Science Policy

Position and Policy Statement on Salivary Biology and Diagnostics

Published on: April 3, 2026

IADR Position and Policy Statement on Salivary Biology and Diagnostics

N. Damé Teixeira, D. Heller, R. Giacaman Sarah, M.L. Laine, A.M. Lynge Pederson, and A. Squassi, M. Charles-Ayinde, and C. Fox.

 

Position Statement on Salivary Biology and Diagnostics 

The International Association for Dental, Oral, and Craniofacial Research (IADR) recognizes saliva as an essential biological fluid in both oral and systemic health and its fundamental role in maintaining key physiological functions within the oral cavity. IADR also supports the use of saliva for diagnostics, health and disease status monitoring, and evaluating therapeutic outcomes. Despite extensive evidence of its importance, salivary biology and diagnostics remain underutilized in clinical dentistry, underrepresented in translational research, and insufficiently integrated into public health frameworks1. Moreover, alterations in salivary quantity and/or quality (salivary gland dysfunction) significantly increase the risk of oral diseases, and contribute to compromised nutrition and quality of life2,3,4. Yet, there is no consensus on reliable standardized clinical tests for assessing salivary gland function, neither efficient evidence-based treatments. This policy statement calls for routine evaluation of salivary function in daily clinical practice and for the development and validation of practical tools that enable early detection of salivary alterations and support timely preventive or therapeutic interventions. It is intended primarily as a resource for clinicians and researchers and will also inform industry stakeholders and policymakers - ultimately benefiting patients. 

The functions of saliva and the impact of salivary gland dysfunction on oral health 

Saliva forms a protective and immunological barrier over the oral mucosa and teeth, shielding tissues from environmental insults, aiding wound healing, providing the first line of defense against pathogens, and preserving tissue integrity5-8. Xerostomia is the subjective sensation of dry mouth, and this symptom is often associated with salivary gland dysfunction however it can also be present in patients with normal salivary flow rates9. Hyposalivation is a term based on objective measures of the salivary flow rates, where the flow rates are significantly lower than the generally accepted normal reference values10,11Both the quantity (flow) of saliva and its composition (quality) play an important role in preventing dental caries12, oral infections13, and erosive tooth wear14, while also supporting essential functions such as lubrication, protection of hard and soft tissues, clearance, pH buffering, initiation of digestion, and facilitation of swallowing speech, and taste3. Saliva regulates oral microbiome and biofilm formation15-21 as well as promoting enamel remineralization22. Salivary quantity and quality also influence the longevity of dental restorations. Thus, in patients with hyposalivation of different etiologies, the survival time of dental fillings is significantly lower than in patients without xerostomia and normal salivary gland function23.

The prevalence of hyposalivation and xerostomia is increasing24-26 particularly among individuals affected by multiple diseases, polypharmacy and certain medications27,28. Medication-induced salivary gland dysfunction and xerostomia, associated with several drug categories, affects up to 30% of patients taking at least one medication28. Emerging evidence also links impaired salivary function to consumption of conventional cigarettes and e-cigarettes29, recreational drug use30,31, and a broader range of commonly prescribed and over-the-counter medications than previously recognized32. Lifestyle factors further contribute to salivary gland dysfunction across all age groups. Despite its growing prevalence, the condition is often underdiagnosed and undertreated, particularly among older adults and patients with chronic diseases24,33. Left unaddressed, salivary gland dysfunction undermines quality of life and increases the risk of oral diseases and preventable complications. 

To recognize and manage salivary gland dysfunction, early detection is essential32. This underscores the need for diagnostic tools that can identify risks at an initial stage and guide preventive care. Validated testing of xerostomia and salivary gland function offers significant potential to pinpoint high-risk patients, support personalized prevention, and enable truly individualized treatment34 Furthermore, incorporating assessment into the first dental appointment for all patients would allow clinicians to establish a personalized baseline before xerostomia and salivary gland dysfunction appear35,36. Such baseline testing enables the early detection of subtle declines in salivary gland function and facilitates more accurate and reliable monitoring of salivary flow rates over time. It also allows for salivary gland dysfunction to be diagnosed against personalized parameters, rather than relying solely on broad and heterogeneous reference values37. Furthermore, there is an urgent need to develop standardized and comparable measurements of salivary and glandular function across populations, communities, and countries. Research initiatives should be promoted to generate harmonized datasets that incorporate age, systemic health conditions, and diverse national and ethnic backgrounds. Such globally comparable data are essential to strengthen epidemiological surveillance, improve diagnostic accuracy, and inform public health policies related to salivary gland dysfunction and oral health.

In clinical practice, care for patients with xerostomia and salivary gland dysfunction is typically limited to those in advanced stages of disease, such as patients with Sjögren’s disease or patients with radiotherapy-associated hyposalivation38,39. However, little is known about the problems that may arise from more subtle reductions in saliva quantity, and quality. Implementing analysis of saliva quantity and quality into clinical practice will support a more integrated, preventive care model - offering significant benefits for patients' oral and overall health and quality of life. This approach is also aligned with public health priorities and the evolving landscape of dental care delivery.

Saliva as a versatile biological fluid 

Saliva is often described as the “mirror of the body”, frequently serving as an early warning sign of systemic disease or change in physical condition40. It has emerged as a promising diagnostic tool, offering insights into disease detection, progression, and prognosis and monitoring results of therapeutic interventions41 Thus, saliva provides a window into both oral and systemic health, due to its diverse components, including nucleic acids (DNA, mRNA, microRNA), epigenetics, proteins, metabolites, and a complex microbial community42-48. Beyond its biological complexity, saliva offers practical advantages: collection is simple, non-invasive, and inexpensive49. These characteristics make it an attractive tool for biomedical research, precision medicine, and routine health monitoring, with the capacity to deliver disease-specific biomarkers that support tailored diagnostic and therapeutic approaches.

Beyond its application in dentistry, saliva has proven diagnostic capabilities for diagnosing systemic and infectious diseases, including those caused by SARS-CoV-241,50,HIV51, immunoinflammatory responses8,52, and certain cancers53,54. Its utility during the COVID-19 pandemic demonstrated the scalability of salivary diagnostics55, reinforcing the need for stronger translational research and clinical integration. Despite this, stakeholder engagement and investment in salivary research remain limited, and there is currently no global policy guidance on its application.

Policy Statement

The IADR recognizes that advancing salivary biology and diagnostics should be aligned with global health priorities, particularly in promoting prevention and personalization of care. IADR therefore recommends:

  • Recognizing salivary gland dysfunction and xerostomia as a public health concern and priority with implications for quality of life, oral and systemic health;
  • Promoting the routine integration of evidence-based diagnosis and management of salivary gland dysfunction and xerostomia into oral care and advocate for their inclusion across public and private health systems through appropriate incentives, reimbursement mechanisms, and policy frameworks that ensure access, implementation, and sustainability.
  • Strengthening the education and awareness of oral healthcare professionals and patients in salivary biology, as well as the diagnosis and therapeutic approaches of salivary gland dysfunction and xerostomia;
  • Developing and validating clinical trials and evidence-based clinical guidelines to standardize protocols for the assessment of salivary gland function and to define effective, standardized therapeutic approaches for glandular and salivary gland functional disorders;
  • Promoting interdisciplinary collaboration among academia, clinicians, patients, policymakers, and industry stakeholders to accelerate translational salivary gland research and implementation of valid salivary tests and treatment for dysfunctions.
     

IADR calls for coordinated global efforts to advance clinically relevant studies that address the significant impact of salivary gland dysfunction and xerostomia on quality of life and oral health, and efficient treatments for that. In parallel, it emphasizes the need for research that bridges basic scientific discoveries of systemic disease biomarkers toward their translation into clinical practice, ensuring that salivary diagnostics evolve into cost-effective and practical tools that can be widely applied.

Adopted 2026

References

  1. Fisic A, Aras HC, Almhöjd U, Almståhl A. (2024). Dental care professionals' awareness of oral dryness and its clinical management: a questionnaire-based study. BMC Oral Health. 24(1):45. 

  2. Aliko A, Wolff A, Dawes C, Aframian D, Proctor G, Ekström J, Narayana N, Villa A, Sia YW, Joshi RK, McGowan R, Beier Jensen S, Kerr AR, Lynge Pedersen AM, Vissink A. (2015). World Workshop on Oral Medicine VI: clinical implications of medication-induced salivary gland dysfunction. Oral Surg Oral Med Oral Pathol Oral Radiol. 120(2):185-206.  

  3. Pedersen AML Sorensen CE, Proctor GB, and Carpenter GH. (2018). Salivary functions in mastication, taste and textural perception, swallowing and initial digestion. Oral Dis. 24(8): 1399-1416. 

  4. Alves LSM, Munduri JM, Lacerda I, Reis LG, da Silva JR, Stefani CM, Guimarães MDCM, Alves LS, Baraldi S, Dame-Teixeira N. (2025). Macronutrient consumption in adults and association with oral and systemic parameters: A cross-sectional study. Arch Oral Biol. 174:106241.

  5. Tabak LA, Levine MJ, Mandel ID, Ellison SA. (1982). Role of salivary mucins in the protection of the oral cavity. J Oral Pathol. 11(1):1-17.  

  6. Okuyama K, Yanamoto S. (2024). Saliva in balancing oral and systemic health, oral cancer, and beyond: A narrative review. Cancers (Basel). 16(24):4276. 

  7. Rodrigues Neves C, Buskermolen J, Roffel S, Waaijman T, Thon M, Veerman E, Gibbs S. (2019). Human saliva stimulates skin and oral wound healing in vitro. J Tissue Eng Regen Med. 13(6):1079-1092. 

  8. Matsuoka M, Soria SA, Pires JR, Campos Passanezi Sant’Ana, Freire M. (2025). Natural and induced immune responses in oral cavity and saliva. BMC Immunol 26(34): doi.org/10.1186/s12865-025-00713-8. 

  9. Fox PC, Busch KA, Baum BJ. (1987). Subjective reports of xerostomia and objective measures of salivary gland performance. J Am Dent Assoc. 115(4):581.

  10. Sreebny LM. (2000). Saliva in health and disease: an appraisal and update. Int Dent J. 50(3):140-61.  

  11. Villa A, Wolff A, Aframian D, Vissink A, Ekström J, Proctor G, McGowan R, Narayana N, Aliko A, Sia YW, Joshi RK, Jensen SB, Kerr AR, Dawes C, Pedersen AM. (2015). World Workshop on Oral Medicine VI: a systematic review of medication-induced salivary gland dysfunction: prevalence, diagnosis, and treatment. Clin Oral Investig. 19(7):1563-80. 

  12. Pedersen AML. (2024). The essential role of saliva for dental caries and erosion. Chapter 7. In: Dental Caries. The disease and its clinical management. 4th Edition, Ole Fejerskov (Editor), Bente Nyvad (Editor), ISBN: 978-1-119-67941-7, Wiley-Blackwell.

  13. Vila T, Rizk AM, Sultan AS, Jabra-Rizk MA. (2019). The power of saliva: Antimicrobial and beyond. PLoS Pathog. 15(11):e1008058. 

  14. Buzalaf MA, Hannas AR, Kato MT. (2012). Saliva and dental erosion. J Appl Oral Sci. 20(5):493-502. 

  15. Marsh PD, Do T, Beighton D, Devine DA. (2016). Influence of saliva on the oral microbiota. Periodontol 2000. 70(1):80-92. 

  16. Lynge Pedersen AM, Belstrøm D. (2019) The role of natural salivary defences in maintaining a healthy oral microbiota. J Dent. 80 (1):S3-S12. 

  17. Hannig M, Balz M. (2001). Protective properties of salivary pellicles from two different intraoral sites on enamel erosion. Caries Res. 35(2):142-148.

  18. Hannig M, Joiner A. (2006). The structure, function and properties of the acquired pellicle. Monographs in Oral Sci. 19:29-64.

  19. Gibbons RJ, Hay DI. (1988). Human salivary acidic proline-rich proteins and statherin promote the attachment of Actinomyces viscosus LY7 to apatitic surfaces. Inf and Imm. 56(2):439-445.

  20. Scannapieco FA. (1994). Saliva-bacterium interactions in oral microbial ecology. Crit Rev Oral Biol Med. 5(3-4):203-48. 

  21. Siqueira WL, Zhang W, Helmerhorst EJ, Gygi SP, Oppenheim FG. (2007). Identification of protein components in in vivo human acquired enamel pellicle using LC-ESI-MS/MS. J Proteome Res. 6(6):2152-2160.

  22. Enax J, Fandrich P, Schulze Zur Wiesche E, Epple M. (2024). The remineralization of enamel from saliva: A chemical perspective. Dent J (Basel). 12(11):339. 

  23. Leinonen J, Vähänikkilä H, Raninen E, Järvelin L, Näpänkangas R, Anttonen V. (2021). The survival time of restorations is shortened in patients with dry mouth. J Dent. 113:103794. 

  24. Agostini BA, Cericato GO, Silveira ERD, Nascimento GG, Costa FDS, Thomson WM, Demarco FF. (2018). How common is dry mouth? systematic review and meta-regression analysis of prevalence estimates. Braz Dent J. 29(6):606-618. 

  25. Pina GMS, Mota Carvalho R, Silva BSF, Almeida FT. (2020). Prevalence of hyposalivation in older people: A systematic review and meta-analysis. Gerodontology. 37(4):317-331.  

  26. Huang S, Zeng X, Deng S, He S, Liu F. (2025). Prevalence of xerostomia in patients with type 2 diabetes mellitus: a systematic review and meta-analysis. BMC Oral Health. 25(1):662. 

  27. Smidt D, Torpet LA, Nauntofte B, Heegaard KM, Pedersen AML. (2010). Associations between labial and whole salivary flow rates, systemic diseases and medications in a sample of elderly people. Community Dent Oral Epidemiol. 38 (5):422-435.  

  28. Thomson WM, Smith MB, Ferguson CA, Moses G. (2021). the challenge of medication-induced dry mouth in residential aged care. Pharmacy (Basel). 9(4):162. 

  29. Carvalho BFDC, Faria NC, Silva KCS, Greenfield E, Alves MGO, Dias M, Mendes MA, Pérez-Sayáns M, Almeida JD. (2024). salivary metabolic pathway alterations in brazilian e-cigarette users. Int J Mol Sci. 25(21):11750.  

  30. Titsas A, Ferguson MM. (2002). Impact of opioid use on dentistry. Aust Dent J. 47(2):94-8. 

  31. Esposito, M. M., Kalinowski, J., & Mikhaeil, M. (2024). The effects of recreational and pharmaceutical substance use on oral microbiomes and health. Bacteria, 3(3), 209-222.

  32. Wolff A, Joshi RK, Ekström J, Aframian D, Pedersen AM, Proctor G, Narayana N, Villa A, Sia YW, Aliko A, McGowan R, Kerr AR, Jensen SB, Vissink A, Dawes C. (2017). A guide to medications inducing salivary gland dysfunction, xerostomia, and subjective sialorrhea: A systematic review sponsored by the World Workshop on oral medicine VI. Drugs R D. 17(1):1-28. 

  33. Rughwani V, Miao Jonasson J, Marklund B, Mossberg K, Almståhl A, Lynge Pedersen AM, Cevik-Aras H. (2025). Xerostomia in primary care: a register-based study of prevalence, medication categories, and associated risk factors. Front Oral Health. 6:1684568. 

  34. Lofgren CD, Wickstrom C, Sonesson M, Lagunas PT, Christersson C. (2012). A systematic review of methods to diagnose oral dryness and salivary gland function. BMC Oral Health. 12:29.

  35. Villa A, Wolff A, Dawes C, Aframian D, Ekström J, Proctor G, McGowan R, Aliko A, Narayana, N, Sia YW, Joshi RK, Jensen SB, Kerr AR, Vissink A, Pedersen AML. (2015). Diagnosis, treatment and prevention of medication-induced salivary gland dysfunction (MISGD): A systematic review. Clin Oral Investig. 19(7):1563-1580. 

  36. Dawes, C. and D.T.W. Wong. (2019). Role of saliva and salivary diagnostics in the advancement of oral health. J Dent Res. 98(2): 133-141.

  37. da Silva JR, Marques RCR, Nunes FPS, Lima AA, Heller D, Stefani CM, Dame-Teixeira N. (2025). What is the normal salivary flow rate in healthy adults? A systematic review with meta-analyses. JDR Clinical & Translational Research. 0(0). 

  38. Wang B, Chen S, Zheng Q, Li Y, Zhang X, Xuan J, Liu Y, Shi G. (2021). Early diagnosis and treatment for Sjögren's syndrome: current challenges, redefined disease stages and future prospects. J Autoimmun. 117:102590.

  39. Hosseini MS, Sanaie S, Mahmoodpoor A, Jabbari Beyrami S, Jabbari Beyrami H, Fattahi S, Jahanshahlou F, Zarei M, Rahimi Mamaghani A, Kuchaki Rafsanjani M. (2024). Cancer treatment-related xerostomia: basics, therapeutics, and future perspectives. Eur J Med Res. 29(1):571. 

  40. Wong D.T. (2006). Towards a simple, saliva-based test for the detection of oral cancer. Expert Rev Mol. Diagn. 6:267–272. 

  41. Fernandes LL, Pacheco VB, Borges L, Athwal HK, de Paula Eduardo F, Bezinelli L, Correa L, Jimenez M, Dame-Teixeira N, Lombaert IMA, Heller D. (2020). saliva in the diagnosis of COVID-19: A review and new research directions. J Dent Res. 99(13):1435-1443. 

  42. Sembler-Møller ML, Belstrøm D, Locht H, Pedersen AML. (2020). Proteomics of saliva, plasma, and salivary gland tissue in Sjögren’s syndrome and non-Sjögren patients identify novel biomarker candidates. J Proteomics. 225:103877.

  43. Liaw A, Liu C, Bartold M, Ivanovski S, Han P. (2024). Effect of non-surgical periodontal therapy on salivary histone deacetylases expression: A prospective clinical study. J Clin Periodontol. 51(7):926-935. 

  44. Han P, Jiao K, Bartold PM, Liaw A, Wei W, Ivanovski S. (2025). Association between salivary circular rnas expression and periodontal disease status. J Periodontal Res. doi: 10.1111/jre.70004. Epub ahead of print. 

  45. Han P, Bartold PM, Salomon C, Ivanovski S. (2021). Salivary outer membrane vesicles and dna methylation of small extracellular vesicles as biomarkers for periodontal status: A pilot study. Int J Mol Sci. 22(5):2423. 

  46. Helmerhorst EJ, Oppenheim FG. (2007). Saliva: a dynamic proteome. J Dent Res. 86(8):680-693.

  47. Levine MJ. (1993). Salivary macromolecules. A structure/function synopsis. Annals of the New York Academy of Sciences. 694(11-16.

  48. Ruhl S. (2012). The scientific exploration of saliva in the post-proteomic era: from database back to basic function. Expert Rev Proteo. 9(1):85-96.

  49. Li Y, Ou Y, Fan K, Liu G. (2024). Salivary diagnostics: opportunities and challenges. Theranostics. 14(18):6969-6990. 

  50. Wang Y, Upadhyay A, Pillai S, Khayambashi P, Tran SD. (2022). Saliva as a diagnostic specimen for SARS-CoV-2 detection: A scoping review. Oral Dis. 28 Suppl 2:2362-2390.

  51. Pant Pai N, Balram B, Shivkumar S, Martinez-Cajas JL, Claessens C, Lambert G, Peeling RW, Joseph L. (2012). Head-to-head comparison of accuracy of a rapid point-of-care HIV test with oral versus whole-blood specimens: a systematic review and meta-analysis. Lancet Infect Dis. 12(5):373-80. 

  52. Costalonga M, Herzberg MC. (2014). The oral microbiome and the immunobiology of periodontal disease and caries. Immunol Lett. 162(2 Pt A):22-38.

  53. Banavar G, Ogundijo O, Toma R, Rajagopal S, Lim YK, Tang K, Camacho F, Torres PJ, Gline S, Parks M, Kenny L, Perlina A, Tily H, Dimitrova N, Amar S, Vuyisich M, Punyadeera C. (2021). The salivary metatranscriptome as an accurate diagnostic indicator of oral cancer. NPJ Genom Med. 6(1):105.

  54. Choi I, Yoshida N, Swarup N, Wong DTW. (2025). Saliva liquid biopsy for detection of early-stage lesions. Expert Rev Mol Diagn. 8:1-6.

  55. Vogels CBF, Watkins AE, Harden CA, Brackney DE, Shafer J, Wang J, Caraballo C, Kalinich CC, Ott IM, Fauver JR, Kudo E, Lu P, Venkataraman A, Tokuyama M, Moore AJ, Muenker MC, Casanovas-Massana A, Fournier J, Bermejo S, Campbell M, Datta R, Nelson A; Yale IMPACT Research Team; Dela Cruz CS, Ko AI, Iwasaki A, Krumholz HM, Matheus JD, Hui P, Liu C, Farhadian SF, Sikka R, Wyllie AL, Grubaugh ND. (2021). SalivaDirect: A simplified and flexible platform to enhance SARS-CoV-2 testing capacity. Med. 2(3):263-280.e6.