Recognition of 7 genes signature (Cirrhosis Risk Score) in the diagnosed non-responders to DAAs therapy by intra-PBMCs nested HCV RNA PCR
- PMID: 37646837
- PMCID: PMC10468448
- DOI: 10.1186/s43141-023-00544-3
Recognition of 7 genes signature (Cirrhosis Risk Score) in the diagnosed non-responders to DAAs therapy by intra-PBMCs nested HCV RNA PCR
Abstract
Background and aims: Predictors of chronic HCV response to oral antiviral therapy (OAT) are related to host genetic variations. Single nucleotide polymorphisms (SNP) and alleles variations of host genes in association with hepatic fibro-cirrhotic changes have a distinct role in OAT outcomes. The current research evaluated the association of Cirrhosis-Risk-Scores (CRS) values, based on the correlation of seven genes signature-SNPs, with sonographic liver parenchymal changes in determining OAT outcomes.
Methods: All study subjects (n = 54) were recruited three months after completing OAT and classified into three groups. Group I (n = 21) had negative HCV PCR, group II (n = 17) showed positive solitary intra-PBMCs HCV infection, and group III(n = 16) was serum HCV RNA PCR-positive. All study-population were subjected to examination by hepatic-ultrasound (US), FIB-4-scoring, and screening for 7 gene-signature that addressed CRS values as low, intermediate, and high depending on gene SNPs identification.
Results: Group I showed a significant association with low CRS values compared to other groups (P < 0.001). Solitary intra- PBMCs HCV infection in group II was significantly combined with intermediate CRS values in comparison to groups I and III (P < 0.001). The high CRS values were significantly found in group III when compared to groups I and II (P < 0.01). On US imaging, low CRS values were common in normally appeared hepatic parenchyma (P < 0.001) and high CRS values were frequent in coarse-liver (P < 0.001), while bright-liver-tissues appearance was mainly detected in the intermediate CRS category (P = 0.09). On FIB-4 scoring, high CRS value were associated with hepatic fibro-cirrhosis compared to intermediate (P < 0.001) and low (P = 0.08) CRS-categories.
Conclusion: The current study concluded the association of (a) high CRS values with coarse liver in viral-RNA serologic relapse, (b) low CRS values with normal liver tissues in sustained virologic response (SVR), (c) intermediate CRS values with bright liver in solitary PBMCs relapse.
Keywords: CRS; DAAs; HCV Relapse; Liver fibro-cirrhosis; PBMCs PCR.
© 2023. Academy of Scientific Research and Technology.
Conflict of interest statement
The authors have no conflicts of interest related to this research. All procedures performed in the current work that involved human participants were in accordance with the ethical standards of the institutional and with the 1964 Helsinki Declaration and its later amendments or comparable ethical standards. Informed consent was obtained from all individual participants included in the current study. This article does not contain any studies with animals performed by any of the authors. Ethical approval certificate Registration number: Trop.Med._17Med.Research_Inf.GIT.Liv.Dis._0000017.
All authors declare that they have no competing interests.
Similar articles
-
HCV treatment outcome depends on SNPs of IFNL3-Gene polymorphisms (rs12979860) and cirrhotic changes in liver parenchyma.Heliyon. 2023 Oct 19;9(11):e21194. doi: 10.1016/j.heliyon.2023.e21194. eCollection 2023 Nov. Heliyon. 2023. PMID: 37928048 Free PMC article.
-
Treatment of hepatitis C virus infection with direct-acting antivirals plus ribavirin eliminates viral RNA from peripheral blood mononuclear cells and reduces virologic relapse in diverse hepatic parenchymal changes.Arch Virol. 2021 Apr;166(4):1071-1081. doi: 10.1007/s00705-021-04969-4. Epub 2021 Feb 3. Arch Virol. 2021. PMID: 33533976
-
Hepatitis C virus serologic relapse after treatment with direct-acting antivirals is dependent on viral RNA levels in peripheral blood mononuclear cells and the grade of liver cirrhosis.Arch Virol. 2018 Oct;163(10):2765-2774. doi: 10.1007/s00705-018-3922-7. Epub 2018 Jul 3. Arch Virol. 2018. PMID: 29971486 Clinical Trial.
-
Hepatitis C virus in chronic liver disease and hepatocellular carcinoma in Taiwan.Princess Takamatsu Symp. 1995;25:27-32. Princess Takamatsu Symp. 1995. PMID: 8875606 Review.
-
[Evaluation of viral hepatitis in solid organ transplantation].Acta Med Croatica. 2014 Apr;68(2):151-9. Acta Med Croatica. 2014. PMID: 26012153 Review. Croatian.
References
-
- Falleti E, Bitetto D, Fabris C, Cussigh A, Fornasiere E, Cmet S, et al. Role of interleukin 28B rs12979860 C/T polymorphism on the histological outcome of chronic hepatitis C: Relationship with gender and viral genotype. J Clin Immunol. 2011;31:891–899. doi: 10.1007/s10875-011-9547-1. - DOI - PubMed
-
- ABD ALLA MDA, EL-DESSOUKY YMM, ABDEL-HAMID MR, ZAIN EL-DEEN ANA. Prevalence of HCV infection among health care employee at Al Azhar University hospitals in Cairo, Egypt. J Egypt Soc Parasitol 2017;47:459–66. 10.21608/jesp.2017.77516
LinkOut - more resources
Full Text Sources