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SCREENING OF EPIGENETIC BIOMARKERS (miRNAs) IN THE GINGIVAL SULCUS

26 aprile 2018 aggiornato da: ANA FUENMAYOR GARCÉS, University of Valencia

Screening of Epigenetic Biomarkers (miRNA) in the Gingival Sulcus

Epigenetics has produced a high impact in biomedical research and is providing new biomarkers for the diagnosis and prognosis of diseases. In addition, epigenetics is also contributing to analyze the molecular causes underlying diseases, even so periodontal diseases as it has been recently reviewed. In this regard, changes in the methylation of genes codifying for pro-inflammatory and anti-inflammatory cytokines has been previously reported. miRNAs are very promising biomolecules to be used as biomarkers because miRNAs act as signaling molecules and participate in many biological processes, such as cellular development, differentiation, and apoptosis. The high stability of circulating miRNAs in the RNase-rich environment of the bloodstream and also in different biospecimens used in clinical routine, make these biomolecules an optimal source of candidate biomarkers. In fact, miRNAs have demonstrated their value as dynamic biomarkers in a wide variety of human diseases. Therefore, miRNAs can be used for the monitoring of periodontal disease.

The objective of this research is to analyze the levels of bone remodeling RANKL / OPG biomolecular markers, and the epigenetic regulation of these proteins to identify promising biomarkers of periodontal disease.

Material and Methods. Levels of RANKL and OPG will be measured in the gingival crevicular fluid (GCF) to assess the state of bone. These samples will be sent to the lab for quantification by ELISA method.

Furthermore, new epigenetic biomarkers based on the identification of high stable microRNAs will be identified by qRT-PCR in GCF as feasible tools for diagnosis and monitoring of wide range of disease, including periodontal disease.

Panoramica dello studio

Tipo di studio

Osservativo

Iscrizione (Anticipato)

40

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Luoghi di studio

      • Valencia, Spagna
        • Reclutamento
        • Ana Fuenmayor Garcés
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

Da 30 anni a 60 anni (Adulto)

Accetta volontari sani

Sessi ammissibili allo studio

Tutto

Metodo di campionamento

Campione non probabilistico

Popolazione di studio

Patients attending to the university who meet the inclusion criteria.

Descrizione

Inclusion Criteria:

Group of periodontal patients:

  1. Clinical criteria: at least 3 locations in unirradicular teeth with PD 6 mm. 3 samples will be taken from each of these 3 locations (9 total samples). Third molars are not included in the study.
  2. Patients not treated periodontally.
  3. 30-60 years.

Periodontally healthy group:

1. Absence of clinical and radiographical periodontal pathology.

Exclusion Criteria:

  • Group of periodontal patients:

    1. Aggressive Periodontal Disease (Armitage, 1999).
    2. Patients with controlled periodontal disease with plaque and gingival indexes ≤20%.
    3. Patients with systemic diseases or taking medications that alter bone metabolism (Osteoporosis, arthritis, hormonal treatment, bisphosphonates, anti-inflammatory, immunosuppressants, etc ...).
    4. Patients with antibiotic, anti-inflammatory or contraceptive treatment in the previous 3 months or taking antiaggregants in the last 7 days before taking the sample.
    5. Smokers (> 10 cig. /day).
    6. Pregnant or breast-feeding.

Periodontally healthy group:

  1. Patients with systemic diseases or taking medications that alter bone metabolism (Osteoporosis, arthritis, hormonal treatment, bisphosphonates, anti-inflammatory, immunosuppressant...).
  2. Patients with antibiotic, anti-inflammatory or contraceptive treatment in the previous 3 months or taking antiaggregants in the last 7 days before taking the sample.
  3. Smokers (> 10 cig/day).
  4. Pregnant or breast-feeding.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

Coorti e interventi

Gruppo / Coorte
Intervento / Trattamento
Periodontal patients.
Taking gingival Crevicular fluid.

Once the anamnesis has been done, all the records corresponding to the Gingival Index and Plaque Index, in both groups are taken.

Subsequently, samples of gingival crevicular fluid are taken for the screening of epigenetic biomarkers.

Periodontally healthy patients.
Taking gingival Crevicular fluid.

Once the anamnesis has been done, all the records corresponding to the Gingival Index and Plaque Index, in both groups are taken.

Subsequently, samples of gingival crevicular fluid are taken for the screening of epigenetic biomarkers.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
microRNA in gingival crevicular fluid (physiological parameter).
Lasso di tempo: 2 years.
Insert the Perio Paper® tip in gingival sulcus until resistance is felt and leave it for 30 seconds.
2 years.

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Probing depth.
Lasso di tempo: 2 years.
Probing depth will be measured in six sites (disto-buccal, mid-buccal, mesio-buccal, disto-palatal, mid-palatal and mesio- palatal) of every teeth with a Williams Probe PQ-OW 208 396. This probe is used by gently hanging pressure into a pocket measuring 20 grams in weight.
2 years.
Bleeding on probing.
Lasso di tempo: 2 years.
Full mouth bleeding score (FMBS) will be calculated based on scores of 0 (no bleeding) or 1 (bleeding) after probing for PD. The usual thing to do is to measure at 4 points for each tooth but we have modified the index and we valorate them at 6 points. (disto-buccal, mid-buccal, mesio-buccal, disto-palatal, mid-palatal and mesio- palatal).
2 years.
Clinical recession.
Lasso di tempo: 2 years.
Clinical recession will be measured in the same six sites as before between the Amelocemental junction and the gingival margin.
2 years.
Plaque score of Silness y löe: (1964)
Lasso di tempo: 2 years.

The Plaque will be scored as follows:

Score 0 = No plaque

Score 1 = A film of plaque adhering to the free gingival margin and adjacent area of the tooth. The plaque may be seen in situ only after application of disclosing solution or by using the probe on the tooth surface.

Score 2 = Moderate accumulation of soft deposits within the gingival pocket, or on the tooth and gingival margin, which can be seen with the naked eye.

Score 3 = Abundance of soft matter within the gingival pocket and/or on the tooth and gingival margin.

The usual thing to do is to evaluate at 4 points for each tooth but we have modified the index and we will evaluate at 6 points. (disto-buccal, mid-buccal, mesio-buccal, disto-palatal, mid-palatal and mesio- palatal)

2 years.
Dental movility of Mïller 1950
Lasso di tempo: 2 years.

Class I

Up to 1 mm of movement in a horizontal direction.

Class II Greater than 1 mm of movement in a horizontal direction. Class III

Excessive horizontal movement and vertical movement.

2 years.
Furcation affection.
Lasso di tempo: 2 years.

Class I:

The level of bone loss allows for the insertion of the periodontal Nabers probe into the concavity of the root trunk. Furcation defect is less than 3 mm is depth.

Class II The level of bone loss allows for the insertion of a periodontal probe into the furcation area between the roots. Furcation defect is at least 3 mm in depth (and thus, in general, surpassing half of the buccolingual thickness of the tooth) but not through-and-through (i.e. there is still some interradicular bone attached to the angle of the furcation.

15

Class III The level of bone loss allows for "through and through" access of the furcation area. Buccal to lingual on lower molars. Buccal to mesio-palatal and disto-palatal on upper molars. Furcation defect encompassing the entire width of the tooth so that no bone is attached to the angle of the furcation.

2 years.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

15 settembre 2017

Completamento primario (Anticipato)

1 luglio 2019

Completamento dello studio (Anticipato)

1 luglio 2019

Date di iscrizione allo studio

Primo inviato

1 aprile 2018

Primo inviato che soddisfa i criteri di controllo qualità

26 aprile 2018

Primo Inserito (Effettivo)

27 aprile 2018

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

27 aprile 2018

Ultimo aggiornamento inviato che soddisfa i criteri QC

26 aprile 2018

Ultimo verificato

1 aprile 2018

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • H1510580113419

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

INDECISO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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