Influence of metabolic syndrome on significant hepatic fibrosis in patients with chronic hepatitis B
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摘要: 目的分析代谢综合征组分疾病对慢性乙型肝炎(CHB)患者显著肝纤维化的影响并探讨其危险因素。方法收集新疆医科大学第四附属医院肝病科2016年1月-2017年5月就诊的CHB患者,按照是否合并非酒精性脂肪性肝病(NAFLD)、糖脂异常分为3组。收集患者的一般资料,所有患者均进行瞬时弹性成像检测,测量身高、体质量,并计算BMI,进行肝功能、血常规、血脂、HBsAg定量、HBV DNA的检测。利用公式计算FIB-4及APRI值。符合正态分布的计量资料多组间比较采用单因素方差分析,进一步两两比较采用LSD-t检验;不符合正态分布的计量资料多组间比较采用Kruskal-Wallis H秩和检验,进一步两两比较采用Wilcoxon秩和检验。计数资料组间比较采用χ2检验。应用单因素和多因素logistic回归模型分析显著肝纤维化的影响因素。结果CHB合并NAFLD组患者脂肪衰减参数[(283. 16±38. 43) dB/m]、肝硬度值(LSM)[9. 40 (7. 50~12. 07) k Pa]值均高于CHB组[(230. 61±29. 97) dB/m、8. 60(6. 37~11. 92) k...Abstract: Objective To investigate the influence of metabolic syndrome components on significant hepatic fibrosis in patients with chronic hepatitis B (CHB) and related risk factors. Methods The patients with CHB who attended Department of Hepatology in The Fourth Affiliated Hospital of Xinjiang Medical University from January 2016 to May 2017 were enrolled and divided into three groups according to the presence or absence of nonalcoholic fatty liver disease (NAFLD) or abnormal glycolipid. The patients' general information was collected, and transient elastography was performed for all patients. Body height and body weight were measured to calculate body mass index (BMI) . Liver function assessment, routine blood test, and HBsAg quantification were performed, and blood lipids and HBV DNA were measured. Fibrosis-4 (FIB-4) and aspartate aminotransferase-to-platelet ratio index (APRI) were calculated according to equations. A one-way analysis of variance was used for comparison of continuous data between groups, and the least significant difference t-test was used for further comparison between two groups; the Kruskal-Wallis H rank sum test was used for comparison of non-normally distributed continuous data between groups, and the Wilcoxon rank-sum test was used for further comparison between two groups. The chi-square test was used for comparison of categorical data between groups. Univariate and multivariate logistic regression analyses were used to identify the influencing factors for significant hepatic fibrosis. Results The CHB-NAFLD group had significantly higher controlled attenuation parameter (CAP) and liver stiffness measurement (LSM) than the CHB group and the CHB-abnormal glycolipid group [CAP: 283. 16 ± 38. 43 d B/m vs 230. 61 ± 29. 97 db/m/237. 82 ± 35. 98 dB/m, P < 0. 05; LSM: 9. 40 (7. 50-12. 07) k Pa vs 8. 60 (6. 37-11. 92) k Pa/8. 20 (6. 00-11. 15) kPa, P < 0. 05], and LSM increased with the increase in the severity of NAFLD (H = 7. 76, P = 0. 02) . The CHB patients with abnormal glucose and lipids had a significantly higher LSM than those with abnormal blood lipid levels alone [9. 6 (8. 22-12. 07) vs7. 5 (5. 7-9. 67) , P < 0. 05]. The multivariate logistic regression analysis showed that increasing age (odds ratio [OR]= 1. 134, 95%confidence interval [CI]: 1. 010-1. 273, P < 0. 05) , an increase in body mass index (OR = 1. 297, 95% CI: 1. 084-1. 553, P <0. 05) , a high gamma-glutamyl transpeptidase (GGT) level (OR = 1. 025, 95% CI: 1. 006-1. 045, P < 0. 05) , a low triglyceride (TG) level (OR = 0. 399, 95% CI: 0. 180-0. 882, P < 0. 05) , and a high HBsAg level (OR = 2. 205, 95% CI: 1. 159-4. 194, P < 0. 05) were independent risk factors for significant hepatic fibrosis in CHB patients. Conclusion Besides age and high HBsAg level, overweight, a high GGT level, and a relatively low TG level also increase the risk of significant hepatic fibrosis in CHB patients.
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Key words:
- hepatitis B, chronic /
- liver cirrhosis /
- metabolic syndrome X
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[1] LIU Y, ZHANG S, ZHAO Y, et al. Development and application of the Chinese (Mainland) version of chronic liver disease questionnaire to assess the health-related quality of life (HRQo L) in patients with chronic hepatitis B[J]. PLo S One, 2016, 11 (9) :e0162763. [2] XIE XC, LIU MH, ZHAO SH, et al. Assessment of therapeutic effect of nuemu pills on the hepatitis-B liver fibrosis[J]. J Changchun Univ Chin Med, 2016, 32 (1) :123-125. (in Chinese) 谢湘春, 刘明晖, 赵树华, 等.疟母丸治疗乙型肝炎肝纤维化的效果[J].长春中医药大学学报, 2016, 32 (1) :123-125 [3] JARCUSKA P, DRAZILOVA S, FEDACKO J, et al. Association between hepatitis B and metabolic syndrome:Current state of the art[J]. World J Gastroenterol, 2016, 22 (1) :155-164. [4] ZHANG YJ, LIU YT, YU XS. Predictive value of serum liver enzyme for the metabolic syndrome[J]. Clin J Med Offic, 2017, 45 (1) :82-85. (in Chinese) 张艳君, 刘奕婷, 于晓松.血清肝酶指标对代谢综合征预测价值[J].临床军医杂志, 2017, 45 (1) :82-85. [5] HASSAN K, BHALLA V, EI REGAL ME, et al. Nonalcoholic fatty liver disease:A comprehensive review of a growing epidemic[J].World J Gastroenterol, 2014, 20 (34) :12082-12101. [6] Chinese Society of Hepatology and Chinese Society of Infectious Diseases. Chinese Medical Association The guideline of prevention and treatment for chronic hepatitis B:A 2015 update[J]. J Clin Hepatol, 2015, 31 (12) :1941-1960. (in Chinese) 中华医学会肝病学分会, 中华医学会感染病学分会慢性乙型肝炎防治指南 (2015年更新版) [J].临床肝胆病杂志, 2015, 31 (12) :1941-1960. [7] Group of Fatty Liver and Alcoholic Liver Diseases, Society of Hepatology, Chinese Medical Association. Guidelines for management of nonalcoholic fatty liver disease[J]. J Clin Hepatol, 2010, 26 (2) :120-124. (in Chinese) 中华医学会肝脏病学分会脂肪肝和酒精性肝病学组.非酒精性脂肪性肝病诊疗指南[J].临床肝胆病杂志, 2010, 26 (2) :120-124. [8] Metabolic Syndrome Study Group, Chinese Diabetes Society, Chinese Medical Association. Recommendations on metabolic Syndrome of Chinese Diabetes Society, Chinese Medical Association[J].Chin J Diabetes, 2004, 12 (3) :5-10. (in Chinese) 中华医学会糖尿病学分会代谢综合征研究协作组.中华医学会糖尿病学分会关于代谢综合征的建议[J].中国糖尿病杂志, 2004, 12 (3) :5-10. [9] LIU W, BAKER RD, BHATIA T, et al. Pathogenesis of nonalcoholic steatohepatitis[J]. Cell Mol Life Sci, 2016, 73 (10) :1969-1987. [10] RAZI B, ALIZADEH S, OMIDKHODA A, et al. Association of chronic hepatitis B infection with metabolic syndrome and its components:Meta-analysis of observational studies[J]. Diabetes Metab Syndr, 2017, 11 (Suppl 2) :s939-s947. [11] WANG CC, TSENG TC, KAO JH. Hepatitis B virus infection and metabolic syndrome:Fact or fiction?[J]. J Gastroenterol Hepatol, 2015, 30 (1) :14-20. [12] CHOI JS, HAN KJ, LEE S, et al. Serum HBV surface antigen positivity is associated with low prevalence of metabolic syndrome in Korean adult men[J]. J Epidemiol, 2015, 25 (1) :74-79. [13] HUANG CY, LU CW, LIU YL, et al. Relationship between chronic hepatitis B and metabolic syndrome:A structural equation modeling approach[J]. Obesity (Silver Spring) , 2016, 24 (2) :483-489. [14] PETTA S, MACALUSO FS, BARCELLONA MR, et al. Serumγ-glutamyl transferase levels, insulin resistance and liver fibrosis in patients with chronic liver diseases[J]. PLo S One, 2012, 7 (12) :e51165. [15] MACHADO MV, OLIVEIRA AG, CORTEZ-PINTO H. Hepatic steatosis in hepatitis B virus infected patients:Meta-analysis of risk factors and comparison with hepatitis C infected patients[J]. J Gastroenterol Hepatol, 2011, 26 (9) :1361-1367. [16] WANG MM, WANG GS, SHEN F, et al. Hepatic steatosis is highly prevalent in hepatitis B patients and negatively associated with virological factors[J]. Dig Dis Sci, 2014, 59 (10) :2571-2579. [17] LESMANA LA, LESMANA CR, PAKASI LS, et al. Prevalence of hepatic steatosis in chronic hepatitis B patients and its association with disease severity[J]. Acta Med Indones, 2012, 44 (1) :35-39. [18] PAIS R, RUSU E, ZILISTEANU D, et al. Prevalence of steatosis and insulin resistance in patients with chronic hepatitis B compared with chronic hepatitis C and non-alcoholic fatty liver disease[J]. Eur J Intern Med, 2015, 26 (1) :30-36. [19] MENA, PEDREIRA JD, CASTRO, et al. Metabolic syndrome association with fibrosis development in chronic hepatitis B virus inactive carriers[J]. J Gastroenterol Hepatol, 2014, 29 (1) :173-178. [20] GARJANI A, SAFAEIYAN A, KHOSHBATEN M. Association between platelet count as a noninvasive marker and ultrasonographic grading in patients with nonalcoholic fatty liver disease[J]. Hepat Mon, 2015, 15 (1) :e24449. [21] SAMAD F, RUF W. Inflammation, obesity, and thrombosis.[J].Blood, 2013, 122 (20) :3415-3422. [22] YANG XZ, GENG AW, XIAO L, et al. Pathological and clinical features of patients with chronic hepatitis B and non-alcoholic fatty liver disease[J]. J Pract Hepatol, 2017, 20 (1) :101-102. (in Chinese) 杨秀珍, 耿爱文, 肖丽, 等.慢性乙型肝炎合并脂肪肝临床与肝组织病理学分析[J].实用肝脏病杂志, 2017, 20 (1) :101-102. [23] MARINO L, JORNAYVAZ FR. Endocrine causes of nonalcoholic fatty liver disease[J]. World J Gastroenterol, 2015, 21 (39) :11053-11076. [24] JIANG ZG, TSUGAWA Y, TAPPER EB, et al. Low-fasting triglyceride levels are associated with non-invasive markers of advanced liver fibrosis among adults in the United States[J]. Aliment Pharmacol Ther, 2015, 42 (1) :106-116. [25] CHUNG TH, KIM MC, KIM CS. Association between hepatitis B surface antigen seropositivity and metabolic syndrome[J]. Korean J Fam Med, 2014, 35 (2) :81-89. [26] FAN JG, YAN SY. Metabolic syndrome and fany liver[J]. J Clin Hepatol, 2016, 32 (3) :407-410. (in Chinese) 范建高, 颜士岩.代谢综合征与脂肪肝[J].临床肝胆病杂志, 2016, 32 (3) :407-410. [27] HSIANG J, WONG GL, CHAN HL, et al. Editorial:Metabolic syndrome delays HBeAg seroclearance in Chinese patients with hepatitis B-authors'reply[J]. Aliment Pharmacol Ther, 2014, 40 (8) :983. [28] HSIANG JC, WONG GL, CHAN HL, et al. Metabolic syndrome delays HBeAg seroclearance in Chinese patients with hepatitis B[J]. Aliment Pharmacol Ther, 2014, 40 (8) :716-726.
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