. This paper will review, summarize, and evaluate original scientific articles linking specific oral health problems (tooth loss, prosthesis, periodontal disease, oral pain, xerostomia, altered taste) and their impact on nutritional outcomes (dietary/nutrient intake, body weight, body composition, blood nutrients). We will describe commonly used nutrition assessment measures used in the studies and address questions regarding how specific oral health characteristics relate to these nutrition outcomes. We will summarize the methodology, findings, and limitations of selected articles. Finally, we will provide suggestions for future research design that might provide better data and lead to better-understood conclusions.
Oral health and nutrition are both defined in multiple ways and described by complex, interrelated measurements. Oral health encompasses gingival status, the well-being of the teeth and jaw, salivary quantity and quality, and sensory dimensions of taste and pain. Likewise, nutritional health includes both the quality and quantity of dietary intake and nutritional status. Dietary intake is comprised of the types of food groups ingested (such as fruits, vegetables, or dairy products) and the nutrient composition of the food eaten (micronutrients-vitamins, minerals, and macronutrients-proportion of calories consumed as protein, carbohydrates, and fats). Nutritional status includes body composition and tissue and blood levels of micronutrients. To highlight these various components of oral health and nutrition, we developed a conceptual model that describes how oral health and nutrition characteristics might relate to each other (Fig.
Both periodontal disease and dental caries can lead to tooth loss. Tooth loss can then result in chewing difficulty because of inadequate occlusive surfaces or the limitations of prostheses. Chewing difficulty may then lead to alteration in food selection and dietary quality, which in turn can affect both body composition and nutritional status. Oral pain can also occur as a result of caries, periodontal disease, soft-tissue lesions, and temporomandibular joint disease. Poorly fitting prostheses may also cause stomatitis and oral pain. Oral pain may lead to changes in diet and subsequent nutritional status. Xerostomia and decreased or altered taste could also, theoretically, contribute to changes in nutrient intake and nutritional status. However, these oral health-nutrition relationships are complicated by the fact that health habits (such as smoking), concurrent illnesses, and attitudes and beliefs about health and health behavior can affect oral health, as well as nutrition. Thus, oral health may appear to be related to nutrition even if it has no impact on nutrition. Hence, it is difficult to distinguish whether the oral characteristics or some of these other confounding characteristics (such as health behavior) are responsible for the relationships seen between oral health and nutrition.
Using this model as a basis for describing oral health and nutrition relationships, we utilized the nutritional and oral health terms noted in the Fig.
We identified many studies that address the relationship between some aspect of oral health and nutrition. Unfortunately, many of these studies have small sample sizes and multiple comparison groups, making them underpowered for the adequate assessment of associations. To maintain brevity in the tables, we listed only those studies with sample sizes over 100.
Following the conceptual model noted in the Fig.
(A) HOW DOES TOOTH LOSS AFFECT DIETARY/NUTRIENT INTAKE?
Hildebrandt et al. (1997) compared dietary behaviors with the number of functional units of teeth (any opposing natural or prosthetic tooth pair). The authors reported that decreased numbers of functional units are associated with the avoidance of stringy (beef/steak), crunchy (carrots), and dry solid food (bread). However, he did not adjust for other known confounders such as education or economic status, nor did he address the presence of xerostomia, which also may contribute to food avoidance. Several studies suggest that edentulous individuals are particularly prone to inappropriate dietary intake (for example, ingesting too few nutrient-dense foods and too much calorie-rich, high fat foods) compared with dentate subjects. In a study of older adults in Sweden, Johansson et al. (1994) found that edentulous men consume fewer fruits and vegetables and have a lower intake of fiber than do dentate men. Edentulous women consumed a higher amount of fat than did dentate women. Both edentulous men and women ate more sweet snacks than their dentate counterparts, after adjustment for age and education. Norlen et al. (1993) confirmed, in his study of older women, an association between edentulousness and ingestion of a larger intake of fat. In neither study, however, was the type of fat differentiated (saturated vs. unsaturated). In three large studies in the United States and Europe, decreasing numbers of teeth were also associated with worse dietary quality. Joshipura et al. (1996) analyzed the association between disease-related nutrients and foods and numbers of teeth. After adjusting for age, smoking, exercise, and profession, they observed that edentulous participants consumed fewer vegetables, less fiber and carotene, and more cholesterol, saturated fat, and calories than participants with 25 or more teeth. In this homogenous population of male health professionals, gender and socio-economic and behavioral factors were inherently controlled. Krall et al. (1998) found that subjects with intact dentition or partially compromised dentition have significantly better masticatory function than subjects with removable partial dentures, compromised dentition, or full dentures. In their analyses, the calorie-adjusted nutrient intakes decreased with progressively impaired dentition status after adjustment for age, smoking status, and alcohol use. They also found that better masticatory function is associated with higher intakes of fiber, vitamin B6, folic acid, vitamins A, C, and D, carotene, thiamin, riboflavin, magnesium, phosphorus, and iron. This study, however, did not control for socio-economic status. In a cross-sectional study of British older adults, subjects with more teeth had higher mean intakes of energy, protein, fat, carbohydrate, fiber, calcium, iron, pantothenic acid, and vitamins C and E (Sheiham et al., 2001). This was the one study that reported a higher intake of fat among individuals with more teeth. The type of fat, however, was not characterized. Smaller cross-sectional studies showed no differences in nutrient intake by dentition status (Baxter, 1984; Gordon et al., 1985). These studies had multiple comparison groups and were probably underpowered for the detection of a difference, if it existed. Several of the larger studies noted above suggest that dentition status is associated with dietary intake. However, most of these studies fail to show whether these associations are independent of common factors (confounders) or total calorie intake. Tooth loss has been found to be associated with factors such as limited financial resources, low education status, and history of smoking that generally reflect negative health behaviors and attitudes (Kay and Blinkhorn, 1987; Burt et al., 1990; Worthington et al., 1999). Subjects concerned with their health might be more conscious about both oral health and eating behaviors, and that might explain the differences in dietary patterns among those with different dentition status. Without adjusting for these confounding effects, we cannot evaluate the independent association between oral health and dietary intakes. Adjusting nutrient intake for total caloric intake is also important because people with higher intake of calories may be expected to have higher intake of most foods and nutrients. It is difficult to interpret differences in nutrient intake when total caloric intake is not controlled (Willett, 1998). Controlling for caloric intake additionally helps reduce extraneous variation in nutrients. In summary, most of the studies relating tooth loss and nutrition suggest that nutrient intake deteriorates in quality with fewer teeth. These changes seen in fruit, vegetable, and micronutrient intake with tooth loss may explain part of the tooth-loss/cardiovascular-disease association. Many of the studies we identified in the literature have various approaches to the assessment of nutrition, making comparisons across studies difficult. Commonly used approaches to eliciting information on food intake in the studies reviewed included the 24-hour recall, food records, and food frequency questionnaires. The 24-hour recall elicits all the foods and beverages the subject has consumed in the preceding 24 hours. Although relatively straightforward to perform, it may not provide enough information to generalize about the individual's usual intake. In addition, it tends to underestimate the person's usual fat and calorie intake. This method is hindered by the subject's memory of what has been consumed in the day before (Gibson, 1990). The food record or diary method consists of a detailed listing of all foods consumed by a subject on one or more days. Food intake is recorded by the subject at the time the food is eaten, to minimize recall error. Portion sizes can be accurately measured; however, the process of keeping a food diary may alter the subject's behavior and not reflect usual intake. With both the 24-hour recall and the food record, multiple dates of intake are needed for usual individual intake to be estimated (Buzzard, 1998). The food frequency questionnaire consists of two components: a food list and a frequency response section for individuals to state how often each food was eaten. This approach relies less on immediate recall and more on generic recall (what usually occurs). It provides a good estimate of usual intake, but provides less detail about cooking methods. It may also not capture foods eaten by ethnic groups that are not mentioned on the questionnaire. A few studies used biochemical indicators of dietary intake. Biochemical measures are objective and thus may appear less error-prone than other nutrition assessment methods. Misclassification may still occur due to inappropriate specimen collection, storage, or analysis. In addition, biochemical measures may not completely reflect intake or tissue levels, depending on the measure's bioavailability and the subject's kinetics with respect to the particular nutrient (Hunter, 1998). A weakness of the studies noted above and many others reviewed is that many of these studies are cross-sectional, making the direction of the oral-health/nutrition relationship difficult to ascertain, and determination regarding causality impossible. The interrelation between dental status and dietary intake is complicated. In addition to dentition status causing a change in dietary pattern, several nutrients—such as vitamins A, B6, C, and D, calcium, niacin, and thiamin—may affect oral health (Midda and König, 1994). The association between dentition status and nutrient intake observed in cross-sectional studies might be partially explained by the potential effect of dietary intake on oral health. Therefore, it is difficult to evaluate the temporal roles of dentition status and dietary intakes in cross-sectional studies. An exception was an analysis by Joshipura et al. (1996) of the longitudinal effect of tooth loss over a four-year period on dietary change adjusted for age, smoking, exercise, and professions. Baseline intake suggested that loss of teeth might lead to detrimental changes in diet. However, there was insufficient tooth loss among the health professionals' population for significant difference to be detected (Joshipura et al., 1996). More longitudinal studies are needed to support and clarify the relationship between oral health and dietary intake, before this association can be implicated in the oral-health/systemic-disease relationship.
(B) HOW DO PROSTHESES AFFECT DIETARY/NUTRIENT INTAKE?
Several investigators have compared nutrient intakes among groups with prostheses. The nutrient assessment varied from crude food groups to specific nutrients derived with the use of nutrient databases and foods selected based on textures. Studies were cross-sectional or compared two groups of people before and after prosthesis, with different prostheses assigned randomly or non-randomly. Overall, prosthesis and type of prosthesis influenced patient satisfaction and chewing efficiency, and variably affected nutrient intake. A group of studies compared subjects having full dentures with dentate subjects. In Krall et al.'s (1998) study of veterans, individuals with full dentures consumed fewer calories, thiamin, iron, folate, vitamin A, and carotene than did individuals with other dentitions. Papas et al. (1998a) evaluated the impact of full dentures and noted lower intake of protein and 19 other nutrients. In a separate population, Papas et al. (1998b) reported that subjects who wore dentures consumed more refined carbohydrates, sugar, and dietary cholesterol than their dentate counterparts. The above studies suggest that the presence of dentures contributes to poorer intake across multiple nutrients compared with dentate subjects. Several studies did not reveal as significant a difference in nutrient content between denture wearers and those who are dentate. Keller et al. (1997) reported decreased calorie intake among dentate men and women, but in men, poorer dietary quality among those with their own teeth. In Appollonio et al.'s (1997) study of older Italian subjects, denture wearers had the same nutrient intake as those who were dentate, with the exception of lower vitamin A intake. Greksa et al. (1995) noted lower intake of vitamins A and C and calcium, but otherwise no other differences between groups in dietary diversity. Hartsook (1974) study showed little difference in diets between patients wearing various combinations of dental prostheses; however, the study was small, and dietary intake was highly variable between the different dental groups. All of these studies are cross-sectional, with only a few controlled adequately for confounding. Many of these studies did not address denture fit among denture wearers, which might explain some of the variability in findings regarding nutrient intake. In a study of denture wearers in Quebec, those who wore dentures that provided poor masticatory performance consumed significantly fewer fruits and vegetables than those with dentures that provided good masticatory performance (Laurin et al., 1994). Likewise, in Swedish older adults, poorly fitting upper dentures were associated with decreased intake of vitamin C (Nordstrom, 1990). In a survey of older Australians, women who reported poorly fitting dentures consumed greater amounts of sweets and dessert items (Horwath, 1990). Future longitudinal studies of the impact of prostheses on diet will need to be performed that address both prosthesis fit and confounding. In comparisons between edentulous subjects without dentures and edentulous subjects with dentures, edentulous subjects without dentures, not surprisingly, consumed more mashed food (Lamy et al., 1999), and in a study of Swedish women, edentulous women consumed more fat (Norlen et al., 1993). Fontijn-Tekamp et al.(1996) reported that edentulous subjects without any prostheses had significantly lower carbohydrate and vitamin B6 intake. None of these studies adjusted for factors other than gender and region in the analysis. Most of the studies of the impact of new dentures on dietary intake are small and with no control group. Garrett et al. (1997) conducted a randomized trial of no dentures, fixed partial dentures (FPD), and removable partial dentures (RPD) among partially edentulous subjects; diet was recorded by seven-day diaries. He evaluated calories and 30 nutrients and found no important differences, other than regression to the mean, among those with extreme intake. Since there was no control group, it was not clear whether the regression to the mean was beyond what might be expected in the control group. Sebring et al. (1995) studied the effect of conventional maxillary + implant-supported or conventional mandibular dentures. He evaluated both caloric intake and 27 nutrients, using three-day diet records and adjusting for body weight. In both groups, caloric intake decreased; percentage of calories from fat also decreased significantly over the subsequent three years. Lindquist (1987) evaluated the impact of prosthetic rehabilitation, using optimized complete dentures and then tissue-integrated mandibular fixed prostheses (TIP) on 64 dissatisfied complete-denture wearers. There was no change in diet after complete dentures were optimized, but there was a persistent increase in fresh fruit consumption after placement of TIP. Hamada et al. (2001) performed a similar study among diabetic patients and again showed no real change in diet except for a slight decrease in mean caloric intake. In contrast to the above studies, where there was a slight improvement in overall dietary quality, in a study by Moynihan et al. (2000), patients receiving either resin-bonded bridges or conventional removable partial dentures demonstrated a significant increase in the proportion of energy obtained from fat, 12 months after treatment in the denture group. There was no significant difference in fruit and vegetable intake between baseline and one year post-intervention in either group. Olivier et al. (1995) conducted the only study that evaluated dietary counseling in addition to prosthetic relining for the edentulous on chewing efficiency, dietary fiber intake from various sources, and gastrointestinal esophageal and colonic symptoms. The authors used food frequency questionnaires and made pre- and post-intervention comparison using paired t test and McNemar's test, thus controlling for subject level factors and increasing efficiency. Chewing ability and fiber intake from fruits and vegetables were significantly improved. However, because there was no group that did not receive dietary counseling, it was not possible to separate the effect of relining from that of the counseling. Sebring et al. (1995) adjusted all nutrients and total calories for body weight; however, none of the studies adjusted nutrients for total caloric intake. None of the above studies considered controlling for potential confounders, which would be an important concern for between-group comparisons, where the prostheses were not assigned randomly. Confounding is not an important concern in randomized clinical trials (RCT) (Garrett et al., 1997) where the prostheses is assigned randomly or in analyses that compare pre- and post-prosthesis (Lindquist, 1987). However, in the studies discussed above, the analyses were often only descriptive or simple between-group analyses. Other than the study by Olivier et al. (1995), studies that compared pre- and post-intervention did not use methods for paired data. Baseline differences in intake of the nutrient under consideration, energy intake, or other potential confounders were not factored into the analyses. Future intervention studies would benefit from larger comparison groups, random assignment, paired data analysis, and consistent adjustment of nutrients for total calories. Given the behavioral aspects of food intake, more studies evaluating the impact of concurrent dietary education concurrent with dental intervention would be informative.
(C) HOW DOES TOOTH LOSS OR PROSTHESES AFFECT NUTRITIONAL STATUS?
Most studies addressing nutritional status do not completely measure every aspect of nutritional status. Indeed, in the nutrition literature, much controversy exists regarding comprehensive measures of nutrition. Most nutrition indices do not fully measure nutrition and often incorporate non-nutritional measures of co-morbidity, physical function, and medication use (Lyne and Prowse, 1999). Given the lack of a well-accepted comprehensive measure of nutritional status, investigators are constrained to look at several separate clinical indicators of nutrition, including body weight and body mass index (an indirect measure of protein, fat, and carbohydrate stores), vitamin levels, indirect measures of vitamin status (hemoglobin) or protein status (visceral protein stores such as albumin), and indicators of energy imbalance (weight change).
(1) Body mass index
(2) Weight
(3) Blood nutrient levels Some investigators have also looked at composite nutritional indices that include both risk factors for poor nutrition (such as multiple medications or depression), anthropometric measures (such as body mass index), and consumption of specific food groups (such as fruits and vegetables). The Mini Nutritional Assessment (MNA) is one such index. The MNA score is based on nutritional status, weight change, and risk factors for nutritional inadequacy (such as appetite, co-morbidity, dementia, and depression). It has been validated in several different older adult populations and correlates well with physician-nutritionists' assessments of overall nutritional status (Vellas et al., 1999). Lamy et al. (1999) and Griep et al. (2000) used the MNA score to measure nutritional status. Lamy et al. (1999) evaluated nursing home residents and found that edentulous subjects without or with only one denture had significantly lower MNA scores, reflecting poorer nutritional status. Griep et al. (2000) noted a relationship between number of teeth and MNA score, in the univariate analysis, but not after adjustment for co-morbidity, medication, and gender. Further combined nutrition scores are hard to interpret and strongly influenced by the patient's severity of illness. All of these studies were cross-sectional, so temporality could not be established.
(D) HOW DOES PERIODONTAL STATUS/DENTAL CARIES AFFECT DIETARY/NUTRIENT INTAKE OR NUTRITIONAL STATUS?
(1) How does periodontal status affect dietary/nutrient intake?
(2) How does periodontal status/dental affect nutritional status?
(E) HOW DOES XEROSTOMIA OR ORAL PAIN AFFECT DIETARY/NUTRIENT INTAKE OR NUTRITIONAL STATUS?
(1) How does xerostomia or oral pain affect dietary/nutrient intake? Three studies of xerostomia have found that diet/nutrition and the quality of saliva were affected by exposure to Sjögren's syndrome and xerogenic medications. Loesche et al. (1995) reported that individuals with complaints of xerostomia were more likely to avoid crunchy vegetables (carrots), dry foods (bread), and sticky foods (peanut butter). Rhodus (1988) studied 28 patients with Sjögren's syndrome and compared them with a group of controls matched for diabetes, depression, cardiovascular disease, arthritis, age, gender, and dental health. Caloric and micronutrient intakes were significantly lower among xerostomic patients. Rhodus and Brown (1990) also evaluated 84 older residents of an extended care facility. Energy, protein, fiber, vitamins A, C, and B6, thiamin, riboflavin, calcium, and iron were significantly lower in the patients with xerostomia than in those without. These studies suggest that xerostomia impairs optimal nutrient intake but are again hampered by their small size, cross-sectional design, and inadequate control for confounding factors.
(2) How does xerostomia or oral pain affect nutritional status? Rhodus (1988) noted that the body mass index for the xerostomic individuals with Sjögren's syndrome was significantly lower than that for the control group. In their study of older extended-care-facility residents, they also noted a significantly lower body mass index among the xerostomic subjects (Rhodus and Brown, 1990). Dormenval et al. (1995) evaluated hospitalized older adults and noted that low unstimulated salivary flow rates were associated with low body mass index, triceps skin-fold thickness, and arm circumference. In the arena of both xerostomia and oral pain, much more research is needed before we will understand the extent to which these oral conditions affect nutrient intake and nutritional status.
(F) HOW DOES ALTERED TASTE AFFECT DIETARY/NUTRIENT INTAKE OR NUTRITIONAL STATUS?
(1) How does altered taste affect dietary/nutrient intake?
(2) How does altered taste affect nutritional status?
In summary, although many studies to date have been small and methodologically flawed, recent larger studies suggest the following regarding the questions raised in this paper:
As stated earlier, health behaviors, co-morbidity, and socio-economic status may confound the nutrition and oral health association. Many of the studies relating nutrition and oral health thus far have been cross-sectional studies with relatively small sample sizes. Nutritional measures were often not standardized, nor were nutrients adjusted for caloric intake. Before we can achieve a better understanding of how nutrition and oral health interrelate, more research is needed to confirm these associations—studies with larger sample sizes and better control of important confounders. These studies will also require inclusion of comprehensive nutrition and oral assessment data. Many of the dietary intake assessment methods used in the studies described are acceptable. Food frequency questionnaires provide optimal dietary information. For ethnically diverse and older adult populations, dietary recalls may be preferable. Dietary recalls, however, estimate usual intake only when multiple days are assessed, so future studies should avoid one 24-hour recall. With both these assessment measures, large sample sizes are required to minimize error. All nutrients reported should be adjusted for calorie intake. Nutritional status assessment measures should include not only height and weight, but preferably indicators of fat and fat-free mass as well. More longitudinal studies would benefit from biochemical indicators of dietary intake. Only a few studies have assessed the nutritional impact of oral pain, xerostomia, and altered taste on nutrition outcomes. In particular, nutrition outcomes of temporomandibular disorders justify further study. Larger dental intervention trials will shed light on how remediable oral-health-related nutritional problems are. The pathophysiologic relationship among oral health status, diet, and systemic health outcomes such as CVD and cancer also warrant further exploration. Nutritional factors, especially anti-oxidants that may be affected by tooth loss, may modulate both periodontal disease and systemic disease by interfering with the inflammatory cascade, and preventing carcinogenesis. Likewise, tooth loss may contribute to the intake of calorie-dense, nutrient-poor diets, leading to decreased intake of anti-oxidants and increased intake of foods that foster obesity. Future studies will require careful assessment of nutritional, inflammatory, and cancer biomarkers to better understand these interrelationships. This review highlights associations between oral health and nutrition that suggest an important potential mediating role in the oral-health/systemic-disease relationship. Ongoing aggressive evaluations of these relationships are needed to improve our understanding of this role and to clarify the exact pathways that relate oral health to cardiovascular and other health outcomes.
The authors thank Tom Barton for assistance with manuscript preparation and review. This work was supported in part by grant K01 AG00691 from the National Institutes of Health.
Critical Reviews in Oral Biology & Medicine, Vol. 13, No. 3,
291-300 (2002) This article has been cited by other articles:
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