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The Cumulative Effects of Known Susceptibility Variants to Predict Primary Biliary Cirrhosis Risk

Multiple genetic variants influence the risk for development of primary biliary cirrhosis (PBC). To explore the cumulative effects of known susceptibility loci on risk, we utilized a weighted genetic risk score (wGRS) to evaluate whether genetic information can predict susceptibility. The wGRS was c...

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Autores principales: Tang, Ruqi, Chen, Haoyan, Miao, Qi, Bian, Zhaolian, Ma, Wansu, Feng, Xiaomei, Seldin, Michael F., Invernizzi, Pietro, Gershwin, M. Eric, Liao, Wilson, Ma, Xiong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5553973/
https://www.ncbi.nlm.nih.gov/pubmed/25569263
http://dx.doi.org/10.1038/gene.2014.76
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author Tang, Ruqi
Chen, Haoyan
Miao, Qi
Bian, Zhaolian
Ma, Wansu
Feng, Xiaomei
Seldin, Michael F.
Invernizzi, Pietro
Gershwin, M. Eric
Liao, Wilson
Ma, Xiong
author_facet Tang, Ruqi
Chen, Haoyan
Miao, Qi
Bian, Zhaolian
Ma, Wansu
Feng, Xiaomei
Seldin, Michael F.
Invernizzi, Pietro
Gershwin, M. Eric
Liao, Wilson
Ma, Xiong
author_sort Tang, Ruqi
collection PubMed
description Multiple genetic variants influence the risk for development of primary biliary cirrhosis (PBC). To explore the cumulative effects of known susceptibility loci on risk, we utilized a weighted genetic risk score (wGRS) to evaluate whether genetic information can predict susceptibility. The wGRS was created using twenty-six known susceptibility loci and investigated in 1840 UK PBC and 5164 controls. Our data indicate that the wGRS was significantly different between PBC and controls (P=1.61E-142). Moreover, we assessed predictive performance of wGRS on disease status by calculating the area under the receiver operator characteristic curve (AUC). The AUC for the purely genetic model was 0.72 and for gender plus genetic model was 0.82, with confidence limits substantially above random predictions. The risk of PBC using logistic regression was estimated after dividing individuals into quartiles. Individuals in the highest risk group disclosed demonstrated a substantially increased risk for PBC, compared to the lowest risk group (OR: 9.3, P=1.91E-084). Finally, we validated our findings in an analysis of an Italian PBC cohort. Our data suggested that the wGRS utilizing genetic variants was significantly associated with increased risk for PBC with consistent discriminant ability. Our study is a first step toward risk prediction for PBC.
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spelling pubmed-55539732017-08-11 The Cumulative Effects of Known Susceptibility Variants to Predict Primary Biliary Cirrhosis Risk Tang, Ruqi Chen, Haoyan Miao, Qi Bian, Zhaolian Ma, Wansu Feng, Xiaomei Seldin, Michael F. Invernizzi, Pietro Gershwin, M. Eric Liao, Wilson Ma, Xiong Genes Immun Article Multiple genetic variants influence the risk for development of primary biliary cirrhosis (PBC). To explore the cumulative effects of known susceptibility loci on risk, we utilized a weighted genetic risk score (wGRS) to evaluate whether genetic information can predict susceptibility. The wGRS was created using twenty-six known susceptibility loci and investigated in 1840 UK PBC and 5164 controls. Our data indicate that the wGRS was significantly different between PBC and controls (P=1.61E-142). Moreover, we assessed predictive performance of wGRS on disease status by calculating the area under the receiver operator characteristic curve (AUC). The AUC for the purely genetic model was 0.72 and for gender plus genetic model was 0.82, with confidence limits substantially above random predictions. The risk of PBC using logistic regression was estimated after dividing individuals into quartiles. Individuals in the highest risk group disclosed demonstrated a substantially increased risk for PBC, compared to the lowest risk group (OR: 9.3, P=1.91E-084). Finally, we validated our findings in an analysis of an Italian PBC cohort. Our data suggested that the wGRS utilizing genetic variants was significantly associated with increased risk for PBC with consistent discriminant ability. Our study is a first step toward risk prediction for PBC. 2015-01-08 2015 /pmc/articles/PMC5553973/ /pubmed/25569263 http://dx.doi.org/10.1038/gene.2014.76 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Tang, Ruqi
Chen, Haoyan
Miao, Qi
Bian, Zhaolian
Ma, Wansu
Feng, Xiaomei
Seldin, Michael F.
Invernizzi, Pietro
Gershwin, M. Eric
Liao, Wilson
Ma, Xiong
The Cumulative Effects of Known Susceptibility Variants to Predict Primary Biliary Cirrhosis Risk
title The Cumulative Effects of Known Susceptibility Variants to Predict Primary Biliary Cirrhosis Risk
title_full The Cumulative Effects of Known Susceptibility Variants to Predict Primary Biliary Cirrhosis Risk
title_fullStr The Cumulative Effects of Known Susceptibility Variants to Predict Primary Biliary Cirrhosis Risk
title_full_unstemmed The Cumulative Effects of Known Susceptibility Variants to Predict Primary Biliary Cirrhosis Risk
title_short The Cumulative Effects of Known Susceptibility Variants to Predict Primary Biliary Cirrhosis Risk
title_sort cumulative effects of known susceptibility variants to predict primary biliary cirrhosis risk
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5553973/
https://www.ncbi.nlm.nih.gov/pubmed/25569263
http://dx.doi.org/10.1038/gene.2014.76
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