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Your search keyword '"Albrecht, J K"' showing total 3 results
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3 results on '"Albrecht, J K"'

1. COMMON GENETIC VARIANTS DO NOT ASSOCIATE WITH IFN-INDUCED NEUTROPENIA IN A GENOME-WIDE ASSOCIATION STUDY OF CHRONIC HEPATITIS C PATIENTS IN THE IDEAL STUDY

Author

Thompson, A. J., Paul Clark, Singh, A., Ge, D., Fellay, J., Sulkowski, M. S., Muir, A. J., Tillman, H. L., Patel, K., Naggie, S., Shianna, K., Afdhal, N. H., Jacobson, I. M., Esteban, R., Poordad, F., Lawitz, E., Mccone, J., Shiffman, M. L., Galler, G. W., King, J. W., Kwo, P. Y., Nyberg, L., Noviello, S., Boparai, N., Koury, K. J., Pedicone, L., Brass, C. A., Albrecht, J. K., Goldstein, D. B., and Mchutchison, J. G.

2. IL28B GENOTYPE IS NOT ASSOCIATED WITH ADVANCED HEPATIC FIBROSIS IN CHRONIC HEPATITIS C PATIENTS ENROLLED IN THE IDEAL STUDY

Author

Thompson, A. J., Paul Clark, Fellay, J., Muir, A. J., Tillmann, H. L., Patel, K., Naggie, S., Afdhal, N. H., Jacobson, I. M., Esteban, R., Poordad, F., Lawitz, E., Mccone, J., Shiffman, M. L., Galler, G. W., King, J. W., Kwo, P. Y., Nyberg, L. M., Goodman, Z., Noviello, S., Boparai, N., Koury, K. J., Pedicone, L., Brass, C. A., Albrecht, J. K., Goldstein, D. B., Mchutchison, J. G., and Sulkowski, M. S.

3. Interleukin 28B polymorphisms are the only common genetic variants associated with low-density lipoprotein cholesterol (LDL-C) in genotype-1 chronic hepatitis C and determine the association between LDL-C and treatment response

Author

Clark, P. J., Thompson, A. J., Zhu, M., Vock, D. M., Zhu, Q., Ge, D., Patel, K., Harrison, S. A., Urban, T. J., Naggie, S., Fellay, J., Tillmann, H. L., Shianna, K., Noviello, S., Pedicone, L. D., Esteban, R., Kwo, P., Sulkowski, M. S., Afdhal, N., Albrecht, J. K., Goldstein, D. B., McHutchison, J. G., and Muir, A. J.

Subjects
Genetic, virus diseases, lipids (amino acids, peptides, and proteins), Polymorphism, digestive system diseases
Abstract

Low-density lipoprotein cholesterol (LDL-C) levels and interleukin 28B (IL28B) polymorphism are associated with sustained viral response (SVR) to peginterferon/ribavirin (pegIFN/RBV) for chronic hepatitis C (CHC) infection. IL28B has been linked with LDL-C levels using a candidate gene approach, but it is not known whether other genetic variants are associated with LDL-C, nor how these factors definitively affect SVR. We assessed genetic predictors of serum lipid and triglyceride levels in 1604 patients with genotype 1 (G1) chronic hepatitis C virus (HCV) infection by genome-wide association study and developed multivariable predictive models of SVR. IL28B polymorphisms were the only common genetic variants associated with pretreatment LDL-C level in Caucasians (rs12980275, P = 4.7 × 10(-17), poor response IL28B variants associated with lower LDL-C). The association was dependent on HCV infection, IL28B genotype was no longer associated with LDL-C in SVR patients after treatment, while the association remained significant in non-SVR patients (P < 0.001). LDL-C was significantly associated with SVR for heterozygous IL28B genotype patients (P < 0.001) but not for homozygous genotypes. SVR modelling suggested that IL28B heterozygotes with LDL-C > 130 mg/dL and HCV RNA ≤600 000 IU/mL may anticipate cure rates >80%, while the absence of these two criteria was associated with an SVR rate of

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