用素食和纯素替代肉类膳食可降低肝硬化患者的氨氮并改变代谢物:随机临床试验

IF 3 3区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY Clinical and Translational Gastroenterology Pub Date : 2024-06-01 DOI:10.14309/ctg.0000000000000707
Bryan D Badal, Andrew Fagan, Victoria Tate, Travis Mousel, Mary Leslie Gallagher, Puneet Puri, Brian Davis, Jennifer Miller, Masoumeh Sikaroodi, Patrick Gillevet, Rolandas Gedguadas, Juozas Kupcinkas, Leroy Thacker, Jasmohan S Bajaj
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引用次数: 0

摘要

导言:饮食会影响肝硬化和肝性脑病(HE)的氨生成,但饮食偏好对肝硬化代谢组学的影响尚不清楚。由于大多数西方人的饮食以肉类为主,我们的目的是确定在以肉类为主食的肝硬化门诊患者中,用等量蛋白质的素食/荤食替代单一肉类膳食对氨和代谢组学的影响:门诊患者中,有肝硬化和无肝硬化的患者均以稳定的西式肉食为基础饮食,按1:1:1的比例随机分为3组。患者食用含 20 克蛋白质的肉类、素食(V)或素食(VG)汉堡。在对患者进行观察期间,在基线和餐后 3 小时内每小时抽血一次,通过液相色谱-质谱法和氨进行代谢组学分析。比较组间/组内的粪便微生物组特征、氨的变化和代谢组学:结果:基线时的粪便微生物组组成相似。肉类组血清氨从基线开始升高,而 VG 或 V 组则没有。与非肉类组相比,肉类组的支链和酰基肉碱代谢物减少。与 VG 组和 VG 组相比,肉类组的脂质概况发生了变化(鞘磷脂增加,溶血磷脂减少):结论:用非肉类替代品替代单一肉类膳食可降低氨生成,并改变肝硬化患者的血清代谢组学,主要是支链氨基酸、酰基肉碱、溶血磷脂和鞘磷脂,与肝脏或粪便微生物组无关。间歇性用素食或纯素替代肉类可能有助于减少肝硬化患者体内氨的生成。
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Substitution of One Meat-Based Meal With Vegetarian and Vegan Alternatives Generates Lower Ammonia and Alters Metabolites in Cirrhosis: A Randomized Clinical Trial.

Introduction: Diet can affect ammoniagenesis in cirrhosis and hepatic encephalopathy (HE), but the impact of dietary preferences on metabolomics in cirrhosis is unclear. As most Western populations follow meat-based diets, we aimed to determine the impact of substituting a single meat-based meal with an equal protein-containing vegan/vegetarian alternative on ammonia and metabolomics in outpatients with cirrhosis on a meat-based diet.

Methods: Outpatients with cirrhosis with and without prior HE on a stable Western meat-based diet were randomized 1:1:1 into 3 groups. Patients were given a burger with 20 g protein of meat, vegan, or vegetarian. Blood for metabolomics via liquid chromatography-mass spectrometry and ammonia was drawn at baseline and hourly for 3 hours after meal while patients under observation. Stool microbiome characteristics, changes in ammonia, and metabolomics were compared between/within groups.

Results: Stool microbiome composition was similar at baseline. Serum ammonia increased from baseline in the meat group but not the vegetarian or vegan group. Metabolites of branched chain and acylcarnitines decreased in the meat group compared with the non-meat groups. Alterations in lipid profile (higher sphingomyelins and lower lysophospholipids) were noted in the meat group when compared with the vegan and vegetarian groups.

Discussion: Substitution of a single meat-based meal with a non-meat alternatives results in lower ammoniagenesis and altered serum metabolomics centered on branched-chain amino acids, acylcarnitines, lysophospholipids, and sphingomyelins in patients with cirrhosis regardless of HE or stool microbiome. Intermittent meat substitution with vegan or vegetarian alternatives could be helpful in reducing ammonia generation in cirrhosis.

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来源期刊
Clinical and Translational Gastroenterology
Clinical and Translational Gastroenterology GASTROENTEROLOGY & HEPATOLOGY-
CiteScore
7.00
自引率
0.00%
发文量
114
审稿时长
16 weeks
期刊介绍: Clinical and Translational Gastroenterology (CTG), published on behalf of the American College of Gastroenterology (ACG), is a peer-reviewed open access online journal dedicated to innovative clinical work in the field of gastroenterology and hepatology. CTG hopes to fulfill an unmet need for clinicians and scientists by welcoming novel cohort studies, early-phase clinical trials, qualitative and quantitative epidemiologic research, hypothesis-generating research, studies of novel mechanisms and methodologies including public health interventions, and integration of approaches across organs and disciplines. CTG also welcomes hypothesis-generating small studies, methods papers, and translational research with clear applications to human physiology or disease. Colon and small bowel Endoscopy and novel diagnostics Esophagus Functional GI disorders Immunology of the GI tract Microbiology of the GI tract Inflammatory bowel disease Pancreas and biliary tract Liver Pathology Pediatrics Preventative medicine Nutrition/obesity Stomach.
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