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SAL_24904 details
Primary information
SALIDSAL_24904
Biomarker namehsa-miR-7108-5p
Biomarker TypeDiagnostic
Sampling MethodEight CP and eight healthy individuals were recruited from Dental Clinic, Universiti Sains Malaysia (USM), Health Campus, Kelantan, Malaysia.
Collection MethodSaliva was collected about 10 ml (or within 20 min) into sterile sample collection container.
Analysis MethodNA
Collection SiteSaliva
Disease CategoryDental Disorder
Disease/ConditionPeriodontitis
Disease SubtypeChronic Periodontitis
Fold Change/ Concentration4 .06
Up/DownregulatedUpregulated
ExosomalNon-exosomal
OrganismHomo sapiens
PMID33329037
Year of Publication2020
Biomarker IDhsa-miR-7108-5p
Biomarker CategorymiRNA
SequenceGUGUGGCCGGCAGGCGGGUGG
Title of studyPlasma- and Saliva Exosome Profile Reveals a Distinct MicroRNA Signature in Chronic Periodontitis
Abstract of studyChronic periodontitis (CP) is an oral cavity disease arising from chronic inflammation of the periodontal tissues. Exosomes are lipid vesicles that are enriched in specific microRNAs (miRNAs), potentially providing a disease-specific diagnostic signature. To assess the value of exosomal miRNAs as biomarkers for CP, 8 plasma- and 8 salivary-exosomal miRNAs samples were profiled using Agilent platform (comparative study). From 2,549 probed miRNAs, 33 miRNAs were significantly down-regulated in CP as compared to healthy plasma samples. Whereas, 1,995 miRNAs (1,985 down-regulated and 10 up-regulated) were differentially expressed in the CP as compared to healthy saliva samples. hsa-miR-let-7d [FC = -26.76; AUC = 1; r = -0.728 [p-value = 0.04]), hsa-miR-126-3p (FC = -24.02; AUC = 1; r = -0.723 [p-value = 0.043]) and hsa-miR-199a-3p (FC = -22.94; AUC = 1; r = -0.731 [p-value = 0.039]) are worth to be furthered studied for plasma-exosomal samples. Meanwhile, for salivary-exosomal samples, hsa-miR-125a-3p (FC = 2.03; AUC = 1; r = 0.91 [p-value = 0.02]) is worth to be furthered studied. These miRNAs are the reliable candidates for the development of periodontitis biomarker, as they were significantly expressed differently between CP and healthy samples, have a good discriminatory value and strongly correlate with the mean of PPD. These findings highlight the potential of exosomal miRNAs profiling in the diagnosis from both sourced as well as provide new insights into the molecular mechanisms involved in CP.