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Featured researches published by Rosmawati Mohamed.


Hepatology International | 2008

Asian-Pacific consensus statement on the management of chronic hepatitis B: A 2012 update

Yun Fan Liaw; Jia-Horng Kao; Teerha Piratvisuth; Henry Lik-Yuen Chan; Rong Nan Chien; Chun-Jen Liu; Ed Gane; Stephen Locarnini; Seng Gee Lim; Kwang Hyub Han; Deepak Amarapurkar; Graham Cooksley; Wasim Jafri; Rosmawati Mohamed; Jin Lin Hou; Wan Long Chuang; Laurentius A. Lesmana; Jose D. Sollano; Dong Jin Suh; Masao Omata

Large amounts of new data on the natural history and treatment of chronic hepatitis B virus (HBV) infection have become available since 2005. These include long-term follow-up studies in large community-based cohorts or asymptomatic subjects with chronic HBV infection, further studies on the role of HBV genotype/naturally occurring HBV mutations, treatment of drug resistance and new therapies. In addition, Pegylated interferon α2a, entecavir and telbivudine have been approved globally. To update HBV management guidelines, relevant new data were reviewed and assessed by experts from the region, and the significance of the reported findings were discussed and debated. The earlier “Asian-Pacific consensus statement on the management of chronic hepatitis B” was revised accordingly. The key terms used in the statement were also defined. The new guidelines include general management, special indications for liver biopsy in patients with persistently normal alanine aminotransferase, time to start or stop drug therapy, choice of drug to initiate therapy, when and how to monitor the patients during and after stopping drug therapy. Recommendations on the therapy of patients in special circumstances, including women in childbearing age, patients with antiviral drug resistance, concurrent viral infection, hepatic decompensation, patients receiving immune-suppressive medications or chemotherapy and patients in the setting of liver transplantation, are also included.


Hepatology International | 2009

Acute-on-chronic liver failure: consensus recommendations of the Asian Pacific Association for the study of the liver (APASL)

Shiv Kumar Sarin; A. Kumar; John Almeida; Yogesh Chawla; Sheung Tat Fan; Hitendra Garg; H. Janaka de Silva; Saeed Hamid; Rajiv Jalan; Piyawat Komolmit; George K. K. Lau; Qing Liu; Kaushal Madan; Rosmawati Mohamed; Qin Ning; Salimur Rahman; Archana Rastogi; Stephen M. Riordan; Puja Sakhuja; Didier Samuel; Samir Shah; Barjesh Chander Sharma; Praveen Sharma; Yasuhiro Takikawa; Babu Ram Thapa; Chun-Tao Wai; Man-Fung Yuen

The Asian Pacific Association for the Study of the Liver (APASL) set up a working party on acute-on-chronic liver failure (ACLF) in 2004, with a mandate to develop consensus guidelines on various aspects of ACLF relevant to disease patterns and clinical practice in the Asia-Pacific region. Experts predominantly from the Asia–Pacific region constituted this working party and were requested to identify different issues of ACLF and develop the consensus guidelines. A 2-day meeting of the working party was held on January 22–23, 2008, at New Delhi, India, to discuss and finalize the consensus statements. Only those statements that were unanimously approved by the experts were accepted. These statements were circulated to all the experts and subsequently presented at the Annual Conference of the APASL at Seoul, Korea, in March 2008. The consensus statements along with relevant background information are presented in this review.


Hepatology International | 2016

Asian-Pacific clinical practice guidelines on the management of hepatitis B: a 2015 update

Shiv Kumar Sarin; Manoj Kumar; G. K. K. Lau; Zaigham Abbas; Henry L. Chan; Chien-Jen Chen; Ding-Shinn Chen; Huey–Ling Chen; Chen Pj; Rong-Nan Chien; A. K. Dokmeci; Ed Gane; Jinlin Hou; Wasim Jafri; Jidong Jia; Jin Hee Kim; Ching-Lung Lai; Han Chu Lee; S.G. Lim; Cheng-Liang Liu; Stephen Locarnini; M. Al Mahtab; Rosmawati Mohamed; Masao Omata; Jun Yong Park; Teerha Piratvisuth; Barjesh Chander Sharma; Jose D. Sollano; F. S. Wang; Lai Wei

Worldwide, some 240 million people have chronic hepatitis B virus (HBV), with the highest rates of infection in Africa and Asia. Our understanding of the natural history of HBV infection and the potential for therapy of the resultant disease is continuously improving. New data have become available since the previous APASL guidelines for management of HBV infection were published in 2012. The objective of this manuscript is to update the recommendations for the optimal management of chronic HBV infection. The 2015 guidelines were developed by a panel of Asian experts chosen by the APASL. The clinical practice guidelines are based on evidence from existing publications or, if evidence was unavailable, on the experts’ personal experience and opinion after deliberations. Manuscripts and abstracts of important meetings published through January 2015 have been evaluated. This guideline covers the full spectrum of care of patients infected with hepatitis B, including new terminology, natural history, screening, vaccination, counseling, diagnosis, assessment of the stage of liver disease, the indications, timing, choice and duration of single or combination of antiviral drugs, screening for HCC, management in special situations like childhood, pregnancy, coinfections, renal impairment and pre- and post-liver transplant, and policy guidelines. However, areas of uncertainty still exist, and clinicians, patients, and public health authorities must therefore continue to make choices on the basis of the evolving evidence. The final clinical practice guidelines and recommendations are presented here, along with the relevant background information.


Journal of Gastroenterology and Hepatology | 2004

Practical difficulties in the management of hepatitis B in the Asia–Pacific region

Rosmawati Mohamed; Paul V. Desmond; DongJin Suh; Deepak Amarapurkar; Edward Gane; Yao Guangbi; Jinlin Hou; Wasim Jafri; Ching-Lung Lai; Chang-Hong Lee; Shou-Dong Lee; Seng Gee Lim; Richard Guan; Pham Hoang Phiet; Teerha Piratvisuth; Jose D. Sollano; Jaw-Ching Wu

The Asia–Pacific Expert Committee on Hepatitis B Management recently reviewed the impact of hepatitis B in the region and assessed the differences and similarities observed in the practical management of the disease in individual Asia–Pacific countries. Hepatitis B is a major health concern in the Asia–Pacific region, and of all chronically infected carriers worldwide, approximately 75% are found in Asia. The disease poses a considerable burden on healthcare systems, and is likely to remain a cause of substantial morbidity and mortality for several decades. Disease prevention activities, including screening and vaccination programs, have been implemented successfully in some Asia–Pacific countries and similar measures are being established in other parts of the region. The management of hepatitis B in the Asia–Pacific varies throughout the region, with each country confronting different issues related to treatment options, disease monitoring and duration of therapy. The influence of cost, availability of diagnostic equipment, and patient awareness and compliance are of additional concern. Although guidelines such as those developed by the Asian Pacific Association for the Study of the Liver have been created to address problems encountered in the management of hepatitis B, many physicians in the region still find it difficult to make satisfactory management decisions because of the treatment choices available. This article examines the different approaches to hepatitis B management in a number of Asia–Pacific countries, and highlights the difficulties that can arise when adhering to treatment guidelines and disease prevention solutions that have proved to be successful in the region.


PLOS ONE | 2012

Ethnic Differences in the Prevalence of Metabolic Syndrome: Results from a Multi-Ethnic Population-Based Survey in Malaysia

Sanjay Rampal; Sanjiv Mahadeva; Eliseo Guallar; Awang Bulgiba; Rosmawati Mohamed; Ramlee Rahmat; Mohamad Taha Arif; Lekhraj Rampal Gyanchand Rampal

Introduction The prevalence of metabolic syndrome is increasing disproportionately among the different ethnicities in Asia compared to the rest of the world. This study aims to determine the differences in the prevalence of metabolic syndrome across ethnicities in Malaysia, a multi-ethnic country. Methods In 2004, we conducted a national cross-sectional population-based study using a stratified two-stage cluster sampling design (N = 17,211). Metabolic syndrome was defined according to the International Diabetes Federation/National Heart, Lung and Blood Institute/American Heart Association (IDF/NHLBI/AHA-2009) criteria. Multivariate models were used to study the independent association between ethnicity and the prevalence of the metabolic syndrome. Results The overall mean age was 36.9 years, and 50.0% participants were female. The ethnic distribution was 57.0% Malay, 28.5% Chinese, 8.9% Indian and 5.0% Indigenous Sarawakians. The overall prevalence of the metabolic syndrome was 27.5%, with a prevalence of central obesity, raised triglycerides, low high density lipoprotein cholesterol, raised blood pressure and raised fasting glucose of 36.9%, 29.3%, 37.2%, 38.0% and 29.1%, respectively. Among those <40 years, the adjusted prevalence ratios for metabolic syndrome for ethnic Chinese, Indians, and Indigenous Sarawakians compared to ethnic Malay were 0.81 (95% CI 0.67 to 0.96), 1.42 (95% CI 1.19 to 1.69) and 1.37 (95% CI 1.08 to 1.73), respectively. Among those aged ≥40 years, the corresponding prevalence ratios were 0.86 (95% CI 0.79 to 0.92), 1.25 (95% CI 1.15 to 1.36), and 0.94 (95% CI 0.80, 1.11). The P-value for the interaction of ethnicity by age was 0.001. Conclusions The overall prevalence of metabolic syndrome in Malaysia was high, with marked differences across ethnicities. Ethnic Chinese had the lowest prevalence of metabolic syndrome, while ethnic Indians had the highest. Indigenous Sarawakians showed a marked increase in metabolic syndrome at young ages.


Antiviral Therapy | 2010

Cost-effectiveness analysis of roadmap models in chronic hepatitis B using tenofovir as the rescue therapy

Yanni Yan Ni Lui; K. K. F. Tsoi; Vincent Wai-Sun Wong; Jia-Horng Kao; Jin Lin Hou; Eng Kiong Teo; Rosmawati Mohamed; Teerha Piratvisuth; Kwang Hyub Han; U. Mihm; Grace Lai-Hung Wong; Henry Lik-Yuen Chan

BACKGROUND The roadmap approach is recommended to guide chronic hepatitis B treatment. We evaluated the cost-effectiveness of various treatment strategies in the global market. METHODS Lamivudine and telbivudine were tested in roadmap models with switch-to tenofovir if HBV was detectable at week 24 or add-on tenofovir if resistance developed at year 1. Tenofovir and entecavir were tested as continuous monotherapy. In the reference arm, lamivudine was used with add-on tenofovir if resistance developed at year 1. The primary measure of effectiveness was undetectable HBV DNA at year 2. Cost-effectiveness was measured by incremental cost-effectiveness ratio (ICER) in US dollars against the reference arm. RESULTS In the US and Germany, costs of the reference arms were US


BMC Public Health | 2012

Knowledge, attitudes and practices among people with chronic hepatitis B attending a hepatology clinic in Malaysia: A cross sectional study

Rosmawati Mohamed; Chirk Jenn Ng; Wen Ting Tong; Suraya Zainol Abidin; Li Ping Wong; Wah Yun Low

14,486 and US


Journal of Gastroenterology and Hepatology | 2013

Impact of leptin receptor gene variants on risk of non-alcoholic fatty liver disease and its interaction with adiponutrin gene.

Shamsul Mohd Zain; Zahurin Mohamed; Sanjiv Mahadeva; Phaik-Leng Cheah; Sanjay Rampal; Kin-Fah Chin; Anis Shafina Mahfudz; Roma Choudhury Basu; Hwa Li Tan; Rosmawati Mohamed

9,998 for hepatitis B e antigen (HBeAg)-positive and US


European Journal of Clinical Investigation | 2016

Peripheral loss of CD8(+) CD161(++) TCRVα7·2(+) mucosal-associated invariant T cells in chronic hepatitis C virus-infected patients.

Muttiah Barathan; Rosmawati Mohamed; Jamuna Vadivelu; Li Y. Chang; Alireza Saeidi; Yean K. Yong; M. Ravishankar Ram; Kaliappan Gopal; Vijayakumar Velu; Marie Larsson; Esaki Muthu Shankar

11,398 and US


PLOS ONE | 2014

Genome-wide analysis of copy number variation identifies candidate gene loci associated with the progression of non-alcoholic fatty liver disease

Shamsul Mohd Zain; Rosmawati Mohamed; David Neil Cooper; Rozaimi Razali; Sanjay Rampal; Sanjiv Mahadeva; Wah-Kheong Chan; Arif Anwar; Nurul Shielawati Binti Mohamed Rosli; Anis Shafina Mahfudz; P C Cheah; Roma Choudhury Basu; Zahurin Mohamed

7,531 for HBeAg-negative patients, respectively. In HBeAg-positive patients, the lamivudine roadmap was most cost-effective (ICER US

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Teerha Piratvisuth

Prince of Songkla University

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Roma Choudhury Basu

University Malaya Medical Centre

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Jia-Horng Kao

National Taiwan University

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