The role of torque teno virus (Ttv) viremia in sarcoidosis etiology

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Objective: To investigate a possible role of torque teno virus (TTV) in the etiology of sarcoidosis Design: Controlled prospective study Setting: Faculty of Meram Medicine, Necmettin Erbakan University, Konya, Turkey Subjects: This cross-sectional, clinical study included 37 sarcoidosis patients and 9 healthy control patients. Intervention: TTV DNA quantification was performed by real-time PCR by the hybridization probe system, and viral load was interpreted by means of the crossing point (CP) value in sera of subjects. Main outcome measures: The prevalence and viral load of TTV Results: TTV DNA was detected in the majority of both patients and healthy controls. The prevalence was 59.5% in patients and 55.6% in controls. This difference was not statistically significant. However, CP values were statistically different in the patient group from the control group (p <0.001); namely, the viral load of TTV was higher in the patient group than in the healthy control group. Conclusions: Overall, these findings demonstrate for the first time that TTV plays a role in the etiology of sarcoidosis. It is likely that the role of TTV in the pathogenesis of sarcoidosis is an aberrant immune response, driven by viral antigens. © 2019, Kuwait Medical Association. All rights reserved.

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AlanDeğerDil
dc.contributor.authorTeke, Turgut
dc.contributor.authorFeyzioglu, Bahadir
dc.contributor.authorTosun, Mustafa
dc.contributor.authorDogan, Metin
dc.contributor.authorYesildag, Kerim
dc.contributor.authorOzdemir, Mehmet
dc.date.accessioned2026-10-18T20:28:27.524947944Z
dc.date.available2026-10-18T20:28:27.524947944Z
dc.date.issued2019
dc.description.abstractObjective: To investigate a possible role of torque teno virus (TTV) in the etiology of sarcoidosis Design: Controlled prospective study Setting: Faculty of Meram Medicine, Necmettin Erbakan University, Konya, Turkey Subjects: This cross-sectional, clinical study included 37 sarcoidosis patients and 9 healthy control patients. Intervention: TTV DNA quantification was performed by real-time PCR by the hybridization probe system, and viral load was interpreted by means of the crossing point (CP) value in sera of subjects. Main outcome measures: The prevalence and viral load of TTV Results: TTV DNA was detected in the majority of both patients and healthy controls. The prevalence was 59.5% in patients and 55.6% in controls. This difference was not statistically significant. However, CP values were statistically different in the patient group from the control group (p <0.001); namely, the viral load of TTV was higher in the patient group than in the healthy control group. Conclusions: Overall, these findings demonstrate for the first time that TTV plays a role in the etiology of sarcoidosis. It is likely that the role of TTV in the pathogenesis of sarcoidosis is an aberrant immune response, driven by viral antigens. © 2019, Kuwait Medical Association. All rights reserved.
dc.identifier.endpage162
dc.identifier.issn0023-5776
dc.identifier.issue2
dc.identifier.scopus2-s2.0-85075281069
dc.identifier.startpage157
dc.identifier.urihttps://rdlopen.rawdatalibrary.net/r/ebyu/13624
dc.identifier.volume51
dc.language.isoen
dc.publisherKuwait Medical Association
dc.relation.ispartofKuwait Medical Journal
dc.rightsinfo:eu-repo/semantics/openAccess
dc.subjectEtiology
dc.subjectInfection
dc.subjectSarcoidosis
dc.subjectTorque teno virus
dc.subjectadult
dc.subjectArticle
dc.subjectcancer staging
dc.subjectclinical article
dc.subjectcontrolled study
dc.subjectDNA determination
dc.subjectDNA purification
dc.subjectfemale
dc.subjecthistology
dc.subjecthuman
dc.subjecthuman tissue
dc.subjecthybridization
dc.subjectmale
dc.subjectmiddle aged
dc.subjectprevalence
dc.subjectprospective study
dc.subjectreal time polymerase chain reaction
dc.subjectthorax radiography
dc.subjectTorque teno virus 1
dc.subjectTorque teno virus infection
dc.subjectvirus load
dc.titleThe role of torque teno virus (Ttv) viremia in sarcoidosis etiology
dc.typeArticle
dspace.entity.typePublication
rdl.citation.scopus0
rdl.source.indexSCOPUS