Impact of Liver Biopsy on the Decision to Treat Patients with Chronic Hepatitis B Genotype D Virus Infection

被引:3
作者
Al-Qahtani, Ahmed Ali [1 ]
Al-Ashgar, Hamad Ibrahim [2 ]
Al-Ahdal, Mohammed Noreen [1 ]
Al Mana, Hadeel [3 ]
Ali, Ali Soliman [4 ]
Hasanain, Ahmed Farouk [4 ]
Helmy, Ahmed [2 ,4 ]
机构
[1] King Faisal Specialist Hosp & Res Ctr, Dept Infect & Immun, Res Ctr, Riyadh 11211, Saudi Arabia
[2] King Faisal Specialist Hosp & Res Ctr, Dept Med, Gastroenterol Sect, Riyadh 11211, Saudi Arabia
[3] King Faisal Specialist Hosp & Res Ctr, Dept Pathol, Riyadh 11211, Saudi Arabia
[4] Assiut Univ Hosp, Dept Trop Med & Gastroenterol, Assiut 71517, Egypt
关键词
Genotype D; Histopathology; Fibrosis; Viral load; Transaminases; Therapy; SERUM HBV-DNA; ALANINE AMINOTRANSFERASE; CONSENSUS STATEMENT; PROMOTER VARIANTS; UNITED-STATES; E-ANTIGEN; DISEASE; EPIDEMIOLOGY; PREVALENCE; MANAGEMENT;
D O I
10.1159/000360858
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Objectives: Patients with chronic hepatitis B virus (HBV) may exhibit significant liver pathology despite alanine aminotransferase (ALT) and HBV DNA levels below the cutoff values advised by treatment guidelines. We evaluated candidacy for HBV therapy when baseline histopathological changes are taken into consideration. Methods: Clinical, biochemical, serological, virological, and histopathological (METAVIR score) data of 117 patients with HBeAg-negative chronic HBV genotype D were collected and analyzed. Results: Significant pathology (>= F2 and/or >= A2) and fibrosis (>= F2 +/- >= A2) were found in 73 (62.4%) and 59 (50.4%) patients, respectively. Based on HBV DNA (>2,000 IU/ml) and ALT levels >2 x 40 U/I (the standard cutoff value), only 31 (26.5%) patients were candidates for therapy. This increased to 58 (49.6%) patients when the new ALT cutoff values (30 U/I for males, and 19 U/I for females) were applied. Relying on either >= F2 and/or A >= 2 or >= F2 +/- >= A2 increases the treatment candidacy to 73 (62.4%) and 59 (50.4%) patients, respectively. Also, when compared with standard ALT cutoff values, applying both new ALT cutoff values with either significant pathology or fibrosis increases treatment candidacy to 28 (23.9%) and 42 (35.9%) patients, respectively. Conclusion: Liver pathology is more reliable than ALT and HBV DNA in the decision to treat patients with HBeAg-negative chronic HBV genotype D. (C) 2014 S. Karger AG, Basel
引用
收藏
页码:248 / 253
页数:6
相关论文
共 33 条
[1]   Hepatitis B genotypes: Relation to clinical outcome in patients with chronic hepatitis B in Saudi Arabia [J].
Abdo, Ayman A. ;
Al-Larallah, Badr M. ;
Sanai, Faisal M. ;
Hersi, Ahmad S. ;
Al-Swat, Khalid ;
Azzam, Nahla A. ;
Al-Dukhayil, Manal ;
Al-Maarik, Amira ;
Al-Faleh, Faleh Z. .
WORLD JOURNAL OF GASTROENTEROLOGY, 2006, 12 (43) :7019-7024
[2]   SEROEPIDEMIOLOGY OF HEPATITIS-B VIRUS-INFECTION IN SAUDI-ARABIAN CHILDREN - A BASE-LINE SURVEY FOR MASS VACCINATION AGAINST HEPATITIS-B [J].
ALFALEH, FZ ;
AYOOLA, EA ;
ARIF, M ;
RAMIA, S ;
ALRASHED, R ;
ALJEFFRY, M ;
ALMOFARREH, M ;
ALKARAWI, M ;
ALSHABRAWY, M .
JOURNAL OF INFECTION, 1992, 24 (02) :197-206
[3]  
BEDOSSA P, 1994, HEPATOLOGY, V20, P15
[4]   CHRONIC HEPATITIS IN HBSAG-CARRIERS WITH SERUM HBV-DNA AND ANTI-HBE [J].
BONINO, F ;
ROSINA, F ;
RIZZETTO, M ;
RIZZI, R ;
CHIABERGE, E ;
TARDANICO, R ;
CALLEA, F ;
VERME, G .
GASTROENTEROLOGY, 1986, 90 (05) :1268-1273
[5]   Outcome of anti-HBe positive chronic hepatitis B in alpha-interferon treated and untreated patients: a long term cohort study [J].
Brunetto, MR ;
Oliveri, F ;
Coco, B ;
Leandro, G ;
Colombatto, P ;
Gorin, JM ;
Bonino, F .
JOURNAL OF HEPATOLOGY, 2002, 36 (02) :263-270
[6]   Noninvasive assessment of liver damage in chronic hepatitis B [J].
Celikbilek, Mehmet ;
Dogan, Serkan ;
Gursoy, Sebnem ;
Zararsiz, Gokmen ;
Yurci, Alper ;
Ozbakir, Omer ;
Guven, Kadri ;
Yucesoy, Mehmet .
WORLD JOURNAL OF HEPATOLOGY, 2013, 5 (08) :439-444
[7]   Prevalence of HBV precore/core promoter variants in the United States [J].
Chu, CJ ;
Keeffe, EB ;
Han, SH ;
Perrillo, RP ;
Min, AD ;
Soldevila-Pico, C ;
Carey, W ;
Brown, RS ;
Luketic, VA ;
Terrault, N ;
Lok, ASF .
HEPATOLOGY, 2003, 38 (03) :619-628
[8]   Quantitative serum HBV DNA levels during different stages of chronic hepatitis B infection [J].
Chu, CJ ;
Hussain, M ;
Lok, ASF .
HEPATOLOGY, 2002, 36 (06) :1408-1415
[9]   Natural history and treatment of hepatitis B virus and hepatitis C virus coinfection [J].
Crockett S.D. ;
Keeffe E.B. .
Annals of Clinical Microbiology and Antimicrobials, 4 (1)
[10]   EASL International Concensus Conference on Hepatitis B -: 13-14 September, 2002 Geneva, Switzerland Consensus Statement (Long version) [J].
de Franchis, R ;
Hadengue, A ;
Lau, G ;
Lavanchy, D ;
Lok, A ;
McIntyre, N ;
Mele, A ;
Paumgartner, G ;
Pietrangelo, A ;
Rodés, J ;
Rosenberg, W ;
Valla, D .
JOURNAL OF HEPATOLOGY, 2003, 39 :S3-S25