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Nutritional therapy for persistent cognitive impairment after resolution of overt hepatic encephalopathy in patients with cirrhosis: A double-blind randomized controlled trial.
Sharma, Barjesh Chander; Maharshi, Sudhir; Sachdeva, Sanjeev; Mahajan, Bhawna; Sharma, Ashok; Bara, Sushma; Srivastava, Siddharth; Kumar, Ajay; Dalal, Ashok; Sonika, Ujjwal.
Afiliação
  • Sharma BC; Department of Gastroenterology, G.B. Pant Hospital, New Delhi, India.
  • Maharshi S; Department of Gastroenterology, SMS Hospital, Jaipur, India.
  • Sachdeva S; Department of Gastroenterology, G.B. Pant Hospital, New Delhi, India.
  • Mahajan B; Department of Biochemistry, G.B. Pant Hospital, New Delhi, India.
  • Sharma A; Department of Radiology, G.B. Pant Hospital, New Delhi, India.
  • Bara S; Department of Gastroenterology, G.B. Pant Hospital, New Delhi, India.
  • Srivastava S; Department of Gastroenterology, G.B. Pant Hospital, New Delhi, India.
  • Kumar A; Department of Gastroenterology, G.B. Pant Hospital, New Delhi, India.
  • Dalal A; Department of Gastroenterology, G.B. Pant Hospital, New Delhi, India.
  • Sonika U; Department of Gastroenterology, G.B. Pant Hospital, New Delhi, India.
J Gastroenterol Hepatol ; 38(11): 1917-1925, 2023 Nov.
Article em En | MEDLINE | ID: mdl-37354045
ABSTRACT
BACKGROUND AND

AIM:

Minimal hepatic encephalopathy (MHE) reflects cognitive impairment in patients with liver cirrhosis and is associated with poor prognosis. We assessed the effects of nutritional therapy on cognitive functions, health-related quality of life (HRQOL), anthropometry, endotoxins, and inflammatory markers in cirrhotic patients with MHE.

METHODS:

In a double-blind randomized controlled trial, cirrhotic patients with MHE were randomized to nutritional therapy (group I 30-35 kcal/kg/day and 1.0-1.5 g of protein/kg/day) and no nutritional therapy (group II diet as patients were taking before) for 6 months. MHE was diagnosed based on psychometric hepatic encephalopathy score (PHES). Anthropometry, ammonia, endotoxins, inflammatory markers, myostatin, and HRQOL were assessed at baseline and after 6 months. Primary endpoints were improvement or worsening in MHE and HRQOL.

RESULTS:

A total of 150 patients were randomized to group I (n = 75, age 46.3 ± 12.5 years, 58 men) and group II (n = 75, age 45.2 ± 9.3 years, 56 men). Baseline PHES (-8.16 ± 1.42 vs -8.24 ± 1.43; P = 0.54) was comparable in both groups. Reversal of MHE was higher in group I (73.2% vs 21.4%; P = 0.001) than group II. Improvement in PHES (Δ PHES 4.0 ± 0.60 vs -4.18 ± 0.40; P = 0.001), HRQOLSickness Impact Profile 3.24 ± 3.63 vs 0.54 ± 3.58; P = 0.001), anthropometry, ammonia, endotoxins, cytokines, and myostatin levels was also significantly higher in group I than group II. Overt hepatic encephalopathy developed in 6 patients in group I and 13 in group II (P = 0.04).

CONCLUSIONS:

Nutritional therapy is effective in treatment of MHE and associated with improvement in nutritional status, HRQOL, ammonia, endotoxins, inflammatory markers, and myostatin levels.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encefalopatia Hepática / Disfunção Cognitiva Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Encefalopatia Hepática / Disfunção Cognitiva Idioma: En Ano de publicação: 2023 Tipo de documento: Article