Allele HLA‐DQB1*06 reduces fibrosis score in patients with non‐alcoholic fatty liver disease. Issue 8 (8th June 2020)
- Record Type:
- Journal Article
- Title:
- Allele HLA‐DQB1*06 reduces fibrosis score in patients with non‐alcoholic fatty liver disease. Issue 8 (8th June 2020)
- Main Title:
- Allele HLA‐DQB1*06 reduces fibrosis score in patients with non‐alcoholic fatty liver disease
- Authors:
- Tan, Hwa‐Li
Zain, Shamsul Mohd
Eng, Hooi‐Sian
Mohamed, Zahurin
Mahadeva, Sanjiv
Chan, Wah‐Kheong
Lau, Peng‐Choong
Basu, Roma Choudhury
Mohamed, Rosmawati - Abstract:
- Abstract : Aim: Human leukocyte antigen (HLA) regions were highlighted as important genetic markers for various liver diseases by hepatology‐related genome‐wide association studies. Replication studies in non‐alcoholic fatty liver disease (NAFLD) are limited and none has investigated the association of HLA alleles with non‐alcoholic steatohepatitis (NASH) and other histological characteristics. In the current study, we examined the association of HLA‐DQA1 and HLA‐DQB1 alleles with NAFLD spectrum and its histological characteristics. Methods: Consecutive biopsy‐proven NAFLD patients ( n = 191) and healthy controls ( n = 188) were enrolled and genotyped for HLA‐DQA1 and HLA‐DQB1 alleles using the sequence‐specific oligonucleotide–polymerase chain reaction method. Results: No association was found between the HLA alleles and NAFLD or NASH in a case–control setting. Nevertheless, among NAFLD patients, the frequency of HLA‐DQB1*06 allele was significantly the lowest in NASH with significant fibrosis (10.4%) and approximately similar for NASH without significant fibrosis (22.9%) and NAFL (22.5%) ( P = 0.004). It is noteworthy that the association remains significant after correction for multiple comparisons (Pc = 0.04). Multivariate analysis revealed that HLA‐DQB1*06 allele is also associated with fibrosis score ( P = 0.001); the result remains significant after correction for multiple comparisons. Conclusion: These findings suggest that HLA‐DQB1*06 is associated with lowerAbstract : Aim: Human leukocyte antigen (HLA) regions were highlighted as important genetic markers for various liver diseases by hepatology‐related genome‐wide association studies. Replication studies in non‐alcoholic fatty liver disease (NAFLD) are limited and none has investigated the association of HLA alleles with non‐alcoholic steatohepatitis (NASH) and other histological characteristics. In the current study, we examined the association of HLA‐DQA1 and HLA‐DQB1 alleles with NAFLD spectrum and its histological characteristics. Methods: Consecutive biopsy‐proven NAFLD patients ( n = 191) and healthy controls ( n = 188) were enrolled and genotyped for HLA‐DQA1 and HLA‐DQB1 alleles using the sequence‐specific oligonucleotide–polymerase chain reaction method. Results: No association was found between the HLA alleles and NAFLD or NASH in a case–control setting. Nevertheless, among NAFLD patients, the frequency of HLA‐DQB1*06 allele was significantly the lowest in NASH with significant fibrosis (10.4%) and approximately similar for NASH without significant fibrosis (22.9%) and NAFL (22.5%) ( P = 0.004). It is noteworthy that the association remains significant after correction for multiple comparisons (Pc = 0.04). Multivariate analysis revealed that HLA‐DQB1*06 allele is also associated with fibrosis score ( P = 0.001); the result remains significant after correction for multiple comparisons. Conclusion: These findings suggest that HLA‐DQB1*06 is associated with lower fibrosis score in NAFLD patients. … (more)
- Is Part Of:
- Hepatology research. Volume 50:Issue 8(2020)
- Journal:
- Hepatology research
- Issue:
- Volume 50:Issue 8(2020)
- Issue Display:
- Volume 50, Issue 8 (2020)
- Year:
- 2020
- Volume:
- 50
- Issue:
- 8
- Issue Sort Value:
- 2020-0050-0008-0000
- Page Start:
- 947
- Page End:
- 954
- Publication Date:
- 2020-06-08
- Subjects:
- fatty liver -- fibrosis -- HLA‐DQ -- human leukocyte antigen -- NAFLD -- NASH
Liver -- Diseases -- Periodicals
Liver Diseases -- Periodicals
Foie -- Maladies -- Périodiques
616.362 - Journal URLs:
- http://www.sciencedirect.com/science/journal/09284346 ↗
http://firstsearch.oclc.org/journal=1386-6346;screen=info;ECOIP ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1872-034X ↗
http://www.sciencedirect.com/science/journal/13866346 ↗
http://www3.interscience.wiley.com/journal/118507311/home ↗
http://www.blackwell-synergy.com/rd.asp?goto=journal&code=hep ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/hepr.13525 ↗
- Languages:
- English
- ISSNs:
- 1386-6346
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 4295.845000
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- 13898.xml