Helen Vidot1, Katharine Kline2, Robert Cheng3,4, Liam Finegan5, Amelia Lin2, Elise Kempler2, Simone I Strasser2,4, David Geoffrey Bowen2,3,4, Geoffrey William McCaughan2,3,4, Sharon Carey1, Margaret Allman-Farinelli6, Nicholas Adam Shackel7. 1. Department Nutrition & Dietetics, Royal Prince Alfred Hospital, Camperdown, NSW 2050, Australia. 2. Sydney Medical School, The University of Sydney, Sydney, NSW 2006, Australia. 3. Liver Injury and Cancer Centre, Centenary Research Institute, The University of Sydney, Sydney, NSW 2006, Australia. 4. A.W. Morrow Gastroenterology and Liver Centre, Royal Prince Alfred Hospital, Camperdown, NSW 2050, Australia. 5. School of Business, The University of Sydney, Sydney, NSW 2006, Australia. 6. School of Life and Environmental Sciences, Charles Perkins Centre, The University of Sydney, Sydney, NSW 2006, Australia. 7. Medicine, University of NSW, Sydney, NSW 2052, Australia.
We thank Drs. Ebadi, Moctezuma-Velazquez, Bhanji and Montano-Loza [1] for their interest and comments on our recent paper [2]. The following is our response to their comments and concerns.Recent European Society for Parenteral and Enteral Nutrition ESPEN consensus guidelines define sarcopenia as a muscle disease that has a low muscle quantity and quality and is associated with poor physical performance [3]. Due to the retrospective nature of this study, frailty assessments for the cohort were not available and the right psoas muscle area, adjusted for height, was used as an indicator of muscle wasting [4]. However, we would contend that the severe extent of muscle wasting seen in our study is such that it is invariably associated with poor physical performance, and hence, is true sarcopenia [5].The cut-off levels used in our study were those previously used in a group of colorectal cancerpatients to predict major surgical complications, and are likely relevant to patients undergoing assessment for liver transplantation. However, we strongly agree that a liver specific sarcopenia assessment should first be independently validated and then applied in future assessment and management of such patients [5]. More recently, the skeletal muscle index has been used to quantify muscle mass and to identify sarcopenia in patients with end-stage liver disease, using the image analysis software application SliceOmatic (TomoVision, Montreal, Canada) [6]. This method is undoubtedly more accurate than the method employed in our study, but due to limited resources, this application was not available to our group. Consequently, we agree that the reported incidence of sarcopenia may be higher in our study. Furthermore, we agree with Drs. Ebadi, Moctezuma-Velazquez, Bhanji and Montano-Loza that our results further support the weak concordance between sarcopenia and subjective global assessment SGA in patients with cirrhosis, particularly in obesepatients with cirrhosis, which has previously been identified [1].Importantly, malnutrition and sarcopenia are very closely linked, but are also separate processes that are increasingly prevalent in obese individuals with cirrhosis, irrespective of disease aetiology [7]. Individually, these conditions are associated with an increased morbidity and mortality, but when they co-exist, they are associated with higher rates of mortality reduced physical function [7]. Our study highlights the poor sensitivity of the widely used nutritional assessment tool, subjective global assessment (SGA), to detect sarcopenia in patients with cirrhosis [8], particularly in obese cirrhoticpatients who are at risk of further muscle wasting and its manifestations [7]. The failure to diagnose sarcopenia in individuals classified as well-nourished using SGA alone potentially results in under-recognition and the progression of sarcopenia [9].There were significantly lower testosterone levels reported in patients without sarcopenia. However, patients without sarcopenia were predominantly female. As expected, the mean value for testosterone, in male patients, was found to be below the normal range across the cohort, regardless of sarcopenia or BMI. Therefore, as is widely accepted, our study is consistent with low testosterone, having a significant contribution to sarcopenia in male patients [10].In conclusion, our study emphasizes the limitations of current body composition assessment tools to diagnose sarcopenia in individuals with cirrhosis. It is important that practitioners recognize the increased prevalence of sarcopenia in this group and utilize a multidisciplinary approach to the diagnosis and management of sarcopenia.
Authors: Elizabeth J Carey; Jennifer C Lai; Connie W Wang; Srinivasan Dasarathy; Iryna Lobach; Aldo J Montano-Loza; Michael A Dunn Journal: Liver Transpl Date: 2017-05 Impact factor: 5.799
Authors: Carlos Moctezuma-Velázquez; Gavin Low; Marina Mourtzakis; Mang Ma; Kelly W Burak; Puneeta Tandon; Aldo J Montano-Loza Journal: Ann Hepatol Date: 2018 July - August , Impact factor: 2.400
Authors: Alfonso J Cruz-Jentoft; Gülistan Bahat; Jürgen Bauer; Yves Boirie; Olivier Bruyère; Tommy Cederholm; Cyrus Cooper; Francesco Landi; Yves Rolland; Avan Aihie Sayer; Stéphane M Schneider; Cornel C Sieber; Eva Topinkova; Maurits Vandewoude; Marjolein Visser; Mauro Zamboni Journal: Age Ageing Date: 2019-01-01 Impact factor: 10.668
Authors: Helen Vidot; Katharine Kline; Robert Cheng; Liam Finegan; Amelia Lin; Elise Kempler; Simone I Strasser; David Geoffrey Bowen; Geoffrey William McCaughan; Sharon Carey; Margaret Allman-Farinelli; Nicholas Adam Shackel Journal: Nutrients Date: 2019-09-04 Impact factor: 5.717