Literature DB >> 17175356

Blood gene expression profiling in liver transplant recipients with hepatitis C virus and posttransplantation diabetes mellitus.

C J Driscoll1, A K Cashion, D K Hathaway, C Thompson, Y Conley, C Riely, L Xu, R Homayouni.   

Abstract

BACKGROUND: Hepatitis C virus (HCV) is a risk factor for developing posttransplantation diabetes mellitus (PTDM) after liver transplantation; little is known about the biological mechanisms involved with this risk. This study investigated gene expression differences to provide insight into potential mechanisms. PATIENTS AND METHODS: Gene expression profiles of blood samples obtained from 6 HCV+ liver transplant recipients were determined using Affymetrix U133 Plus 2.0 microarrays. Differential gene expression was assessed between HCV+ recipients with PTDM (n = 3) and without PTDM (n = 3) using the GeneSpring 7.3 software package. The Welch t test was used to identify significant differences (P < .05) between groups. Gene expression profiles for 6 HCV- liver transplant recipients (with PTDM = 3, without PTDM = 3) were used as a blind test set to evaluate a subset of genes to predict PTDM.
RESULTS: Expression levels of 347 genes were significantly different between recipients with PTDM and those without PTDM. Seventy-four genes were up-regulated and 270 were down-regulated in PTDM. Genes were categorized into functional classes: apoptosis (n = 69 genes); immune function (n = 110); diabetes (n = 17); hepatitis C (n = 12); liver transplant (n = 69). The expression profile of a subset of genes was evaluated for predicting PTDM in 6 HCV- transplant recipients. We accurately predicted the presence or absence of PTDM in 5/6 recipients.
CONCLUSIONS: PTDM in HCV+ liver transplant recipients was associated with down-regulated expression of a large number of genes. A subset of these genes was useful to predict PTDM in HCV- recipients. Most genes were associated with apoptosis and immune function. HCV may act as a primer by affecting a group of genes involved in developing diabetes.

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Year:  2006        PMID: 17175356      PMCID: PMC1847576          DOI: 10.1016/j.transproceed.2006.10.116

Source DB:  PubMed          Journal:  Transplant Proc        ISSN: 0041-1345            Impact factor:   1.066


  6 in total

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Review 2.  Glucose abnormalities in patients with hepatitis C virus infection: Epidemiology and pathogenesis.

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Journal:  Diabetes Care       Date:  2006-05       Impact factor: 19.112

3.  Hepatitis C infection increases the risk of new-onset diabetes after transplantation in liver allograft recipients.

Authors:  Jordana L Soule; Ali J Olyaei; Tobin A Boslaugh; Ann M H Busch; Jonathan M Schwartz; Samuel H Morehouse; John M Ham; Susan L Orloff
Journal:  Am J Surg       Date:  2005-05       Impact factor: 2.565

4.  Correlation of genetic markers of rejection with biopsy findings following human pancreas transplant.

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5.  Hepatitis C virus is independently associated with increased insulin resistance after liver transplantation.

Authors:  Aymin Delgado-Borrego; Deborah Casson; David Schoenfeld; Ma Somsouk; Adam Terella; Sergio H Jordan; Atul Bhan; Seema Baid; A Benedict Cosimi; Manuel Pascual; Raymond T Chung
Journal:  Transplantation       Date:  2004-03-15       Impact factor: 4.939

6.  Posttransplant diabetes mellitus in liver transplant recipients.

Authors:  Carolyn J Driscoll; Ann K Cashion; Donna K Hathaway; Carol Thompson; Yvette Conley; Osama Gaber; Santiago Vera; Hosein Shokouh-Amiri
Journal:  Prog Transplant       Date:  2006-06       Impact factor: 1.065

  6 in total
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1.  Collection and storage of human blood and adipose for genomic analysis of clinical samples.

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2.  Integrating genomics into biobehavioral research: a transplantation exemplar.

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3.  Peripheral blood gene expression profiling for cardiovascular disease assessment.

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  3 in total

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