In:
Journal of Medical Virology, Wiley, Vol. 85, No. 3 ( 2013-03), p. 449-458
Abstract:
This study aimed to develop a model for predicting anemia using the inosine triphosphatase ( ITPA ) genotype and to evaluate its relationship with treatment outcome. Patients with genotype 1b chronic hepatitis C (n = 446) treated with peg‐interferon alpha and ribavirin (RBV) for 48 weeks were genotyped for the ITPA (rs1127354) and IL28B (rs8099917) genes. Data mining analysis generated a predictive model for anemia (hemoglobin (Hb) concentration 〈 10 g/dl); the CC genotype of ITPA , baseline Hb 〈 14.0 g/dl, and low creatinine clearance (CLcr) were predictors of anemia. The incidence of anemia was highest in patients with Hb 〈 14.0 g/dl and CLcr 〈 90 ml/min (76%), followed by Hb 〈 14.0 g/dl and ITPA CC (57%). Patients with Hb ≥14.0 g/dl and ITPA AA/CA had the lowest incidence of anemia (17%). Patients with two predictors (high‐risk) had a higher incidence of anemia than the others (64% vs. 28%, P 〈 0.0001). At baseline, the IL28B genotype was a predictor of a sustained virological response [adjusted odds ratio 9.88 (95% confidence interval 5.01–19.48), P 〈 0.0001]. In patients who achieved an early virological response, the IL28B genotype was not associated with a sustained virological response, while a high risk of anemia was a significant negative predictor of a sustained virological response [0.47 (0.24–0.91), P = 0.026]. For high‐risk patients with an early virological response, giving 〉 80% of the planned RBV dose increased sustained virological responses by 24%. In conclusion, a predictive model incorporating the ITPA genotype could identify patients with a high risk of anemia and reduced probability of sustained virological response. J. Med. Virol. 85:449–458, 2013. © 2013 Wiley Periodicals, Inc.
Type of Medium:
Online Resource
ISSN:
0146-6615
,
1096-9071
Language:
English
Publisher:
Wiley
Publication Date:
2013
detail.hit.zdb_id:
752392-0
detail.hit.zdb_id:
1475090-9
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