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A systematic review of methods to diagnose oral dryness and salivary gland function
BMC Oral Healthvolume 12, Article number: 29 (2012)
The most advocated clinical method for diagnosing salivary dysfunction is to quantitate unstimulated and stimulated whole saliva (sialometry). Since there is an expected and wide variation in salivary flow rates among individuals, the assessment of dysfunction can be difficult. The aim of this systematic review is to evaluate the quality of the evidence for the efficacy of diagnostic methods used to identify oral dryness.
A literature search, with specific indexing terms and a hand search, was conducted for publications that described a method to diagnose oral dryness. The electronic databases of PubMed, Cochrane Library, and Web of Science were used as data sources. Four reviewers selected publications on the basis of predetermined inclusion and exclusion criteria. Data were extracted from the selected publications using a protocol. Original studies were interpreted with the aid of Quality Assessment of Diagnostic Accuracy Studies (QUADAS) tool.
The database searches resulted in 224 titles and abstracts. Of these abstracts, 80 publications were judged to meet the inclusion criteria and read in full. A total of 18 original studies were judged relevant and interpreted for this review. In all studies, the results of the test method were compared to those of a reference method.
Based on the interpretation (with the aid of the QUADAS tool) it can be reported that the patient selection criteria were not clearly described and the test or reference methods were not described in sufficient detail for it to be reproduced. None of the included studies reported information on uninterpretable/intermediate results nor data on observer or instrument variation. Seven of the studies presented their results as a percentage of correct diagnoses.
The evidence for the efficacy of clinical methods to assess oral dryness is sparse and it can be stated that improved standards for the reporting of diagnostic accuracy are needed in order to assure the methodological quality of studies. There is need for effective diagnostic criteria and functional tests in order to detect those individuals with oral dryness who may require oral treatment, such as alleviation of discomfort and/or prevention of diseases.
Oral dryness is a complex condition, expressed as a physiological deficiency with or without perceived dysfunction. Clinically, oral dryness may vary from a slight reduction in salivary flow with transient inconvenience to severe impairment of oral health and concomitant psychological indisposition. Salivary dysfunction has mainly been related to a decrease in salivary flow rate, but the molecular composition of saliva has gained more attention in understanding the complexity of the condition. Saliva has been shown to have multi- functional characteristics as expressed by several families of salivary molecules, each comprising multiple members that are multifunctional and overlapping . This explains the presence of a compensatory mechanism in saliva and that the expression of salivary dysfunction is most likely to be multi-facetted.
Part of this variation might be explained by the fact that there is no global consensus regarding the terminology associated with oral dryness, although many authors distinguish between xerostomia, denoting the subjective feeling and hyposalivation, denoting a decreased salivary flow rate [13–17].
Oral dryness may be caused by many factors. One factor of importance is pharmacotherapy. Decreased salivary flow rate has been reported as a consequence of treatment with various types of drugs but as for the subjective feeling of oral dryness the total number of drugs taken seems to be more important . No age-dependent decrease in salivary flow rate has been established [19, 20] although a higher prevalence of perceived oral dryness has been reported with increased age . This might be explained by an increased intake of medication with increasing age.
Several systemic disorders such as Sjögren’s syndrome, diabetes mellitus, rheumatoid arthritis, and systemic lupus erythematosus are also known to cause oral dryness. In addition, radiotherapy to the head and neck region is a factor of importance.
With regard to an increasingly elderly population and its dependent use of medication, a multitude of negative side effects associated with disturbed salivary function will present a medico-socio-economic problem not only for the individual per se but also for society in the near future.
The most advocated clinical method for diagnosing salivary gland dysfunction is to quantitate unstimulated and stimulated whole saliva flow rates (sialometry). The cut-off value for a very low unstimulated and stimulated whole saliva flow rate is claimed to be ≤ 0.1 ml/min and ≤ 0.7 ml/min, respectively which is generally referred in the literature to studies by Ericsson and Hardwick  and Sreebny and Valdini . Attempts have also been made to correlate perceived oral dryness to salivary output with varying results. However, reports where the patients describe their oral comfort/discomfort levels, suggest weak to no correlation between measures of salivary flow rates and an individual’s own subjective description [4, 22–24]. Symptoms of dry mouth often occur when the salivary flow rate is reduced by about 50%, but can also be experienced within what is regarded as the normal salivary flow rate range . Unless the mouth is almost dry, without proper individual baseline information it is almost impossible to ascertain if the level of a patient’s salivary flow rate is actually below ‘normal’. Since there is a great variability in individual salivary flow rate and a wide range of flow rate is accepted, the accurate assessment of dysfunction can be difficult. With this in mind, it can be argued if measurements of salivary flow rates can be used as a discriminating diagnostic tool.
Ghezzi et al.  studied the variation of stimulated parotid and submandibular flow rates in a healthy population of adults over a six-hour period. In accordance with other investigators [25, 27], they demonstrated that salivary flow rates are not constant and that there exists a broad range of stimulated parotid and submandibular flow rates among healthy individuals. These findings were confirmed in the study by Burlage et al. . They determined the variation in stimulated parotid flow rate for repeated collections. They also found a large degree of similarity between the flow rates of the left and right parotid glands in healthy subjects as well as in patients with Sjögren’s syndrome.
Responses to standardized questions have been compared to objective measures of major salivary gland output in order to identify certain questions that with a high degree of reliability predict true salivary gland dysfunction . The results showed that questions focusing on perceived oral dryness associated with eating were highly indicative of salivary performance whilst the most commonly heard complaints such as perceived oral dryness at night and during the day had no significant correlation with reduced salivary flow rate.
Furthermore, the individuals’ assessment of the quantity of saliva as “too little” was highly predictive of decreased salivary output.
The aim of this systematic review is to evaluate the quality of the evidence for the efficacy of diagnostic methods used to identify oral dryness.
The systematic approach of the literature review was adapted according to Goodman  and consisted of the following steps: specification of the problem, formulation of a plan to conduct the literature search with specified indexing terms, retrieval of publications and interpretation of the evidence from the literature studied.
Specification of the problem
The following question was developed to articulate the problem: What methods are used to diagnose oral dryness and what is the efficacy of these methods?
Formulation of a plan, literature search, and retrieval
The first step of the search was to use Medical Subject Headings (MeSH) and free text words to search the electronic databases PubMed (including MeSH Subheadings and [All fields]), Cochrane Library, and Web of Science.”
The following search terms were identified on the basis of Medical Subject Headings (MeSH) and within the MeSH database these terms are defined as:
Saliva: the clear, viscous fluid secreted by the salivary glands and mucous glands of the mouth and containing mucins, water, organic salts, and ptylin.
Xerostomia: decreased salivary flow.
Diagnostic techniques and procedures: methods, procedures, and tests performed to diagnose disease, disordered function, or disability. Year introduced: 1998.
Pilocarpine: a slowly hydrolyzed muscarinic agonist with no nicotinic effects. Pilocarpine is used as a miotic and in the treatment of glaucoma.
The above mentioned MeSH terms were combined by using the Boolean operator ‘OR’ with free text words within a search facet.
Since this review focused on diagnostic methods and an initial search resulted in a number of publications on intervention with pilocarpine, the decision was made to confine the search by excluding those studies.
Exclusion of studies on intervention with pilocarpine was obtained by using the Boolean operator ‘NOT’ in the search.
To be included in this review, publications that described a method for diagnosing oral dryness were searched. The inclusion and exclusion criteria are presented in Table 1.
The search was limited to publications with an Entrez date in the period from January 1, 1966 to February 22, 2011.
The decision to include the article was made by reading the title and the abstract. Four authors (CDL, CW, MS and CC) screened all titles and abstracts independently for possible inclusion. When an abstract was considered by at least one author to be relevant, the full text was obtained for independent assessment against the stated inclusion criteria (Table 1) with the aid of a protocol (Additional file 1: Table S1). Any disagreement was resolved by discussion among the reviewers.
The protocol used in the assessment against the stated inclusion criteria.
Will the study be included in the systematic review? Yes No.
The second step was to search by hand the reference lists of the original studies that had been found relevant in the first step. Reference lists of reviews were also searched. Titles containing words suggesting diagnostic measures and techniques of oral dryness were sought.
Inclusion and exclusion criteria were also considered in the hand search. The abstracts of the selected references were obtained and when considered relevant by at least one author, the publication was ordered in full text. Book chapters and reviews were excluded, since the search focused on original studies.
Data were extracted on the following items: year of publication; study objectives; study design; study population; control group; test method; reference method; and authors’ conclusion.
Original studies that presented a method for diagnosing oral dryness were interpreted according to the Quality Assessment of Diagnostic Accuracy Studies (QUADAS) tool .
In the present review, a modified protocol comprising 15 questions was applied, as presented in Table 2.
The same reviewers assessed the articles separately. Any interexaminer disagreements were resolved by discussion on each article to reach a consensus.
The number of publications retrieved, read and interpreted is presented in Figure 1.
The database searches resulted in 224 titles and abstracts. Of these abstracts, 80 publications were judged to meet the inclusion criteria and read in full. Data were extracted according to the pre-established protocol. Animal studies and publications in a language other than English were excluded. Publications using a sialogogue (not only pilocarpine) as intervention were excluded. Furthermore, studies where oral dryness was not described as a primary condition, studies where the conditions for the donors were not standardised and studies that did not include a control group were excluded. Studies were oral dryness was a secondary outcome variable, i.e. studies reporting oral dryness as a secondary finding to e.g. treatment or medication, but not to general diseases e.g. Sjögren’s syndrome, were also excluded.
This resulted in 11 original studies being considered relevant for the review. The hand search of the reference lists of 11 original studies and 20 reviews resulted in an additional 60 abstracts. After these abstracts had been read, 24 publications were selected and read in full and data were extracted. After the publications had been read in detail, seven were selected.
Preliminary evaluation of the included studies revealed heterogeneity with respect to inclusion criteria, test method and reference method. Consequently, it was not possible to conduct a quantitative data synthesis leading to a meta-analysis.
Study objectives and study design
Seven of the included studies [31, 33, 34, 36, 37, 43, 44] aimed at examining the potential use of different tests or a combination of tests for the diagnosis of Sjögren’s syndrome. The remaining 11 studies [4, 32, 35, 38–42, 45–47] described different methods for determining salivary hypofunction.
Five studies were performed in the USA [4, 31, 39, 42, 46], two in The Netherlands [36, 37], two in Sweden [32, 34], one in Egypt , one in Great Britain , one in Japan , one in South Korea , one in Spain , one in Denmark , one in France , one in Mexico  and one in Israel .
Study populations and control groups
The majority of de individuals included in the study groups were individuals with Sjögren’s syndrome (Table 3). In six studies [4, 38, 40, 42, 46, 47] the study population consisted of individuals with symptoms of and/or findings of oral dryness. In one study , subjects were participants in a cross sectional general health survey, randomly selected from a population register.
The control groups consisted mainly of age- and gender-matched healthy individuals. In two studies, the control group consisted of individuals with normal salivary secretion rates [32, 42]. One study  included individuals with symptoms of dry mouth in the control group, and in one study  the control group consisted of individuals with Sjögren’s syndrome.
The number of included individuals in the study populations varied between 16 and 341 and in the control groups between 12 and 372.
Two studies did not report age and gender [31, 47] for individuals included in the study populations or control groups. Two studies [33, 44] did not state gender for individuals included in the control groups. Two studies [38, 42] reported age and gender for all included subjects.
Index test methods and reference methods
A variety of index test methods were used in the included articles (Table 4)..
In general terms, the index tests could be divided into five categories:
Secretion tests; including sialometry and sialochemistry,Oral Schirmer’s test, secretion composition using protein separation techniques, total protein content, electrolyte content and specific protein content with immunological tests or iodine starch reactions (amylase) [31, 32, 36–38, 41]
Some studies used a combination of tests to assess salivary gland hypofunction [40, 42–44]. All studies used sialometry as a reference standard when evaluating the different index tests. However, different secretions, including stimulated and unstimulated glandular saliva, as well as unstimulated whole saliva were used (Table 5).
Eleven of the included studies [31–37, 41, 43–45] used established criteria for the classification of Sjögren’s syndrome as reference methods. Seven of these studies [31, 35–37, 41, 43, 44] used the European Community Study Group on diagnostic criteria for Sjögren’s syndrome as reference method [48–52]. Two studies [32, 34] used the Copenhagen Criteria for the classification of Sjögren’s syndrome  as reference method and two studies [33, 45] used the proposed criteria for Sjögren’s syndrome according to Fox et al.  as a reference method. The cut-off values defining salivary gland hypofunction in the studies not using the above mentioned reference methods are presented in Table 4.
Based on this, it can be reported that the patient selection criteria were not clearly described [38–40, 47], and the test method  or the reference method [4, 33, 39, 41, 44] were not described in sufficient detail to allow the study to be reproduced. None of the included studies reported uninterpretable/intermediate results or data on observer or instrument variation. Authors’ judgements regarding seven of the quality items in the QUADAS tool (Table 2, questions no 1,4,6,9,10,11,12 and 13) are presented in Figure 2.
One study  examined the application of three different gel electrophoresis systems (SDS-PAGE, anionic-PAGE, immobilized pH gradient (IPG)) in the diagnosis of Sjögren’s syndrome. Tests of accuracy revealed that the immobilized pH grading system had a specificity of 97%, sensitivity of 95%, positive predictive value of 97% and negative predictive value of 95% in the diagnosis of Sjögren’s syndrome.
In the study by Kalk et al. , reference values of several salivary variables, i.e. sodium, chloride and phosphate concentration in stimulated parotid and submandibular/sublingual saliva, unstimulated and stimulated submandibular/sublingual flow rates and lag phase of parotid secretion were defined in order to diagnose Sjögren’s syndrome. The most accurate test, with a sensitivity of 85% and specificity of 96%, combined stimulated submandibular/sublingual flow rate and parotid sodium and chloride concentration.
Oral Schirmer’s test was used as test method in one study  for detecting salivary gland hypofunction. Cut-off values for the unstimulated test (≤ 30 mm/5 min, ≤ 40 mm/5 min, ≤ 50 mm/5 min, ≤ 60 mm/5 min), and for the stimulated test (≤ 50 mm/5 min, ≤ 60 mm/5 min, ≤ 70 mm/5 min, ≤ 80 mm/5 min) were examined and sensitivity, specificity, positive predictive values and negative predictive values were calculated. A cut-off value of ≤30 mm/5 min for the unstimulated sialometric test using Oral Shirmer’s test provided a sensitivity of 67.9% and a specificity of 62.8%. A cut-off value of ≤ 80 mm/5 min for the stimulated test showed a sensitivity of 87.6%, specificity of 67.5%, positive predictive value of 55.7% and a negative predictive value of 7.8%.
A wafer test was used as a test method in one study  to predict early salivary gland dysfunction and xerostomia. Different cut-off values (3–7 min) were examined and the best balance between sensitivity and specificity was seen with a cut-off value of 4 min (wafer 4). This cut-off value exhibited a sensitivity of 92.9%, specificity of 71.7%, positive predictive value of 31.7%, negative predictive value of 98.6% and accuracy of 74.3%. With increasing time, the specificity for reduced salivary flow increased. Wafer 4 was compared with the European questionnaire  in order to validate the test as a screening instrument for low salivary flow and xerostomia. For low salivary flow, the European questionnaire  and the wafer 4 showed identical sensitivity. However, wafer 4 showed higher specificity, positive predictive value, negative predictive value, and accuracy. For xerostomia, wafer 4 showed higher sensitivity and negative predictive value when compared to the European questionnaire .
An indirect method (candy weight loss) was used as a test method in one study  to determine salivary output level. Significant associations were found when comparing candy weight loss with stimulated parotid and submandibular and sublingual saliva. When using a cut-off value of 0.23 g candy loss, the sensitivity was 92%, specificity 85% and the positive predictive value 82%.
Sreebny and Valdini  determined the validity of using symptoms related to dry mouth by using a questionnaire, to screen patients for salivary gland hypofunction. The study population was classified into three groups according to their ability to produce unstimulated whole saliva. Flow rates of ≤ 0.1 ml/min were characterised as “abnormal”, between 0.11 and 0.2 ml/min as “low normal”, and > 0.2 ml/min as “normal”. Determinations of sensitivity, specificity and negative and positive predictive values were made for xerostomia alone and for xerostomia in combination with three symptoms that were closely associated with it. A positive answer to the question “Does your mouth usually feel dry” showed a sensitivity of 93%, specificity of 68%, positive predictive value of 54% and negative predictive value of 98%. When an additional three symptoms were taken into account (difficulty with speech, trying to keep mouth moist and getting out of bed to drink), the specificity increased to 91% and the positive predictive value increased to 75%.
A combination of tests for the classification of the oral component of Sjögren’s syndrome was examined in the study by Pennec et al. . The tests examined were salivary flow rate (unstimulated whole saliva), salivary lysozyme, salivary lactoferrin, sialography, salivary gland scintigraphy and labial salivary gland biopsy. The authors concluded that the most efficient combination of test for the oral component of Sjögren’s syndrome was salivary gland biopsy (sensitivity 95%, specificity 75%, positive predictive value 90%, negative predictive value 14%) plus salivary flow rate (sensitivity 68%, specificity 81%, positive predictive value 90%, negative predictive value 50%) or salivary lactoferrin (sensitivity 58%, specificity 75%, positive predictive value 82%, negative predictive value 53%).
The aim of systematic reviews is to identify and evaluate all available research evidence relating to a particular objective. An essential part of any systematic review is the quality assessment of individual studies. Aspects such as study design, methods of sample recruitment, the execution of the tests and the completeness of the study report relate to the overall quality. The results of a systematic review will be biased if the results of individual studies are synthesised without any consideration of quality in terms of potential for bias, lack of applicability and the quality of reporting.
QUADAS  was the first systematically developed, evidence based quality assessment tool to be used in systematic reviews of diagnostic accuracy studies. The QUADAS tool  contains a detailed explanation of the intention of each item, situations when the item does not apply and how to score items. This allows for minor adaptations in specific areas. The QUADAS tool  does not incorporate quality scores to assess the level of evidence. Since the importance of individual items and their potential biases may vary according to the context in which they are applied, incorporation of quality scores into the results of a review may generate different magnitudes of bias and lead to different conclusions regarding the effect of study quality on estimates of diagnostic accuracy. Instead, it has been proposed that a systematic review should involve a component approach, where the association of individual quality items with test accuracy are investigated individually .
The QUADAS tool  was used in the present systematic review since it is a standardised approach to quality assessment and since the criteria needed to assess the quality of diagnostic test evaluations differ from those needed to assess evaluations of therapeutic interventions .
In the present review, modifications were done to adapt the QUADAS tool  to better correspond to the objectives of the study. Two questions (numbers 6 and 7) were excluded from the 14 questions of the final QUADAS tool  and two were added from the original list of 28. In addition, question number 3 was modified into two sub-questions.
When interpreting the studies with the aid of the QUADAS tool  it could be established that some studies showed shortcomings in describing the selection criteria clearly and in describing the test method or the reference method in such detail that it could be reproduced. A sufficient description of the tests is important since variations in measures of diagnostic accuracy can be traced back to differences in the execution of the tests. A clear description is also needed in order to implement the test in another setting. None of the included studies reported uninterpretable/intermediate results or data on observer or instrument variation. A diagnostic test can produce uninterpretable/intermediate results with varying frequency. If these results are removed from the analysis, it may lead to biased assessments of the test characteristics. Furthermore, it can be questioned if some of the studies presented appropriate results.
When scoring QUADAS items  as unclear it is difficult to be certain if this indicates poor methods with the attendant consequences for bias and/or variation, or simply poor reporting of a methodologically sound study. The STARD initiative  has proposed standards for the reporting of diagnostic accuracy studies. If these standards are widely adopted, reviewers might be able to assess methodological quality rather than the quality of reporting. The aim of test accuracy studies is to assess how well a test can distinguish between subjects with and without the disease/condition of interest. There are two basic types of test accuracy study: (1) The single-gate design which includes participants in whom the disease status is unknown, and compares the results of the index test with those of a reference standard used to confirm diagnosis. This design is broadly representative of the setting in which the test would be used in practice. (2) The two-gate design compares the results of the index test in patients with an established diagnosis of the target condition with its results in healthy controls or controls with another diagnosis. This design has inherent problems that may lead to bias. The inclusion of healthy controls is likely to lead to over estimations of specificity and the selective inclusion of cases with more advanced disease is likely to lead to over estimations of sensitivity . The two-gate studies can however be useful in the earlier phases of test development.
Addressing the question formulated to specify the problem, it can be concluded that whilst a variety of tests to diagnose oral dryness have been examined, only a few have been validated in terms of diagnostic accuracy. Eight of the included studies presented their results as percentage of correct diagnoses. Four of these studies used European Community Study Group on classification criteria for Sjögren’s syndrome [48–52] as reference method. The European classification criteria for Sjögren’s syndrome were developed and validated between 1989 and 1996 and have received broad acceptance by the scientific community. Since the reference standard is an important determinant of the diagnostic accuracy of a test, it raises the question of why all of studies aimed at the evaluation of tests for the diagnosis of Sjögren’s syndrome did not use the same reference method.
Although these criteria have received a broad acceptance, some criticism has been raised concerning the inclusion of subjective test (symptoms), physiologic measures that lack specificity and alternate objective tests that are not diagnostically equivalent.
Recently, the American College of Rheumatology  proposed new classification criteria for Sjögren’s syndrome. These criteria are based on expert opinion elicited using the nominal group technique and analyses of data from the Sjögren’s International Collaborative Clinical Alliance . The proposed criteria are: 1) positive serum anti-SSA and/or anti-SSB or (positive rheumatoid factor and antinuclear antibody titer ≥1:320), 2) ocular staining score ≥3, or 3) presence of focal lymphocytic sialadenitis with a focus score ≥1 focus/4 mm2 in salivary gland biopsy samples. Case definition requires at least 2 of the 3 above mentioned objective features. Thus, only objective tests and not subjective tests (symptoms) are included since symptoms of dry mouth and/or eyes can lead to misclassification of asymptomatic patients. For the salivary and ocular phenotypic features of Sjögren’s syndrome the results did not identify any suitable alternate tests besides labial salivary gland biopsy. While unstimulated salivary flow rate <0.1 ml/min had good sensitivity, it had low specificity compared to the labial salivary gland biopsy to measure focal lymphocytic sialadenitis with a focus score ≥1 . Seven of the studies interpreted in this review evaluated different tests for determining decreased salivary flow and used sialometry as a reference method. These studies revealed heterogeneity with respect to source of secretion whether unstimulated or stimulated. Cut-off values defining salivary gland hypofunction also varied. As stated earlier, without proper individual baseline information, it is almost impossible to ascertain if the level of a patient’s salivary flow rate is below the ‘normal’. When using sialometry for diagnosing salivary dysfunction it can be argued if the method is used as a diagnostic tool or rather as a verification of an already established condition. Sreebny  proposed that the low cut-off values should be viewed as values which “flag” or “raise suspicion” about the presence of a disease. They do not indicate that the person who demonstrates such values definitely has a disease.
The fact that there is no global consensus regarding the terminology of oral dryness, although many authors distinguish between xerostomia, denoting the subjective feeling, and hyposalivation, denoting a decreased salivary flow rate, creates a problem for research, diagnosis, and therapy. As for research, this problem is illustrated when using Medical Subject Headings (MeSH). MeSH is the National Library of Medicine’s controlled vocabulary thesaurus used for indexing articles for PubMed. The MeSH database defines xerostomia as decreased salivary flow, which is incorrect since a sensation of oral dryness can occur in subjects with a normal salivary flow. Nederfors  proposed to divide the term “salivary gland hypofunction” into 3 different entities: xerostomia, denoting the subjective feeling; hyposalivation, denoting the decreased salivary flow rate; and altered saliva composition. This classification accepts that xerostomia may exist without signs of hyposalivation, that hyposalivation may be a symptomless condition and that an altered saliva composition may exist even if the saliva secretion rate is unaffected and without subjective symptoms. These three entities are inter-related and can influence each other in different ways.
Over the last decade, advances have been made regarding proteomic and genomic approaches to identify potential biomarkers that may be used in the detection of different diseases, e.g. Sjögren’s syndrome . Saliva is a biofluid that is readily accessible via noninvasive methods, and therefore a perfect medium to be explored for purposes to monitor health status, disease onset and progression, and treatment outcome. Salivary diagnostic technologies identifying specific biomarkers associated with disease may in the future be used to verify general diseases behind salivary gland hypofunction . It should also be mentioned that in the absence of an efficient treatment, a diagnostic method has little value. The basic causes of oral dryness are difficult to treat and many methods have been tested to stimulate saliva secretion and ease the patient’s discomfort, e.g., saliva-stimulating tablets and artificial saliva. Several studies have evaluated the efficacy of such preparations but there is no documented evidence of their effect on oral health [64–66].
Currently, diagnostic methods are addressing quantity and content of saliva in bulk and few qualitative tests of saliva, in bulk or of saliva as an adsorbed thin film, are at this date available for describing the protective functions of saliva.
Since changes in the protective functions of saliva may occur, there is a need for effective diagnostic criteria and functional tests in order to discern which individuals with oral dryness will require oral treatment, such as alleviation of discomfort and/or prevention of diseases.
An important component in determining the usefulness of a test is the evaluation of the diagnostic accuracy, but the clinical value lies in improving a patient’s condition or health. The clinical value, i.e. how the results of a test affects the clinical decision-making and the effect on the patient’s wellbeing are important factors when evaluating diagnostic tests or methods. A method with high diagnostic accuracy may not always be efficient and useful for the patient. Studies that investigate the value of diagnostic interventions are scarce and seldom available for new test methods. In addition, appropriate reference standards for many disorders are lacking.
The aim of this systematic review was to evaluate the quality of evidence for diagnostic methods used to identify oral dryness and their clinical application.
After assessing the quality of the retrieved studies, it may be concluded that the evidence for the efficacy of clinical methods to assess oral dryness is sparse. When evaluating the retrieved studies by using the QUADAS tool , many of the studies exhibited shortcomings. Standards for the reporting of diagnostic accuracy studies have been suggested, such as the STARD initiative . If these standards are widely adopted, the quality of reporting will be improved and the methodological quality of diagnostic accuracy studies will be easier to assess. This will, as a consequence, benefit patients.
A global consensus regarding the terminology of oral dryness is needed in order to facilitate diagnosis and treatment and continued research.
Changes in the protective functions of saliva may occur, which might affect oral health.
There is a need for effective diagnostic criteria and functional tests in order to detect those individuals with oral dryness who may require treatment, such as alleviation of discomfort and/or prevention of diseases.
Levine MJ: Salivary molecules. A structure/function synopsis. Saliva as a Diagnostic Fluid. Edited by: Malamud D, Tabak LA. 1993, New York: Annals of the New York Academy of Sciences, 11-16.
Osterberg T, Landahl S, Hedegard B: Salivary flow, saliva, pH and buffering capacity in 70-year-old men and women. Correlation to dental health, dryness in the mouth, disease and drug treatment. J Oral Rehabil. 1984, 11: 157-170. 10.1111/j.1365-2842.1984.tb00565.x.
Ben-Aryeh H, Miron D, Berdicevsky I, Szargel R, Gutman D: Xerostomia in the elderly: prevalence, diagnosis, complications and treatment. Gerodontology. 1985, 4: 77-82. 10.1111/j.1741-2358.1985.tb00373.x.
Sreebny LM, Valdini A: Xerostomia: Part I: Relationship to other oral symptoms and salivary gland hypofunction. Oral Surg Oral Med Oral Pathol. 1988, 66: 451-458. 10.1016/0030-4220(88)90268-X.
Thorselius I, Emilson CG, Osterberg T: Salivary conditions and drug consumption in older age groups of elderly Swedish individuals. Gerodontics. 1988, 4: 66-70.
Gilbert GH, Heft MW, Duncan RP: Mouth dryness as reported by older Floridians. Community Dent Oral Epidemiol. 1993, 21: 390-397. 10.1111/j.1600-0528.1993.tb01105.x.
Locker D: Subjective reports of oral dryness in an older adult population. Community Dent Oral Epidemiol. 1993, 21: 165-168. 10.1111/j.1600-0528.1993.tb00744.x.
Narhi TO: Prevalence of subjective feelings of dry mouth in the elderly. J Dent Res. 1994, 73: 20-25. 10.1177/00220345940730010301.
Loesche WJ, Bromberg J, Terpenning MS, Bretz WA, Dominguez BL, Grossman NS, et al: Xerostomia, xerogenic medications and food avoidances in selected geriatric groups. J Am Geriatr Soc. 1995, 43: 401-407.
Billings RJ, Proskin HM, Moss ME: Xerostomia and associated factors in a community-dwelling adult population. Community Dent Oral Epidemiol. 1996, 24 (Billings RJ, Proskin HM, Moss ME): 312-316.
Hochberg MC, Tielsch J, Munoz B, Bandeen-Roche K, West SK, Schein OD: Prevalence of symptoms of dry mouth and their relationship to saliva production in community dwelling elderly: the SEE project, Salisbury Eye Evaluation. J Rheumatol. 1998, 25: 486-491.
Nederfors T: Xerostomia and hyposalivation. Adv Dent Res. 2000, 14: 48-56. 10.1177/08959374000140010701.
Field EA, Longman LP, Bucknall R, Kaye SB, Higham SM, Edgar WM: The establishment of a xerostomia clinic: a prospective study. Br J Oral Maxillofac Surg. 1997, 35: 96-103. 10.1016/S0266-4356(97)90683-5.
Fox PC: Management of dry mouth. Dent Clin North Am. 1996, 41: 863-875.
Fox PC, van der Ven PF, Sonies BC, Weiffenbach JM, Baum BJ: Xerostomia: evaluation of a symptom with increasing significance. J Am Dent Assoc. 1985, 110: 519-525.
Jensen JL, Barkvoll P: Clinical implications of the dry mouth. Ann NY Acad Sci. 1998, 842: 156-162. 10.1111/j.1749-6632.1998.tb09643.x.
Locker D: Xerostomia in older adults: a longitudinal study. Gerodontology. 1995, 12: 18-25. 10.1111/j.1741-2358.1995.tb00125.x.
Nederfors T, Isaksson R, Mörnstad H, Dahlöf C: Prevalence of perceived symptoms of dry mouth in an adult Swedish population- relation to age, sex and pharmacotherapy. Community Dent Oral Epidemiol. 1997, 25: 211-216. 10.1111/j.1600-0528.1997.tb00928.x.
Ship JA, Baum BJ: Is reduced salivary flow normal in old people?. Lancet. 1990, 336: 1507-
Osterberg T, Birkhed D, Johansson C, Svanborg A: Longitudinal study of stimulated whole saliva in an elderly population. Scand J Dent Res. 1992, 100: 340-345.
Ericsson Y, Hardwick L: Individual diagnosis, prognosis and counseling for caries prevention. Caries Res. 1978, 12: 94-102. 10.1159/000260369.
Fox PC, Busch KA, Baum BJ: Subjective reports of xerostomia and objective measures of salivary gland performance. J Am Dent Assoc. 1987, 115: 581-584.
Sreebny LM, Valdini A, Yu A: Xerostomia. Part II: Relationship to nonoral symptoms, drugs, and diseases. Oral Surg Oral Med Oral Pathol. 1989, 68: 419-427. 10.1016/0030-4220(89)90140-0.
Löfgren CD, Isberg PE, Christersson C: Screening for oral dryness in relation to salivary flow rate addresses the need for functional tests of saliva. Oral Health Prev Dent. 2010, 8: 243-252.
Ship JA, Fox PC, Baum BJ: How much saliva is enough?. J Am Dent Assoc. 1991, 122: 63-69.
Ghezzi EM, Lange LA, Ship JA: Determination of Variation of Stimulated Salivary Flow Rates. J Dent Res. 2000, 11: 1874-1878.
Dawes C: Circadian rhythms in human salivary flow rate and composition. J Physiol. 1972, 220: 529-545.
Burlage FR, Pijpe J, Coppes RP, Hemels MEW, Meertens H, Canrinus A, Vissink A: Variability of flow rate when collecting stimulated parotid saliva. Eur J Oral Sci. 2005, 113: 386-390. 10.1111/j.1600-0722.2005.00241.x.
Goodman C: Literature Searching and Evidence Interpretation for Assessing Health Care Practices. 1993, Stockholm: Swedish Council on Technology Assessment in Health Care
Whiting P, Rutjes AWS, Reitsma JB, Bossuyt PMM, Kleijnen J: The development of QUADAS: a tool for the quality assessment of studies of diagnostic accuracy included in systematic reviews. BMC Med Res Methodol. 2003, 3: 25-10.1186/1471-2288-3-25.
Al-Hashimi I, Haghighat N, Fox PC: Salivary electrophoresis in the diagnosis of Sjogren’s syndrome. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 1998, 85: 542-547. 10.1016/S1079-2104(98)90288-8.
Almståhl A, Wickström M: Electrolytes in stimulated whole saliva in individuals with hyposalivation of different origins. Arch Oral Biol. 2003, 48: 337-344. 10.1016/S0003-9969(02)00200-5.
El-Miedany Y, El-Hady SM, El-Baddin MA: Validity of the Saliva Ferning Test for the Diagnosis of Dry Mouth in Sjögren’s Syndrome. Rev Rhum Engl Ed. 1999, 66: 73-78.
Håkansson U, Jacobsson L, Lilja B, Manthorpe R, Henriksson V: Salivary Gland Scintigraphy in Subjects with and without Symptoms of Dry Mouth and/or Eyes, and in Patients with primary Sjögren’s syndrome. Scand J Rheumatol. 1994, 23: 326-333. 10.3109/03009749409099282.
Hay EM, Thomas E, Pal B, Hajeer A, Chambers H, Silman AJ: Weak association between subjective symptoms of and objective testing for dry eyes and dry mouth: results from a population based study. Ann Rheum Dis. 1998, 57: 20-24. 10.1136/ard.57.1.20.
Kalk WWI, Vissink A, Spijkervet FKL, Bootsma H, Kallenberg CGM, Amerongen AVN: Sialometry and sialochemistry: diagnostic tools for Sjögren’s syndrome. Ann Rheum Dis. 2001, 60: 1110-1116. 10.1136/ard.60.12.1110.
Kalk WWI, Vissink A, Stegenga B, Bootsma H, Amerongen AVN, Kallenberg CGM: Sialometry and sialochemistry: a non-invasive approach for diagnosing Sjögren’s syndrome. Ann Rheum Dis. 2002, 61: 137-144. 10.1136/ard.61.2.137.
Kanehira T, Yamaguchi T, Takehara J, Kashiwazaki H, Abe T, Morita M, Asano K, Fujii Y, Sakamoto W: A pilot study of a simple screening technique for estimation of salivary flow. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2009, 108: 389-393. 10.1016/j.tripleo.2009.04.019.
Kohn WG, Ship JA, Atkinson JC, Patton LL, Fox PC: Salivary gland 99mTc-scintigraphy: a grading scale and correlation with major salivary gland flow rates. J oral Pathol Med. 1992, 21: 70-74. 10.1111/j.1600-0714.1992.tb00982.x.
Lee SK, Lee SW, Chung SC, Kim YK, Kho HS: Analysis of residual saliva and minor salivary gland secretions in patients with dry mouth. Arch Oral Biol. 2002, 47: 637-641. 10.1016/S0003-9969(02)00053-5.
López-Jornet P, Camacho-Alonso F, Bermejo-Fenoll A: A simple test for salivary gland hypofunction using Oral Schirmer’s test. J Oral Pathol Med. 2006, 35: 244-248. 10.1111/j.1600-0714.2006.00411.x.
Navazesh M, Christensen C, Brightman V: Clinical Criteria for the Diagnosis of Salivary Gland Hypofunction. J Dent Res. 1992, 7: 1363-1369.
Pedersen AM, Reibel J, Nauntofte B: Primary Sjögren’s syndrome (pSS): subjective symptoms and salivary findings. J Oral Pathol Med. 1999, 28: 303-311.
Pennec YL, Letoux G, Leroy JP, Youinou P: Reappraisal of tests for xerostomia. Clin Exp Rheumatol. 1993, 11: 523-528.
Sánchez-Guerrero J, Aguirre-Garcia E, Pérez-Dosal MR, Kraus A: The wafer test: a semi-quantitative test to screen for xerostomia. Rheumatology. 2002, 41: 381-389. 10.1093/rheumatology/41.4.381.
Wolff M, Kleinberg I: Oral mucosal wetness in hypo- and normosalivators. Arch Oral Biol. 1998, 43: 455-462. 10.1016/S0003-9969(98)00022-3.
Wolff A, Herscovivi D, Rosenberg M: A simple technique for determination of salivary gland hypofunction. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2002, 94: 175-178. 10.1067/moe.2002.126023.
Vitali C, Bombardieri S, Moutsopoulos HM, Balestrieri G, Bencivelli W, Bernstein RM, et al: Preliminary criteria for the classification of Sjögren’s syndrome. Results of a prospective concerted action supported by the European Community. Arthritis Rheum. 1993, 36: 340-347. 10.1002/art.1780360309.
Vitali C, Moutsopoulos HM, Bombardieri S: The European Study Group on diagnostic criteria for Sjögren’s syndrome. Sensitivity and specificity of tests for ocular and oral involvement of Sjögren’s syndrome. Ann Rheum Dis. 1994, 53: 637-647. 10.1136/ard.53.10.637.
Vitali C, Bombardieri S, Moutsopoulos HM, Coll J, Gerli L, Hatron PY, et al: Assessment of the European classification criteria for Sjögren’s syndrome in a series of clinically defined cases; results of a prospective multicentre study. The European Study Group on Diagnostic Criteria for Sjögren’s syndrome. Ann Rheum Dis. 1996, 55: 116-121. 10.1136/ard.55.2.116.
Vitali C, Bombardieri S, Moutsopoulos HM, the European Study Group on Diagnostic Criteria for Sjögren’s syndrome: The European classification criteria for Sjögren’s syndrome (SS). Proposal for a modification of the rules for classification suggested by the analysis of the receiver operating characteristic (ROC) curve of the criteria performance [abstract]. J Rheumatol. 1997, 24: 38-
Vitali C, Bombardieri S, Jonsson R, Moutsopoulos HM, Alexander EL, Carsons SE, Daniels TE, Fox PC, Fox RI, Kassan SS, Pillemer SR, Talal N, Weisman MH, the European Study Group on Diagnostic Criteria for Sjögren’s syndrome: Classification criteria for Sjögren’s syndrome: a revised version of the European criteria proposed by the American-European Consensus Group. Ann Rheum Dis. 2002, 61: 554-558. 10.1136/ard.61.6.554.
Manthorpe R, Oxholm P, Prause J, Schiødt M: The Copenhagen criteria for Sjögren’s syndrome. Scand J Rheumatol. 1986, 61: 19-21.
Fox RI, Robinson CA, Curd JG, Kozin F, Howell FV: Sjögren’s syndrome. Proposed Criteria for Classification. Arthritis Rheum. 1986, 29: 577-585. 10.1002/art.1780290501.
Whiting P, Harbord R, Kleijnen J: No role for quality scores in systematic reviews of diagnostic accuracy studies. BMC Med Res Methodol. 2005, 5: 19-10.1186/1471-2288-5-19.
Deeks JJ: Systematic reviews of evaluations of diagnostic and screening tests. In Systematic Reviews in Health Care BMJ. 2001, 323: 157-162.
Bossuyt PM, Reitsma JB, Bruns DE, Gatsonis CA, Glasziou PP, Irwing LM, Lijmer JG, Moher D, Rennie D, de Vet HC: Towards complete and accurate reporting of studies of diagnostic accuracy. Radiol. 2003, 226: 24-28. 10.1148/radiol.2261021292.
Lijmer JG, Mol BW, Heisterkamp S, Bonsel GJ, Prins MH, van der Meulen JH, Bossuyt PM: Empirical evidence of design-related bias in studies of diagnostic tests. JAMA. 1999, 282: 1061-1066. 10.1001/jama.282.11.1061.
Shiboski SC, Shiboski CH, Criswell A, Baer AN, Challacombe S, Lanfranchi H, et al: American College of Rheumatology Classification Criteria for Sjögren’s Syndrome: a Data-Driven, Expert Consensus Approach in the Sjögren’s International Collaborative Clinical Alliance Cohort. Arthritis Care Res. 2012, 64: 475-487. 10.1002/acr.21591.
Daniels TE, Criswell LA, Shiboski C, Shiboski S, Lanfranchi H, Dong Y, the Sjögren’s International Collaborative Clinical Alliance Research Groups, et al: An early view of the international Sjögren’s syndrome registry. Arthritis Rheum. 2009, 61: 711-714. 10.1002/art.24397.
Sreebny LM: Saliva in health and disease: an appraisal and update. Int Dent J. 2000, 50: 140-161. 10.1111/j.1875-595X.2000.tb00554.x.
Hu S, Wang J, Meijer J, Ieong S, Xie Y, Yu T, et al: Salivary Proteomic and Genomic Biomarkers for Primary Sjögren’s Syndrome. Arthritis Rheum. 2007, 56: 3588-3600. 10.1002/art.22954.
Wong DT: Salivary diagnostics powered by nanotechnologies, proteomics and genomics. J Am Dent Assoc. 2006, 137: 313-321.
Johnson G, Barenthin I, Westphal P: Mouthdryness among patients in longterm hospitals. Gerodontology. 1984, 3: 197-203. 10.1111/j.1741-2358.1984.tb00420.x.
van der Reijden WA, van der Kwaak H, Vissink A, Veerman ECI, Amerongen AVN: Treatment of xerostomia with polymer-based saliva substitutes in patients with Sjögren’s syndrome. Arthritis and Rheumatism. 1996, 39: 57-63. 10.1002/art.1780390108.
Kaarela K, Mutrtu O: Xerostomia in Sjögren’s syndrome treated with sali-synt. Scan J Rheumatol. 1982, 11: 39-40. 10.3109/03009748209098112.
The pre-publication history for this paper can be accessed here:http://www.biomedcentral.com/1472-6831/12/29/prepub
This study was supported by the Faculty of Odontology, Malmö University and the Swedish Dental Society.
The authors declare that they have no competing interests.
CDL and CC conceived the study. CDL, CW, MS and CC designed the study and CDL was responsible for the literature search. PTL was responsible for the search strategy. CDL, CW, MS and CC appraised the identified publications. CDL drafted the manuscript. All authors read and approved the final manuscript.