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Assessment of Alpha-1-Acid Glycoprotein as a new Biomarker for Hepatocellular Carcinoma

• 2018
العودة
معلومات البحث
المؤلفون Badawy A. Abdul Aziz1, Maha Zein-Elabedin Omar1, Abdelmoneam Ahmed2, Medhat A. Khalil2 and Amira MN Abdelrahman
الكلمات المفتاحية Not Available
المجلة العلمية Not Available
الناشر Not Available
المجلد Not Available
العدد Not Available
الصفحات Not Available
publication.type Local
رابط البحث Not Available
المواد المرفقة Not Available
الملخص
Background and study aim: The outcome
of patients with hepatocellular carcinoma
(HCC) remains poor because of late
diagnosis. We aimed to evaluate the
performances of serum alpha -1-acid
glycoprotein (AAG) for the diagnosis of
HCC, especially for HCC with low alphafetoprotein
(AFP).
Patients and Methods: Ninety patients
included in this study, 60 had HCC, and
30 (50%) of these were AFP low HCC
(AFP ≤20 ng/mL). The remaining 30 patients
were chronic hepatitis C and cirrhosis
without HCC as control group. Plasma
AAG was analyzed using quantitative
enzyme immunoassay technique.
Results: Serum level of AAG was
significantly elevated in low AFP HCC
group compared with high AFP HCC and
cirrhotic without HCC group, 1307.20 ±
9627 vs (850.82 ± 795.14 and 309.77±
220.17 respectively). Receiver operating
characteristic (ROC) curve showed that
the best cut off for AAG and AFP was
740 μg/ml and 20 ng/mL respectively.
The area under the curve of AAG was
significantly higher than that for AFP (0.95
vs 0.92) respectively. AAG at a cut-off value
of 740 μg/ml provides higher sensitivity
(73.3% vs 62%, respectively) and specificity
(74.0%, and 71%, respectively) in low
AFP HCC than high AFP HCC
Conclusion: The role of AFP in the
diagnosis of HCC is limited; AAG had
better performance in diagnosing HCC
patients with low AFP. So Serum level of
AAG might be used as a potential diagnostic
marker for hepatocellular carcinoma.