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VİRAL ETİYOLOJİLİ KRONİK KARACİĞER HASTALARINDA KARACİĞER FİBROZİSİ İÇİN BİYOKİMYASAL GÖSTERGELER

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Abstract (2. Language): 
Biochemical markers of Uver fibrosis in patients witlı ehronic viral /iver disease. Liver biopsy is the gold standard for the diagnosis of ehronic viral liver disease. Bccause liver biopsy is an invasive procedure, development of noninvasİve biochemical markers reflecting liver fibrosis is a necessity. The aim of our study is to determine the diagnostjc accuracy of serum hyaluronat and procoHagen III N-terminal peptide (PIIINP) levels for the evahıation of liver fibrosis in ehronic viral liver disease. 183 ehronic hepatitis patients with viral etiology were ineluded in our study (112 male, mean 44.4+13.7 year) and liver biopsy and/or laparoseopy were done in eacb. When the valucs of "the area under the receiver operating characterİstic (AUROC)" were calculated, (hey were found to be 0.892 + 0.027 for hyaluronat and 0.658 + 0.048 for PIIINP İn seperence cirrhosİs. The dİagnostic accuracy of serum hyaluronate and PIIINP for severe fibrosis (F3-F4) were 76% (cut-off value, 60 ng/ml) and 53.7% (cut-off value, 6.4 pg/1) and for cirrhosis werc 75.2% (cut-off value, 60 ng/ml) and 60,5% (cut-off value, 6.4 pg/1) res-pectivcly, Accordİng to our resuttSj it should bc considered that serum hyaluronat levels nıay be uscd as a noninvasive marker for diagnosis of chirrosis or severe fibrosis in viral liver disease.
Abstract (Original Language): 
Karaciğer biyopsisi, kronik karaciğer hastalığının tanısında altın standarttır. Ancak biyopsinin invaziv bir işlem olması, karaciğer fibrozisini yansıtan noninvaziv biyokimyasal göstergelerin geliştirilmesini zorunlu kılmaktadır. Çalışmamızın amacı, vira! etiyolojili kronik karaciğer hastalığında serum hyaluronat vc prokoliajen III N-terminal peptid (PII1NP) düzeylerinin karaciğer fibrozisini göstermedeki tanısal doğruluğunu saptamaktır. Çalışmaya viral etiyolojili 183 kronik hepatitÜ hasta afındı (112 erkek, ortalama yaş 44.4+13.7 yıl) ve hepsine karaciğer ponksiyon biyopsisi ve/veya laparoskopi yapıldı. ROC eğrileri ile hesaplandığında "the area under the receiver operating characterİstic (AUROC)" değerleri, sirozu göstermede hyaluronat için 0.892 ± 0.027, PIIINP için 0.658 ± 0.048 olarak bulundu. İleri fibrozisi (F3-F4) saptamada tanısal doğruluk oranları hyaluronat için (eşik değer 60 ng/ml) %76, PIIINP için (eşik değer 6.4 ug/1) %53.7, sirozu saptamada tanısal doğruluk oranları hyaluronat için (eşik değer 100 ng/ml) %75.2, PIIINP için (eşik değer 6.4 ug/i) %60.5 saptandı. Sonuçlarımız serum hyaluronat düzeylerinin viral etiyolojili karaciğer sirozunun veya ileri fibrozisinin tanısında noninvaziv bir gösterge olarak kullanılabileceği düşündürmektedir.
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