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Nutrients 2013, 5(4), 1110-1121; doi:10.3390/nu5041110

Use of Dietary Supplements in Patients Seeking Treatment at a Periodontal Clinic
Faculty of Applied Health Sciences, Brock University, St. Catharines, Ontario, L2S 3A1, Canada
Reconstructive Periodontics and Implant Surgery Clinic, Fonthill, Ontario, L0S 1E5, Canada
Author to whom correspondence should be addressed.
Received: 16 February 2013; in revised form: 7 March 2013 / Accepted: 20 March 2013 / Published: 2 April 2013


: Dietary supplement use may modify the risk of periodontal disease but effects on wound healing after periodontal procedures are less clear. This study characterized dietary supplement use by male and female patients (n = 376) attending a periodontal clinic—information that is essential for evidence-based intervention studies that may improve patient outcomes after periodontal procedures. Calcium, vitamin D, multivitamin and vitamin C were most commonly used. A greater (p ≤ 0.05) number of males took no supplements compared to females, and more (p ≤ 0.05) females than males took ≥ four supplements. Females took more (p ≤ 0.05) calcium, vitamin D, fish oil, green tea, magnesium, omega 3,6,9 and B vitamin complex. Younger patients (31–50 years) had the highest (p ≤ 0.05) frequency of no supplement use compared to older age groups. Patients over age 50 had a higher (p ≤ 0.05) frequency of using ≥ four supplements including calcium and vitamin D. Supplement use was lower (p ≤ 0.05) in smokers, particularly for calcium, fish oil, green tea and vitamin D. In conclusion, females, older individuals and non-smokers have higher supplement use. Future dietary intervention studies can focus on supplements with known biological activities—anti-inflammatory, antioxidant or osteogenic activity—that may enhance wound healing after reconstructive periodontal procedures.
dietary supplements; periodontal disease; supplement use; wound healing

1. Introduction

Periodontitis is the component of periodontal disease [1] associated with inflammation of the periodontium resulting in progressive bone and soft tissue destruction, ultimately leading to tooth loss [2]. The etiology of periodontitis originates with the development of a bacterial biofilm, or plaque, on the tooth surface and oral epithelia [2,3]. The host response to the pathogenic biofilm is to initiate periodontal inflammation and recruit polymorphonuclear neutrophils (PMNs) to the infection site [2,3]. PMNs respond to the microbial threats via the creation of reactive oxygen species (ROS), which in chronic inflammation, results in a state of oxidative stress [4].

Dietary supplement use may modify the risk for the development and progression of periodontal disease [5,6,7,8,9]. The antioxidant activity [4] of nutrients such as vitamin C [10,11], and α-tocopherol [12], and the anti-inflammatory activity [7] of polyunsaturated fatty acids (docosahexaeonic acid (DHA) [13,14]) may attenuate the development of periodontal disease. Studies using the NHANES III-a large cross-sectional survey study-have demonstrated that lower vitamin C intake is associated with a higher risk (OR 1.19) of having periodontal disease [10], and that higher vitamin C intake is associated with a reduced risk (OR 0.53) of severe periodontitis [11]. Additionally, using data from the NHANES III, the highest quintile of serum total antioxidant activity (TAOC) was associated with reduced risk (OR 0.63) of severe periodontitis [11]. Association studies have also shown that low intakes of α-tocopherol or DHA are associated with an increased risk of periodontal disease [12,13,14]. Large cross-sectional survey studies have identified that periodontal disease affects a substantial number of individuals and given the potential systemic health effects linked to periodontal disease (i.e., cardiovascular disease and preterm birth), periodontal disease represents a pubic health concern [3]. The Canadian Health Measures Survey from 2007 to 2009 reports that 21% of Canadian adults with natural teeth have experienced a moderate to severe periodontal problem [15], and current estimates from the United States (2009–2010 NHANES) report that periodontitis affects 47% of the adult population over 30 years of age [16]. At present, it is unclear exactly how much of the periodontal disease burden may be exacerbated by poor nutrition. Furthermore, there is limited data regarding whether dietary interventions may enhance recovery from periodontal disease.

Physical disruption of the microbial biofilm at hygiene appointments is the first-line intervention toward periodontal disease [2]. However, emerging data from dietary intervention studies suggest a functional role for diet or dietary supplements in supporting periodontal health and attenuating periodontal disease [17,18,19]. For instance, a diet focusing on whole fresh foods—fruits, vegetables and whole-grains—while limiting processed foods, reduced periodontal inflammation in 20 women with metabolic syndrome [17]. Dietary intervention of two grapefruits per day for two weeks was associated with lower sulcus bleeding in patients with chronic periodontitis [18]. A diet rich in whole-grains has also been shown to reduce the risk of periodontitis by 23% in a prospective study of male health professionals [19]. Moreover, dietary supplements have been shown to have beneficial effects. Supplementation with a fruit and vegetable concentrate in capsules resulted in improvements in probing depth, bleeding on probing, and plaque scores [20]. Another supplementation study, using borage oil that contains high levels of omega-6, improved both probing depth and gingival inflammation in adults with periodontitis [21]. Supplementation with lycopene, in combination with oral prophylaxis, has also been shown to attenuate gingival inflammation more effectively than oral prophylaxis alone [22]. Together, the studies discussed highlight the potential importance of diet or dietary supplements in reducing periodontal inflammation in combination with regular hygiene maintenance.

In addition to maintenance of periodontal health, a few studies have shown that diet may assist with wound healing from periodontal procedures. These few studies have shown that micronutrients (vitamin D and the B vitamins) [23,24,25] and macronutrients (DHA and eicosapentaenoic acid (EPA)) [26,27] can improve patient recovery following periodontal therapy. Being vitamin D sufficient (serum 25(OH)D > 50 nmol/L) before open flap debridement surgery resulted in greater clinical attachment levels and reductions in probing depths post-surgery than patients with lower levels of serum 25(OH)D [23]. Likewise, patients receiving access flap surgery experienced better clinical attachment levels when treated post-operatively with a vitamin-B complex (50 mg thiamine HCl, riboflavin, niacinamide, d-calcium pantothenate, pyridoxine HCl; 50 μg d-biotin, cyanocobalamin; 400 μg folate) [24]. Vitamin B12 as a component of post-surgical medication also resulted in less patient pain at 6 and 120 h post third molar extraction than in control patients [25]. In patients requiring sanative therapy, a combination of acetylsalicylic acid (81 mg) and fish oil (containing 900 mg DHA and EPA) decreased probing depths while increasing clinical attachment and reducing levels of salivary RANKL and MMP-8, markers of inflammation [26]. Similarly, in patients with a furcation defect requiring bone allograft, a combination therapy of acetylsalicylic acid (75 mg) and DHA (900 mg) and EPA (450 mg) resulted in greater clinical attachment, probing depth reductions, and decreased amounts of IL-1β present in the gingival crevicular fluid [27].

Together, findings from these studies suggest that use of dietary supplements during and after periodontal procedures may improve periodontal health outcomes following periodontal procedures. However, randomized controlled trials are needed to more definitively determine how dietary supplements may enhance outcomes after periodontal procedures. The objective of this study was to characterize the use of dietary supplements by patients who attend a periodontal clinic for one of three reasons: comprehensive general examination, implant consultation or other surgical consultation. By understanding the pattern of intakes, researchers will be better informed to design intervention studies that will support better long-term outcomes after periodontal procedures.

2. Methods

A sample of 442 surveys was collected from a periodontal clinic in Southern Ontario. The surveys were administered as part of the routine patient information collected before a periodontal procedure was performed. Patients with uncommon reasons for visiting the periodontal clinic and those in the 19–30 years of age category were removed from the dataset due to small sample group sizes. The final dataset contained 376 surveys with the following three most frequent ‘reason for visit’ categories: Comprehensive General Examination (n = 90), Implant Consultation (n = 126), and Other Surgical Consultation (n = 160). The surgical consult group contained the following procedures: crown lengthening, flap surgery, and grafting. A supplement was considered used if the patient indicated any use of the supplement, irrespective of brand, dose, frequency, or duration. The frequency of supplement use among groups was assessed using a Chi-square test with significance defined as p ≤ 0.05. This study was approved by the Human Ethics Board at Brock University, St. Catharines, Ontario (File #11-161-Ward).

3. Results

3.1. Characteristics of the Study Population

The study population of 376 patients consisted of 152 males (40.4%) and 224 females (59.6%). Approximately 57% of patients were between the ages of 51 and 70 years and most were receiving a surgical consultation (42.6%). A smoking frequency of 16.0% was reported for males and females combined (Table 1).

Table 1. Characteristics of Study Population.
Table 1. Characteristics of Study Population.
n = 152n = 224n =376
n (%)n (%)n (%)
31–50 years45 (29.6)70 (31.2)115 (30.6)
51–70 years85 (55.9)131 (58.5)216 (57.5)
≥70 years22 (14.5)23 (10.3)45 (12.0)
Smoking Status
Ever Smoker28 (18.4)32 (14.3)60 (16.0)
Never Smoker124 (81.6)192 (85.7)316 (84.0)
Reason for Visit
Comprehensive General Examination37 (24.3)53 (23.7)90 (23.9)
Implant Consultation56 (36.8)70 (31.2)126 (33.5)
Other Surgical Consultation59 (38.8)101 (45.1)160 (42.6)

3.2. Number of Supplements Used According to Sex, Age and Smoking Status

There were a greater (p ≤ 0.05) number of males taking no supplements compared to females. Likewise, there were more (p ≤ 0.05) females taking ≥ four supplements than males (Table 2). Taking no supplements depended on the participant age. The youngest age group (31–50 years) had the highest (p ≤ 0.05) frequency of no supplement use compared to the 51–70 years group, which was in turn higher (p ≤ 0.05) than the ≥70 years of age group (Table 2). The 30–51 years group had a higher (p ≤ 0.05) frequency of using one supplement compared to the 51–70 years group but not the ≥70 years of age group (Table 2). Complementary to the pattern of younger participants not using supplements, the older age groups (≥70 years and 51–70 years) had a higher (p ≤ 0.05) frequency of using four or more supplements (Table 2). Supplement use was lower (p ≤ 0.05) in smokers than non-smokers (Table 2).

Table 2. Total Supplements Used by Sex, Age and Smoking Status.
Table 2. Total Supplements Used by Sex, Age and Smoking Status.
Total SupplementsMaleFemale31-50 years51-70 years≥ 70 yearsCurrent SmokerNon-Smoker
n = 152n = 224n = 115n = 216n = 45n = 60n = 316
n (%)n (%)n (%)n (%)n (%)n (%)n (%)
070 (46.1) a65 (29.0) b55 (47.8) a73 (33.8) b7 (15.6) c35 (58.3) a100 (31.6) b
128 (18.4)36 (16.1)26 (22.6) a29 (13.4) b9 (20.0) a,b6 (10.0)58 (18.4)
214 (9.2)30 (13.4)11 (9.6)26 (12.0)7 (15.6)5 (8.3)39 (12.3)
314 (9.2)29 (12.9)11 (9.6)27 (12.5)5 (11.1)5 (8.3)38 (12.0)
≥426 (17.1) b64 (28.6) a12 (10.4) b61 (28.2) a17 (37.8) a9 (15.0)81 (25.6)

Within sex, age, and smoking status, different superscripts in a row denote significant differences among groups (p ≤ 0.05).

3.3. 10 Most Frequently Used Supplements by Total Population and by Sex

The 10 most frequently used supplements by the entire population were vitamin D, multivitamin, calcium, vitamin C, omega 3,6,9, vitamin B12, B vitamin complex, fish oil, magnesium, and green tea (Table 3). Although not in the same order, both males and females reported the same four supplements as those most frequently used (calcium, multivitamin, vitamin C, vitamin D). Omega 3,6,9 was ranked the fifth most used supplement for both males and females. Glucosamine, ground flaxseed, and garlic were unique to the 10 most frequently used supplements in the male population. The female population reported the same 10 most frequently used supplements as the general population, but not in the same ranked order (Table 3). Specifically, females reported greater frequency of use for B vitamin complex (p = 0.020), calcium (p ≤ 0.001), fish oil (p = 0.041), green tea (p = 0.003), magnesium (p = 0.001), omega 3,6,9 (p = 0.042), and vitamin D (p = 0.001) compared to males (Table 4).

Table 3. 10 Most Frequently Used Supplements.
Table 3. 10 Most Frequently Used Supplements.
Supplement NameTotal PopulationSupplement NameMaleSupplement NameFemale
n = 376n = 152
n = 224
n (%)n (%)
n (%)
Vitamin D117 (31.1)Multivitamin45 (29.6)Vitamin D84 (37.5)
Multivitamin117 (31.1)Vitamin D33 (21.7)Calcium83 (37.1)
Calcium97 (25.8)Vitamin C22 (14.5)Multivitamin72 (32.1)
Vitamin C61 (16.2)Calcium14 (9.2)Vitamin C39 (17.4)
Omega 3,6,949 (13.0)Omega 3,6,913 (8.6)Omega 3,6,936 (16.1)
Vitamin B1245 (12.0)Vitamin B1213 (8.6)B Vitamin Complex32 (14.3)
B Vitamin Complex42 (11.2)Glucosamine11 (7.2)Vitamin B1232 (14.3)
Fish Oil40 (10.6)B Vitamin Complex10 (6.6)Magnesium31 (13.8)
Magnesium37 (9.8)Fish Oil10 (6.6)Fish Oil30 (13.4)
Green Tea35 (9.3)Flaxseed Ground *6 (3.9)Green Tea29 (12.9)
Garlic *6 (3.9)
Green Tea *6 (3.9)
Magnesium *6 (3.9)

* Supplements with same frequency of use in 10th position.

Table 4. Sex Differences in Supplements Used.
Table 4. Sex Differences in Supplements Used.
Supplement NameMale, n = 152, n (%)Female, n = 224, n (%)p value
B Vitamin Complex10 (6.6) b32 (14.3) a0.020
Calcium14 (9.2) b83 (37.1) a<0.001
Fish Oil10 (6.6) b30 (13.4) a0.041
Green Tea6 (3.9) b29 (12.9) a0.003
Magnesium6 (3.9) b31 (13.8) a0.001
Omega 3,6,913 (8.6) b36 (16.1) a0.042
Vitamin D33 (21.7) b84 (37.5) a0.001

Different superscripts in a row denote significant differences among groups (p ≤ 0.05); Use of other supplements did not significantly differ by sex.

3.4. 10 Most Frequently Used Supplements by Age

Calcium, multivitamin, vitamin C, and vitamin D were the four most frequently used supplements across the age categories, although they were not in the same order for each category, except vitamin C in the forth ranked position (Table 5). In the 31–50 years group, a multivitamin was the most frequently used supplement followed by vitamin D and calcium. In the 51–70 years group, multivitamin was replaced by vitamin D as the most used frequently used supplement and calcium use remained the same in the third position. In the oldest age group, ≥70 years, a multivitamin was replaced by calcium as the second most used supplement while vitamin D remained the most used supplement. Unlike the 51–70 and ≥70 years of age categories, the 31–50 years of age category did not include magnesium. Similarly, the 51–70 years of age group, unlike the other age categories, did not include ground flaxseed. The ≥70 years of age group was unique in listing glucosamine as one of its 10 most frequently used supplements (Table 5). Both calcium (p = 0.001) and vitamin D (p ≤ 0.001) use were dependent on the age of the study participant, as the older age categories ≥70 years and 51–70 years reported a higher usage frequency than the 31–50 years of age group (Table 6).

Table 5. 10Most Frequently Used Supplements by Age.
Table 5. 10Most Frequently Used Supplements by Age.
Supplement Name31–50 yearsSupplement Name51–70 yearsSupplement Name≥70 years
n = 115n = 216n = 45
n (%)n (%)n (%)
Multivitamin32 (27.8)Vitamin D77 (35.6)Vitamin D20 (44.4)
Vitamin D20 (17.4)Multivitamin73 (33.8)Calcium18 (40.0)
Calcium16 (13.9)Calcium63 (29.2)Multivitamin12 (26.7)
Vitamin C15 (13.0)Vitamin C35 (16.2)Vitamin C11 (24.4)
B Vitamin Complex10 (8.7)Omega 3,6,930 (13.9)Magnesium9 (20.0)
Fish Oil10 (8.7)Vitamin B1230 (13.9)Omega 3,6,99 (20.0)
Omega 3,6,910 (8.7)B Vitamin Complex28 (13.0)Fish Oil7 (15.6)
Green Tea8 (7.0)Magnesium24 (11.1)Vitamin B127 (15.6)
Vitamin B128 (7.0)Fish Oil23 (10.6)Glucosamine6 (13.3)
Flaxseed Ground5 (4.3)Green Tea23 (10.6)B Vitamin Complex *4 (8.9)
Flaxseed Ground *4 (8.9)
Green Tea *4 (8.9)

* Supplements with same frequency of use in 10th position.

Table 6. Age and Supplements Used.
Table 6. Age and Supplements Used.
Supplement Name31–50 years51–70 years≥70 yearsp value
n = 115n = 216n = 45
n (%)n (%)n (%)
Calcium16 (13.9) b63 (29.2) a18 (40.0) a0.001
Vitamin D20 (17.4) b77 (35.6) a20 (44.4) a<0.001

Different superscripts in a row denote significant differences among groups (p ≤ 0.05); Use of other supplements did not significantly differ by age.

3.5. 10 Most Frequently Used Supplements by Smoking Status

Current smokers reported the same four most frequently used supplements (calcium, multivitamin, vitamin C, and vitamin D) as non-smokers (Table 7). Both the current smoker and non-smoker populations reported using omega 3,6,9 as the fifth most used supplement, as well and both vitamin B12 and B vitamin complex as the seventh and eighth most used supplements. Unlike the current smokers, the non-smokers reported using fish oil and green tea while current smokers reported using cod liver oil and garlic in their 10 most frequently used supplements. Despite the differences in the ranking of the 10 most frequently used supplements, the usage frequencies for supplements were not the same. Current smokers reported using less calcium (p = 0.006), fish oil (p = 0.011), green tea (p = 0.027) and vitamin D (p = 0.022) than non-smokers (Table 8).

Table 7. 10 Most Frequently Used Supplements By Smoking Status.
Table 7. 10 Most Frequently Used Supplements By Smoking Status.
Supplement NameCurrent SmokerSupplement NameNon-Smoker
n = 60
n = 316
n (%)n (%)
Multivitamin14 (23.3)Vitamin D106 (33.5)
Vitamin D11 (18.3)Multivitamin103 (32.6)
Vitamin C9 (15.0)Calcium90 (28.5)
Calcium7 (11.7)Vitamin C52 (16.5)
Omega 3,6,97 (11.7)Omega 3,6,942 (13.3)
Magnesium6 (10.0)Fish Oil39 (12.3)
Vitamin B126 (10.0)Vitamin B1239 (12.3)
B Vitamin Complex4 (6.7)B Vitamin Complex38 (12.0)
Cod Liver Oil3 (5.0)Green Tea34 (10.8)
Garlic3 (5.0)Magnesium31 (9.8)
Table 8. Smoking and Supplements Used.
Table 8. Smoking and Supplements Used.
Supplement NameCurrent Smoker, n = 60, n (%)Non-Smoker, n = 316, n (%)p value
Calcium7 (11.7) b90 (28.5) a0.006
Fish Oil1 (1.7) b39 (12.3) a0.011
Green Tea1 (1.7) b34 (10.8) a0.027
Vitamin D11 (18.3) b106 (33.5) a0.022

Different superscripts in a row denote significant differences among groups (p ≤ 0.05); Use of other supplements did not significantly differ between current and non-smokers.

3.6. 10 Most Frequently Used Supplements by Reason for Visit

For the three reasons for visit, the 10 most frequently used supplements were similar and included calcium, multivitamin and vitamin D (Table 9). Only the comprehensive general examination group reported using glucosamine as one of their 10 most frequently used supplements. Similarly, the implant consultation group was unique in reporting ground flaxseed as one of its 10 most frequently used supplements (Table 9). Patients receiving a surgical consultation had a lower (p = 0.009) usage frequency for glucosamine than either the comprehensive general examination or implant consultation categories.

Table 9. 10 Most Frequently Used Supplements by Reason for Visit.
Table 9. 10 Most Frequently Used Supplements by Reason for Visit.
Supplement NameComprehensive General ExaminationSupplement NameImplant ConsultationSupplement NameOther Surgical Consultation
n = 90n = 126n = 160
n (%)n (%)n (%)
Multivitamin30 (33.3)Vitamin D43 (34.1)Vitamin D49 (30.6)
Vitamin D25 (27.8)Multivitamin42 (33.3)Calcium45 (28.1)
Calcium24 (26.7)Calcium28 (22.2)Multivitamin45 (28.1)
Omega 3,6,915 (16.7)Omega 3,6,919 (15.1)Vitamin C29 (18.1)
Vitamin C13 (14.4)Vitamin C19 (15.1)B Vitamin Complex21 (13.1)
B Vitamin Complex12 (13.3)Fish Oil17 (13.5)Vitamin B1221 (13.1)
Glucosamine12 (13.3)Vitamin B1216 (12.7)Magnesium17 (10.6)
Green Tea9 (10.0)Green Tea12 (9.5)Fish Oil15 (9.4)
Fish Oil8 (8.9)Magnesium12 (9.5)Omega 3,6,915 (9.4)
Magnesium *8 (8.9)Flaxseed Ground10 (7.9)Green Tea14 (8.8)
Vitamin B12 *8 (8.9)

* Supplements with same frequency of use in 10th position.

4. Discussion

This study showed that females used more supplements than males, and that general supplement use increased with subject age, regardless of sex. Moreover, smokers used fewer supplements than non-smokers. Interestingly, the list of the 10 most commonly used dietary supplements was relatively similar when comparing by sex, age, smoking status or reason for visit.

The finding that females used more supplements than males, and that supplement use increased with subject age, was not surprising based on data from the Canadian Community Health Survey (2004–2005). The Canadian Community Health Survey (CCHS) cycle 2.2 is a nationwide cross-sectional nutrition survey representing 98% of all province-dwelling Canadians (n = 35,107). The CCHS cycle 2.2 had a response rate of 76.5% and as part of its design included an assessment of the nutritional supplements used by each participant [28]. According to the CCHS 2.2, total supplement use by Canadians was 40.1% [29] and multivitamin use, defined as ≥ three supplements, was 28% [30]. Total supplement use in the present study was 64.1%, much greater than the CCHS but may be explained by the fact that patients visiting the periodontal clinic had a higher proportion of older individuals in which supplement use is higher. Another reason for the difference may be the fact that we used a detailed list of supplements whereas the CCHS focused on multivitamin use without consideration of herbals or botanicals [28]. Similar to our findings, Shakur et al., 2012 reported greater supplement use between the NHANES survey and the CCHS 2.2, with the difference being attributed to the fact that NHANES examines a greater variety of supplements (such as herbals or botanicals) than the CCHS 2.2 [30]. The fact that our survey contained a wide variety of possible nutritional supplements, not limited to vitamins and minerals, may explain our greater percentage of total supplement use compared to the CCHS 2.2. However, good agreement between the studies was observed for individual supplement use such as multivitamin (28.0% vs. 31.1%), vitamin D (28.0% vs. 31.1%), and calcium (28.0% vs. 25.8%), in which the first percentage is from the CCHS 2.2 [30]. Additionally, the CCHS 2.2 and NHANES (2003–2006) studies, similar to the findings of the present study, reported greater supplement use among women compared to men, and greater supplement use with older age [29,30,31] .

Given the challenge of attaining the dietary reference intake for calcium and vitamin D from diet alone in the Canadian elderly [32,33,34,35,36] and public health messages encouraging use of vitamin D supplements, it was not surprising that calcium and vitamin D supplement use increased in the post-50 age categories. As part of the Canada’s Food Guide, Health Canada advises that all Canadians 50 years or older consume a vitamin D supplement containing 400 IU per day [37]. Moreover, other organizations such as the Canadian Cancer Society suggest Canadians consume a vitamin D supplement containing 1000 IU in the winter months [38]. In addition to calcium and vitamin D, multivitamin and vitamin C supplement use were also included in the four most used supplements after age 50 years. This is supported by a survey of Canadian community-living older adults in which calcium, vitamin C and D were frequently used micronutrients and overall multivitamin use was high (43.5%) [35]. In a study of Ontario seniors living in long term care facilities, supplementation with the recommended vitamin D dose (>400 IU/day) was effective in ensuring that >90% of the seniors achieved optimum serum 25(OH)D levels (>75 nmol/L) [36].

Vitamin C is critical for the maintenance of periodontal health. It is well known that smoking depletes vitamin C stores and thus smokers should consume a vitamin C supplement or increase their dietary intake of vitamin C [39]. However, use of vitamin C supplements was not higher among smokers in this study. This finding is similar to findings from the CCHS 2.2 that reported no difference in vitamin C supplement use between smokers and non-smokers [39]. Whether supplementation with vitamin C improves wound healing after periodontal surgery in smokers requires investigation. Our study also showed that current smokers used less calcium, vitamin D, green tea and fish oil supplements. The effect of these supplements in smokers versus non-smokers at improving wound healing after periodontal procedures is an area for future investigation.

Supplement use was largely similar among patients regardless of their reason for visit. The only difference was that patients receiving a surgical consultation had lower usage frequency of glucosamine than patients receiving comprehensive general examination or implant consultation. There is no clear link between glucosamine supplement use and the different reasons for visiting the periodontist. However, males and those over 70 years of age did report glucosamine as one of the most commonly used supplements and may have been more represented in the comprehensive general examination or implant consultation groups.

5. Conclusions

Supplement usage in this sample of patients seeking periodontal care was similar to the general Canadian population and was not dependent on the patient’s reason for visiting the periodontist. Future dietary intervention studies to optimize periodontal health can focus on supplements with known biological activities that may enhance wound healing after periodontal procedures. Dietary supplements such as those with known anti-inflammatory, antioxidant or osteogenic activity are of interest.


The authors thank R. Hamm and C. Hamm for assistance with data collection. W.E. Ward holds a Canada Research Chair in Bone and Muscle Development.

Conflict of Interest

The authors declare no conflict of interest.


  1. Armitage, G.C. Development of a classification system for periodontal diseases and conditions. Ann. Periodontol. 1999, 4, 1–6. [Google Scholar] [CrossRef]
  2. Darveau, R.P. Periodontitis: A polymicrobial disruption of host homeostasis. Nat. Rev. Microbiol. 2010, 8, 481–490. [Google Scholar] [CrossRef]
  3. Dentino, A.; Lee, S.; Mailhot, J.; Hefti, A.F. Principles of periodontology. Periodontol. 2000 2013, 61, 16–53. [Google Scholar] [CrossRef]
  4. Chapple, I.L.; Matthews, J.B. The role of reactive oxygen and antioxidant species in periodontal tissue destruction. Periodontol. 2000 2007, 43, 160–232. [Google Scholar] [CrossRef]
  5. Lau, B.Y.; Johnston, B.D.; Fritz, P.C.; Ward, W.E. Dietary strategies to optimize wound healing after periodontal and dental implant surgery: An evidence-based review. Open Dent. J. 2013. in press. [Google Scholar]
  6. Kaye, E.K. Nutrition, dietary guidelines and optimal periodontal health. Periodontol. 2000 2012, 58, 93–111. [Google Scholar] [CrossRef]
  7. Chapple, I.L. Potential mechanisms underpinning the nutritional modulation of periodontal inflammation. J. Am. Dent. Assoc. 2009, 140, 178–184. [Google Scholar]
  8. Davis, K. Understanding antioxidants: Using various arsenals to impact the oral environment. Dent. Today 2012, 31, 92, 94, 96–97. [Google Scholar]
  9. Van der Velden, U.; Kuzmanova, D.; Chapple, I.L. Micronutritional approaches to periodontal therapy. J. Clin. Periodontol. 2011, 38, 142–158. [Google Scholar]
  10. Nishida, M.; Grossi, S.G.; Dunford, R.G.; Ho, A.W.; Trevisan, M.; Genco, R.J. Dietary vitamin C and the risk for periodontal disease. J. Periodontol. 2000, 71, 1215–1223. [Google Scholar] [CrossRef]
  11. Chapple, I.L.; Milward, M.R.; Dietrich, T. The prevalence of inflammatory periodontitis is negatively associated with serum antioxidant concentrations. J. Nutr. 2007, 137, 657–664. [Google Scholar]
  12. Iwasaki, M.; Manz, M.C.; Taylor, G.W.; Yoshihara, A.; Miyazaki, H. Relations of serum ascorbic acid and alpha-tocopherol to periodontal disease. J. Dent. Res. 2012, 91, 167–172. [Google Scholar] [CrossRef]
  13. Iwasaki, M.; Yoshihara, A.; Moynihan, P.; Watanabe, R.; Taylor, G.W.; Miyazaki, H. Longitudinal relationship between dietary ω-3 fatty acids and periodontal disease. Nutrition 2010, 26, 1105–1109. [Google Scholar] [CrossRef]
  14. Naqvi, A.Z.; Buettner, C.; Phillips, R.S.; Davis, R.B.; Mukamal, K.J. n-3 fatty acids and periodontitis in US adults. J. Am. Diet. Assoc. 2010, 110, 1669–1675. [Google Scholar] [CrossRef]
  15. Health Canada. Canadian Health Measures Survey results—oral health statistics, 2007–2009. Chronic Dis. Can. 2010, 30, 117–118.
  16. Eke, P.I.; Dye, B.A.; Wei, L.; Thornton-Evans, G.O.; Genco, R.J. Prevalence of periodontitis in adults in the United States: 2009 and 2010. J. Dent. Res. 2012, 91, 914–920. [Google Scholar] [CrossRef]
  17. Jenzsch, A.; Eick, S.; Rassoul, F.; Purschwitz, R.; Jentsch, H. Nutritional intervention in patients with periodontal disease: Clinical, immunological and microbiological variables during 12 months. Br. J. Nutr. 2009, 101, 879–885. [Google Scholar] [CrossRef]
  18. Staudte, H.; Sigusch, B.W.; Glockmann, E. Grapefruit consumption improves vitamin C status in periodontitis patients. Br. Dent. J. 2005, 199, 213–217. [Google Scholar] [CrossRef]
  19. Merchant, A.T.; Pitiphat, W.; Franz, M.; Joshipura, K.J. Whole-grain and fiber intakes and periodontitis risk in men. Am. J. Clin. Nutr. 2006, 83, 1395–1400. [Google Scholar]
  20. Chapple, I.L.; Milward, M.R.; Ling-Mountford, N.; Weston, P.; Carter, K.; Askey, K.; Dallal, G.E.; de Spirt, S.; Sies, H.; Patel, D.; Matthews, J.B. Adjunctive daily supplementation with encapsulated fruit, vegetable and berry juice powder concentrates and clinical periodontal outcomes: A double-blind RCT. J. Clin. Periodontol. 2012, 39, 62–72. [Google Scholar] [CrossRef]
  21. Rosenstein, E.D.; Kushner, L.J.; Kramer, N.; Kazandjian, G. Pilot study of dietary fatty acid supplementation in the treatment of adult periodontitis. Prostaglandins Leukot. Essent. Fatty Acids 2003, 68, 213–218. [Google Scholar] [CrossRef]
  22. Chandra, R.V.; Prabhuji, M.L.; Roopa, D.A.; Ravirajan, S.; Kishore, H.C. Efficacy of lycopene in the treatment of gingivitis: A randomised, placebo-controlled clinical trial. Oral Health Prev. Dent. 2007, 5, 327–336. [Google Scholar]
  23. Bashutski, J.D.; Eber, R.M.; Kinney, J.S.; Benavides, E.; Maitra, S.; Braun, T.M.; Giannobile, W.V.; McCauley, L.K. The impact of vitamin D status on periodontal surgery outcomes. J. Dent. Res. 2011, 90, 1007–1012. [Google Scholar] [CrossRef]
  24. Neiva, R.F.; Al-Shammari, K.; Nociti, F.H., Jr.; Soehren, S.; Wang, H.L. Effects of vitamin-B complex supplementation on periodontal wound healing. J. Periodontol. 2005, 76, 1084–1091. [Google Scholar] [CrossRef]
  25. Barroso, A.B.; Lima, V.; Guzzo, G.C.; Moraes, R.A.; Vasconcellos, M.C.; Bezerra, M.M.; Viana, F.A.; Bezerra, R.C.; Santana, G.S.; Frota-Bezerra, F.A.; et al. Efficacy and safety of combined piroxicam, dexamethasone, orphenadrine, and cyanocobalamin treatment in mandibular molar surgery. Braz. J. Med. Biol. Res. 2006, 39, 1241–1247. [Google Scholar] [CrossRef]
  26. El-Sharkawy, H.; Aboelsaad, N.; Eliwa, M.; Darweesh, M.; Alshahat, M.; Kantarci, A.; Hasturk, H.; van Dyke, T.E. Adjunctive treatment of chronic periodontitis with daily dietary supplementation with omega-3 Fatty acids and low-dose aspirin. J. Periodontol. 2010, 81, 1635–1643. [Google Scholar] [CrossRef]
  27. Elkhouli, A.M. The efficacy of host response modulation therapy (omega-3 plus low-dose aspirin) as an adjunctive treatment of chronic periodontitis (clinical and biochemical study). J. Periodontal. Res. 2011, 46, 261–268. [Google Scholar] [CrossRef]
  28. Health Canada. Canadian Community Health Survey Cycle 2.2 Nutrition (2004): A guide to accessing and interpreting the data, 2006. Available online: fn-an/alt_formats/hpfb-dgpsa/pdf/surveill/cchs-guide-escc-eng.pdf (accessed on 7 February 2013).
  29. Guo, X.; Willows, N.; Kuhle, S.; Jhangri, G.; Veugelers, P.J. Use of vitamin and mineral supplements among Canadian adults. Can. J. Public Health 2009, 100, 357–360. [Google Scholar]
  30. Shakur, Y.A.; Tarasuk, V.; Corey, P.; O’Connor, D.L. A comparison of micronutrient inadequacy and risk of high micronutrient intakes among vitamin and mineral supplement users and nonusers in Canada. J. Nutr. 2012, 142, 534–540. [Google Scholar] [CrossRef]
  31. Bailey, R.L.; Gahche, J.J.; Lentino, C.V.; Dwyer, J.T.; Engel, J.S.; Thomas, P.R.; Betz, J.M.; Sempos, C.T.; Picciano, M.F. Dietary supplement use in the United States, 2003–2006. J. Nutr. 2011, 141, 261–266. [Google Scholar] [CrossRef]
  32. Vatanparast, H.; Adolphe, J.L.; Whiting, S.J. Socio-economic status and vitamin/mineral supplement use in Canada. Health Rep. 2010, 21, 19–25. [Google Scholar]
  33. Garriguet, D. Bone health: Osteoporosis, calcium and vitamin D. Health Rep. 2011, 22, 7–14. [Google Scholar]
  34. Vatanparast, H.; Dolega-Cieszkowski, J.H.; Whiting, S.J. Many adult Canadians are not meeting current calcium recommendations from food and supplement intake. Appl. Physiol. Nutr. Metab. 2009, 34, 191–196. [Google Scholar] [CrossRef]
  35. McKenzie, J.; Keller, H.H. Vitamin-mineral supplementation and use of herbal preparations among community-living older adults. Can. J. Public Health 2001, 92, 286–290. [Google Scholar]
  36. Ioannidis, G.; Kennedy, C.C.; Dykeman, J.; Dudziak, S.; Papaioannou, A. Association between vitamin D3 supplementation and serum 25-hydroxyvitamin D levels in older individuals residing in long-term care in Ontario, Canada. J. Am. Geriatr. Soc. 2012, 60, 985–987. [Google Scholar] [CrossRef]
  37. Health Canada. Eating Well with Canada’s Food Guide, 2007. Available online: (accessed on 7 Febuary 2013).
  38. Whiting, S.J.; Langlois, K.A.; Vatanparast, H.; Greene-Finestone, L.S. The vitamin D status of Canadians relative to the 2011 Dietary Reference Intakes: An examination in children and adults with and without supplement use. Am. J. Clin. Nutr. 2011, 94, 128–135. [Google Scholar] [CrossRef]
  39. Garriguet, D. The effect of supplement use on vitamin C intake. Health Rep. 2010, 21, 57–62. [Google Scholar]
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