Salivary Glands and Periodontal Changes in a Population of Sjögren's and Sicca Syndrome Treated by Pilocarpine: A Pilot Study

Thibaud Depinoy, Alain Saraux, Jacques-Olivier Pers, Sylvie Boisramé, Divi Cornec, Thierry Marhadour, Dewi Guellec, Valérie Devauchelle-Pensec, Luc Bressollette, Sandrine Jousse-Joulin, Thibaud Depinoy, Alain Saraux, Jacques-Olivier Pers, Sylvie Boisramé, Divi Cornec, Thierry Marhadour, Dewi Guellec, Valérie Devauchelle-Pensec, Luc Bressollette, Sandrine Jousse-Joulin

Abstract

Introduction: Oral administration of pilocarpine enhances salivary flow in sicca patients but its effect upstream on ultrasound (US) of salivary glands (SG) and downstream on periodontium remain unknown.

Methods: Sicca patients were prospectively included. Echostructural and vascularization of SG were assessed using B mode and pulsed Doppler (USPD). Vascularization of SG was measured using resistive index (RI) before and after stimulation by lemon juice. Echostructure (measure of glandular length in cm2, evaluation of parotid and submandibular glands parenchymal abnormalities) was assessed at baseline (M0) and after 3 months (M3) of treatment with pilocarpine. A dental consultation was performed at M0 and M3 to evaluate changes in unstimulated salivary flow (USSF), stimulated salivary flow (SSF), and periodontal parameters such as modified gingival index (Lobene), plaque index (Silness), bleeding index, pocket depth, and pH.

Results: Nineteen patients were included but only 11 received pilocarpine treatment for 3 months, as six stopped pilocarpine due to side effects and two were excluded for other causes. Among the 11 patients who completed the 3-month follow-up, five had primary Sjögren's syndrome according to the American-European's classification criteria. As expected, statistical differences were found concerning SSF (p = 0.018) and USSF (p = 0.027) between M0 and M3 while no statistical change in both SG echostructure and vascularization or periodontal evaluation was shown.

Conclusions: Pilocarpine improved SSF and USSF measurements in sicca syndrome but no ultrasonography of major salivary glands (SGUS) structural and vascular changes were detected as well as periodontal evaluation.

Keywords: Pilocarpine; Salivary glands; Sjögren’s syndrome; Ultrasonography.

Figures

Fig. 1
Fig. 1
Doppler waveform analysis of arterial supply in parotid gland (Pathologic Resistive Index: 0.58). The Doppler waveform analysis shows a decrease of the systolic peak, which explains the low resistive index (IR: 0.57) result in pSS patients
Fig. 2
Fig. 2
Flowchart of the screening patients from October 2012 and November 2014

References

    1. Delli K, Spijkervet FK, Kroese FG, Bootsma H, Vissink A. Xerostomia. Monogr Oral Sci. 2014;24:109–125. doi: 10.1159/000358792.
    1. Milin M, Cornec D, Chastaing M, et al. Sicca symptoms are associated with similar fatigue, anxiety, depression, and quality-of-life impairments in patients with and without primary Sjögren’s syndrome. Joint Bone Spine. 2016;83(6):681–685. doi: 10.1016/j.jbspin.2015.10.005.
    1. Takagi Y, Sumi M, Nakamura H, Sato S, Kawakami A, Nakamura T. Salivary gland ultrasonography as a primary imaging tool for predicting efficacy of xerostomia treatment in patients with Sjögren’s syndrome. Rheumatology (Oxford) 2016;55(2):237–245. doi: 10.1093/rheumatology/kev278.
    1. Kim JW, Lee H, Park SH, Kim SK, Choe JY, Kim JK. Salivary gland ultrasonography findings are associated with clinical, histological, and serologic features of Sjögren’s syndrome. Scand J Rheumatol. 2018;7:1–8.
    1. De Vita S, Lorenzon G, Rossi G, Sabella M, Fossaluzza V. Salivary gland echography in primary and secondary Sjögren’s syndrome. Clin Exp Rheumatol. 1992;10(4):351–356.
    1. Chikui T, Yonetsu K, Izumi M, Eguchi K, Nakamura T. Abnormal blood flow to the submandibular glands of patients with Sjögren’s syndrome: doppler waveform analysis. J Rheumatol. 2000;27(5):1222–1228.
    1. Martinoli C, Derchi LE, Solbiati L, Rizzatto G, Silvestri E, Giannoni M. Color Doppler sonography of salivary glands. AJR Am J Roentgenol. 1994;163(4):933–941. doi: 10.2214/ajr.163.4.8092039.
    1. Jousse-Joulin S, Devauchelle-Pensec V, Morvan J, et al. Ultrasound assessment of salivary glands in patients with primary Sjögren’s syndrome treated with rituximab: quantitative and Doppler waveform analysis. Biologics. 2007;1(3):311–319.
    1. Saraux A, Pers JO, Devauchelle-Pensec V. Treatment of primary Sjögren syndrome. Nat Rev Rheumatol. 2016;12(8):456–471. doi: 10.1038/nrrheum.2016.100.
    1. Vivino FB, Al-Hashimi I, Khan Z, et al. Pilocarpine tablets for the treatment of dry mouth and dry eye symptoms in patients with Sjögren syndrome: a randomized, placebo-controlled, fixed-dose, multicenter trial. P92–01 study group. Arch Intern Med. 1999;159(2):174–181. doi: 10.1001/archinte.159.2.174.
    1. Wu CH, Hsieh SC, Lee KL, Li KJ, Lu MC, Yu CL. Pilocarpine hydrochloride for the treatment of xerostomia in patients with Sjögren’s syndrome in Taiwan–a double-blind placebo-controlled trial. J Formos Med Assoc. 2006;105(10):796–803. doi: 10.1016/S0929-6646(09)60266-7.
    1. Nakamura N, Sasano N, Yamashita H, et al. Oral pilocarpine (5mg t.i.d) used for xerostomia causes adverse effects in Japanese. Auris Nasus Larynx. 2009;36(3):310–313. doi: 10.1016/j.anl.2008.04.008.
    1. Berk L. Systemic pilocarpine for treatment of xerostomia. Expert Opin Drug Metab Toxicol. 2008;4(10):1333–1340. doi: 10.1517/17425255.4.10.1333.
    1. Tanigawa T, Yamashita J, Sato T, et al. Efficacy and safety of pilocarpine mouthwash in elderly patients with xerostomia. Spec Care Dentist. 2015;35(4):164–169. doi: 10.1111/scd.12105.
    1. Cifuentes M, Del Barrio-Díaz P, et Vera-Kellet C. Pilocarpine and artificial saliva for the treatment of xerostomia and xerophthalmia of Sjögren’s syndrome: a double-blind control trial. Br J Dermatol. 2018.
    1. Carotti M, Salaffi F, Manganelli P, Argalia G. Ultrasonography and colour Doppler sonography of salivary glands in primary Sjögren’s syndrome. Clin Rheumatol. 2001;20(3):213–219. doi: 10.1007/s100670170068.
    1. Cornec D, Jousse-Joulin S, Pers JO, et al. Contribution of salivary gland ultrasonography to the diagnosis of Sjögren’s syndrome: toward new diagnostic criteria? Arthritis Rheum. 2013;65(1):216–225. doi: 10.1002/art.37698.
    1. Jousse-Joulin S, D'Agostino MA, Nicolas C, et al. Video clip assessment of a salivary gland ultrasound scoring system in Sjögren’s syndrome using consensual definitions: an OMERACT ultrasound working group reliability exercise. Ann Rheum Dis. 2019;78(7):967–973. doi: 10.1136/annrheumdis-2019-215024.
    1. Ramfjord SP. The periodontal disease index (PDI) J Periodontol. 1967;38(Suppl):602–610. doi: 10.1902/jop.1967.38.6.602.
    1. Pers JO, Saraux A, Pierre R, Youinou P. Anti-TNF-alpha immunotherapy is associated with increased gingival inflammation without clinical attachment loss in subjects with rheumatoid arthritis. J Periodontol. 2008;79(9):1645–1651. doi: 10.1902/jop.2008.070616.
    1. Silness J, Loe H. Periodontal disease in pregnancy. Ii. Correlation between oral hygiene and periodontal condition. Acta Odontol Scand. 1964;22:121–135. doi: 10.3109/00016356408993968.
    1. Lobene RR, Weatherford T, Ross NM, Lamm RA, Menaker L. A modified gingival index for use in clinical trials. Clin Prev Dent. 1986;8(1):3–6.
    1. Le Gall M, Cornec D, Pers JO, et al. A prospective evaluation of dental and periodontal status in patients with suspected Sjögren’s syndrome. Joint Bone Spine. 2016;83(2):235–236. doi: 10.1016/j.jbspin.2015.02.015.
    1. Le Goff M, Cornec D, Jousse-Joulin S, et al. Comparison of 2002 AECG and 2016 ACR/EULAR classification criteria and added value of salivary gland ultrasonography in a patient cohort with suspected primary Sjögren’s syndrome. Arthritis Res Ther. 2017;19(1):269. doi: 10.1186/s13075-017-1475-x.
    1. Fisher BA, Everett CC, Rout J, et al. Effect of rituximab on a salivary gland ultrasound score in primary Sjögren’s syndrome: results of the TRACTISS randomised double-blind multicentre substudy. Ann Rheum Dis. 2018;77(3):412–416. doi: 10.1136/annrheumdis-2017-212268.
    1. Luciano N, Baldini C, Tarantini G, et al. Ultrasonography of major salivary glands: a highly specific tool for distinguishing primary Sjögren’s syndrome from undifferentiated connective tissue diseases. Rheumatology (Oxford) 2015;54(12):2198–2204.
    1. Carotti M, Ciapetti A, Jousse-Joulin S, Salaffi F. Ultrasonography of the salivary glands: the role of grey-scale and colour/power Doppler. Clin Exp Rheumatol. 2014;32(1 Suppl 80):S61–70.
    1. Hendrickson RG, Morocco AP, Greenberg MI. Pilocarpine toxicity and the treatment of xerostomia. J Emerg Med. 2004;26(4):429–432. doi: 10.1016/j.jemermed.2003.09.013.
    1. Zimmerman TJ, Wheeler TM. Miotics: side effects and ways to avoid them. Ophthalmology. 1982;89(1):76–80. doi: 10.1016/S0161-6420(82)34866-6.
    1. Noaiseh G, Baker JF, Vivino FB. Comparison of the discontinuation rates and side-effect profiles of pilocarpine and cevimeline for xerostomia in primary Sjögren’s syndrome. Clin Exp Rheumatol. 2014;32(4):575–577.
    1. Brimhall J, Jhaveri MA, Yepes JF. Efficacy of cevimeline vs. pilocarpine in the secretion of saliva: a pilot study. Spec Care Dentist. 2013;33(3):123–127. doi: 10.1111/scd.12010.
    1. Bernardi R, Perin C, Becker FL, et al. Effect of pilocarpine mouthwash on salivary flow. Braz J Med Biol Res. 2002;35(1):105–110. doi: 10.1590/S0100-879X2002000100015.
    1. Christensen LB, Petersen PE, Torn JJ, Schiodt M. Dental caries and dental health behavior of patients with primary Sjögren syndrome. Acta Odontol Scand. 2001;59(3):116–120. doi: 10.1080/000163501750266684.
    1. Pijpe J, Kalk WW, Bootsma H, Spijkervet FK, Kallenberg CG, Vissink A. Progression of salivary gland dysfunction in patients with Sjögren’s syndrome. Ann Rheum Dis. 2007;66(1):107–112. doi: 10.1136/ard.2006.052647.

Source: PubMed

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