Cited by 12Tryptophan and brain disordersDental materials and restorationsImmunotoxicology and immune responses

Elevated Systemic L-Kynurenine/L-Tryptophan Ratio and Increased IL-1 Beta and Chemokine (CX3CL1, MCP-1) Proinflammatory Mediators in Patients with Long-Term Titanium Dental Implants

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Merino, José Joaquín, Cabaña-Muñoz, María Eugenia, Toledano Gasca, Adolfo, Garcimartín, Alba, Benedí, Juana, Camacho-Alonso, Fabio, Parmigiani-Izquierdo, José María·2019·Journal of Clinical Medicine

Abstract

Titanium is the mean biocompatible metal found in dental titanium alloys (Ti-6Al-4V). The safety of certain dental biomaterial amalgams has been questioned in patients. The levels of several systemic cytokines (interleukin (IL)-1 beta, IL-4: pg/mL) and chemokines (monocyte chemoattractant protein-1 (MCP-1), soluble fractalkine (CX3CL1: pg/mL) were determined using ELISA and compared between these study groups. The study included 30 controls without dental materials (cont), 57 patients with long-term titanium dental implants plus amalgams (A + I group) as well as 55 patients with long-term dental amalgam alone (A group). All patients (except controls) have had dental titanium implants (Ti-6Al-4V) and/or amalgams for at least 10 years (average: 15 years). We evaluated whether systemic levels of cytokines/chemokines, kyn/L-trp ratio and aromatic amino acid levels (HPLC: mM/L, Phe, L-Trp, His, Treo) could be altered in patients with long-term dental titanium and/or amalgams. These systemic markers were evaluated in 142 patients. The A + I group had higher L-Kynurenine/L-Tryptophan ratios than patients with long-term dental amalgam fillings alone (A). In addition, levels of IL-1 Beta cytokine, CX3CL1 and MCP-1 chemokines were higher in the A + I group than in the A group (A). The increased L-kyn/L-trp ratio and MCP-1 and fractalkine receptor (CX3CR1) elevations could suggest enhanced chemotactic responses by these chemokines in the A + I group.

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  • CX3CL1 levels are significantly higher in patients with titanium implants and dental amalgam restorations compared to patients with only long-standing dental amalgam restorations.

    “Thus, it has been shown that CX3CL1 levels are significantly higher in patients with titanium implants and dental amalgam restorations compared to patients with only long-standing dental amalgam restorations [171].”

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Authors
Merino, J. J., Cabaña-Muñoz, M. E., Toledano Gasca, A., Garcimartín, A., Benedí, J., Camacho-Alonso, F., & Parmigiani-Izquierdo, J. M.
Affiliations
  • Departamento de Farmacología, Farmacognosia y Botánica, Facultad de Farmacia, Universidad Complutense de Madrid (U.C.M), c/Plaza Ramón y Cajal s/n, 28040 Madrid, Spain
  • Centro CIROM, Centro de Implantología y Rehabilitación Oral Multidisciplinaria, 30001 Murcia, Spain
  • Department of Neuroanatomy, Instituto Cajal (CSIC), 28040 Madrid, Spain
  • Universidad Complutense de Madrid (ES)
  • Faculty of Medicine, University of Murcia, 30100 Murcia, Spain
Venue
Journal of Clinical Medicine
Publisher
MDPI AG
Published
2019-09-02
Volume
8
Issue
9
Pages
1368
ISSN
2077-0383 (ISSN-L)
OpenAlex
W2970906987
Cited by
12
References
56
Citations by year
2026: 2 · 2024: 2 · 2023: 2 · 2022: 2 · 2021: 2 · 2020: 2
FWCI
0.49
Type
journal article
Language
en
Open access
Locations
  • Journal of Clinical Medicine (publishedVersion, cc-by)
  • PubMed Central (publishedVersion, cc-by)
  • PubMed (publishedVersion)
  • Docta Complutense (Universidad Complutense de Madrid) (submittedVersion, cc-by)
  • DIGITAL.CSIC (Spanish National Research Council (CSIC)) (submittedVersion, cc-by)
  • DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion)
Topics
  • Life Sciences › Neuroscience › Biological Psychiatry › Tryptophan and brain disorders
  • Health Sciences › Dentistry › Orthodontics › Dental materials and restorations
  • Life Sciences › Immunology and Microbiology › Immunology › Immunotoxicology and immune responses
Keywords
kynurenine/tryptophan ratio, dental amalgam, Ti-6Al-4V, IL-1β, MCP-1, CX3CR1, chemokines, cytokines, aromatic amino acids, systemic inflammation, biomaterial biocompatibility

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