» Articles » PMID: 25652148

Post-allogeneic Hematopoietic Stem Cell Transplantation (HSCT) Changes in Inorganic Salivary Components

Overview
Specialties Critical Care
Oncology
Date 2015 Feb 6
PMID 25652148
Citations 9
Authors
Affiliations
Soon will be listed here.
Abstract

Recent studies have considered the qualitative and quantitative assessment of salivary flow, as well the biochemical components of saliva, as possible biomarkers that might contribute to the pathogenesis of chronic graft-versus-host disease (cGHVD) in hematopoietic stem cell transplantation (HSCT) patients. The aim of this study was to evaluate prospectively the inorganic salivary status at different periods of allogeneic HSCT. Saliva collection and oral examination were performed prior to the HSCT, ​between days 8 and 10, days 80 and 100, and at the cGVHD onset. Concentrations of calcium (Ca), phosphate (Pi), chloride (Cl), magnesium (Mg), potassium (K), and sodium (Na) were performed using colorimetric reactions and atomic absorption. Fifty-five consecutive patients undergoing first allogeneic HSCT were included in this study. Between days 8 and 10, the salivary flow rate was significantly higher (p = 0.05), Pi concentration was decreased (p = 0.007), and Na and Cl were increased (p = 0.001 and p = 0.001, respectively), compared with the baseline. Salivary flow rate during the same period showed a negative correlation with Pi concentration (p = 0.02) and a positive correlation with Na and Cl concentrations (p = 0.003 and p = 0.001, respectively). The salivary flow rate was decreased between days 80 and 100 (p = 0.02) and Na, Cl, and K concentrations were increased (p = 0.03, p = 0.02, and p = 0.003, respectively). Salivary flow rate showed a negative correlation with Na and Cl (p = 0.01 and p = 0.013, respectively). At cGVHD onset, the salivary flow rate showed no statistical difference compared with the other studied periods. A trend was observed in the higher Na concentration compared with the baseline (p = 0.06) and Pi concentration presented a significant decrease (p = 0.004). Ca and Mg concentrations showed no changes during all evaluation periods. The present study showed changes in inorganic salivary components in post-HSCT periods, mainly during the early period post-HSCT and at the cGVHD onset. We speculate that Na, Cl, and Pi in saliva could be used as a potential biomarker in further studies.

Citing Articles

Salivary flow rate, subjective oral dryness and dental caries 5 years after haematopoietic cell transplantation.

Bulthuis M, van Gennip L, Thomas R, van Leeuwen S, Bronkhorst E, Laheij A BMC Oral Health. 2024; 24(1):1058.

PMID: 39256697 PMC: 11389434. DOI: 10.1186/s12903-024-04804-7.


Assessment of the Salivary Concentrations of Selected Immunological Components in Adult Patients in the Late Period after Allogeneic Hematopoietic Stem Cell Transplantation-A Translational Study.

Brodzikowska A, Kochanska B, Boguslawska-Kapala A, Struzycka I, Gorski B, Miskiewicz A Int J Mol Sci. 2024; 25(3).

PMID: 38338734 PMC: 10855433. DOI: 10.3390/ijms25031457.


The effect of conditioning regimen and prescribed medications on hyposalivation in haematopoietic cell transplantation (HCT) patients: an 18-month prospective longitudinal study.

Bulthuis M, van Gennip L, Thomas R, Bronkhorst E, Laheij A, Raber-Durlacher J Clin Oral Investig. 2023; 27(12):7369-7381.

PMID: 37853264 PMC: 10713764. DOI: 10.1007/s00784-023-05327-1.


Perspectives on oral chronic graft-versus-host disease from immunobiology to morbid diagnoses.

Tollemar V, Legert K, Sugars R Front Immunol. 2023; 14:1151493.

PMID: 37449200 PMC: 10338056. DOI: 10.3389/fimmu.2023.1151493.


Dental consensus on HSCT - Part II: dental Care during HSCT.

Gobbi M, Ferreira M, de Carvalho D, Silva G, Macari K, Neves L Hematol Transfus Cell Ther. 2023; 45(3):368-378.

PMID: 37321878 PMC: 10499574. DOI: 10.1016/j.htct.2023.04.003.


References
1.
Horn T, Rest E, Mirenski Y, Corio R, Zahurak M, Vogelsang G . The significance of oral mucosal and salivary gland pathology after allogeneic bone marrow transplantation. Arch Dermatol. 1995; 131(8):964-5. DOI: 10.1001/archderm.131.8.964. View

2.
Yamagata K, Arai C, Sasaki H, Takeuchi Y, Onizawa K, Yanagawa T . The effect of oral management on the severity of oral mucositis during hematopoietic SCT. Bone Marrow Transplant. 2011; 47(5):725-30. DOI: 10.1038/bmt.2011.171. View

3.
Izutsu K, Sullivan K, Schubert M, Truelove E, Shulman H, Sale G . Disordered salivary immunoglobulin secretion and sodium transport in human chronic graft-versus-host disease. Transplantation. 1983; 35(5):441-6. DOI: 10.1097/00007890-198305000-00010. View

4.
Imanguli M, Pavletic S, Guadagnini J, Brahim J, Atkinson J . Chronic graft versus host disease of oral mucosa: review of available therapies. Oral Surg Oral Med Oral Pathol Oral Radiol Endod. 2006; 101(2):175-83. DOI: 10.1016/j.tripleo.2005.08.028. View

5.
Sonis S, Oster G, Fuchs H, Bellm L, BRADFORD W, Edelsberg J . Oral mucositis and the clinical and economic outcomes of hematopoietic stem-cell transplantation. J Clin Oncol. 2001; 19(8):2201-5. DOI: 10.1200/JCO.2001.19.8.2201. View