期刊文献+

Hepatitis C virus G1b infection decreases the number of small low-density lipoprotein particles 被引量:1

Hepatitis C virus G1b infection decreases the number of small low-density lipoprotein particles
下载PDF
导出
摘要 AIM: To investigate how hepatitis C virus(HCV) G1 b infection influences the particle number of lipoproteins.METHODS: The numbers of lipoprotein particles in fasting sera from 173 Japanese subjects, 82 with active HCV G1 b infection(active HCV group) and 91 with cleared HCV infection(SVR group), were examined. Serum lipoprotein was fractionated by high-performance liquid chromatography into twenty fractions. The cholesterol and triglyceride concentrations in each fraction were measured using Lipo SEARCH. The number of lipoprotein particles in each fraction was calculated using a newly developed algorithm, and the relationship between chronic HCV G1 b infection and the lipoprotein particle number was determined by multiple linear regression analysis.RESULTS: The median number of low-density lipoprotein(LDL) particles was significantly lower in the active HCV group [1182 nmol/L, interquartile range(IQR): 444 nmol/L] than in the SVR group(1363 nmol/L, IQR: 472 nmol/L, P < 0.001), as was that of highdensity lipoprotein(HDL) particles(14168 nmol/L vs 15054 nmol/L, IQR: 4114 nmol/L vs 3385 nmol/L, P = 0.042). The number of very low-density lipoprotein(VLDL) particles was similar between the two groups. Among the four LDL sub-fractions, the number of large LDL particles was similar between the two groups. However, the numbers of medium(median: 533.0 nmol/L, IQR: 214.7 nmol/L vs median: 633.5 nmol/L, IQR: 229.6 nmol/L, P < 0.001), small(median: 190.9 nmol/L, IQR: 152.4 nmol/L vs median: 263.2 nmol/L, IQR: 159.9 nmol/L; P < 0.001), and very small LDL particles(median: 103.5 nmol/L, IQR: 66.8 nmol/L vs median: 139.3 nmol/L, IQR: 67.3 nmol/L, P < 0.001) were significantly lower in the active HCV group than in the SVR group, respectively. Multiple linear regression analysis indicated an association between HCV G1 b infection and the decreased numbers of medium, small, and very small LDL particles. However, active HCV infection did not affect the number of large LDL particles or any sub-fractions of VLDL and HDL particles.CONCLUSION: HCV G1 b infection decreases the numbers of medium, small, and very small LDL particles. AIM: To investigate how hepatitis C virus (HCV) G1b infection influences the particle number of lipoproteins.METHODS: The numbers of lipoprotein particles in fasting sera from 173 Japanese subjects, 82 with active HCV G1b infection (active HCV group) and 91 with cleared HCV infection (SVR group), were examined. Serum lipoprotein was fractionated by high-performance liquid chromatography into twenty fractions. The cholesterol and triglyceride concentrations in each fraction were measured using LipoSEARCH. The number of lipoprotein particles in each fraction was calculated using a newly developed algorithm, and the relationship between chronic HCV G1b infection and the lipoprotein particle number was determined by multiple linear regression analysis.RESULTS: The median number of low-density lipoprotein (LDL) particles was significantly lower in the active HCV group [1182 nmol/L, interquartile range (IQR): 444 nmol/L] than in the SVR group (1363 nmol/L, IQR: 472 nmol/L, P &#x0003c; 0.001), as was that of high-density lipoprotein (HDL) particles (14168 nmol/L vs 15054 nmol/L, IQR: 4114 nmol/L vs 3385 nmol/L, P = 0.042). The number of very low-density lipoprotein (VLDL) particles was similar between the two groups. Among the four LDL sub-fractions, the number of large LDL particles was similar between the two groups. However, the numbers of medium (median: 533.0 nmol/L, IQR: 214.7 nmol/L vs median: 633.5 nmol/L, IQR: 229.6 nmol/L, P &#x0003c; 0.001), small (median: 190.9 nmol/L, IQR: 152.4 nmol/L vs median: 263.2 nmol/L, IQR: 159.9 nmol/L; P &#x0003c; 0.001), and very small LDL particles (median: 103.5 nmol/L, IQR: 66.8 nmol/L vs median: 139.3 nmol/L, IQR: 67.3 nmol/L, P &#x0003c; 0.001) were significantly lower in the active HCV group than in the SVR group, respectively. Multiple linear regression analysis indicated an association between HCV G1b infection and the decreased numbers of medium, small, and very small LDL particles. However, active HCV infection did not affect the number of large LDL particles or any sub-fractions of VLDL and HDL particles.CONCLUSION: HCV G1b infection decreases the numbers of medium, small, and very small LDL particles.
出处 《World Journal of Gastroenterology》 SCIE CAS 2016年第29期6716-6725,共10页 世界胃肠病学杂志(英文版)
基金 Supported by Shionogi Pharmaceutical KK
关键词 Chronic hepatitis C LIPOPROTEIN PARTICLES LOW-DENSITY LIPOPROTEINS Very LOW-DENSITY LIPOPROTEINS Tri Chronic hepatitis C Lipoprotein particles Low-density lipoproteins Very low-density lipoproteins Triglycerides Cholesterol Regression analysis
  • 相关文献

参考文献62

  • 1Lerat Hervé,Higgs Martin,Pawlotsky Jean-Michel.Animal models in the study of hepatitis C virus-associated liver pathologies. Expert review of gastroenterology & hepatology . 2011
  • 2Jean-Christophe Meunier,Rodney S. Russell,Ronald E. Engle,Kristina N. Faulk,Robert H. Purcell,Suzanne U. Emerson.Apolipoprotein C1 Association with Hepatitis C Virus. Journal of Virology . 2008
  • 3Bruno Sainz,Naina Barretto,Danyelle N Martin,Nobuhiko Hiraga,Michio Imamura,Snawar Hussain,Katherine A Marsh,Xuemei Yu,Kazuaki Chayama,Waddah A Alrefai,Susan L Uprichard.Identification of the Niemann-Pick C1–like 1 cholesterol absorption receptor as a new hepatitis C virus entry factor. Nature Medicine . 2012
  • 4Packard C J,Munro A,Lorimer A R,Gotto A M,Shepherd J.Metabolism of apolipoprotein B in large triglyceride-rich very low density lipoproteins of normal and hypertriglyceridemic subjects. The Journal of Clinical Investigation . 1984
  • 5Ye Jin.Reliance of host cholesterol metabolic pathways for the life cycle of hepatitis C virus. PLoS pathogens . 2007
  • 6Chia-Yen Dai,Wan-Long Chuang,Chi-Kung Ho,Ming-Yen Hsieh,Jee-Fu Huang,Li-Po Lee,Nai-Jen Hou,Zu-Yau Lin,Shinn-Cherng Chen,Ming-Yuh Hsieh,Liang-Yen Wang,Jun-Fa Tsai,Wen-Yu Chang,Ming-Lung Yu.??Associations between hepatitis C viremia and low serum triglyceride and cholesterol levels: A community-based study(J)Journal of Hepatology . 2008 (1)
  • 7Tanaka, Naoki,Moriya, Kyoji,Kiyosawa, Kendo,Koike, Kazuhiko,Gonzalez, Frank J,Aoyama, Toshifumi.PPAR[alpha] activation is essential for HCV core protein-induced hepatic steatosis and hepatocellular carcinoma in mice[J]. Journal of Clinical Investigation . 2008 (2)
  • 8Neumann AU,Lam NP,Dahari H,et al.Hepatitis C viral dynamics in vivo and the antiviral efficacy of interferon-alpha therapy. Science . 1998
  • 9Cole TG,Contois JH,Csako G,Mc Connell JP,Remaley AT,Devaraj S,Hoefner DM,Mallory T,Sethi AA,Warnick GR.Association of apolipoprotein B and nuclear magnetic resonance spectroscopy-derived LDL particle number with outcomes in25 clinical studies:assessment by the AACC Lipoprotein and Vascular Diseases Division Working Group on Best Practices. Clinical Chemistry . 2013
  • 10Packard C J,Gaw A,Demant T,Shepherd J.Development and application of a multicompartmental model to study very low density lipoprotein subfraction metabolism. Journal of Lipid Research . 1995

共引文献18

同被引文献11

引证文献1

二级引证文献4

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部