Approach to Protein-losing Enteropathy and Nutritional Management
Keywords:
protein-losing enteropathy, hypoalbuminemia, anasarca, nutritional managementAbstract
Patients with protein-losing enteropathy (PLE) usually present with anasarca from severe hypoalbuminemia. Clinical manifestations of PLE have to be differentiated from other causes of generalized edema including hepatic cirrhosis, proteinuria, and severe malnutrition. The diagnosis of PLE need a demonstration of abnormal gastrointestinal protein loss using either technetium-99m-, or indium-111-, labeled protein scintigraphy or -1 antitrypsin clearance. The etiologies of PLE can be grouped into 3 categories; the erosive gastrointestinal diseases, the non-erosive gastrointestinal diseases, and the diseases with increase lymphatic and interstitial pressure. The common investigations to identify cause of PLE usually involve fecal examination, test for fecal fat, computerized tomography of abdomen, gastrointestinal endoscopy and biopsy. The resolution of PLE is usually achieved by the control of primary disease. Proper nutritional management includes provision of adequate energy and higher protein intake up to 2-3 g/kg/day to combat the ongoing protein loss. Low fat diet with or without medium chained triglyceride supplement may help to reduce the symptoms of edema. Micronutrients statuses, particular those of fat-soluble vitamins, should be assessed and treated if deficient state is presence.
References
Goldberg DJ, Dodds K, Rychik J. Rare problems associated with the Fontan circulation. Cardiol Young 2010; 20 Suppl 3: 113–119.
Rychik J. Protein-losing enteropathy after Fontan operation. Congenit Heart Dis 2007; 2: 288–300.
Feldt RH, Driscoll DJ, Offord KP, et al. Protein-losing enteropathy after the Fontan operation. J Thorac Cardiovasc Surg 1996; 112: 672–680.
Mok CC, Ying KY, Mak A, et al. Outcome of protein-losing gastroenteropathy in systemic lupus erythematosus treated with prednisolone and azathioprine. Rheumatology 2006; 45: 425–429.
Tian X-P, Zhang X. Gastrointestinal involvement in systemic lupus erythematosus: insight into pathogenesis, diagnosis and treatment. World J Gastroenterol 2010; 16: 2971–2977.
John AS, Johnson JA, Khan M, et al. Clinical outcomes and improved survival in patients with protein-losing enteropathy after the Fontan operation. J Am Coll Cardiol 2014; 64: 54–62.
Al-Mogairen SM. Lupus protein-losing enteropathy (LUPLE): a systematic review. Rheumatol Int 2011; 31: 995–1001.
Van Kruiningen HJ, Colombel J-F. The forgotten role of lymphangitis in Crohn’s disease. Gut 2008; 57: 1–4.
Lenz D, Hambsch J, Schneider P, et al. Protein-losing enteropathy in patients with Fontan circulation: is it triggered by infection? Crit Care 2003; 7: 185–190.
Umar SB, DiBaise JK. Protein-losing enteropathy: case illustrations and clinical review. Am J Gastroenterol 2010; 105: 43–49; quiz 50.
Levitt DG, Levitt MD. Protein losing enteropathy: comprehensive review of the mechanistic association with clinical and subclinical disease states. Clin Exp Gastroenterol 2017; 10: 147–168.
Takeda H, Ishihama K, Fukui T, et al. Significance of rapid turnover proteins in protein-losing gastroenteropathy. Hepatogastroenterology 2003; 50: 1963–1965.
Chiu NT, Lee BF, Hwang SJ, et al. Protein-losing enteropathy: diagnosis with (99m)Tc-labeled human serum albumin scintigraphy. Radiology 2001; 219: 86–90.
Khalesi M, Nakhaei AA, Seyed AJ, et al. Diagnostic accuracy of nuclear medicine imaging in protein losing enteropathy : systematic review and meta-analysis of the literature. Acta Gastro-Enterol Belg 2013; 76: 413–422.
Itoi K, Sasaki T, Sawai T, et al. Protein-losing gastroenteropathy in association with immune deposits in gastrointestinal mucosal capillaries. Am J Gastroenterol 1989; 84: 187–191.
Florent C, L’Hirondel C, Desmazures C, et al. Intestinal clearance of alpha 1-antitrypsin. A sensitive method for the detection of protein-losing enteropathy. Gastroenterology 1981; 81: 777–780.
Strygler B, Nicar MJ, Santangelo WC, et al. Alpha 1-antitrypsin excretion in stool in normal subjects and in patients with gastrointestinal disorders. Gastroenterology 1990; 99: 1380–1387.
Fuss IJ, Strober W, Cuccherini BA, et al. Intestinal lymphangiectasia, a disease characterized by selective loss of naive CD45RA+ lymphocytes into the gastrointestinal tract. Eur J Immunol 1998; 28: 4275–4285.
Müller C, Wolf H, Göttlicher J, et al. Cellular immunodeficiency in protein-losing enteropathy. Predominant reduction of CD3+ and CD4+ lymphocytes. Dig Dis Sci 1991; 36: 116–122.
Prakitrittranon W, Eua-Ananta YU, Dhiensiri T, et al. Intestinal capillariasis from Maha Sarakham Province, northeast Thailand: report of a case. Southeast Asian J Trop Med Public Health 1980; 11: 496–497.
Tsourdi E, Heidrich FM, Winzer M, et al. An exotic cause of exudative enteropathy. Am J Case Rep 2014; 15: 226–229.
Furtado AK, Cabral VLR, Santos TN, et al. Giardia infection: protein-losing enteropathy in an adult with immunodeficiency. World J Gastroenterol 2012; 18: 2430–2433.
Chamouard P, Nehme-Schuster H, Simler J-M, et al. Videocapsule endoscopy is useful for the diagnosis of intestinal lymphangiectasia. Dig Liver Dis 2006; 38: 699–703.
Takenaka H, Ohmiya N, Hirooka Y, et al. Endoscopic and imaging findings in protein-losing enteropathy. J Clin Gastroenterol 2012; 46: 575–580.
Chen Z, Li M-T, Xu D, et al. Protein-losing enteropathy in systemic lupus erythematosus: 12 years experience from a Chinese academic center. PloS One 2014; 9: e114684.
Law ST, Ma KM, Li KK. The clinical characteristics of lupus related protein-losing enteropathy in Hong Kong Chinese population: 10 years of experience from a regional hospital. Lupus 2012; 21: 840–847.
Sansinanea P, Carrica SA, Marcos J, et al. Protein-losing enteropathy associated with refractory systemic lupus erythematosus with a good response to rituximab. Reumatol Clin 2016; 12: 47–49.
Johnson JN, Driscoll DJ, O’Leary PW. Protein-losing enteropathy and the Fontan operation. Nutr Clin Pract 2012; 27: 375–384.
Shima T, Ozeki M, Kinoshita T, et al. Protein-losing enteropathy secondary to nonocclusive mesenteric ischemia: A case report. Medicine (Baltimore) 2018; 97: e13403.
Gomes F, Schuetz P, Bounoure L, et al. ESPEN guidelines on nutritional support for polymorbid internal medicine patients. Clin Nutr 2018; 37: 336–353.
Desai AP, Guvenc BH, Carachi R. Evidence for medium chain triglycerides in the treatment of primary intestinal lymphangiectasia. Eur J Pediatr Surg 2009; 19: 241–245.
Lai Y, Yu T, Qiao X-Y, et al. Primary intestinal lymphangiectasia diagnosed by double-balloon enteroscopy and treated by medium-chain triglycerides: a case report. J Med Case Reports 2013; 7: 19.
McClave SA, Taylor BE, Martindale RG, et al. Guidelines for the Provision and Assessment of Nutrition Support Therapy in the Adult Critically Ill Patient: Society of Critical Care Medicine (SCCM) and American Society for Parenteral and Enteral Nutrition (A.S.P.E.N.). J Parenter Enter Nutr 2016; 40: 159–211.
Weimann A, Braga M, Carli F, et al. ESPEN guideline: Clinical nutrition in surgery. Clin Nutr 2017; 36: 623–650.
Downloads
Published
How to Cite
Issue
Section
License
The content and information in the articles published in Thai JPEN วารสารโภชนบำบัด, are the opinions and responsibility of the authors directly. The editorial team is not obliged to agree or take any responsibility.
All articles, content, figures, etc. that have been published in Thai JPEN วารสารโภชนบำบัด are the copyright of Thai JPEN วารสารโภชนบำบัด. If any person or organization require distribution of all or any part of them, please send the request for the written permission from Thai JPEN วารสารโภชนบำบัด only.