Skip to main content

Thank you for visiting nature.com. You are using a browser version with limited support for CSS. To obtain the best experience, we recommend you use a more up to date browser (or turn off compatibility mode in Internet Explorer). In the meantime, to ensure continued support, we are displaying the site without styles and JavaScript.

Relationship of hyposalivation and xerostomia in Mexican elderly with socioeconomic, sociodemographic and dental factors

Abstract

We determined the prevalence of hyposalivation and xerostomia in older Mexicans (≥60 years), and its relationship with diverse factors. A cross-sectional study was realized in elderly subjects from Pachuca, Mexico. Chewing-stimulated saliva was collected under standardized conditions and salivary flow was measured; subjects were considered to have hyposalivation if their stimulated salivary flow was less than 0.7 mL per minute. Xerostomia was evaluated by asking subjects ‘Does your mouth feel dry?’. Hyposalivation was present in 59.7%, and xerostomia in 25.2% of subjects. 16.5% of subjects had both conditions. Xerostomia was present in 27.7% of subjects with hyposalivation and 21.4% of subjects without hyposalivation, but the difference was not significant (p > 0.05). Thus, 68.3% of older Mexicans had xerostomia and/or hyposalivation. Factors associated with hyposalivation were: using fewer devices in oral hygiene, lacking social benefits for retirement/pension, living in a public retirement home, brushing teeth less than twice a day and lacking teeth without dentures. None of the factors included in this study were associated with xerostomia. We concluded that several variables studied were associated with hyposalivation, but none for xerostomia. Additional research should examine the amount of hyposalivation and factors associated with hyposalivation especially in elderly with increased risk for hyposalivation.

Introduction

Healthy humans produce 0.5–1.5 liters of saliva each day. About 90% of the saliva is derived from three pairs of major salivary glands (parotid, submandibular and sublingual) and the remaining 10% comes from numerous minor salivary glands distributed in the oral mucosa1. Saliva is vital for the maintenance of normal oral physiology and mucosal and dental health, and is of paramount importance for the maintenance of oral and general homeostasis. Saliva plays a crucial role in digestive function, speaking, chewing, swallowing, tasting, phonation, cleaning, hydration of the oral mucosa and protection of the teeth, due to buffering and remineralization properties. In addition, saliva controls the composition of the oral microflora due to antibacterial, antifungal and antiviral properties. The loss of salivary function (“dry mouth”) can have far-reaching consequences, such as increased buccodental disease (including dental caries, periodontal disease, gingivitis, erosion and ulceration of mucosal tissues, mucositis and angular cheilitis, and oral candidiasis), speech impairment, denture wearing, less enjoyment and ingestion of food and decreased quality-of-life2,3,4,5,6,7. Dry mouth is most commonly caused by alterations in salivary gland function, dehydration, and cognitive alterations in older people. Salivary dysfunctions can be divided into three alterations: xerostomia (subjective alteration), hyposalivation (reduction of salivary flow), and alterations in salivary composition. Most authors agree that xerostomia and hyposalivation are two separate entities: xerostomia denotes the subjective feeling, the symptom, of dry mouth, whereas hyposalivation denotes the sign, a decreased saliva flow rate3,8. The term “dry mouth” has been used to describe both conditions9.

The diagnosis of salivary dysfunctions can be obtained by means of subjective and objective methods. Xerostomia is primarily evaluated through the use of questionnaires, using either single-item approaches or multi-item scales. Several authors have suggested using instruments to broaden the analysis of xerostomia, in grading aspects related to chewing, swallowing, speech, sleep and quality-of-life. Although a consensus has not been reached on the definition of low salivary flow7,10, hyposalivation is considered when the salivary flow rate is <0.1 mL/min at rest or <0.7 mL/min under stimulation. Salivary flow rates are measured by sialometry, which is a technique that collects whole saliva or the fluid produced by each major gland individually, either at rest or during stimulation3.

The exact nature of the relationship between xerostomia and hyposalivation in the elderly is unknown11. Not all people who have hyposalivation report xerostomia, and people who report xerostomia may have normal or high salivary flow. Mouth dryness is a common clinical complaint in the elderly, more so than in other age groups. It is important to comprehensively establish the current status of xerostomia and hyposalivation in the elderly. However, only a few studies have investigated the prevalence of both xerostomia and hyposalivation within the same elderly populations6. A recent review by Liu et al.9 indicated that the prevalence of xerostomia ranged from 5.5% to 39% in the general public and from 17% to 40% among community-dwelling elders. In institutionalized elders, the prevalence of xerostomia ranged from 20% to 72%. The prevalence of hyposalivation ranged from 15% to 23% in community-dwelling elders and from 17% to 50% in institutionalized elders. Some researchers found that unstimulated whole saliva indicated a higher prevalence of hyposalivation than did stimulated whole saliva, whereas other researchers found the opposite results.

Many factors have been identified as possible causes of reduced salivary flow rates: medications, systemic diseases, aging12,13, the female gender6,11,12,13, agents affecting digestive organs6, nutritional or general health status, diagnosed diseases13,14, depression14, body mass index13, the number of remaining teeth, having fewer than 20 teeth13, periodontal condition, xerogenic drugs13, consumption of certain nutrients14, and bite force4. Variables associated with xerostomia include sex11,15, age15, various diseases (such as diabetes, hypertension, cardiovascular disorders, neurological disorders and psychological disorders)15,16, various drugs15, hypnotics6, smoking habits6 and depression6.

To our knowledge, no studies have identified risk factors for reduced salivary flow rate and xerostomia in the Mexican elderly. The aim of this study was to determine the prevalence of hyposalivation and xerostomia in a sample of older Mexicans, and to evaluate its association with sociodemographic, socioeconomic, behavioral and dental variables.

Materials and Methods

Study design and sample

A study was conducted in subjects ≥60 years-old recruited from two retirement homes (one public and one private) and one group of community-dwelling, independently-living people. The group meets three days a week in the city of Pachuca, in the Hidalgo province of Mexico, for recreation, culture and entertainment. The study design and subjects have been described in detail17,18,19,20. Briefly, a cross-sectional study was conducted. Nowadays, in the Hidalgo province are living 250,715 people with 60 years or older; only In Pachuca City about 23, 340 elder people are living. Otherwise in this City there are eight homes for elderly, but only three with different type of subsidy were chosen for this study. After obtaining the relevant permits, we invited the subjects to participate in the study, informing them about the aims of the research, the confidentiality in data management, and the fact that they could stop participating at any moment. Inclusion criteria were: 1) either sex, 2) 60 years and older, 3) a wish to participate in the research, and 4) coming from the above-mentioned groups. Exclusion criteria were: 1) under 60 years-old, 2) having a hearing or language impairment that could affect the interview, and 3) having a physical or mental disability that could preclude the oral exam. We did not use any sampling approach. From the initial sample of 151 subjects, 12 refused to participate in the study or did not meet the inclusion/exclusion criteria, for that reason, in the final sample just participated 139 subjects.

Variables and data collection

The dependent variables used in this analysis were hyposalivation and xerostomia. To determine stimulated salivary flow, standardized procedures were applied21. Stimulated saliva samples were taken under resting conditions in a quiet room between 7:30 a.m. and 9:30 a.m., at least one hour after the last intake of food and beverages or smoking too, for this study, tooth brushing and rinsing were not allowed; because these variables could modify the salivary pH grade. The subjects chewed a piece of paraffin wax of fixed size (Merck 7159) for five minutes, during which the whole saliva was swallowed and expectorated into a calibrated dry plastic tube. The flow rate was calculated in milliliters per minute (mL/min). When the stimulated salivary flow was lower than 0.7 mL/min, the subjects were considered to exhibit hyposalivation. In addition, the subjects were evaluated for xerostomia with the question ‘Does your mouth feel dry?22,23 and were operationally categorized as 0 (subjects without xerostomia, who answered “no” to the question) and 1 (subjects with xerostomia, who responded “yes” to the question).

Questionnaires were used to collect information on demographic variables such as age, sex and marital status, as well as indicators of socioeconomic position such as home type, social security, pension/retirement and education. Questionnaires also addressed various other exposures and behavioral factors such as the frequency of tooth brushing, use of aids in oral hygiene, smoking, consumption of soda, number of drugs, number of hyposalivation-inducing medications, presence of chronic diseases and whether the subject had received radiation in the head or neck. A thorough clinical examination by one examiner was used to determine the number of missing teeth and use of dentures. In this regard, the subjects were coded as 0 (subjects who had lost all of their teeth (edentulous) and used dentures), 1 (subjects who had lost at least one tooth and used fixed or removable prostheses), 2 (subjects who were edentulous and did not use dentures), 3 (subjects with at least 20 natural teeth and no prostheses), and 4 (subjects who had less than 20 natural teeth and no prostheses).

Data analysis

Statistical analysis was performed using Stata statistical package version 11.0 (StataCorp, Texas, United States). Subjects’ characteristics were summarized as means (±standard deviation) and range (minimum to maximum) for continuous variables, as well as frequency counts and percentages for categorical data. Subsequently, a bivariate analysis was performed; chi-squared and Fisher’s exact tests were used to analyze categorical variables, and the Mann-Whitney test was used to compare quantitative data between the groups. P values <0.05 were considered to be statistically significant.

Ethical considerations

The study protocol followed the Declaration of Helsinki for research involving human subjects and was approved by the local ethics committee of the Post Graduate and Research Unit of the Academic Area of Dentistry of Health Sciences Institute at Autonomous University of Hidalgo State. Written informed consent was obtained from all participants who agreed to participate in this study as volunteers.

Results

In total, the study included 139 adults over 60 years of age. The characteristics of the subjects are shown in Table 1. The average age was 79.06 ± 9.78 years, and 69% of the subjects were female. The prevalence of hyposalivation was 59.7% (95% CI: 51.5–68.0), whereas the prevalence of xerostomia was 25.2% (95%CI: 17.9–32.5) (Table 2). The salivary flow rate of the whole study group was 0.75 ± 0.80 mL/min. Additionally, 16.5% of the subjects had both hyposalivation and xerostomia. Hence, 68.3% of the subjects in the present study had xerostomia and/or hyposalivation.

Table 1 Univariate analysis of the characteristics of the subjects included in the study.
Table 2 Hyposalivation and xerostomia prevalence in the study.

The results of the bivariate analysis of hyposalivation can be seen in Table 3 and are related to xerostomia in Table 4. We observed that hyposalivation correlated with using fewer auxiliaries in oral hygiene, lacking social benefits for retirement/pension, living in a public retirement home, brushing teeth less than two times a day, and being edentulous without dentures (p <0.05). None of the variables analyzed in this study correlated with xerostomia. Xerostomia was reported by 27.7% of subjects with hyposalivation and 21.4% of subjects who did not have hyposalivation; this difference was not significant (Table 5).

Table 3 Bivariate analysis between hyposalivation and the characteristics of the study subjects.
Table 4 Bivariate analysis between xerostomia and the characteristics of the study subjects.
Table 5 Analysis between hyposalivation and xerostomia.

Discussion

This cross-sectional study was conducted in elderly Mexican people to investigate the prevalence of hyposalivation and xerostomia, as well as the factors associated with these conditions. Our findings revealed that 59.7% of the subjects had hyposalivation and 25.2% self-reported xerostomia. Liu et al.9 observed that the prevalence of xerostomia ranged from 17% to 40% among community-dwelling elders and 20% to 72% among institutionalized elders. The prevalence of hyposalivation ranged from 15% to 23% in the community-dwelling elders and 17% to 50% among institutionalized elders. Previous studies suggested that not all people who had hyposalivation reported xerostomia, and people who reported xerostomia could have a normal or high salivary flow6,12. This was also observed in our study; although subjects with hyposalivation presented a higher prevalence of xerostomia rather than those subjects with lacking of hyposalivation, anyway, the difference was not significant. It has been suggested that hyposalivation can exist in people who have no complaint of xerostomia, while people with sufficient salivary secretion can have xerostomia6. However, we measured salivary flow rates during stimulation; studies have shown that oral dryness is more significantly associated with the resting salivary flow rate than the stimulated salivary flow rate13,14.

In recent decades, studies have analyzed the impact of socioeconomic position on the general health of the population. Health is, to a large extent, determined by social class and socioeconomic position, referred to as health inequalities. This health stratification produces differences in outcomes of morbidity and mortality, depending on which stratification measure is used. The exact mechanism by which health and socioeconomic status are associated is unclear, because this variable is part of a multidimensional construct24. Possible mechanisms between socioeconomic position and differences in health involve health behaviors, affordability of a healthy lifestyle and healthcare, and absence of physically demanding work and hazardous working conditions or distress. Indeed, the associations of socioeconomic position and health are so strong that several researchers have put forward the hypothesis that social standing may indeed be the fundamental cause for health25. Krieger26 introduced the concept of “biological expression of social inequality”, which refers to how people biologically incorporate and express their experiences of economic and social inequality, from in utero to death, thereby manifesting social inequalities across a wide range of health aspects. Another hypothesis to explain this association is that hyposalivation may fit into the ‘Life course perspective’27. According to this concept, during growth the individual passes through critical periods when socioeconomic and biological factors may affect the development of organs and body tissues. Deficiencies in certain factors may lead to a permanently reduced function of the salivary glands and to an increased susceptibility to disease during adulthood13. In fact, various studies worldwide have found that the best socioeconomic position is associated with better oral health events28,29,30,31. We analyzed diverse indicators of socioeconomic position and found two of them to be significant: having a pension/retirement and living in a private retirement home or and one group of community-dwelling (the club of day). Similar to our study, a study in Japan found that subjects with hyposalivation were more likely to have a lower socioeconomic position14. In contrast, a study in Brazil did not obtain the same results32.

In general, daily tooth brushing has a positive effect on oral health by preventing major oral diseases, Studies have shown that daily tooth brushing also has a beneficial impact on salivary flow, which our results support. In the Netherlands, Ligtenberg et al.33 found that tooth brushing induced transient changes in salivary flow. After brushing with water, the subjects’ salivary secretion rate increased significantly for 60 minutes, suggesting that tooth brushing mechanically stimulates saliva secretion. The secretion rates were further enhanced after brushing with different types of toothpastes, probably as a result of additional gustatory stimulation. A study conducted in Japan by Inenaga et al.34 found that tooth brushing in different oral regions (surface of the molars, gingiva, tongue, and palatal rugae) increased the flow rate of the parotid salivary gland, probably via the activation of periodontal mechanoreceptors. Hoek et al.35 found that tooth brushing increased the saliva flow rate by 15%, but the flow rate returned to baseline within 30 minutes; thus, the brushing of teeth induces a transient increase in saliva secretion. Since no toothpaste was used, the increase was probably due to mechanical, not gustatory, stimulation. Similarly, other studies have shown that brushing teeth with a manual or electric toothbrush significantly improves the feeling of xerostomia and the amount of salivary flow. Mechanical and electrical stimulation have been used in the past to increase salivary flow. Sonic vibration stimulation with an electric toothbrush is another useful way to stimulate saliva secretion36.

The association between hyposalivation and the number of teeth in the mouth has been observed in various studies around the world. In Sweden, Flink et al.13 found that subjects with less than 20 teeth had a higher risk of hyposalivation (<0.70 mL/min). Studies by Samnieng et al.37 (community-dwelling elderly Thai) and Sawair et al.38. (Jordanian Arabs 15 years and older) found that subjects with hyposalivation had fewer teeth than control subjects. Our results are consistent with both of these studies. Bite force is a key determinant of masticatory performance, and correlates with chewing efficiency in subjects with overdentures, full dentures, and natural dentitions. Bite force is involved in the mastication of food, and the force required to chew food is related to the firmness of one’s diet. An increase in the frequency of chewing or a change in diet to more rigid foods results in increased salivary flow rates39. Although not explicitly studied, we observed that when missing teeth were replaced with prostheses, the salivary flow was higher. It has been suggested that both chewing and bite force are involved in salivary gland secretion39; multiple authors consider the loss of teeth to be responsible for the decrease in bite force and subsequent decrease in salivary flow rate. Matzuda et al.40 found that the replacement of complete dentures for elderly patients improved maximal occlusal force and increased both the stimulated and unstimulated salivary flow rates; consequently, the number of subjects with hyposalivation decreased significantly. Prosthetic treatment providing more functional complete dentures may increase salivary flow by allowing more frequent or forceful mastication and stimulation of mechanoreceptors in the oral mucosa. An increase in salivary flow rate accompanying the insertion of an initial set of complete dentures is a well-known phenomenon36. Our study suggests that there is an increased stimulation in subjects with more natural or prosthetic teeth. In any regard, our results reinforce the need to rehabilitate individuals with missing teeth and hyposalivation to improve oral health and quality-of-life.

Studies have investigated the effects of aging on salivary gland secretion, but these effects remain unclear. Many functional studies found that there is no decrease in the flow of whole or parotid saliva with age in healthy, non-medicated individuals1. The results of our study reinforce this notion because we did not observe a significant association between age and xerostomia or hyposalivation. However, we used only elderly subjects, so younger individuals are needed to verify the hypothesis. In our study, none of the independent variables correlated with xerostomia, as seen in other studies.

The limitations of this study should be recognized for a correct interpretation of the results. We used a cross-sectional study design, which provides only statistical associations and cannot establish causal relationships between the variables. In the other hand, in this study we only measured stimulated salivary flow rate, and other studies demonstrated that the oral dryness is more significantly associated with unstimulated whole saliva flow rate, so, in the future studies this situation should be considered. Finally, nowadays there are other ways to evaluate xerostomia, so, we propose apply this measure system in other questionnaires with more sensibility for xerostomia.

In conclusion, the results show that the prevalences of hyposalivation and xerostomia were 59.7% and 25.2%, respectively. Only 16.5% of the subjects had both hyposalivation and xerostomia. In total, 68.3% of the subjects had xerostomia and/or hyposalivation. Several variables were found to be associated with hyposalivation, but none were associated with xerostomia. These results indicate clear inequalities in hyposalivation by socioeconomic variables. Additional research should examine the prevalence and consequences in high-risk older.

Additional Information

How to cite this article: Islas-Granillo, H. et al. Relationship of hyposalivation and xerostomia in Mexican elderly with socioeconomic, sociodemographic and dental factors. Sci. Rep. 7, 40686; doi: 10.1038/srep40686 (2017).

Publisher's note: Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  1. 1

    Mese, H. & Matsuo, R. Salivary secretion, taste and hyposalivation. J. Oral Rehabil. 34, 711–723 (2007).

    CAS  Article  Google Scholar 

  2. 2

    Chaudhury, N. M., Shirlaw, P., Pramanik, R., Carpenter, G. H. & Proctor, G. B. Changes in saliva rheological properties and mucin glycosylation in dry mouth. J. Dent. Res. 94, 1660–1667 (2015).

    CAS  Article  Google Scholar 

  3. 3

    Saleh, J., Figueiredo, M. A., Cherubini, K. & Salum, F. G. Salivary hypofunction: an update on aetiology, diagnosis and therapeutics. Arch. Oral Biol. 60, 242–255 (2015).

    Article  Google Scholar 

  4. 4

    Takeuchi, K. et al. Risk factors for reduced salivary flow rate in a Japanese population: the Hisayama Study. Biomed. Res. Int. 2015, 381821 (2015).

    Article  Google Scholar 

  5. 5

    Enoki, K. et al. Influence of xerostomia on oral health-related quality of life in the elderly: a 5-year longitudinal study. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. 117, 716–721 (2014).

    Article  Google Scholar 

  6. 6

    Ohara, Y. et al. Prevalence and factors associated with xerostomia and hyposalivation among community-dwelling older people in Japan. Gerodontology 33, 20–27 (2016).

    Article  Google Scholar 

  7. 7

    Navazesh, M., Christensen, C. & Brightman, V. Clinical criteria for the diagnosis of salivary gland hypofunction. J. Dent. Res. 71, 1363–1369 (1992).

    CAS  Article  Google Scholar 

  8. 8

    Nederfors, T. Xerostomia and Hyposalivation. Adv. Dent. Res. 14, 48–56 (2000).

    CAS  Article  Google Scholar 

  9. 9

    Liu, B., Dion, M. R., Jurasic, M. M., Gibson, G. & Jones, J. A. Xerostomia and salivary hypofunction in vulnerable elders: prevalence and etiology. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. 114, 52–60 (2012).

    Article  Google Scholar 

  10. 10

    Sánchez-Guerrero, J., Aguirre-García, E., Pérez-Dosal, M. R., Kraus, A., Cardiel, M. H. & Soto-Rojas, A. E. The wafer test: a semi-quantitative test to screen for xerostomia. Rheumatology (Oxford) 41, 381–389 (2002).

    Article  Google Scholar 

  11. 11

    Thomson, W. M., Chalmers, J. M., Spencer, A. J. & Ketabi, M. The occurrence of xerostomia and salivary gland hypofunction in a population-based sample of older South Australians. Spec. Care Dentist. 19, 20–23 (1999).

    CAS  Article  Google Scholar 

  12. 12

    van der Putten, G. J., Brand, H. S., Bots, C. P. & van Nieuw Amerongen, A. [Prevalence of xerostomia and hyposalivation in the nursing home and the relation with number of prescribed medication]. Tijdschr. Gerontol. Geriatr. 34, 30–36 (2003).

    CAS  Google Scholar 

  13. 13

    Flink, H., Bergdahl, M., Tegelberg, A., Rosenblad, A. & Lagerlöf, F. Prevalence of hyposalivation in relation to general health, body mass index and remaining teeth in different age groups of adults. Community Dent. Oral Epidemiol. 36, 523–531 (2008).

    Article  Google Scholar 

  14. 14

    Iwasaki, M. et al. Hyposalivation and dietary nutrient intake among community-based older Japanese. Geriatr Gerontol Int. 16, 500–507 (2016).

    Article  Google Scholar 

  15. 15

    Abdullah, M. J. Prevalence of xerostomia in patients attending Shorish dental speciality in Sulaimani city. J. Clin. Exp. Dent. 7, e45–53 (2015).

    Article  Google Scholar 

  16. 16

    Lee, T. F. et al. Patient- and therapy-related factors associated with the incidence of xerostomia in nasopharyngeal carcinoma patients receiving parotid-sparing helical tomotherapy. Sci Rep 5, 13165 (2015).

    ADS  CAS  Article  Google Scholar 

  17. 17

    Islas-Granillo, H. et al. Socioeconomic, sociodemographic and clinical variables associated with root caries in a group of persons age 60 years and older in Mexico. Geriatr. Gerontol. Int. 12, 271–276 (2012).

    Article  Google Scholar 

  18. 18

    Islas-Granillo, H. et al. Salivary parameters (salivary flow, pH and buffering capacity) in stimulated saliva of Mexican elders 60 years old and older. West Indian Med. J. 63, 758–765 (2014).

    CAS  Google Scholar 

  19. 19

    Islas-Granillo, H. et al. Prevalence of functional dentition in mexican elders. Rev. Clin. Periodoncia Implantol. Rehabil. Oral. 8, 150–156 (2015).

    Article  Google Scholar 

  20. 20

    Islas-Granillo, H. et al. Tooth loss experience and associated variables among adult mexicans 60 years and older. P. R. Health Sci. J. 35, 88–92 (2016).

    Google Scholar 

  21. 21

    Närhi, T. O., Vehkalahti, M. M., Siukosaari, P. & Ainamo, A. Salivary findings, daily medication and root caries in the old elderly. Caries Res 32, 5–9 (1998).

    Article  Google Scholar 

  22. 22

    Sreebny, L. M. & Valdini, A. Xerostomia. Part I: Relationship to other oral symptoms and salivary gland hypofunction. Oral Surg Oral Med Oral Pathol. 66, 451–458. (1988).

    CAS  Article  Google Scholar 

  23. 23

    Närhi, T. O. Prevalence of subjective feelings of dry mouth in the elderly. J Dent Res. 73, 20–5 (1994).

    Article  Google Scholar 

  24. 24

    Laaksonen, M., Rahkonen, O., Martikainen, P. & Lahelma, E. Socioeconomic Position and Self-Rated Health: The Contribution of Childhood Socioeconomic Circumstances, Adult Socioeconomic Status, and Material Resources. Am. J. Public Health 95, 1403–1409 (2005).

    Article  Google Scholar 

  25. 25

    Chauvel, L. & Leist, A. K. Socioeconomic hierarchy and health gradient in Europe: the role of income inequality and of social origins. Int. J. Equity Health 14, 132 (2015).

    Article  Google Scholar 

  26. 26

    Krieger, N. A glossary for social epidemiology. J. Epidemiol. Community Health 55, 693–700 (2001).

    CAS  Article  Google Scholar 

  27. 27

    Ben-Shlomo, Y. & Kuh, D. A life course approach to chronic disease epidemiology: conceptual models, empirical challenges and interdisciplinary perspectives. Int. J. Epidemiol. 31, 285–293 (2002).

    Article  Google Scholar 

  28. 28

    Ghorbani, Z. & Peres, K. G. Is the association between socioeconomic status and nonreplaced extracted teeth mediated by dental care behaviours in adults? Community Dent. Oral Epidemiol. 43, 532–539 (2015).

    Article  Google Scholar 

  29. 29

    Bhandari, B., Newton, J. T. & Bernabé, E. Income Inequality and Use of Dental Services in 66 Countries. J. Dent. Res. 94, 1048–1054 (2015).

    CAS  Article  Google Scholar 

  30. 30

    Liang, J., Wu, B., Plassman, B., Bennett, J. M. & Beck, J. Social stratification, oral hygiene, and trajectories of dental caries among old Americans. J. Aging Health 26, 900–923 (2014).

    Article  Google Scholar 

  31. 31

    Friedman, P. K., Kaufman, L. B. & Karpas, S. L. Oral health disparity in older adults: dental decay and tooth loss. Dent. Clin. North Am. 58, 757–770 (2014).

    Article  Google Scholar 

  32. 32

    Borges, B. C., Fulco, G. M., Souza, A. J. & de Lima, K. C. Xerostomia and hyposalivation: a preliminary report of their prevalence and associated factors in Brazilian elderly diabetic patients. Oral Health Prev. Dent. 8, 153–158 (2010).

    Google Scholar 

  33. 33

    Ligtenberg, A. J., Brand, H. S., Bots, C. P. & Nieuw Amerongen, A. V. The effect of toothbrushing on secretion rate, pH and buffering capacity of saliva. Int. J. Dent. Hyg. 4, 104–105 (2006).

    CAS  Article  Google Scholar 

  34. 34

    Inenaga, K., Inangaki, T., Hosokawa, R. & Ono, K. Parotid salivary secretion induced by stimulation of periodontal regions with toothbrush in humans. J. Med. Invest. 56, 277 (2009).

    Article  Google Scholar 

  35. 35

    Hoek, G. H., Brand, H. S., Veerman, E. C. I. & Nieuw Amerongen, A. V. Toothbrushing affects the protein composition of whole saliva. Eur. J. Oral Sci. 110, 480–481 (2002).

    Article  Google Scholar 

  36. 36

    Papas, A. et al. Stimulation of salivary flow with a powered toothbrush in a xerostomic population. Spec. Care Dentist. 26, 241–246 (2006).

    Article  Google Scholar 

  37. 37

    Samnieng, P., Ueno, M., Shinada, K., Zaitsu, T., Wright, F. A. & Kawaguchi, Y. Association of hyposalivation with oral function, nutrition and oral health in community-dwelling elderly Thai. Community Dent. Health 29, 117–123 (2012).

    CAS  Google Scholar 

  38. 38

    Sawair, F. A., Ryalat, S., Shayyab, M. & Saku, T. The unstimulated salivary flow rate in a jordanian healthy adult population. J. Clin. Med. Res. 1, 219–225 (2009).

    Google Scholar 

  39. 39

    Ikebe, K. et al. Relationship between bite force and salivary flow in older adults. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod. 104, 510–515 (2007).

    Article  Google Scholar 

  40. 40

    Matsuda, K., Ikebe, K., Ogawa, T., Kagawa, R. & Maeda, Y. Increase of salivary flow rate along with improved occlusal force after the replacement of complete dentures. Oral Surg. Oral Med. Oral Pathol. Oral Radiol. Endod. 108, 211–215 (2009).

    Article  Google Scholar 

Download references

Acknowledgements

Publication supported by the Ministry of Education, Mexican Federal Government, through of The Faculty Development Program (PRODEP).

Author information

Affiliations

Authors

Contributions

H.I.G., A.B.Y. and C.E.M.S. were involved in the design and development of the study. C.E.M.S. designed the study, did the analysis of the data and wrote the first draft of the manuscript. M.A.F.B., L.A.B., N.P.M., M.L.M.-C. and M.M.R. were involved in the conception of the paper, analysis and interpretation of the results. All the authors were involved in the critical review and made intellectual contributions, they also accepted the final version.

Corresponding author

Correspondence to Carlo Eduardo Medina-Solís.

Ethics declarations

Competing interests

The authors declare no competing financial interests.

Rights and permissions

This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/

Reprints and Permissions

About this article

Verify currency and authenticity via CrossMark

Cite this article

Islas-Granillo, H., Borges-Yáñez, A., Fernández-Barrera, M. et al. Relationship of hyposalivation and xerostomia in Mexican elderly with socioeconomic, sociodemographic and dental factors. Sci Rep 7, 40686 (2017). https://doi.org/10.1038/srep40686

Download citation

Further reading

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.

Search

Quick links

Nature Briefing

Sign up for the Nature Briefing newsletter — what matters in science, free to your inbox daily.

Get the most important science stories of the day, free in your inbox. Sign up for Nature Briefing