Objective: Our main aim was to investigate the serum lipid levels in a series of patients with liver cirrhosis of viral origin. Subjects and Methods: The study comprised 90 patients, 60 with viral liver cirrhosis, equally divided between hepatitis virus C (HCV) and B (HBV) etiologies, and 30 control patients with no known liver pathology. Patients were investigated during a 5-year period in the 1st Medical Clinic of the Emergency County Hospital of Craiova, Romania. The following series of serum lipid parameters were recorded: lipemia, total cholesterol and cholesteryl ester, high-density lipoprotein (HDL) cholesterol, low-density lipoprotein (LDL) cholesterol, very-low-density lipoprotein (VLDL) cholesterol and triglyceride (TG) values. Statistical analysis of these parameters was performed using the ANOVA test followed by Tukey multiple comparison tests to compare replicate means; p < 0.05 was considered statistically significant. Results: We observed significantly lower values for serum lipids (543.5 and 549.37 mg/dl in the HBV and HCV cirrhosis subgroups, compared with 649.9 mg/dl in controls), total cholesterol (143.6 and 147.9 vs. 198.0 mg/dl, respectively), cholesteryl esters (83.6 and 80, compared to 147.9 mg/dl, respectively), LDL cholesterol (91.6 and 88.5 vs. 132.4 mg/dl) in both cirrhosis groups when compared with controls (p < 0.001), as well as HDL cholesterol (32.1 and 36.9 vs. 47.3 mg/dl, p < 0.05). However, TG and VLDL cholesterol values of controls and cirrhosis groups were similar (p > 0.05). We did not register any differences between the two cirrhosis groups (p > 0.05). Conclusion: Our data showed that both HCV and HBV cirrhosis severely impaired liver lipid metabolism. Late stages of the disease resulted in a pseudonormalization of VLDL cholesterol and TG values.

1.
Nguyen P, Leray V, Diez M, Serisier S, Le Bloc’h J, Siliart B, Dumon H: Liver lipid metabolism. J Anim Physiol Anim Nutr 2008;92:272–283.
2.
Cicognani C, Malavolti M, Morselli-Labate AM, Zamboni L, Sama C, Barbara L: Serum lipid and lipoprotein patterns in patients with liver cirrhosis and chronic active hepatitis. Arch Intern Med 1997;157:792–796.
3.
Cimminiello C, Soncini M, Gerosa MC, Toschi V, Motta A, Bonfardeci G: Lipoprotein (a) and fibrinolytic system in liver cirrhosis. Coagulation Abnormalities in Liver Cirrhosis (CALC) Study Group. Biomed Pharmacother 1995;49:364–368.
4.
Jarmay K, Karacsony G, Nagy A, Schaff Z: Changes in lipid metabolism in chronic hepatitis C. World J Gastroenterol 2005;11:6422–6428.
5.
Kaye GL, Kruszynska YT, Harry DS, Heslop K, Johnston DG, McIntyre N: Lipid metabolism and insulin resistance in cirrhosis. J Hepatol 1994;20:782–791.
6.
Hiraoka H, Yamashita S, Matsuzawa Y, Kubo M, Nozaki S, Sakai N, Hirano K, Kawata S, Tarui S: Decrease of hepatic triglyceride lipase levels and increase of cholesteryl ester transfer protein levels in patients with primary biliary cirrhosis: relationship to abnormalities in high-density lipoprotein. Hepatology 1993;18:103–110.
7.
Irshad M, Dube R, Joshi YK: Impact of viral hepatitis on apo- and lipoprotein status in blood. Med Princ Pract 2007;16:310–314.
8.
Siagris D, Christofidou M, Theocharis GJ, Pagoni N, Papadimitriou C, Lekkou A, Thomopoulos K, Starakis I, Tsamandas AC, Labropoulou-Karatza C: Serum lipid pattern in chronic hepatitis C: histological and virological correlations. J Viral Hepat 2006;13:56–61.
9.
Vere CC, Neagoe D, Streba CT, Prejbeanu I, Ianosi G, Comanescu V, Pirici D: Steatosis and serum lipid patterns in patients with chronic viral hepatitis: differences related to viral etiology. Rom J Morphol Embryol 2010;51:509–514.
10.
Ramcharran D, Wahed AS, Conjeevaram HS, Evans RW, Wang T, Belle SH, Yee LJ: Serum lipids and their associations with viral levels and liver disease severity in a treatment-naive chronic hepatitis C type 1-infected cohort. J Viral Hepat 2011;18:e144–e152.
11.
Moritani M, Adachi K, Arima N, Takashima T, Miyaoka Y, Niigaki M, Furuta K, Sato S, Kinoshita Y: A study of arteriosclerosis in healthy subjects with HBV and HCV infection. J Gastroenterol 2005;40:1049–1053.
12.
Perales J, Angel Lasuncion M, Cano A, Martin-Scapa MA, Maties M, Herrera E: Changes in the lipid profile in chronic hepatopathies. Med Clin 1994;102:364–368.
13.
Tan TC, Crawford DH, Jaskowski LA, Murphy TM, Heritage ML, Subramaniam VN, Clouston AD, Anderson GJ, Fletcher LM: Altered lipid metabolism in Hfe-knockout mice promotes severe NAFLD and early fibrosis. Am J Physiol Gastrointest Liver Physiol 2011;301:G865–G876.
14.
Man EB, Kartin BL, Durlacher SH, Peters JP: The lipids of serum and liver in patients with hepatic diseases. J Clin Invest 1945;24:623–643.
15.
Petrides AS, Groop LC, Riely CA, DeFronzo RA: Effect of physiologic hyperinsulinemia on glucose and lipid metabolism in cirrhosis. J Clin Invest 1991;88:561–570.
16.
Onuegbu AJ, Olisekodiaka JM, Adebolu OE, Adesiyan A, Ayodele OE: Coffee consumption could affect the activity of some liver enzymes and other biochemical parameters in healthy drinkers. Med Princ Pract 2011;20:514–518.
17.
Al-Qabandi W, Owayed AF, Dhaunsi GS: Cellular oxidative stress and peroxisomal enzyme activities in pediatric liver transplant patients. Med Princ Pract 2012;21:264–270.
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