Conference Papers

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This collection contains abstracts of conference papers, presented at local and international conferences by the staff of the Faculty of Medicine

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    The value of brunt scoring in predicting the short term outcome of non-alcohlic steatohepatitis
    (Wiley Blackwell Scientific Publications, 2004) Hewavisenthi, S.J.de S.; Pathmeswaran, A.; de Silva, H.J.
    BACKGROUND: Brunt scoring is currently used in the grading and staging of liver biopsies in non-alcoholic steatohepatitis (NASH). Its value in predicting the outcome of patients following modifications in lifestyle, the cornerstone of management in NASH, needs evaluation. OBJECTIVES: To determine whether Brunt grades correlate with Aspartate transaminase (AST) and Alanine transaminase (ALT) levels, and outcome following lifestyle modifications in NASH. METHOD: In a prospective study from May 1999 to May 2003 the biopsies of 79 patients diagnosed as having NASH were assigned 3 necroinflammatory grades based on the Brunt system. The mean serum transaminase values at presentation for each necroinflammatory grade were compared using ANOVA. 77/79 patients were given advice on lifestyle modifications and then followed up for a median 2.5 years. The time taken for serum transaminases to return to normal was correlated with the necroinflammatory grades, AST and ALT values at presentation using Kendall tau b. RESULTS : The mean AST and ALT values (IU/L) in the three necroinflammatory grades were - grade 1:62.4 and 102:1, grade 2: 87.6 and 139.4 and grade 3: 90.9 and 164.5. There was a significant difference in the AST and ALT values between grades 1 and 2, and grades 1 and 3, but not between grades 2 and 3. In 51/77 patients serum transaminases returned to normal levels after a median 6 months (range 3– 14 months). There was no significant correlation between the time taken for serum transaminases to return to normal and the transaminase values or necroinflammatory grades at presentation. CONCLUSION: Brunt grading correlates with both AST and ALT levels. However, neither necroinflammatory grades nor serum transaminase values at first presentation are predictors of the duration to normalization of liver enzymes in NASH patients managed with life style modifications
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    Genetic variants of NAFLD in an urban Sri Lankan community
    (Wiley Blackwell Scientific Publications, 2013) Niriella, M.A.; Kasturiratne, A.; Akiyama, K.; Takeuchi, F.; Isono, M.; Dassanayake, A.S.; de Silva, A.P.; Wickremasinghe, A.R.; Kato, N.; de Silva, H.J.
    OBJECTIVE: Recently, genome-wide association studies (GWAS) have successfully identified loci associated with susceptibility to non-alcoholic fatty liver disease (NAFLD) in populations of European descent. No large-scale genetic studies have been performed thus far in South Asian populations. Therefore, as part of a community-based cohort study in an urban adult population of Sri Lankans, we investigated associations of genetic variants with NAFLD, diagnosed on established ultrasound criteria, and its related phenotypes. METHODS: We selected 10 single nucleotide polymorphisms (SNPs), all previously reported to be associated with NAFLD in populations of European and/or South Asian ancestry, for a case-control replication study. They included loci derived from GWAS [PNPLA3 (rs738409), LYPLAL1 (rs12137855), GCKR (rs780094), PPP1R3B (rs4240624) and NCAN (rs2228603)] plus those from candidate gene studies [APOC3 (rs2854117 and rs2854116), ADIPOR2 (rs767870) and STAT3 (rs6503695 and rs9891119)]. Genotype data of 2988 participants were used for the analysis. RESULTS: A significant NAFLD association was observed for PNPLA3 (rs738409) [OR = 1.25, 95% CI 1.08–1.44, P = 0.003)]; rs738409 was also associated with a trend towards lower serum triglycerides APOC3 variants were significantly (P = 7.3–7.5 × 10–8) associated with higher triglycerides, but not with NAFLD (OR = 0.86). Apart from SNP–lipid associations previously reported at the GCKR, PPP1R3B and NCAN loci, there were no other prominent associations. CONCLUSION: Our data confirm that the PNPLA3 gene variant is significantly associated with NAFLD in the general Sri Lankan population but could not replicate previously reported disease associations at other loci, reinforcing the importance of further large-scale study on genetic variants in diverse populations to better understand the pathophysiology of NAFLD.