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[威尔逊病临床营养的新进展:现状与展望]

[The new aspects of clinical nutrition at Wilson disease: actuality and perspectives].

作者信息

Baranovsky A Yu, Belodedova A S, Fedorova T F, Palgova L K, Grigoreva E Yu

机构信息

Saint Petersburg University, Saint Petersburg, Russia.

Saint Petersburg Clinical Hospital of the Russian Academy of Sciences, Saint Petersburg, Russia.

出版信息

Vopr Pitan. 2019;88(4):12-17. doi: 10.24411/0042-8833-2019-10036. Epub 2019 Jul 15.

Abstract

Wilson disease is hereditary disorder of copper metabolism, based on defect of cooper excretion, which leads to accumulation of cooper in the liver and brain. This disease is one of the most difficult to diagnose. Without treatment disease brings to early disability and lethal outcome. In the article, domestic and foreign approaches to dietary management of Wilson disease have been compared. Diet is not recommended as sole therapy. The degree of restriction of the products containing copper now is discussed. According to the Russian clinical guidelines of diagnosis and treatment of Wilson disease exception of products, copper content in which exceeds 0.5 mg/100 g (liver, shellfish, nuts, cocoa products, mushrooms, bean and some grains) is recommended, while in EASL clinical guidelines there are no any information about restriction of the products containing copper. It is necessary to pay attention not only to cooper restriction, but also to qualitative components of diet. Protein is important part of nutrition under liver disease. According to ESPEN guidelines, the recommended protein intake at chronic hepatitis and cirrhosis is 1.2-1.5 g/kg/day. Dairy products and whey protein are good sources of protein, they almost do not contain cooper, therefore they can be used without restrictions at Wilson disease (in case of normal lactose and milk protein tolerance). The reduce of consumption of sugar, refined carbohydrates and trans fats is also recommended. Dietary recommendations must take into consideration the nutrition status of the patient (protein energy malnutrition, normal body weight, obesity) and degree of liver damage (chronic hepatitis, cirrhosis). It is necessary to develop individualization of diet, increasing efficiency of medicinal treatment of Wilson disease.

摘要

威尔逊病是一种铜代谢的遗传性疾病,基于铜排泄缺陷,导致铜在肝脏和大脑中蓄积。这种疾病是最难诊断的疾病之一。未经治疗,该病会导致早期残疾和致命后果。在本文中,对国内外威尔逊病饮食管理方法进行了比较。不建议将饮食作为唯一的治疗方法。目前正在讨论含铜产品的限制程度。根据俄罗斯威尔逊病诊断和治疗临床指南,建议排除铜含量超过0.5毫克/100克的产品(肝脏、贝类、坚果、可可制品、蘑菇、豆类和一些谷物),而欧洲肝脏研究学会(EASL)临床指南中没有关于含铜产品限制的任何信息。不仅要注意铜的限制,还要注意饮食的质量成分。蛋白质是肝病营养的重要组成部分。根据欧洲临床营养和代谢学会(ESPEN)指南,慢性肝炎和肝硬化时推荐的蛋白质摄入量为1.2 - 1.5克/千克/天。乳制品和乳清蛋白是优质蛋白质来源,它们几乎不含铜,因此在威尔逊病时(在乳糖和乳蛋白耐受性正常的情况下)可以无限制使用。还建议减少糖、精制碳水化合物和反式脂肪的摄入。饮食建议必须考虑患者的营养状况(蛋白质能量营养不良、正常体重、肥胖)和肝损伤程度(慢性肝炎、肝硬化)。有必要制定个性化饮食,提高威尔逊病药物治疗的效果。

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