The best anti-HCV S/Co values for reflecting HCV infection in a university hospital in the eastern part of Turkey
Özet
Introduction: The measurement of hepatitis C virus (HCV) RNA is a test that requires high cost, advanced technique, and qualified personnel. Diagnosis and treatment of patients may be delayed due to the high rate of false-positive results. This study aims to predict true antibody positivity and viremia by determining the most appropriate anti-HCV signal-to-cutoff (S/Co) value reflecting HCV infection. Methodology: The presence of anti-HCV antibodies and HCV RNA levels were examined in 72341 people who applied to the Mengücek Gazi Training and Research Hospital between January 2018 and December 2020. The anti-HCV levels were determined by using the Abbot Architect i2000 SR device (Abbot Diagnostics, Chicago, IL, USA). The levels of HCV RNA were determined in the COBAS AmpliPrep/COBAS, TaqMan 48 (Roche, Diagnostics, Pleasanton, USA) devices using serum samples from patients. Our study is a retrospective and methodological study. Results: Of the 150 patients with anti-HCV antibodies, 50 (33.3%) were HCV RNA positive, and 100 (66.7%) were HCV RNA negative. Anti-HCV levels of HCV RNA-positive patients were statistically higher than HCV RNA-negative patients. The most appropriate anti-HCV S/Co value for diagnosing hepatitis C patients was 15.4. The sensitivity of this value was 72%, specificity 88%, positive predictive value (PPV) 73.5%, and negative predictive value (NPV) 86.1%. Receiver operating characteristic (ROC) curve was significantly higher than 0.5 (95% confidence interval 0.938-0.827). Conclusions: Correct approaches can be applied in the diagnosis of HCV infection using the anti-HCV S/Co value found in our study. © 2024 Dabanlioǧlu et al.
Anahtar Kelimeler
Tam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Dabanlioǧlu, Bülent | |
| dc.contributor.author | Yilmaz, Aysun | |
| dc.contributor.author | Akyüz, Sümeyye | |
| dc.contributor.author | Gülhan, Bariş | |
| dc.date.accessioned | 2026-10-18T20:26:58.211003592Z | |
| dc.date.available | 2026-10-18T20:26:58.211003592Z | |
| dc.date.issued | 2024 | |
| dc.description.abstract | Introduction: The measurement of hepatitis C virus (HCV) RNA is a test that requires high cost, advanced technique, and qualified personnel. Diagnosis and treatment of patients may be delayed due to the high rate of false-positive results. This study aims to predict true antibody positivity and viremia by determining the most appropriate anti-HCV signal-to-cutoff (S/Co) value reflecting HCV infection. Methodology: The presence of anti-HCV antibodies and HCV RNA levels were examined in 72341 people who applied to the Mengücek Gazi Training and Research Hospital between January 2018 and December 2020. The anti-HCV levels were determined by using the Abbot Architect i2000 SR device (Abbot Diagnostics, Chicago, IL, USA). The levels of HCV RNA were determined in the COBAS AmpliPrep/COBAS, TaqMan 48 (Roche, Diagnostics, Pleasanton, USA) devices using serum samples from patients. Our study is a retrospective and methodological study. Results: Of the 150 patients with anti-HCV antibodies, 50 (33.3%) were HCV RNA positive, and 100 (66.7%) were HCV RNA negative. Anti-HCV levels of HCV RNA-positive patients were statistically higher than HCV RNA-negative patients. The most appropriate anti-HCV S/Co value for diagnosing hepatitis C patients was 15.4. The sensitivity of this value was 72%, specificity 88%, positive predictive value (PPV) 73.5%, and negative predictive value (NPV) 86.1%. Receiver operating characteristic (ROC) curve was significantly higher than 0.5 (95% confidence interval 0.938-0.827). Conclusions: Correct approaches can be applied in the diagnosis of HCV infection using the anti-HCV S/Co value found in our study. © 2024 Dabanlioǧlu et al. | |
| dc.identifier.doi | 10.3855/jidc.18105 | |
| dc.identifier.endpage | 135 | |
| dc.identifier.issn | 2036-6590 | |
| dc.identifier.issue | 1 | |
| dc.identifier.pmid | 38377100 | |
| dc.identifier.scopus | 2-s2.0-85185718387 | |
| dc.identifier.startpage | 131 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/12007 | |
| dc.identifier.volume | 18 | |
| dc.identifier.wos | WOS:001171532700002 | |
| dc.language.iso | en | |
| dc.publisher | Journal of Infection in Developing Countries | |
| dc.relation.ispartof | Journal of Infection in Developing Countries | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | anti-HCV | |
| dc.subject | HCV RNA | |
| dc.subject | S/Co | |
| dc.subject | Hepacivirus | |
| dc.subject | Hepatitis C | |
| dc.subject | Hepatitis C Antibodies | |
| dc.subject | Hospitals | |
| dc.subject | Humans | |
| dc.subject | Retrospective Studies | |
| dc.subject | RNA, Viral | |
| dc.subject | Sensitivity and Specificity | |
| dc.subject | Turkey | |
| dc.subject | adult | |
| dc.subject | aged | |
| dc.subject | Article | |
| dc.subject | chemiluminescent microparticle immunoassay | |
| dc.subject | false positive result | |
| dc.subject | female | |
| dc.subject | Hepatitis C virus | |
| dc.subject | human | |
| dc.subject | major clinical study | |
| dc.subject | male | |
| dc.subject | predictive value | |
| dc.subject | real time polymerase chain reaction | |
| dc.subject | receiver operating characteristic | |
| dc.subject | retrospective study | |
| dc.subject | university hospital | |
| dc.subject | viremia | |
| dc.subject | architect | |
| dc.subject | diagnosis | |
| dc.title | The best anti-HCV S/Co values for reflecting HCV infection in a university hospital in the eastern part of Turkey | |
| dc.type | Article | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 1 | |
| rdl.citation.wos | 2 | |
| rdl.department | Erzincan Binali Yıldırım University, Faculty of Medicine, Department of Medical Microbiology, Erzincan, Turkey. | |
| rdl.oa.status | gold | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
