Mia RAKIC

Dr. Mia RAKIC

Facultad de Odontologia, Etiology and Therapy of Periodontal Diseases (ETEP) Research Group, Universidad Complutense de Madrid, Madrid, Spain
orcid

Research Focus & Metrics

Academic Career Length

17Years (2010-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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7 December 2017 in Clinical Oral Investigations
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Journal Article
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Mia RAKICMia RAKIC
Mia RAKIC
PGPablo Galindo-Moreno
Pablo Galindo-Moreno
AMAlberto Monje
Alberto Monje
SRSandro Radovanovic
Sandro Radovanovic
HWHom-Lay Wang
Hom-Lay Wang
Luigi CanulloLuigi Canullo
Luigi Canullo

20 November 2015 in Clinical Oral Implants Research
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Luigi CanulloLuigi Canullo
Luigi Canullo
Marco TallaricoMarco Tallarico
Marco Tallarico
SRSandro Radovanovic
Sandro Radovanovic
BDBoris Delibasic
Boris Delibasic
UCUgo Covani
Ugo Covani
Mia RAKICMia RAKIC
Mia RAKIC

1 March 2016 in The International Journal of Oral and Maxillofacial Implants
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Mia RAKICMia RAKIC
Mia RAKIC
MGMaria Grusovin
Maria Grusovin
LCLuigi Canullo
Luigi Canullo
Mia Rakic, DDS, PhD/Maria Gabriella Grusovin, DDS/Luigi Canullo, DDS, PhD: Purpose: To qualitatively investigate the microbiologic profile in peri-implantitis by systematically reviewing the published literature on peri-implant infection. Materials and Methods: Searches of the US National Institutes of Health free digital archives of the biomedical and life sciences journal literature (PubMed) and The Cochrane Library of the Cochrane Collaboration (CENTRAL), as well as a hand search of other literature, were conducted to identify articles potentially relevant for the review. Randomized clinical trials, prospective cohort studies, longitudinal studies, case-control studies, and cross-sectional studies in humans reporting microbiologic findings in patients with diagnosed peri-implantitis were considered eligible for this review. Screening, data extraction, and quality assessment were conducted independently and in duplicate. Results: Twenty-one articles were eligible for inclusion in this review. Early studies focused on the identification of target periopathogens, whereas more recent studies used advanced molecular techniques for comprehensive overview of the peri-implantitis?associated microbiome. In summary, the microbiologic profile in peri-implantitis (1) is complex and variable, (2) consists of gram-negative anaerobic periopathogens and opportunistic microorganisms in almost the same ratio, (3) is frequently associated with the Epstein-Barr virus and nonsaccharolytic anaerobic gram-positive rods, (4) is not so strictly associated with Staphylococcus aureus, and (5) is different from that of periodontitis. A meta-analysis could not be performed because of the heterogeneity of the reviewed studies. Conclusion: Although a comparison of the published results was limited because of the inhomogeneity of the studies, it is clear that the microbiologic profile of peri-implantitis consists of aggressive and resistant microorganisms and is distinct from that of periodontitis. It seems that the quantitative characteristics of the microflora cohabitants represent the key determinant of disease, rather than the qualitative composition, which is very similar in healthy and peri-implantitis states.

28 May 2013 in Journal of Periodontal Research
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NNN. Novakovic
N. Novakovic
TTT. Todorovic
T. Todorovic
Mia RAKICMia RAKIC
Mia RAKIC
IMI. Milinkovic
I. Milinkovic
IDI. Dozic
I. Dozic
SCS. Cakic
S. Cakic

1 November 2014 in Journal of Periodontology
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Mia RAKICMia RAKIC
Mia RAKIC
XSXavier Struillou
Xavier Struillou
APAleksandra Petkovic‐Curcin
Aleksandra Petkovic‐Curcin
SMSmiljana Matic
Smiljana Matic
Luigi CanulloLuigi Canullo
Luigi Canullo
DVDanillo Vladimir Vojvodic
Danillo Vladimir Vojvodic
Background: The aims of this study are to estimate the profile of bone loss biomarkers in peri‐implant tissues and to identify potential prognostic biomarkers of peri‐implantitis.Methods: Peri‐implant crevicular fluid samples collected from 164 participants (52 patients with peri‐implantitis, 54 with mucositis, and 58 with healthy peri‐implant tissues) were analyzed using enzyme‐linked immunosorbent assays to evaluate concentrations of the receptor activator of nuclear factor‐κB (RANK), soluble RANK ligand (sRANKL), osteoprotegerin (OPG), cathepsin‐K, and sclerostin.Results: Concentrations of RANK, sRANKL, OPG, and sclerostin were significantly increased in patients with peri‐implantitis compared with patients with healthy peri‐implant tissues. Comparisons between peri‐implantitis and mucositis demonstrated significantly higher values of sclerostin in peri‐implantitis samples. Comparisons between mucositis and healthy peri‐implant tissues showed significantly increased levels of RANK and cathepsin‐K in mucositis.Conclusion: These results are suggestive of a role of sRANKL, OPG, and sclerostin as prognostic biomarkers in peri‐implantitis.

18 June 2012 in Clinical Oral Implants Research
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Mia RAKICMia RAKIC
Mia RAKIC
VLVojislav Lekovic
Vojislav Lekovic
NNNatasa Nikolic‐Jakoba
Natasa Nikolic‐Jakoba
DVDanillo Vladimir Vojvodic
Danillo Vladimir Vojvodic
APAleksandra Petkovic‐Curcin
Aleksandra Petkovic‐Curcin
MSMariano Sanz
Mariano Sanz