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. 2022 Oct 21;2022:4498613. doi: 10.1155/2022/4498613

Table 2.

Various toxic effects of titanium particles.

Authors Type of study Influence on oral cavity
Correa et al. 2009 [26] In vitro (i) Greater S. mutans adherence
Makihira et al. 2010 [27] In vitro (i) Increased cytotoxicity and inflammation
Olmedo et al. 2012 [28] Ex-vivo (i) Increased number of macrophages and T lymphocytes cause bone loss and implant failure
Barao et al. 2013 [29] In vitro (i) Increased LPS adherence
Olmedo et al. 2013 [5] Ex-vivo (i) Metal particles exfoliated in peri-implant mucosa trigger inflammatory reactions
Barao et al. 2014 [30] In vitro (i) Increased P. gingivalis attachment on implant surface
Safioti et al. 2017 [31] Observational study (i) Peri-implantitis
Chandar et al. 2017 [32] In vitro (i) Greater cell viability of CpTi than Ti6Al4V
(ii) Aluminum and vanadium in Ti6Al4V induce cytotoxicity
(iii) Cytotoxicity decreases due to the formation of TiO2
Pettersson et al. 2017 [33] In vitro (i) Increased Ti ions near Ti implants stimulate human macrophages to release IL-1β specifically from LPS stimulated macrophages
Daubert et al. 2018 [34] Observational study (i) Ti ions modify peri-implant microbiome structure and diversity
(ii) Increased Peri-implantitis
Zhu et al. 2018 [35] In vitro (i) Ti ions (10 ppm) suppressed osteoblasts and trigger nuclear expression of YAP pathway
(ii) Its activation suppresses osteogenic differentiation
Hosoki et al. 2018 [36] Observational study (i) Ti allergy occurred in 6.3% of all cases
Daubert et al. 2019 [37] Case control study (i) Increased methylated DNA cytosine in peri-implantitis due to epigenetic alterations in the tissues
(ii) Increased association between Ti concentration and global methylation levels independent of peri-implantitis
(iii) Methylation of DNA influenced by Ti dissolution
Berryman et al. 2020 [38] Ex-vivo (i) Increased bone loss and peri-implantitis
Kotsakis et al. 2020 [39] In vitro (i) Cytotoxic effects of Ti on fibroblasts
De Lima-Souza et al. 2021 [40] Case report (i) Erythematous-papular-nodular lesions in mandibular and submandibular region
(ii) Histopathologically chronic fistula with foreign body reaction and Ti ions along fistula wall