scholarly journals Elevated serum immunoglobulin G levels in patients with chronic liver disease in comparison to patients with autoimmune hepatitis

2010 ◽  
Vol 5 (1) ◽  
pp. 4857 ◽  
Author(s):  
Hind I. Fallatah ◽  
Hisham O. Akbar
2015 ◽  
Vol 2015 ◽  
pp. 1-8 ◽  
Author(s):  
Andreia Silva Evangelista ◽  
Maria Cristina Nakhle ◽  
Thiago Ferreira de Araújo ◽  
Clarice Pires Abrantes-Lemos ◽  
Marta Mitiko Deguti ◽  
...  

Iron abnormalities in chronic liver disease may be the result of genetic diseases or secondary factors. The present study aimed to identify subjects with HFE-HH in order to describe the frequency of clinical manifestations, identify risk factors for iron elevation, and compare the iron profile of HFE-HH to other genotypes in liver disease patients. A total of 108 individuals with hepatic disease, transferrin saturation (TS) > 45%, and serum ferritin (SF) > 350 ng/mL were tested for HFE mutations. Two groups were characterized: C282Y/C282Y or C282Y/H63D genotypes (n=16) were the HFE hereditary hemochromatosis (HFE-HH) group; and C282Y and H63D single heterozygotes, the H63D/H63D genotype, and wild-type were considered group 2 (n=92). Nonalcoholic liver disease, alcoholism, and chronic hepatitis C were detected more frequently in group 2, whereas arthropathy, hepatocarcinoma, diabetes, and osteoporosis rates were significantly higher in the HFE-HH group. TS > 82%, SF > 2685 ng/mL, and serum iron > 178 μg/dL were the cutoffs for diagnosis of HFE-HH in patients with liver disease. Thus, in non-Caucasian populations with chronic liver disease, HFE-HH diagnosis is more predictable in those with iron levels higher than those proposed in current guidelines for the general population.


2021 ◽  
Vol 12 (06) ◽  
pp. 251-260
Author(s):  
Rajaa M. Alshanketi ◽  
Reem Jabbad ◽  
Bayan Baghlaf ◽  
Romaysaa Al-Yamani ◽  
Majed Alsahafi ◽  
...  

2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
Giorgos Bamias ◽  
Michalis Gizis ◽  
Ioanna Delladetsima ◽  
Eyfrosyni Laoudi ◽  
Spyros I. Siakavellas ◽  
...  

Background. Decoy-receptor 3 (DcR3) exerts antiapoptotic and immunomodulatory function and is overexpressed in neoplastic and inflammatory conditions. Serum DcR3 (sDcR3) levels during the chronic hepatitis/cirrhosis/hepatocellular carcinoma (HCC) sequence have not been explored.Objective. To assess the levels and significance of sDcR3 protein in various stages of chronic liver disease.Methods. We compared sDcR3 levels between healthy controls and patients with chronic viral hepatitis (CVH), decompensated cirrhosis (DC), and HCC. Correlations between sDcR3 levels and various patient- and disease-related factors were analyzed.Results. sDcR3 levels were significantly higher in patients with CVH than in controls (P<0.01). sDcR3 levels were elevated in DC and HCC, being significantly higher compared not only to controls (P<0.001for both) but to CVH patients as well (P<0.001for both). In addition, DcR3 protein was detected in large quantities in the ascitic fluid of cirrhotics. In patients with CVH, sDcR3 significantly correlated to fibrosis severity, as estimated by Ishak score (P=0.019) or by liver stiffness measured with elastography (Spearmanr=0.698,P<0.001). In cirrhotic patients, significant positive correlations were observed between sDcR3 levels and markers of severity of hepatic impairment, including MELD score (r=0.653,P<0.001).Conclusions. Circulating levels of DcR3 are elevated during chronic liver disease and correlate with severity of liver damage. sDcR3 may serve as marker for liver fibrosis severity and progression to end-stage liver disease.


2019 ◽  
Vol 39 (9) ◽  
pp. 1641-1651
Author(s):  
Yuichi Honma ◽  
Michihiko Shibata ◽  
Tsuguru Hayashi ◽  
Masashi Kusanaga ◽  
Noriyoshi Ogino ◽  
...  

Hepatology ◽  
2016 ◽  
Vol 65 (2) ◽  
pp. 661-677 ◽  
Author(s):  
Dana Tedesco ◽  
Manoj Thapa ◽  
Sanjeev Gumber ◽  
Elizabeth J. Elrod ◽  
Khalidur Rahman ◽  
...  

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