The use of urinary fluoride excretion to facilitate monitoring fluoride intake: A systematic scoping review


Authors: Oladipo S. Idowu aff001;  Liane B. Azevedo aff001;  Ruth A. Valentine aff002;  Josie Swan aff002;  Priyanka V. Vasantavada aff001;  Anne Maguire aff002;  Fatemeh V. Zohoori aff001
Authors place of work: School of Health and Social Care, Teesside University, Middlesbrough Tees Valley, United Kingdom aff001;  School of Dental Sciences, Newcastle University, Framlington Place, Newcastle Upon Tyne, United Kingdom aff002
Published in the journal: PLoS ONE 14(9)
Category: Research Article
doi: 10.1371/journal.pone.0222260

Summary

Background

As a recognised effective and economical agent for dental caries prevention, fluoride has been used in many different fluoridation schemes implemented across the world. Considering the narrow ‘dose-gap’ between the benefit of caries reduction and the risk of dental fluorosis, it is recommended that fluoride intake is monitored by measuring urinary fluoride excretion. The aim of this scoping review is to map the current literature/evidence on fluoride intake and excretion studies in relation to the study population, settings, type of study design, methodology, and analytical approach.

Methods

Embase/Ovid, MEDLINE/Ovid, CINAHL/EBSCO, Scopus/Elsevier were searched for relevant articles until April 2018. Studies were included if they reported intake and excretion of fluoride in healthy humans of all age groups. Findings were explored using a narrative synthesis to summarise studies characteristics and outcome measures.

Results

Removal of duplicates from the originally 2295 identified records yielded 1093 studies of which 206 articles were included. Only 21.6% of the studies were conducted in children (<8-year-olds). Most studies (38.8%) used drinking water concentration as a proxy for fluoride intake, whereas only 11.7% measured fluoride intake from all sources. Of the 72 studies that measured dietary fluoride intake, only 10 reported the validity of the employed dietary assessment method. Only 14 studies validated the urine sample collection methods. No information on the validity of the employed analytical method was reported by the majority (64.6%) of studies. Only a small proportion (8.7%) of the included studies investigated the association between fluoride intake and excretion.

Conclusion

The findings reveal much variability in terms of conducting the studies and reporting the findings, illustrating a high heterogeneity in data collection across settings and populations. Future studies should provide more detail on sampling technique, measurement protocols (including validation), and on clearly defining the relationship between intake and urinary excretion of fluoride.

Keywords:

Physical sciences – Chemistry – Chemical compounds – Fluorides – Biology and life sciences – Physiology – Physiological processes – Excretion – Ingestion – Body fluids – Urine – Anatomy – Body fluids – Urine – Nutrition – Diet – Medicine and health sciences – Physiology – Physiological processes – Excretion – Ingestion – Body fluids – Urine – Anatomy – Body fluids – Urine – Nutrition – Diet – Infectious diseases – Bacterial diseases – Caries – People and places – Population groupings – Age groups – Research and analysis methods – Database and informatics methods – Database searching

Introduction

While dental caries is a largely preventable condition, it still remains an important global public health problem, affecting 60–90% of schoolchildren and the vast majority of adults [1]. The World Health Organisation (WHO) has officially endorsed the use of fluorides for population-based prevention of dental caries since the late 1960s [1]. The goals of community-based public health programmes are generally to provide regular, low-level exposure to fluoride in the community through appropriate means such as fluoridated water, salt, milk and fluoride toothpaste. Studies have shown that it can be quite challenging to attain effective fluoride-based caries prevention without the development of some degree of dental fluorosis, which can occur as a result of excessive ingestion of fluoride during tooth development. A key oral health promotion strategy is therefore to maximise caries reduction while minimising fluorosis. A fluoride intake of 0.05–0.07 mg/kg body weight (BW)/day in children <12 years of age has been suggested as optimum for caries prevention; whereas an intake of more than 0.1 mg/kg BW/day could increase the risk of occurrence of dental fluorosis [2]. Despite the widespread use of these guidelines in authoritative advisory recommendations for many years, the associated values and thresholds have been recently questioned due to their empirical origin [35]. Recent studies have also shown changes in the sources of ingested fluoride as well as in the prevalence and severity of dental fluorosis [3]. The Iowa Fluoride Study (IFS), which is the most comprehensive longitudinal cohort study on the association between fluoride intake, dental caries, and dental fluorosis, has also reported an overlap in mean fluoride intake between groups with dental caries and groups with fluorosis [6]. These reports indicate the need for research to clearly establish an optimum (or adequate) and upper limit of fluoride intake. The recent fluoride symposium on appropriateness of guidelines for fluoride intake [3] also highlighted the need for more nuanced guidelines on fluoride intake to help inform policy with the aim of introducing change in fluoride intake or leading to the adjustment of the timing of fluoride intake across the critical period of ages 0 to 6 years to reduce the risk of occurrence of fluorosis [4]. Assessment of total fluoride intake in the population is quite challenging due to exposure to multiple dietary and non-dietary sources of fluoride as well as the difficulty in measurement of the amount of unintentional swallowing of toothpaste by young children.

As urine is the most important metabolic pathway for elimination of fluoride from the body, it has been considered as a useful biomarker for contemporary fluoride exposure at a population- but not individual- level [7]. The relationships between intake and urinary excretion of fluoride have been examined for different age groups to establish the value of urine for prediction of fluoride intake according to age. A strong correlation between fluoride intake and urinary fluoride excretion has been reported for a pooled sample of children aged 7 years or younger as well as for adults aged 18 to 75 years [8]. However, no such correlation was found with a narrower age group of 6 to 7 year olds [9]; indicating the need for more fluoride intake and excretion studies in specific age groups. One of the conclusions of the recent fluoride symposium [3] was that “… there is not enough evidence to use biomarkers of fluoride exposure such as urine and nails, despite the fact that they take into account the absorption rate” along with the suggestion of more research being needed to establish a reliable biomarker of fluoride exposure [5].

Many factors can modify fluoride metabolism and consequently alter the relationship between fluoride intake and excretion, including age (skeletal growth), dose and form of fluoride as well as acid-base disturbances (e.g. altitude of residence), renal impairment, physical activity, nutritional status, composition of diet, and genetics [10]. Nevertheless, the implementation of fluoride interventions vary considerably across countries. For instance, community water fluoridation has currently been implemented in 25 countries and fluoridated salt is available in 23 countries [11]. Fluoridated milk is also given to school children in a few countries [12]. In addition, fluoridated toothpastes are widely used globally and many populations have naturally occurring fluoride in their drinking water supply. A mix of all these potential fluoride vehicles, with a complex fluoride availability, can influence fluoride excretion.

Fluoride intake and excretion studies also have the potential to reach erroneous conclusions if they use an unfocussed study design, invalid methods of data collection (particularly fluoride exposure data) or non-standardised analytical techniques. For example, a study in which the existing analytical techniques for fluoride analysis were examined amongst nine internationally recognised laboratories, showed inconsistencies in the use of these fluoride assay techniques [13]. The latter study also reported a statistically significantly difference in the average fluoride concentration of urine and beverage samples amongst the nine laboratories when using their own standard operating protocols and assay techniques. Future research should be able to add more nuanced understanding on fluoride intake in specific situations by ideally following standard operating protocols.

Direct assessment of total fluoride exposure in a population (particularly children) can be difficult and expensive. Measurement of fluoride levels in urine has been suggested as an alternative method for estimation of fluoride exposure in populations and consequently as a basis for decisions on the use of fluoride for caries prevention. However, a clearer perspective is needed to better understand the association between fluoride intake and urinary fluoride excretion and specific situations in which urinary fluoride excretion is strongly associated with intake. Therefore, the aim of this scoping review was to map the current literature/evidence on the association between fluoride intake and excretion. The specific objectives of this review were to map this association in relation to the study population, setting, type of study design and methodology, including the analytical approach used. The ultimate aim of this systematic scoping review is to review the observational data found in fluoride intake and excretion studies in humans to provide a basis for more targeted research questions to address any research gaps and inform the design of future interventions.

Methods

This systematic scoping review was guided by the Joanna Briggs Institute for systematic scoping reviews [1416]; and reported according to the Preferred Reporting of Items for Systematic Reviews and Meta- Analyses (PRISMA) Statement [17]. A detailed review protocol can be obtained from the Open Science Framework (DOI 10.17605/OSF.IO/9CQGE).

Search strategy

A three-step approach was applied for the search [1416]. The initial search was performed with MEDLINE (through Ovid) and CINAHL databases using the terms identified based on PEO (Population, Exposure, Outcome). A second search was then undertaken across four electronic databases using all identified reports and articles until April 30, 2018: Embase/Ovid (1974–2018), MEDLINE/Ovid (1946–2018), CINAHL/EBSCO (1997–2018), Scopus/Elsevier (1950–2018) (S1 File). No limits were set for years of publication on the database search. All citations were then imported into the web-based bibliographic manager Endnote X8, and duplicate citations were removed.

Eligibility criteria

Searches were limited to studies in English and were included if they; (a) were conducted with heathy participants of any age group, gender or ethnicity; (b) were carried out at nursery, schools, preschool, kindergarten, child care centres, hospitals or community settings; (c) estimated fluoride intake from any customary sources of fluoride including water, diets, dental products and supplements and; (d) estimated urinary fluoride concentration or excretion.

Studies were excluded if they measured occupational fluoride exposure. Studies were also excluded if they were reviews, opinion papers, policy documents, case reports, editorials or letters.

Process of study selection

A two-stage screening process was used to assess the relevant studies. The first level of screening involved only the study title and abstract by two reviewers (IO and JS). Afterwards, the full texts of the included studies were examined independently by two reviewers: IO and one of the co-authors (VZ, LA, RV, PV). Discrepancies were resolved by discussions and consensus or by consultation with a third reviewer (VZ or LA).

Data charting process

A standardised data extraction tool was developed by the research team and included the following information: author(s); year; title; aim of study; study design; country; setting; number of participants; age; gender; intake and excretion data; methods of data collection, analytical procedures, and outcome(s). The developed data extraction tool was tested with 10% of the articles before implementation. Data extraction was then carried out by one reviewer (IO) and verified by another (PV). Due to the work undertaken being a scoping review, no quality appraisal was undertaken [16].

Data synthesis

The extracted data were originally recorded in Excel and then imported to SPSS (version 22). Descriptive analysis was used to report the studies by their characteristics and outcome measures:

A. Studies’ characteristics:

  • Year: which was divided into two groups according to the year of publication; “prior to-” and “at or after-” 1999. This was based on the year of release of the 1999 World Health Organisation (WHO) manual guidelines on monitoring fluoride excretion in community prevention programmes [18];

  • Country: which was divided into low income economy, lower middle income economy, upper middle income economy and higher income economy, according to the World Bank Group classification [19];

  • Setting: nursery/schools, hospitals, community or unclear;

  • Age: 0–8 years, 9–16 years, 17 years and above, or a combination of age groups;

  • Gender; male, female, or both;

  • Study design (non-randomised controlled trial, randomised controlled trial, uncontrolled before and after studies, cross-sectional, or longitudinal studies.

B. Outcome measures

  • Reporting of fluoride concentration in the area;

  • Fluoride intake and sources: water, diet, dental products, supplements, or a specific combination of two or more sources—such as water and dental products, diet and supplement, diet and dental products, a combination of diet, supplement and dental products;

  • Method of assessment of dietary fluoride intake: 24-h dietary recall, diet history, duplicate method, food diary, food frequency questionnaire (FFQ),semi-FFQ, household survey, observed food frequency, or not reported;

  • Method of assessment of fluoride intake from dental products: sample collection–i.e. toothpaste applied/expectorate collected, toothbrushing questionnaire, or not reported;

  • Fluoride excretion: urine, or urine and faeces;

  • Assessment of fluoride in urine: urinary fluoride concentration, urinary fluoride excretion (by collecting 24-h urine, or spot urine, or time controlled urine), or not specified.

  • Analytical method: fluoride-ion selective electrode, gas chromatography, spectrophotometry, titration, ion-exchange chromatography, or not reported;

  • Validity of data and methods: fluoride intake, fluoride excretion (urine collection) and fluoride analytical method, or not reported;

  • Reporting of the investigation of any relationship between fluoride intake and fluoride excretion.

Findings were then further explored using a narrative synthesis.

Results

Studies’ characteristics

The search of four databases yielded 2295 records (Fig 1): Ovid Medline, 613; Ovid Embase, 763; Scopus, 867; CINAHL, 52. After removal of duplicates, the titles and abstracts of 1093 studies were screened for eligibility and 718 studies were excluded. The full text of 375 potentially relevant articles were further screened for eligibility. A total of 169 studies were excluded for different reasons (Fig 1) and 206 studies met the inclusion criteria described above.

<h2>Flowchart outlining identification of papers for inclusion following the Prisma flow diagram.</h2>
Fig. 1.

Flowchart outlining identification of papers for inclusion following the Prisma flow diagram.


Studies originated from 43 countries across most continents, with the majority from India (n = 36), USA (n = 35) and China (n = 24) (Fig 2). Table 1 presents the characteristics of the included studies. A higher proportion (57%) of the studies was published after 1999: on average, five papers were published per year between 1999 and 2018 compared to two papers per year in the years up to 1999. The vast majority of the studies (79.1%) were conducted in either higher- or upper-middle- income economy countries and the predominant setting was at community (56.3%). More studies were conducted in adults (30.4%) or combining different age groups (39.2%) and predominately on both genders (82.6%). While a range of study designs were applied, the majority used a cross-sectional design (64.6%).

<h2>Distribution of included studies according to continent.</h2>
Fig. 2.

Distribution of included studies according to continent.


Tab. 1.

Studies’ (n = 206) characteristics.

<h2>Studies’ (n = 206) characteristics.</h2>

Outcome measures

Tables 24 show the assessed variables and employed methodology of the included studies.

Tab. 2.

Outcome measures related to fluoride intake, specified in the included studies (n = 206).

<h2>Outcome measures related to fluoride intake, specified in the included studies (n = 206).</h2>
Tab. 3.

Outcome measures related to fluoride excretion (n = 206 studies).

<h2>Outcome measures related to fluoride excretion (n = 206 studies).</h2>
Tab. 4.

Studies which explored relationships between fluoride intake and excretion data.

<h2>Studies which explored relationships between fluoride intake and excretion data.</h2>

A considerable number of studies (n = 113; 53.9%) included in the review did not report the water fluoride concentration of the area investigated (Table 2). Most studies used water as a proxy for fluoride intake, while only 24 (11.7%) studies measured fluoride intake from all sources. In the 72 studies that measured dietary fluoride intake, the most frequently used assessment methods were duplicate method (n = 16), food diary (n = 17) and food frequency questionnaire (n = 16). Only 10 studies (out of the 72) reported the validity of the employed dietary assessment method: duplicate method (n = 5), 24-hour dietary recall (n = 3) and food dietary assessment method (n = 2). Only 36 (27.5%) studies measured fluoride intake from ingestion of dental products of which 20 (55.5%) studies used a questionnaire as the assessment tool.

A small proportion (n = 23; 11.2%) of studies measured fluoride excretion from both urine and faeces (Table 3), whereas the majority (n = 183; 88.8%) assessed fluoride excretion from urine alone. Almost one-fifth of the studies did not specify the method of urine collection and, when reported, most used either a 24-hour (35%) or spot urine (34.5%) collection method. Out of the 72 studies in which 24-hour urine collection was collected, only 13 (18.1%) studies validated the sample collection either by urinary flow rate (n = 3), urinary volume (n = 1), creatinine ratio (n = 5) or any combination (n = 4). Most of the included studies (88.8%) measured urinary fluoride concentration using a fluoride ion selective electrode (F-ISE). However, no information on the validity and reliability of the employed analytical method was reported by the majority of the studies (n = 133; 64.6%).

Less than half (45%; n = 93) of the included studies reported the investigation of any relationship between fluoride intake and excretion. Of the studies [8, 9, 20100] that investigated the intake/excretion relationship, the majority (30%; n = 28) reported the association between fluoride concentration of water and fluoride excretion, whereas only 18 studies (19%) reported the association between fluoride intake and fluoride excretion (Table 4).

Discussion

This systematic scoping review synthesised the evidence for the association between fluoride intake and fluoride excretion in healthy human participants including the characteristics of the studies and findings of the existing research.

The review showed that number of published studies increased post 1999; which might be due to a publication by the World Health Organisation (WHO) on “Monitoring of renal fluoride excretion in community prevention programmes in oral health” [18] in 1999. In that WHO guideline only 11 fluoride intake and/or excretion studies were cited and this may have led to a re-attraction of the attention of researchers around the world to the paucity of data, stimulating research on the suitability of urine for monitoring fluoride exposure. As a result, the latest WHO guidance [7], published in 2014, cited more than 34 studies on fluoride intake/excretion in children. However, the main conclusion of the 2014 WHO guidance on assessment of renal fluoride excretion was mainly based on a study [8] in which the ability of 24-hour urine sample to predict fluoride exposure was investigated by examining the 17 published reports of the simultaneous measurement of fluoride intake and excretion for 212 pooled samples of children aged less than 7 years (taken from 9 studies in children) and for 283 adults aged 18–75 years (taken from 8 studies in adults) who consumed ‘westernised’ diets.

The findings of this scoping review show an unbalanced geographical distribution of articles and heavy concentration of studies from higher-income-economy countries. Interestingly, many studies were conducted in Asia, particularly in China and India. This could be related to; i) an increase in budgets for research and development [101] and/or; ii) a need for research and monitoring of fluoride exposure due to the extent of fluoride toxicity from contaminated water and polluted air, in those countries.

Studies suggest that the first two years of life are the most important period for development of fluorosis in early-erupting teeth, whereas the first eight years of life appear to be the most important period for development of dental fluorosis in late-erupting permanent teeth [102]. However, the findings of this review show that of the 206 included studies, only 44 (21.6%) were conducted in children younger than 8 years old. The lower number of studies involving children could be due to the various challenges (such as ethical conduct as well as cooperation of children and their parents) and costs of conducting paediatric research. However, more studies involving children are essential as research with adults in not easily generalized or extrapolated to infants and young children due to their anatomical and physiological differences.

The findings also reveal great variability in terms of study conduct and the reporting of findings, illustrating a high heterogeneity in data collection across settings and populations. One of the main sources of heterogeneity was the methods of assessment of fluoride intake (from diet and toothpaste ingestion). In particular, the methods of dietary data collection widely differed between the studies (Table 2), emphasizing the need for the development of a gold standard method for more accurate estimation of the systemic ingestion of fluoride from diet. Furthermore, few studies reported detailed information on the validity of dietary data collection (Table 3). Since gastric absorption and renal excretion of fluoride are pH-dependent, any diet-induced changes in the pH of the stomach as well as urinary pH could decrease or increase the concentration of fluoride in urine. For example; i) the bioavailability of fluoride from water is almost 100%, whereas a mixed diet may reduce absorption of fluoride by 47% [103] and; ii) a vegetarian-based diet increases fluoride excretion. To establish an exact association between fluoride intake and excretion, the type of diet should, therefore, be evaluated and reported accurately.

This scoping review also shows the heterogeneous nature of the methods used to collect urine samples (Table 3). When spot urine samples were collected, few studies provided detailed information on the time of sample collection (e.g. fasting or non-fasting; before/after meal/brushing, etc). The fluoride concentration of a spot urine sample can be influenced by factors such as hydration status, time of collection (in relation to time of fluoride ingestion) and length of accumulation of urine (and fluoride) in the bladder. A single spot urine sample, collected after overnight fasting, could be a potentially useful indicator of chronic fluoride exposure for water fluoridation schemes, in which the community ingests a constant low level of fluoride throughout the day. However, when monitoring inadvertent F ingestion, such as through swallowed toothpaste, or through community-based milk fluoridation programmes when participants receive a single fluoride dose at a particular time of day, it is important that more spot urine samples are collected to allow the most appropriate and accurate evaluation of the programme. Although creatinine-adjustment methods have been reported [20, 104] as an appropriate method for estimation of urine fluoride concentration of spot urine samples, and consequently urinary fluoride excretion, they have not been widely explored with different populations and intakes (i.e. different age groups, diet, etc). Likewise, although the majority of the included studies measured fluoride concentration of samples using a fluoride ion-selective-electrode, the validity of the method used was reported in very few studies (Table 3) and this information is essential to accurately compare and understand the findings of the various studies.

Any relationship between fluoride intake and urinary fluoride excretion was explored in only 45% of the studies. The association between fluoride concentration of water and fluoride excretion was reported in 28 studies, whereas only 18 studies (9%) reported the association between fluoride intake and fluoride excretion (Table 4). Considering the multiple and increasing sources of fluoride exposure, and the rise in the “halo effect” of fluoride through globalisation of the food and drink industry [105], the relevance of studies in which fluoride concentration of water is used as a proxy for fluoride intake could be questionable. In addition, due to the diversity of the methods of data collection and analysis, geographical locations and age groups, as well as the small number of studies (n = 18) in which the relationship between fluoride intake and fluoride excretion was investigated, no firm conclusion on the appropriateness of urine as a biomarker for fluoride exposure for all age groups and all dietary/oral hygiene habits can be drawn.

The main limitations of this review were that; i) the searches were limited to studies published in English which may lead to language bias and the omission of relevant reports published in other languages, ii) the “grey literature”, which could reduce the impact of publication bias, was not included (mainly due to the concern with the manageability of overwhelming volume of identified peer-reviewed articles) and; iii) being a scoping review, the quality of the included studies was not assessed and the conclusion was mainly based on the existence of studies rather than their quality.

Conclusions

The diversity of the included studies in this review and their findings highlight the need for strong evidence (collected via reliable reproducible methods) on appropriateness of urinary fluoride as a suitable measure of fluoride exposure for different situations; e.g. different age groups and types of fluoride-based caries-prevention programmes across diverse communities with their different geographical locations and wide ranges of dietary and oral hygiene habits.

Future studies

Future research should focus on: i) development (and validation) of gold standard universal methods for assessing fluoride intake from diet and toothpaste ingestion according to age group and dietary/oral hygiene habits; ii) development (and validation) of alternative methods for 24-hour urine collection such as urinary fluoride: creatinine ratio and urinary fluoride: specific gravity ratio in spot urine samples and iii) assessment of the ability of spot urine sample(s) to predict fluoride intake, according to age group, sources of fluoride exposure including fluoridation scheme.

Likewise, future studies should fully report detail on sampling technique (e.g. fluoride exposure, fluoride excretion), measurement protocols (including validation of the employed methodology), and clearly defined outcomes. Studies should also include reporting on the investigation of the relationship between total fluoride intake and urinary excretion of fluoride. Furthermore, researchers should ensure that potential differences between their findings and other studies/situations are included in their reporting.

Supporting information

S1 File [pdf]
Search history conducted in four electronic databases.

S2 File [pdf]
PRISMA-ScR Fillable checklist.


Zdroje

1. Petersen PE, Ogawa H. Prevention of dental caries through the use of fluoride—the WHO approach. Community Dent. Health. 2016;33(2):66–8. doi: 10.1922/CDH_Petersen03 WOS:000377644900001. 27352461

2. Burt BA. The changing patterns of systemic fluoride intake. J Dent Res. 1992;71(5):1228–37. 1607439

3. Rugg-Gunn AJ. Introduction: Guidelines for Fluoride Intake-Are They Appropriate? Adv Dent Res. 2018;29(2):142–3. doi: 10.1177/0022034517750588 29461107.

4. Spencer AJ, Do LG, Mueller U, Baines J, Foley M, Peres MA. Understanding Optimum Fluoride Intake from Population-Level Evidence. Adv Dent Res. 2018;29(2):144–56. doi: 10.1177/0022034517750592 29461108.

5. Zohoori FV. Summary of General Discussion and Conclusions. Adv Dent Res. 2018;29(2):183–5. doi: 10.1177/0022034517750591 29461109.

6. Warren JJ, Levy SM, Broffitt B, Cavanaugh JE, Kanellis MJ, Weber-Gasparoni K. Considerations on optimal fluoride intake using dental fluorosis and dental caries outcomes—a longitudinal study. J Public Health Dent. 2009;69(2):111–5. doi: 10.1111/j.1752-7325.2008.00108.x 19054310.

7. World Health Organization. Basic methods for assessing renal fluoride excretion in community prevention programmes for oral health Geneva, Switzerland: World Health Organization, 2014.

8. Villa A, Anabalon M, Zohouri V, Maguire A, Franco AM, Rugg-Gunn A. Relationships between fluoride intake, urinary fluoride excretion and fluoride retention in children and adults: an analysis of available data. Caries Res. 2010;44(1):60–8. doi: 10.1159/000279325 20130402.

9. Zohoori FV, Walls R, Teasdale L, Landes D, Steen IN, Moynihan P, et al. Fractional urinary fluoride excretion of 6-7-year-old children attending schools in low-fluoride and naturally fluoridated areas in the UK. Br J Nutr. 2013;109(10):1903–9. doi: 10.1017/S0007114512003583 22974716.

10. Whitford GM. Intake and metabolism of fluoride. Adv Dent Res. 1994;8(1):5–14. 7993560

11. Pollick HF. Salt fluoridation: a review. J Calif Dent Assoc. 2013;41(6):395–7, 400–4. 23875431.

12. Banoczy J, Petersen PE, Rugg-Gunn A, editors. Milk fluoridation for the prevention of dental caries. Geneva: World Health Organization; 2009.

13. Martínez-Mier EA, Cury JA, Heilman JR, Katz BP, Levy SM, Li Y, et al. Development of gold standard ion-selective electrode-based methods for fluoride analysis. Caries Res. 2011;45:3–12. doi: 10.1159/000321657 21160184

14. Arksey H, O'Malley L. Scoping studies: towards a methodological framework. Int J Soc Res Methodol. 2005;8(1):19–32.

15. Levac D, Colquhoun H, O'Brien KK. Scoping studies: advancing the methodology. Implement Sci. 2010;5(1):69.

16. Peters MDJ, Godfrey CM, Khalil H, McInerney P, Parker D, Soares CB. Guidance for conducting systematic scoping reviews. Int J Evid Based Healthc. 2015;13(3):141–6. doi: 10.1097/XEB.0000000000000050 01787381-201509000-00005. 26134548

17. Liberati A, Altman DG, Tetzlaff J, Mulrow C, Gotzsche PC, Ioannidis JPA, et al. The PRISMA Statement for Reporting Systematic Reviews and Meta-Analyses of Studies That Evaluate Health Care Interventions: Explanation and Elaboration. Plos Med. 2009;6(7). ARTN e100010010.1371/journal.pmed.1000100. WOS:000268452400006.

18. Marthaler TM, editor. Monitoring of renal fluoride excretion in community preventive programmes on oral health. World Health Organisation; 1999.

19. World Bank Group, World Bank. Development Data Group. Atlas of sustainable development goals 2018: from world development indicators. Washington, DC: World Bank Group; 2018. xi, 76 pages.

20. Zohoori FV, Maguire A. Determining an upper reference value for the urinary fluoride-creatinine ratio in healthy children younger than 7 years. Caries Res. 2017;51(4):283–9. doi: 10.1159/000472263 28535503

21. Lee JR. Optimal fluoridation—The concept and its application to municipal water fluoridation. West J Med. 1975;122(5):431–6. 1130041.

22. Abuhaloob L, Maguire A, Moynihan P. Fractional Urinary Fluoride Excretion (FUFE) of 3–4 year children in the Gaza Strip. Community Dent Health. 2015;32(1):8–15. 26263586.

23. Buzalaf MA, Rodrigues MH, Pessan JP, Leite AL, Arana A, Villena RS, et al. Biomarkers of fluoride in children exposed to different sources of systemic fluoride. J Dent Res. 2011;90(2):215–9. doi: 10.1177/0022034510385937 21270463.

24. Cury JA, Del Fiol FS, Tenuta LM, Rosalen PL. Low-fluoride dentifrice and gastrointestinal fluoride absorption after meals. J Dent Res. 2005;84(12):1133–7. 16304442.

25. Das K, Mondal NK. Dental fluorosis and urinary fluoride concentration as a reflection of fluoride exposure and its impact on IQ level and BMI of children of Laxmisagar, Simlapal Block of Bankura District, W.B., India. Environ Monit Assess. 2016;188(4):218. doi: 10.1007/s10661-016-5219-1 26960765.

26. Haftenberger M, Viergutz G, Neumeister V, Hetzer G. Total fluoride intake and urinary excretion in German children aged 3–6 years. Caries Res. 2001;35(6):451–7. 11799286.

27. Ketley CE, Lennon MA. Determination of fluoride intake from urinary fluoride excretion data in children drinking fluoridated school milk. Caries Res. 2001;35(4):252–7. 11423720.

28. Li M, Gao Y, Cui J, Li Y, Li B, Liu Y, et al. Cognitive Impairment and Risk Factors in Elderly People Living in Fluorosis Areas in China. Biol Trace Elem Res. 2016;172(1):53–60. doi: 10.1007/s12011-015-0568-0 26606914.

29. Linhares DP, Garcia PV, Amaral L, Ferreira T, Cury JA, Vieira W, et al. Sensitivity of two biomarkers for biomonitoring exposure to fluoride in children and women: A study in a volcanic area. Chemosphere. 2016;155:614–20. doi: 10.1016/j.chemosphere.2016.04.092 27155929.

30. Watanabe M, Kono K, Orita Y, Dote T, Usuda K, Takahashi Y, et al. Influence of dietary fluoride intake on urinary fluoride concentration and evaluation of corrected levels in spot urine. Fluoride—Quarterly Reports. 1995;28(2):61–70. 25152295.

31. Wu JH, Qin M, Li DD, Yang D, Li BY, Liu XN, et al. Correlation analysis of urinary fluoride levels and the daily intake of fluoride in brick tea type fluorosis areas. Fluoride. 2016;(4):449–57. 614336484.

32. Zheng Y, Wu J, Ng JC, Wang G, Lian W. The absorption and excretion of fluoride and arsenic in humans. Toxicology Lett. 2002;133(1):77–82. 12076512.

33. Zohoori FV, Rugg-Gunn AJ. Total fluoride intake and urinary excretion in 4-year-old Iranian children residing in low-fluoride areas. Br J Nutr. 2000;83(01):15–25. doi: 10.1017/S0007114500000040

34. Zohoori FV, Buzalaf MA, Cardoso CA, Olympio KP, Levy FM, Grizzo LT, et al. Total fluoride intake and excretion in children up to 4 years of age living in fluoridated and non-fluoridated areas. Eur J Oral Sci. 2013;121(5):457–64. doi: 10.1111/eos.12070 24028594.

35. Al-Saleh I, Al-Doush I. Urinary fluoride levels in Saudi individuals drinking tap and bottled water. Int J Environ Health Res. 2000;10(1):21–6. 30184590.

36. Antonijevic E, M, inic Z, Curcic M, Djukic-Cosic D, Milicevic N, et al. “Borderline” fluorotic region in Serbia: correlations among fluoride in drinking water, biomarkers of exposure and dental fluorosis in schoolchildren. Environ Geochem Health. 2016;38(3):885–96. doi: 10.1007/s10653-015-9769-x 26423526.

37. Cardenas-Gonzalez M, Osorio-Yanez C, Gaspar-Ramirez O, Pavkovic M, Ochoa-Martinez A, Lopez-Ventura D, et al. Environmental exposure to arsenic and chromium in children is associated with kidney injury molecule-1. Environ Res. 2016;150:653–62. doi: 10.1016/j.envres.2016.06.032 27431456.

38. Choi AL, Zhang Y, Sun G, Bellinger DC, Wang K, Yang XJ, et al. Association of lifetime exposure to fluoride and cognitive functions in Chinese children: a pilot study.[Erratum appears in Neurotoxicol Teratol. 2015 Sep-Oct;51:89]. Neurotoxicol Teratol. 2015;47:96–101. doi: 10.1016/j.ntt.2014.11.001 25446012.

39. Collins EM, Segreto VA. Urinary fluoride levels of children residing in communities with naturally occurring fluorides in the drinking water. J Dent Child. 1984;51(5):352–5. 6592187.

40. Czarnowski W, Krechniak J, Urbanska B, Stolarska K, Taraszewska-Czarnowska M, Muraszko-Klaudel A. The impact of water-borne fluoride on bone density. Fluoride. 1999;32(2):91–5. 29394840.

41. Czarnowski W, Wrzesniowska K, Krechniak J. Fluoride in water, urine and egg shells as an indicator of environmental contamination. Fluoride—Quarterly Reports. 1994;27(3):141–4. 24236569.

42. Czarnowski W, Wrzesniowska K, Krechniak J. Fluoride in drinking water and human urine in northern and central Poland. Sci Total Environ. 1996;191(1):177–84. 8885430.

43. Escobar-Garcia D, Mejia-Saavedra J, Jarquin-Yanez L, Molina-Frechero N, Pozos-Guillen A. Collagenase 1A2 (COL1A2) gene A/C polymorphism in relation to severity of dental fluorosis. Community Dent Oral Epidemiol. 2016;44(2):162–8. doi: 10.1111/cdoe.12201 26564713.

44. Gonzalez-Horta C, Ballinas-Casarrubias L, Sanchez-Ramirez B, Ishida MC, B-H, ez A, et al. A concurrent exposure to arsenic and fluoride from drinking water in Chihuahua, Mexico. Int J Environ Res Public Health [Electronic Resource]. 2015;12(5):4587–601. doi: 10.3390/ijerph120504587 25918912.

45. Grimaldo M, Borja-Aburto VH, Ramirez AL, Ponce M, Rosas M, Diaz-Barriga F. Endemic fluorosis in San Luis Potosi, Mexico. I. Identification of risk factors associated with human exposure to fluoride. Environ Res. 1995;68(1):25–30. 7729383.

46. Kertesz P, Banoczy J, Ritlop B, Brody A, Peter M. The determination of urinary fluoride/creatinine ratio (Q) in monitoring fluoride intake. Acta Physiol Hung. 1989;74(3):209–14. 2640404.

47. Konieczka P, Zygmunt B, Namieśnik J. Determination of and relationship between content of fluorides in drinking water and in urine of pre-school children. Chem Anal Warsaw. 2000;45(4):561–73. rayyan-20105340.

48. Konieczka P, Zygmunt B, Namieśnik J. Effect of fluoride content in drinking water in tricity on its concentration in urine of pre-school children. Toxicol Environ Chem. 2000;74(1):125–30. rayyan-20105341.

49. Maguire A, Zohouri FV, Hindmarch PN, Hatts J, Moynihan PJ. Fluoride intake and urinary excretion in 6- to 7-year-old children living in optimally, sub-optimally and non-fluoridated areas. Community Dent Oral Epidemiol. 2007;35(6):479–88. 18039290.

50. Martinez-Mier EA, Soto-Rojas AE. Differences in exposure and biological markers of fluoride among White and African American children. J Public Health Dent. 2010;70(3):234–40. doi: 10.1111/j.1752-7325.2010.00173.x 20545831.

51. Phantumvanit P, Songpaisan Y, Schamschula RG. Community dental fluorosis and the fluoride content of saliva and urine in thai children. Studies in Environmental Science. 1986;27:173–80. rayyan-20105547.

52. Qayyum M, Waheed Uz Z, Rehman R, Ahmad B, Ahmad M, Ali S, et al. Statistical analysis of fluoride levels in human urine and drinking water samples of fluorinated area of Punjab (Pakistan). J Chem Soc Pakistan. 2013;35(3):1029–33. rayyan-20105567.

53. Rango T, Vengosh AJ, Tekle-Haimanot R, Weinthal E, et al. Fluoride exposure from groundwater as reflected by urinary fluoride and children’s dental fluorosis in the Main Ethiopian Rift Valley. Sci Total Environ. 2014;496:188–97. doi: 10.1016/j.scitotenv.2014.07.048 25084227.

54. Rathee N, Garg P, Pundir CS. Correlative study of fluoride content in urine, serum and urinary calculi. Indian J Clin Biochem. 19(2):100–2. doi: 10.1007/BF02894265 23105464.

55. Rocha-Amador D, Navarro M, Trejo-Acevedo A, Carrizales L, Perez-Maldonado I, Diaz-Barriga F, et al. Use of the Rey-Osterrieth Complex Figure Test for neurotoxicity evaluation of mixtures in children. Neurotoxicology. 2009;30(6):1149–54. doi: 10.1016/j.neuro.2009.09.003 19770001.

56. Rocha-Amador DO, Calderon J, Carrizales L, Costilla-Salazar R, Perez-Maldonado IN. Apoptosis of peripheral blood mononuclear cells in children exposed to arsenic and fluoride. Environ Toxicol Phar 2011;32(3):399–405. 22004959.

57. Saxena S, Sahay A, Goel P. Effect of fluoride exposure on the intelligence of school children in Madhya Pradesh, India. J Neurosci Rural Pract. 2012;3(2):144–9. doi: 10.4103/0976-3147.98213 22865964.

58. Trivedi MH, Sangai NP, Patel RS, Payak M, Vyas SJ. Assessment of groundwater quality with special reference to fluoride and its impact on iq of schoolchildren in six villages of the mundra region, kachchh, gujarat, India. Fluoride. 2012;45(4):377–83. 368958766.

59. Wang B, Zheng B, Lian W, Yang L, Huang R, Ruan J. Fluorine in drinking water and urine in the urban and rural areas of northwestern China—Its determination by a fluoride ion selective electrode. Chin J Geochem. 2009;28(2):172–5. rayyan-20105796.

60. Wang C, Gao Y, Wang W, Zhao L, Zhang W, Han H, et al. A national cross-sectional study on effects of fluoride-safe water supply on the prevalence of fluorosis in China. BMJ Open. 2012;2. 366100963.

61. Yadav JP, Lata S. Urinary fluoride levels and prevalence of dental fluorosis in children of Jhajjar District, Haryana. Indian J Med Sci. 2003;57(9):394–9. 14515029.

62. Villa A, Anabalon M, Cabezas L. The fractional urinary fluoride excretion in young children under stable fluoride intake conditions. Community Dent Oral Epidemiol. 2000;28(5):344–55. 11014511.

63. Villa A, Anabalon M, Cabezas L, Rugg-Gunn A. Fractional urinary fluoride excretion of young female adults during the diurnal and nocturnal periods. Caries Res. 2008;42(4):275–81. doi: 10.1159/000135673 18523387.

64. Villa A, Cabezas L, Anabalon M, Garza E. The fractional urinary fluoride excretion of adolescents and adults under customary fluoride intake conditions, in a community with 0.6-mg F/L in its drinking water. Community Dental Health. 2004;21(1):11–8. 15074867.

65. Villa A, Cabezas L, Anabalon M, Rugg-Gunn A. The fractional urinary fluoride excretion of adults consuming naturally and artificially fluoridated water and the influence of water hardness: a randomized trial. Community Dent Health. 2009;26(3):132–7. 19780352.

66. Villa AE, Salazar G, Anabalon M, Cabezas L. Estimation of the fraction of an ingested dose of fluoride excreted through urine in pre-school children. Community Dent Oral Epidemiol. 1999;27(4):305–12. 10403091.

67. Warneke G, Setnikar I. Effects of meal on the pharmacokinetics of fluoride from oral monofluorophosphate. Arzneimittelforschung. 1993;43(5):590–5. 8329005.

68. Franco AM, Saldarriaga A, Martignon S, Gonzalez MC, Villa AE. Fluoride intake and fractional urinary fluoride excretion of Colombian preschool children. Community Dent Health. 2005;22(4):272–8. 16379167.

69. Ketley CE, Lennon MA. Urinary fluoride excretion in children drinking fluoridated school milk. Int J Paediatr Dent. 2000;10(4):260–70. 11310239.

70. Pessan JP, Pin ML, Martinhon CC, de Silva SM, Granjeiro JM, Buzalaf MA. Analysis of fingernails and urine as biomarkers of fluoride exposure from dentifrice and varnish in 4- to 7-year-old children. Caries Res. 2005;39(5):363–70. 16110207.

71. Szekely M, Banoczy J, Fazakas Z, Hobai S, Villa A. A comparison of two methods for the evaluation of the daily urinary fluoride excretion in Romanian pre-school children. Community Dent Health. 2008;25(1):23–7. 18435230.

72. Maguire A, Zohouri FV, Hindmarch PN, Hatts J, Moynihan PJ. Fluoride intake and urinary excretion in 6- to 7-year-old children living in optimally, sub-optimally and non-fluoridated areas. Community Dent Oral Epidemiol. 2007;35(6):479–88. 18039290

73. Omid N, Maguire A, O'Hare WT, Zohoori FV. Total daily fluoride intake and fractional urinary fluoride excretion in 4- to 6-year-old children living in a fluoridated area: weekly variation? Community Dent Oral Epidemiol. 2016;45:12–9. doi: 10.1111/cdoe.12254 27649844.

74. Largent EJ, Heyroth FF. The absorption and excretion of fluorides; further observations on metabolism of fluorides at high levels of intake. J Ind Hyg & Toxicol. 1949;31(3):134–8. 18151204.

75. Spencer H, Kramer L, Norris C, Wiatrowski E. Effect of aluminum hydroxide on fluoride metabolism. Clin Pharmacol Ther. 1980;28(4):529–35. 7408412.

76. Spencer H, Kramer L, Norris C, Wiatrowski E. Effect of aluminum hydroxide on plasma fluoride and fluoride excretion during a high fluoride intake in man. Toxicol Appl Pharmacol. 1981;58(1):140–4. 7233433.

77. Spencer H, Kramer L, Wiatrowski E, Osis D. Magnesium-fluoride interrelationships in man. I. Effect of fluoride on magnesium metabolism. Am J Physiol. 1977;233(3):E165–9. 910903.

78. Spencer H, Kramer L, Wiatrowski E, Osis D. Magnesium-fluoride interrelationships in man II. Effect of magnesium on fluoride metabolism. Am J Physiol. 1978;234(4):E343–7. 645849.

79. Spencer H, Lewin I, Wistrowski E, Samachson J. Fluoride metabolism in man. Am J Med. 1970;49(6):807–13. rayyan-20105689. 5006619

80. Spencer H, Osis D, Kramer L, Wiatrowski E, Norris C. Effect of calcium and phosphorus on fluoride metabolism in man. J Nutr. 1975;105(6):733–40. 1142003.

81. Spencer H, Osis D, Wiatrowski E, Samachson J. Availability of fluoride from fish protein concentrate and from sodium fluoride in man. J Nutr. 1970;100(12):1415–24. 5481676.

82. Ericsson Y, Hellstrom I, H, er Y. Pilot studies on the fluoride metabolism in infants on different feedings. Acta Paediatr Scand. 1972;61(4):459–64. 5068006.

83. Jolly SS. Fluoride balance studies in endemic fluorosis. Fluoride—Quarterly Reports. 1976;9(3):138–47. 7138941.

84. Ketley CE, Cochran JA, Holbrook WP, Sanches L, van Loveren C, Oila AM, et al. Urinary fluoride excretion by preschool children in six European countries. Community Dent Oral Epidemiol. 2004;32:62–8. 15016119.

85. Maheshwari UR, King JC, Leybin L, Newbrun E, Hodge HC. Fluoride balances during early and late pregnancy. J Occup Med. 1983;25(8):587–90. 6886867.

86. Maheshwari UR, Leybin L, Hodge HC, Newbrun E, Schneider VS, McDonald J. Comparison of fluoride balances during ambulation and bed rest. Proc West Pharmacol Soc. 1981;24:151–3. 7255440.

87. Maheshwari UR, McDonald JT, Schneider VS, Brunetti AJ, Leybin L, Newbrun E, et al. Fluoride balance studies in ambulatory healthy men with and without fluoride supplements. Am J Clin Nutr. 1981;34(12):2679–84. 7315769.

88. Maheshwari UR, Schneider VS, McDonald JT, Brunetti AJ, Leybin L, Newbrun E, et al. Fluoride balance studies in healthy men during bed rest with and without a fluoride supplement. Am J Clin Nutr. 1982;36(2):211–8. 7102580.

89. Ekstrand J, Spak CJ, Ehrnebo M. Renal clearance of fluoride in a steady state condition in man: influence of urinary flow and pH changes by diet. Acta Pharmacol Toxicol (Copenh). 1982;50(5):321–5. 7113707

90. Trautner K, Siebert G. An experimental study of bio-availability of fluoride from dietary sources in man. Arch Oral Biol. 1986;31(4):223–8. 3459412.

91. Hattab FN. Pharmacokinetics of fluoride absorbed from dried seafoods by healthy adults. Eur J Clin Pharmacol. 1988;34(5):489–93. 3203709

92. Trautner K. Influence of food on relative bioavailability of fluoride in man from Na2FPO3-containing tablets for the treatment of osteoporosis. Int J Clin Pharmacol. 1989;27(5):242–9. 2737790.

93. Villa A, Guerrero S, Cisternas P, Monckeberg F. Fluoride bioavailability from disodium monofluorophosphate fluoridated milk in children and rats. Caries Res. 1989;23(3):179–83. 2736581.

94. Liote F, Bardin C, Liou A, Brouard A, Terrier JL, Kuntz D. Bioavailability of fluoride in postmenopausal women: comparative study between sodium fluoride and disodium monofluorophosphate-calcium carbonate. Calcif Tissue Int. 1992;50(3):209–13. 1617494.

95. Spencer H, Kramer L, Osis D, Wiatrowski E. Excretion of retained fluoride in man. J Appl Physiol. 1975;38(2):282–7. 1120753.

96. Puche RC, Rigalli A, Trumper L, Dip O, Pereyra JL, Poudes G, et al. Estimation of bone turnover in climacteric women by the whole body retention of fluoride. Maturitas. 1991;14(1):57–64. 1791773.

97. Tsunoda H, Tsunoda N. Fluoride absorption and excretion in human subjects following ingestion of F-contaminated agricultural products. Studies in Environmental Science. 1986;27:107–12. rayyan-20105759.

98. Zohoori FV, Walls R, Teasdale L, L, es D, Steen IN, et al. Fractional urinary fluoride excretion of 6-7-year-old children attending schools in low-fluoride and naturally fluoridated areas in the UK. Br J Nutr. 2013;109(10):1903–9. doi: 10.1017/S0007114512003583 22974716.

99. Ekstrand J, Ziegler EE, Nelson SE, Fomon SJ. Absorption and retention of dietary and supplemental fluoride by infants. Adv Dent Res. 1994;8(2):175–80. 7865072.

100. Ekstrand J, Fomon SJ, Ziegler EE, Nelson SE. Fluoride pharmacokinetics in infancy. Pediatr Res. 1994;35(2):157–63. 8165049

101. Organisation for Economic Co-operation and Development. Main science and technology indicators in 2016. Available from: http://www.oecd.org/science/msti.htm.

102. Bhagavatula P, Levy SM, Broffitt B, Weber-Gasparoni K, Warren JJ. Timing of fluoride intake and dental fluorosis on late-erupting permanent teeth. Community Dent Oral Epidemiol. 2016;44(1):32–45. doi: 10.1111/cdoe.12187 WOS:000368346900004. 26198477

103. Shulman ER, Vallejo M. Effect of gastric contents on the bioavailability of fluoride in humans. Pediatr Dent. 1990;12(4):237–40. 2077500

104. Zohouri FV, Swinbank CM, Maguire A, Moynihan PJ. Is the fluoride/creatinine ratio of a spot urine sample indicative of 24-h urinary fluoride? Community Dent Oral Epidemiol. 2006;34(2):130–8. doi: 10.1111/j.1600-0528.2006.00269.x 16515677

105. Zohoori FV, Maguire A. Are there good reasons for fluoride labelling of food and drink? Bri Dent J. 2018;224(4):215–7.


Článek vyšel v časopise

PLOS One


2019 Číslo 9

Nejčtenější v tomto čísle

Tomuto tématu se dále věnují…


Kurzy

Zvyšte si kvalifikaci online z pohodlí domova

Léčba bolesti v ordinaci praktického lékaře
nový kurz
Autoři: MUDr. PhDr. Zdeňka Nováková, Ph.D.

Revmatoidní artritida: včas a k cíli
Autoři: MUDr. Heřman Mann

Jistoty a nástrahy antikoagulační léčby aneb kardiolog - neurolog - farmakolog - nefrolog - právník diskutují
Autoři: doc. MUDr. Štěpán Havránek, Ph.D., prof. MUDr. Roman Herzig, Ph.D., doc. MUDr. Karel Urbánek, Ph.D., prim. MUDr. Jan Vachek, MUDr. et Mgr. Jolana Těšínová, Ph.D.

Léčba akutní pooperační bolesti
Autoři: doc. MUDr. Jiří Málek, CSc.

Nové antipsychotikum kariprazin v léčbě schizofrenie
Autoři: prof. MUDr. Cyril Höschl, DrSc., FRCPsych.

Všechny kurzy
Kurzy