Periradicular tissue fluid-derived biomarkers for apical periodontitis: An in vitro methodological and in vivo cross-sectional study.

absorbance apical periodontitis biomarkers elution inflammation periradicular tissue fluid

Journal

International endodontic journal
ISSN: 1365-2591
Titre abrégé: Int Endod J
Pays: England
ID NLM: 8004996

Informations de publication

Date de publication:
Oct 2023
Historique:
revised: 04 07 2023
received: 15 03 2023
accepted: 14 07 2023
medline: 12 9 2023
pubmed: 19 7 2023
entrez: 19 7 2023
Statut: ppublish

Résumé

Periradicular tissue fluid (PTF) offers a source of diagnostic, prognostic and predictive biomarkers for endodontic disease. (1) To optimize basic parameters for PTF paper point sampling in vitro for subsequent in vivo application. (2) To compare proteomes of PTF from teeth with normal apical tissues (NAT) and asymptomatic apical periodontitis (AAP) using high-throughput panels. (1) To assess volume absorbance, paper points (n = 20) of multiple brands, sizes and sampling durations were inserted into PBS/1%BSA at several depths. Wetted lengths (mm) were measured against standard curves to determine volume absorbance (μL). To assess analyte recovery, paper points (n = 6) loaded with 2 μL recombinant IL-1β (15.6 ng/mL) were eluted into 250 μL: (i) PBS; (ii) PBS/1% BSA; (iii) PBS/0.1% Tween20; (iv) PBS/0.25 M NaCl. These then underwent: (i) vortexing; (ii) vortexing/centrifugation; (iii) centrifugation; (iv) incubation/vortexing/centrifugation. Sandwich-ELISAs determined analyte recovery (%) against positive controls. (2) Using optimized protocols, PTF was retrieved from permanent teeth with NAT or AAP after accessing root canals. Samples, normalized to total fluid volume (TFV), were analysed to determine proteomic profiles (pg/TFV) of NAT and AAP via O-link Target-48 panel. Correlations between AAP and diagnostic accuracy were explored using principal-component analysis (PCA) and area under receive-operating-characteristic curves (AUC [95% CI]), respectively. Statistical comparisons were made using Mann-Whitney U, anova and post hoc Bonferonni tests (α < .01). (1) UnoDent's 'Classic' points facilitated maximum volume absorbance (p < .05), with no significant differences after 60 s (1.6 μL [1.30-1.73]), 1 mm depth and up to 40/0.02 (2.2 μL [1.98-2.20]). For elution, vortexing (89.3%) and PBS/1% BSA (86.9%) yielded the largest IL-1β recovery (p < .05). (2) 41 (NAT: 13; AAP: 31) PTF samples proceeded to analysis. The panel detected 18 analytes (CCL-2, -3, -4; CSF-1; CXCL-8, -9; HGF; IL-1β, -6, -17A, -18; MMP-1, -12; OLR-1; OSM; TNFSF-10, -12; VEGF-A) in ≥75% of AAP samples at statistically higher concentrations (p < .01). CXCL-8, IL-1β, OLR-1, OSM and TNFSF-12 were strongly correlated to AAP. 'Excellent' diagnostic performance was observed for TNFSF-12 (AUC: 0.94 [95% CI: 0.86-1.00]) and the PCA-derived cluster (AUC: 0.96 [95% CI: 0.89-1.00]). Optimized PTF sampling parameters were identified in this study. When applied clinically, high-throughput proteomic analyses revealed complex interconnected networks of potential biomarkers. TNFSF-12 discriminated periradicular disease from health the greatest; however, clustering analytes further improved diagnostic accuracy. Additional independent investigations are required to validate these findings.

Sections du résumé

BACKGROUND BACKGROUND
Periradicular tissue fluid (PTF) offers a source of diagnostic, prognostic and predictive biomarkers for endodontic disease.
AIMS OBJECTIVE
(1) To optimize basic parameters for PTF paper point sampling in vitro for subsequent in vivo application. (2) To compare proteomes of PTF from teeth with normal apical tissues (NAT) and asymptomatic apical periodontitis (AAP) using high-throughput panels.
METHODOLOGY METHODS
(1) To assess volume absorbance, paper points (n = 20) of multiple brands, sizes and sampling durations were inserted into PBS/1%BSA at several depths. Wetted lengths (mm) were measured against standard curves to determine volume absorbance (μL). To assess analyte recovery, paper points (n = 6) loaded with 2 μL recombinant IL-1β (15.6 ng/mL) were eluted into 250 μL: (i) PBS; (ii) PBS/1% BSA; (iii) PBS/0.1% Tween20; (iv) PBS/0.25 M NaCl. These then underwent: (i) vortexing; (ii) vortexing/centrifugation; (iii) centrifugation; (iv) incubation/vortexing/centrifugation. Sandwich-ELISAs determined analyte recovery (%) against positive controls. (2) Using optimized protocols, PTF was retrieved from permanent teeth with NAT or AAP after accessing root canals. Samples, normalized to total fluid volume (TFV), were analysed to determine proteomic profiles (pg/TFV) of NAT and AAP via O-link Target-48 panel. Correlations between AAP and diagnostic accuracy were explored using principal-component analysis (PCA) and area under receive-operating-characteristic curves (AUC [95% CI]), respectively. Statistical comparisons were made using Mann-Whitney U, anova and post hoc Bonferonni tests (α < .01).
RESULTS RESULTS
(1) UnoDent's 'Classic' points facilitated maximum volume absorbance (p < .05), with no significant differences after 60 s (1.6 μL [1.30-1.73]), 1 mm depth and up to 40/0.02 (2.2 μL [1.98-2.20]). For elution, vortexing (89.3%) and PBS/1% BSA (86.9%) yielded the largest IL-1β recovery (p < .05). (2) 41 (NAT: 13; AAP: 31) PTF samples proceeded to analysis. The panel detected 18 analytes (CCL-2, -3, -4; CSF-1; CXCL-8, -9; HGF; IL-1β, -6, -17A, -18; MMP-1, -12; OLR-1; OSM; TNFSF-10, -12; VEGF-A) in ≥75% of AAP samples at statistically higher concentrations (p < .01). CXCL-8, IL-1β, OLR-1, OSM and TNFSF-12 were strongly correlated to AAP. 'Excellent' diagnostic performance was observed for TNFSF-12 (AUC: 0.94 [95% CI: 0.86-1.00]) and the PCA-derived cluster (AUC: 0.96 [95% CI: 0.89-1.00]).
CONCLUSIONS CONCLUSIONS
Optimized PTF sampling parameters were identified in this study. When applied clinically, high-throughput proteomic analyses revealed complex interconnected networks of potential biomarkers. TNFSF-12 discriminated periradicular disease from health the greatest; however, clustering analytes further improved diagnostic accuracy. Additional independent investigations are required to validate these findings.

Identifiants

pubmed: 37464545
doi: 10.1111/iej.13956
doi:

Substances chimiques

Biomarkers 0

Types de publication

Journal Article

Langues

eng

Pagination

1222-1240

Subventions

Organisme : British Endodontic Society
Organisme : European Society of Endodontology
Organisme : Oral & Dental Research Trust

Informations de copyright

© 2023 The Authors. International Endodontic Journal published by John Wiley & Sons Ltd on behalf of British Endodontic Society.

Références

Alptekin, N.O., Ari, H., Haliloglu, S., Alptekin, T., Serpek, B. & Ataoglu, T. (2005) The effect of endodontic therapy on periapical exudate neutrophil elastase and prostaglandin-E2 levels. Journal of Endodontia, 31(11), 791-795.
Ataoğlu, T., Ungör, M., Serpek, B., Haliloğlu, S., Ataoğlu, H. & Ari, H. (2002) Interleukin-1beta and tumour necrosis factor-alpha levels in periapical exudates. International Endodontic Journal, 35(2), 181-185.
Ballal, V., Rao, S., Bagheri, A., Bhat, V., Attin, T. & Zehnder, M. (2017) MMP-9 in dentinal fluid correlates with caries lesion depth. Caries Research, 51(5), 460-465.
Brown, D.W.P. (2017) Paper points revisited: risk of cellulose fibre shedding during canal length confirmation. International Endodontic Journal, 50(6), 620-626.
Chapman, C.E. (1969) A microscopic study of the apical region ofhhuman anterior teeth. Journal of the British Endodontic Society, 3(4), 52-58.
Connert, T., Judenhofer, M.S., Hülber-J, M., Schell, S., Mannheim, J.G., Pichler, B.J. et al. (2018) Evaluation of the accuracy of nine electronic apex locators by using micro-CT. International Endodontic Journal, 51(2), 223-232.
Corazza, B.J.M., Martinho, F.C., Khoury, R.D., Toia, C.C., Orozco, E.I.F., Prado, R.F. et al. (2021) Clinical influence of calcium hydroxide and N acetylcysteine on the levels of resolvins E1 and D2 in apical periodontitis. International Endodontic Journal, 54(1), 61-73.
da Cunha, P.C., Gomes, M.S., Della Bona, A., Vanni, J.R., Kopper, P.M. & de Figueiredo, J.A. (2008) Evaluation of two methods of measuring the absorbing capacity of paper points. Dental Materials, 24(3), 399-402.
Dummer, P.M., Hicks, R. & Huws, D. (1980) Clinical signs and symptoms in pulp disease. International Endodontic Journal, 13(1), 27-35.
Dummer, P.M., McGinn, J.H. & Rees, D.G. (1984) The position and topography of the apical canal constriction and apical foramen. International Endodontic Journal, 17(4), 192-198.
ESE. (2006) Quality guidelines for endodontic treatment: consensus report of the European Society of Endodontology. International Endodontic Journal, 39(12), 921-930.
Ferreira, L.G., Rosin, F.C. & Corrêa, L. (2016) Analysis of interleukin 17A in periapical abscess and granuloma lesions. Brazilian Oral Research, 30, S1806-83242016000100235.
Glickman, G.N. (2009) AAE Consensus Conference on Diagnostic Terminology: background and perspectives. Journal of Endodontia, 35(12), 1619-1620.
Grant, D.S., Kleinman, H.K., Goldberg, I.D., Bhargava, M.M., Nickoloff, B.J., Kinsella, J.L. et al. (1993) Scatter factor induces blood vessel formation in vivo. Proceedings of the National Academy of Sciences of the United States of America, 90(5), 1937-1941.
Grant, M.M., Taylor, J.J., Jaedicke, K., Creese, A., Gowland, C., Burke, B. et al. (2022) Discovery, validation, and diagnostic ability of multiple protein-based biomarkers in saliva and gingival crevicular fluid to distinguish between health and periodontal diseases. Journal of Clinical Periodontology, 49(7), 622-632.
Grga, D., Dzeletović, B., Damjanov, M. & Hajduković-Dragojlović, L. (2013) Prostaglandin E2 in apical tissue fluid and postoperative pain in intact and teeth with large restorations in two endodontic treatment visits. Srpski Arhiv za Celokupno Lekarstvo, 141(1-2), 17-21.
Hama, S., Takeichi, O., Hayashi, M., Komiyama, K. & Ito, K. (2006) Co-production of vascular endothelial cadherin and inducible nitric oxide synthase by endothelial cells in periapical granuloma. International Endodontic Journal, 39(3), 179-184.
Hartroth, B., Seyfahrt, I. & Conrads, G. (1999) Sampling of periodontal pathogens by paper points: evaluation of basic parameters. Oral Microbiology and Immunology, 14(5), 326-330.
Hasegawa, T., Venkata Suresh, V., Yahata, Y., Nakano, M., Suzuki, S., Suzuki, S. et al. (2021) Inhibition of the CXCL9-CXCR3 axis suppresses the progression of experimental apical periodontitis by blocking macrophage migration and activation. Scientific Reports, 11(1), 2613.
Inic-Kanada, A., Nussbaumer, A., Montanaro, J., Belij, S., Schlacher, S., Stein, E. et al. (2012) Comparison of ophthalmic sponges and extraction buffers for quantifying cytokine profiles in tears using Luminex technology. Molecular Vision, 18, 2717-2725.
Kabashima, H., Yoneda, M., Nagata, K., Hirofuji, T., Ishihara, Y., Yamashita, M. et al. (2001) The presence of chemokine receptor (CCR5, CXCR3, CCR3)-positive cells and chemokine (MCP1, MIP-1alpha, MIP-1beta, IP-10)-positive cells in human periapical granulomas. Cytokine, 16(2), 62-66.
Karamifar, K., Khayat, A., Mogharrabi, S., Rajaei, Y. & Saghiri, M.A. (2012) Effect of gravity and capillarity on human saliva penetration in coronally unsealed obturated root canals. The Saudi Dental Journal, 24(3-4), 157-162.
Kataria, N.G., Bartold, P.M., Dharmapatni, A.A., Atkins, G.J., Holding, C.A. & Haynes, D.R. (2010) Expression of tumor necrosis factor-like weak inducer of apoptosis (TWEAK) and its receptor, fibroblast growth factor-inducible 14 protein (Fn14), in healthy tissues and in tissues affected by periodontitis. Journal of Periodontal Research, 45(4), 564-573.
Katz, D.H., Robbins, J.M., Deng, S., Tahir, U.A., Bick, A.G., Pampana, A. et al. (2022) Proteomic profiling platforms head to head: leveraging genetics and clinical traits to compare aptamer- and antibody-based methods. Science Advances, 8(33), eabm5164.
Klausen, B., Helbo, M. & Dabelsteen, E. (1985) A differential diagnostic approach to the symptomatology of acute dental pain. Oral Surgery, Oral Medicine, and Oral Pathology, 59(3), 297-301.
Kwak, H.B., Lee, S.W., Jin, H.M., Ha, H., Lee, S.H., Takeshita, S. et al. (2005) Monokine induced by interferon-gamma is induced by receptor activator of nuclear factor kappa B ligand and is involved in osteoclast adhesion and migration. Blood, 105(7), 2963-2969.
Liu, W., Yu, J. & Zhou, H. (2003) Changes of prostaglandin E2 levels in periapical exudates after root canal treatment. Hua Xi Kou Qiang Yi Xue Za Zhi, 21(1), 39-40.
Lofthag-Hansen, S., Huumonen, S., Gröndahl, K. & Gröndahl, H.G. (2007) Limited cone-beam CT and intraoral radiography for the diagnosis of periapical pathology. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics, 103(1), 114-119.
Majeed, Z., Philip, K., Alabsi, A.M., Pushparajan, S. & Swaminathan, D. (2016) Identification of gingival Crevicular fluid sampling, analytical methods, and oral biomarkers for the diagnosis and monitoring of periodontal diseases: a systematic review. Disease Markers, 2016, 1804727.
Mao, Y.J., Sheng, X.R. & Pan, X.M. (2007) The effects of NaCl concentration and pH on the stability of hyperthermophilic protein Ssh10b. BMC Biochemistry, 8, 28.
Martinho, F.C., Nascimento, G.G., Leite, F.R., Gomes, A.P., Freitas, L.F. & Camões, I.C. (2015) Clinical influence of different intracanal medications on Th1-type and Th2-type cytokine responses in apical periodontitis. Journal of Endodontia, 41(2), 169-175.
Martinho, F.C., Teixeira, F.F., Cardoso, F.G., Ferreira, N.S., Nascimento, G.G., Carvalho, C.A. et al. (2016) Clinical investigation of matrix metalloproteinases, tissue inhibitors of matrix metalloproteinases, and matrix metalloproteinase/tissue inhibitors of matrix metalloproteinase complexes and their networks in apical periodontitis. Journal of Endodontia, 42(7), 1082-1088.
Marton, I.J. & Kiss, C. (1993) Characterization of inflammatory cell infiltrate in dental periapical lesions. International Endodontic Journal, 26(2), 131-136.
Márton, I.J. & Kiss, C. (2000) Protective and destructive immune reactions in apical periodontitis. Oral Microbiology and Immunology, 15(3), 139-150.
Márton, I.J. & Kiss, C. (2014) Overlapping protective and destructive regulatory pathways in apical periodontitis. Journal of Endodontia, 40(2), 155-163.
Matsuo, T., Ebisu, S., Nakanishi, T., Yonemura, K., Harada, Y. & Okada, H. (1994) Interleukin-1 alpha and interleukin-1 beta periapical exudates of infected root canals: correlations with the clinical findings of the involved teeth. Journal of Endodontia, 20(9), 432-435.
Mente, J., Petrovic, J., Gehrig, H., Rampf, S., Michel, A., Schürz, A. et al. (2016) A prospective clinical pilot study on the level of matrix metalloproteinase-9 in dental pulpal blood as a marker for the state of inflammation in the pulp tissue. Journal of Endodontia, 42(2), 190-197.
Nagendrababu, V., Duncan, H.F., Fouad, A.F., Kirkevang, L.L., Parashos, P., Pigg, M. et al. (2023) PROBE 2023 guidelines for reporting observational studies in Endodontics: a consensus-based development study. International Endodontic Journal, 56(3), 308-317.
Nagendrababu, V., Murray, P.E., Ordinola-Zapata, R., Peters, O.A., Rôças, I.N., Siqueira, J.F., Jr. et al. (2021) PRILE 2021 guidelines for reporting laboratory studies in Endodontology: a consensus-based development. International Endodontic Journal, 54(9), 1482-1490.
Nair, P.N. (2004) Pathogenesis of apical periodontitis and the causes of endodontic failures. Critical Reviews in Oral Biology and Medicine, 15(6), 348-381.
Nakanishi, K., Yoshimoto, T., Tsutsui, H. & Okamura, H. (2001) Interleukin-18 regulates both Th1 and Th2 responses. Annual Review of Immunology, 19, 423-474.
Nonaka, C.F., Maia, A.P., Nascimento, G.J., de Almeida, F.R., Batista de Souza, L. & Galvão, H.C. (2008) Immunoexpression of vascular endothelial growth factor in periapical granulomas, radicular cysts, and residual radicular cysts. Oral Surgery, Oral Medicine, Oral Pathology, Oral Radiology, and Endodontics, 106(6), 896-902.
Ohgi, K., Kajiya, H., Goto, T.K., Okamoto, F., Yoshinaga, Y., Okabe, K. et al. (2018) Toll-like receptor 2 activation primes and upregulates osteoclastogenesis via lox-1. Lipids in Health and Disease, 17(1), 132.
Patel, S., Dawood, A., Mannocci, F., Wilson, R. & Pitt Ford, T. (2009) Detection of periapical bone defects in human jaws using cone beam computed tomography and intraoral radiography. International Endodontic Journal, 42(6), 507-515.
Pezelj-Ribarić, S., Magasić, K., Prpić, J., Miletić, I. & Karlović, Z. (2007) Tumor necrosis factor-alpha in peripical tissue exudates of teeth with apical periodontitis. Mediators of Inflammation, 2007, 69416.
Pumarola-Suñé, J., Solá-Vicens, L., Sentís-Vilalta, J., Canalda-Sahli, C. & Brau-Aguadé, E. (1998) Absorbency properties of different brands of standardized endodontic paper points. Journal of Endodontia, 24(12), 796-798.
Rechenberg, D.K., Bostanci, N., Zehnder, M. & Belibasakis, G.N. (2014) Periapical fluid RANKL and IL-8 are differentially regulated in pulpitis and apical periodontitis. Cytokine, 69(1), 116-119.
Reisinger, K., Kaufmann, R. & Gille, J. (2003) Increased Sp1 phosphorylation as a mechanism of hepatocyte growth factor (HGF/SF)-induced vascular endothelial growth factor (VEGF/VPF) transcription. Journal of Cell Science, 116(Pt 2), 225-238.
Repeke, C.E., Ferreira, S.B., Jr., Claudino, M., Silveira, E.M., de Assis, G.F., Avila-Campos, M.J. et al. (2010) Evidences of the cooperative role of the chemokines CCL3, CCL4 and CCL5 and its receptors CCR1+ and CCR5+ in RANKL+ cell migration throughout experimental periodontitis in mice. Bone, 46(4), 1122-1130.
Ricucci, D. & Bergenholtz, G. (2004) Histologic features of apical periodontitis in human biopsies. Endodontic Topics, 8(1), 68-87.
Safavi, K.E. & Rossomando, E.F. (1991) Tumor necrosis factor identified in periapical tissue exudates of teeth with apical periodontitis. Journal of Endodontia, 17(1), 12-14.
Sette-Dias, A.C., Maciel, K.F., Abdo, E.N., Brito, L.C.N., Carvalho, M.A.R., Vieira, L.Q. et al. (2016) Cytokine expression in patients hospitalized for severe odontogenic infection in Brazil. Journal of Endodontia, 42(5), 706-710.
Shimauchi, H., Miki, Y., Takayama, S., Imai, T. & Okada, H. (1996) Development of a quantitative sampling method for periapical exudates from human root canals. Journal of Endodontia, 22(11), 612-615.
Shimauchi, H., Takayama, S., Imai-Tanaka, T. & Okada, H. (1998) Balance of interleukin-1 beta and interleukin-1 receptor antagonist in human periapical lesions. Journal of Endodontia, 24(2), 116-119.
Silva, T.A., Garlet, G.P., Fukada, S.Y., Silva, J.S. & Cunha, F.Q. (2007) Chemokines in oral inflammatory diseases: apical periodontitis and periodontal disease. Journal of Dental Research, 86(4), 306-319.
Šimundić, A.M. (2009) Measures of diagnostic accuracy: basic definitions. EJIFCC, 19(4), 203-211.
Sorsa, T., Alassiri, S., Grigoriadis, A., Räisänen, I.T., Pärnänen, P., Nwhator, S.O. et al. (2020) Active MMP-8 (aMMP-8) as a grading and staging biomarker in the periodontitis classification. Diagnostics, 10(2), 61.
Steinitz, M. (2000) Quantitation of the blocking effect of tween 20 and bovine serum albumin in ELISA microwells. Analytical Biochemistry, 282(2), 232-238.
Teixeira, F.F.C., Cardoso, F.G.R., Ferreira, N.S., Corazza, B.J.M., Valera, M.M.C., Nascimento, G.G. et al. (2022) Effects of calcium hydroxide Intracanal medications on T helper (Th1, Th2, Th9, Th17, and Tfh) and regulatory T (Treg) cell cytokines in apical periodontitis: a CONSORT RCT. Journal of Endodontia, 48(8), 975-984.
Tsai, C.H., Huang, F.M. & Chang, Y.C. (2008) Immunohistochemical localization of oncostatin M in epithelialized apical periodontitis lesions. International Endodontic Journal, 41(9), 772-776.
Virdee, S.S., Butt, K., Grant, M., Camilleri, J., Cooper, P.R. & Tomson, P.L. (2019) A systematic review of methods used to sample and analyse periradicular tissue fluid during root canal treatment. International Endodontic Journal, 52(8), 1108-1127.
Wahlgren, J., Salo, T., Teronen, O., Luoto, H., Sorsa, T. & Tjäderhane, L. (2002) Matrix metalloproteinase-8 (MMP-8) in pulpal and periapical inflammation and periapical root-canal exudates. International Endodontic Journal, 35(11), 897-904.
Weber, M., Ries, J., Büttner-Herold, M., Geppert, C.I., Kesting, M. & Wehrhan, F. (2019) Differences in inflammation and bone resorption between apical granulomas, radicular cysts, and dentigerous cysts. Journal of Endodontia, 45(10), 1200-1208.
Wik, L., Nordberg, N., Broberg, J., Björkesten, J., Assarsson, E., Henriksson, S. et al. (2021) Proximity extension assay in combination with next-generation sequencing for high-throughput proteome-wide analysis. Molecular & Cellular Proteomics, 20, 100168.
Yakar, N., Guncu, G.N., Akman, A.C., Pınar, A., Karabulut, E. & Nohutcu, R.M. (2019) Evaluation of gingival crevicular fluid and peri-implant crevicular fluid levels of sclerostin, TWEAK, RANKL and OPG. Cytokine, 113, 433-439.
Youden, W.J. (1950) Index for rating diagnostic tests. Cancer, 3(1), 32-5.
Zehnder, M. & Belibasakis, G.N. (2022) A critical analysis of research methods to study clinical molecular biomarkers in Endodontic research. International Endodontic Journal, 55(Suppl 1), 37-45.
Zehnder, M., Rechenberg, D.K., Bostanci, N., Sisman, F. & Attin, T. (2014) Comparison of vehicles to collect dentinal fluid for molecular analysis. Journal of Dentistry, 42(8), 1027-1032.
Zhi, J., Yu, D., Yuan, D. & Chen, J. (2017) Interleukin-17 in apical exudates of periapical periodontitis treated with minocycline controlled-release formulation. Chinese Journal of Tissue Engineering Research, 21(10), 1508-1513.
Zhou, H., Yuen, P.S., Pisitkun, T., Gonzales, P.A., Yasuda, H., Dear, J.W. et al. (2006) Collection, storage, preservation, and normalization of human urinary exosomes for biomarker discovery. Kidney International, 69(8), 1471-1476.

Auteurs

Satnam S Virdee (SS)

Institute of Clinical Sciences, School of Dentistry & Birmingham Dental Hospital, University of Birmingham, Birmingham, UK.

Nasir Z Bashir (NZ)

School of Dentistry, University of Leeds, Leeds, UK.

Milan Krstic (M)

Institute of Clinical Sciences, School of Dentistry & Birmingham Dental Hospital, University of Birmingham, Birmingham, UK.

Josette Camilleri (J)

Institute of Clinical Sciences, School of Dentistry & Birmingham Dental Hospital, University of Birmingham, Birmingham, UK.

Melissa M Grant (MM)

Institute of Clinical Sciences, School of Dentistry & Birmingham Dental Hospital, University of Birmingham, Birmingham, UK.

Paul R Cooper (PR)

Department of Oral Sciences, Faculty of Dentistry, University of Otago, Dunedin, New Zealand.

Phillip L Tomson (PL)

Institute of Clinical Sciences, School of Dentistry & Birmingham Dental Hospital, University of Birmingham, Birmingham, UK.

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