Noninvasive prediction of hepatitis C-associated hepatocellular carcinoma using circulating apolipoproteins
Background and aims Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related mortality worldwide. We investigated the potential usefulness of circulating apolipoproteins (Apo-A1 and Apo-A4) in HCC screening and diagnosis. Patients and methods We included 60 adult patients with h...
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Format: | Article |
Language: | English |
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SpringerOpen
2019-01-01
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Series: | The Egyptian Journal of Internal Medicine |
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Online Access: | http://www.esim.eg.net/article.asp?issn=1110-7782;year=2019;volume=31;issue=4;spage=451;epage=457;aulast=El |
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author | Hasan El Garem Gamal Esmat Rabab Salama Hanan Fouad Dina Sabry Yomna Mostafa Dalia Omran Heba Omar |
author_facet | Hasan El Garem Gamal Esmat Rabab Salama Hanan Fouad Dina Sabry Yomna Mostafa Dalia Omran Heba Omar |
author_sort | Hasan El Garem |
collection | DOAJ |
description | Background and aims Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related mortality worldwide. We investigated the potential usefulness of circulating apolipoproteins (Apo-A1 and Apo-A4) in HCC screening and diagnosis.
Patients and methods We included 60 adult patients with hepatitis C virus-related chronic liver disease including HCC, in addition to 20 healthy controls. Patients were stratified into three equal groups, with 20 patients each: chronic hepatitis C, posthepatitis C cirrhosis (liver cirrhosis), and HCC. All patients and controls underwent full clinical assessment, laboratory investigations, and evaluation of candidate apolipoproteins by enzyme-linked immunoassay.
Results Significantly higher Apo-A1 and Apo-A4 levels were detected in patients with HCC than in those with liver cirrhosis (P<0.001). Receiver operator characteristic curve showed that for HCC diagnosis, a cutoff of 78.6 mg/dl for Apo-A1 yielded 90% sensitivity and 100% specificity and a cutoff of 16.5 mg/dl for Apo-A4 yielded 85% sensitivity and 80% specificity. Furthermore, within HCC group, Apo-A1 was significantly higher in patients with small HCC (>2 cm) than those with large tumors (P=0.01). Lower Apo-A1 level correlated significantly with pylethrombosis (P=0.007).
Conclusion Apo-A1 and Apo-A4 are novel biomarkers for HCC screening and diagnosis, with a special discriminative ability for Apo-A1 for those with small tumors and those with pylethrombosis. |
first_indexed | 2024-12-23T04:43:14Z |
format | Article |
id | doaj.art-ab3ea91286f14d8b8531c6e27eac961d |
institution | Directory Open Access Journal |
issn | 1110-7782 2090-9098 |
language | English |
last_indexed | 2024-12-23T04:43:14Z |
publishDate | 2019-01-01 |
publisher | SpringerOpen |
record_format | Article |
series | The Egyptian Journal of Internal Medicine |
spelling | doaj.art-ab3ea91286f14d8b8531c6e27eac961d2022-12-21T17:59:44ZengSpringerOpenThe Egyptian Journal of Internal Medicine1110-77822090-90982019-01-0131445145710.4103/ejim.ejim_26_19Noninvasive prediction of hepatitis C-associated hepatocellular carcinoma using circulating apolipoproteinsHasan El GaremGamal EsmatRabab SalamaHanan FouadDina SabryYomna MostafaDalia OmranHeba OmarBackground and aims Hepatocellular carcinoma (HCC) is one of the leading causes of cancer-related mortality worldwide. We investigated the potential usefulness of circulating apolipoproteins (Apo-A1 and Apo-A4) in HCC screening and diagnosis. Patients and methods We included 60 adult patients with hepatitis C virus-related chronic liver disease including HCC, in addition to 20 healthy controls. Patients were stratified into three equal groups, with 20 patients each: chronic hepatitis C, posthepatitis C cirrhosis (liver cirrhosis), and HCC. All patients and controls underwent full clinical assessment, laboratory investigations, and evaluation of candidate apolipoproteins by enzyme-linked immunoassay. Results Significantly higher Apo-A1 and Apo-A4 levels were detected in patients with HCC than in those with liver cirrhosis (P<0.001). Receiver operator characteristic curve showed that for HCC diagnosis, a cutoff of 78.6 mg/dl for Apo-A1 yielded 90% sensitivity and 100% specificity and a cutoff of 16.5 mg/dl for Apo-A4 yielded 85% sensitivity and 80% specificity. Furthermore, within HCC group, Apo-A1 was significantly higher in patients with small HCC (>2 cm) than those with large tumors (P=0.01). Lower Apo-A1 level correlated significantly with pylethrombosis (P=0.007). Conclusion Apo-A1 and Apo-A4 are novel biomarkers for HCC screening and diagnosis, with a special discriminative ability for Apo-A1 for those with small tumors and those with pylethrombosis.http://www.esim.eg.net/article.asp?issn=1110-7782;year=2019;volume=31;issue=4;spage=451;epage=457;aulast=Elapolipoprotein-a1apolipoprotein-a4diagnosispylethrombosisscreeningsmall hepatocellular carcinoma |
spellingShingle | Hasan El Garem Gamal Esmat Rabab Salama Hanan Fouad Dina Sabry Yomna Mostafa Dalia Omran Heba Omar Noninvasive prediction of hepatitis C-associated hepatocellular carcinoma using circulating apolipoproteins The Egyptian Journal of Internal Medicine apolipoprotein-a1 apolipoprotein-a4 diagnosis pylethrombosis screening small hepatocellular carcinoma |
title | Noninvasive prediction of hepatitis C-associated hepatocellular carcinoma using circulating apolipoproteins |
title_full | Noninvasive prediction of hepatitis C-associated hepatocellular carcinoma using circulating apolipoproteins |
title_fullStr | Noninvasive prediction of hepatitis C-associated hepatocellular carcinoma using circulating apolipoproteins |
title_full_unstemmed | Noninvasive prediction of hepatitis C-associated hepatocellular carcinoma using circulating apolipoproteins |
title_short | Noninvasive prediction of hepatitis C-associated hepatocellular carcinoma using circulating apolipoproteins |
title_sort | noninvasive prediction of hepatitis c associated hepatocellular carcinoma using circulating apolipoproteins |
topic | apolipoprotein-a1 apolipoprotein-a4 diagnosis pylethrombosis screening small hepatocellular carcinoma |
url | http://www.esim.eg.net/article.asp?issn=1110-7782;year=2019;volume=31;issue=4;spage=451;epage=457;aulast=El |
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