Revitalizing liver health: Human placental extract shows promise in chronic liver disease management
This editorial provided commentaries on an article titled "Liver function improvement after human placental extract injections in patients with chronic liver disease: Thirty case reports". The first clinical application of an innovative therapeutic protocol was comprehensively described in this case report by Lee, in which 30 patients with chronic liver disease (CLD) received intravenous administration of 10 mL human placental extract (HPE). Notably, significant improvements in liver function could be observed in these patients, which underscored the potential of this novel treatment for CLD management. However, the rising prevalence of CLD around the world underscored the limitations of conventional therapies (such as antiviral agents and lifestyle modifications) in addressing advanced fibrosis or metabolic dysfunction-associated steatotic liver disease. Additionally, emerging regenerative therapies (including HPE) have garnered more attention due to their bioactive components, which could modulate the hepatic microenvironment based on antioxidant, anti-inflammatory, and pro-regenerative mechanisms. Although the existing evidence remains relatively lacking, the multi-targeted action of HPE highlights its potential as a novel therapeutic strategy. Overall, this editorial outlines the research advancements of HPE, alongside the critical analysis of existing limitations and the proposal of future research directions.
- Research Article
- 10.12998/wjcc.v13.i23.102937
- Aug 16, 2025
- World journal of clinical cases
This case report describes a protocol developed by Danaun Medical Clinic for the introduction of a pioneering intervention comprising intravenous human placental extract (HPE) therapy to improve the liver function of patients with chronic liver disease (CLD). This study involved data from patients whose chief complaint was reduced quality of life attributable to CLD. The new treatment approach resulted in improvements in the liver function and fatty liver of 30 patients with CLD. Improvements were observed using abdominal ultrasonography. Unlike traditional methods, this protocol provided more sustainable and meaningful results. Treatment with 10 mL of HPE administered intravenously once or twice per week significantly improved liver function. The observed improvements in fatty liver and liver function suggest the utility of this approach for the management of patients with CLD. This case series highlights the potential of innovative treatments for patients with CLD that could improve the quality of life of the patients.
- Research Article
11
- 10.1097/00005176-200207001-00013
- Jul 1, 2002
- Journal of Pediatric Gastroenterology and Nutrition
The Impact of Liver Disease on Growth and Nutrition
- Research Article
74
- 10.1053/j.gastro.2004.12.004
- Mar 1, 2005
- Gastroenterology
Contribution of metabolic factors to alanine aminotransferase activity in persons with other causes of liver disease
- Front Matter
16
- 10.1111/jan.13350
- Jul 5, 2017
- Journal of Advanced Nursing
Chronic liver diseases are very common worldwide and represent a major healthcare issue (GBD 2013 Mortality and Causes of Death Collaborators, 2015). Chronic liver diseases are characterized by inflammation of the liver, which may be secondary to distinct etiological factors, including hepatitis C or B infection, increased alcohol consumption, or non-alcoholic fatty liver disease (NAFLD). This article is protected by copyright. All rights reserved.
- Front Matter
91
- 10.1097/00007890-199810150-00034
- Oct 1, 1998
- Transplantation
Minimal criteria for placement of adults on the liver transplant waiting list: a report of a national conference organized by the American Society of Transplant Physicians and the American Association for the Study of Liver Diseases.
- Research Article
36
- 10.1016/j.amjmed.2010.08.014
- Dec 25, 2010
- The American Journal of Medicine
Venous Thromboembolism with Chronic Liver Disease
- Research Article
21
- 10.1046/j.1365-2141.1998.00855.x
- Oct 1, 1998
- British journal of haematology
Hepatitis in haemophilia.
- Research Article
184
- 10.1053/j.gastro.2012.02.011
- Apr 23, 2012
- Gastroenterology
Viral Hepatitis in Liver Transplantation
- Front Matter
7
- 10.1016/j.cgh.2011.10.036
- Nov 4, 2011
- Clinical Gastroenterology and Hepatology
Fatigue in Cirrhosis: Is Transplant the Answer?
- Research Article
135
- 10.1016/j.jhepr.2020.100169
- Aug 4, 2020
- JHEP Reports
Impact of COVID-19 on the care of patients with liver disease: EASL-ESCMID position paper after 6 months of the pandemic.
- Research Article
9
- 10.1016/j.jep.2023.117514
- Nov 30, 2023
- Journal of Ethnopharmacology
Recent progress on the application of compound formulas of traditional Chinese medicine in clinical trials and basic research in vivo for chronic liver disease
- Discussion
19
- 10.1016/j.jhep.2020.11.004
- Dec 16, 2020
- Journal of Hepatology
“Dual aetiology fatty liver disease”: A recently proposed term associated with potential pitfalls
- Research Article
128
- 10.1097/mpg.0b013e31826f2760
- Jan 1, 2013
- Journal of Pediatric Gastroenterology and Nutrition
Outcome of liver disease in children is mainly determined by severity and progression of liver fibrosis. Liver biopsy is the accepted standard for evaluating fibrosis but is limited by the need for sedation in children, sampling error, and risks including bleeding. The aim of the present study was to compare tools for noninvasive assessment of liver fibrosis in a paediatric cohort. Children undergoing liver biopsy for chronic liver disease were recruited and underwent transient elastography (TE). Liver biopsies were scored by a hepatohistopathologist from F0 (no fibrosis) to F4 (cirrhosis). TE was compared with biopsy score. During the study period, 104 children (62 boys) were enrolled (median age 13.6 years). Diagnosis was autoimmune liver disease in 27; nonalcoholic fatty liver disease in 37; posttransplant in 16; hepatitis B/C in 8; Wilson disease in 5; and the remainder, miscellaneous. TE was successful in all but 7 patients and was a good discriminator of significant fibrosis (≥ F2) (P < 0.001), severe fibrosis (≥ F3) (P < 0.001), and cirrhosis (F4) (P = 0.003). The area under the receiver operating characteristic curve for the prediction of ≥ F2, ≥ F3, and F4 using TE was 0.78, 0.79, and 0.96, respectively. TE performed best in children with autoimmune liver disease and in those posttransplant. The present study demonstrates that TE is a reliable tool in distinguishing different stages of liver fibrosis in paediatric patients. Thus, TE may serve as a useful adjunct to liver biopsy for diagnostic purposes providing a reliable method of noninvasively monitoring liver disease progression in children.
- Research Article
4
- 10.1542/neo.2-9-e215
- Sep 1, 2001
- NeoReviews
After completing this article, readers should be able to: 1. Describe the caloric requirements of a neonate who has chronic liver disease. 2. Identify the vitamin and mineral deficiencies associated with cholestasis and the methods used to correct these deficits. 3. Describe the relationship between total parenteral nutrition and the development of chronic liver disease. 4. Delineate the relationship between malnutrition at the time of liver transplantation and subsequent morbidity and mortality. 5. List the best measurements of nutrition assessment in infants who have chronic liver disease. The liver is involved in many of the body’s metabolic processes, including: regulation of protein, fat, and carbohydrate metabolism; vitamin storage and activation; and detoxification and excretion of waste products. The healthy liver synthesizes and excretes bile salts. With cholestatic liver diseases, poor bile flow results in fat malabsorption because micelles, which solubilize long-chain fatty acids, cannot form without bile salts. Fat malabsorption results in enteric losses of the fat-soluble vitamins A, D, E, and K. Impaired liver function can lead to nutrient deficiencies and eventually protein-energy malnutrition. All of these factors, combined with the common symptoms of anorexia and poor dietary intake, make malnutrition common in chronic liver disease, particularly if it occurs in infants, who are more vulnerable to the debilitating effects of malnutrition because of their higher energy and growth requirements. A wide range of deficits occurs in most chronic liver diseases of children (Table 1⇓ ). Malnutrition itself may induce further derangements of liver function because the liver requires energy for a number of synthetic, storage, and detoxification functions. View this table: Table 1. Nutritional Risk Factors in Acute and Chronic Liver Disease The need for aggressive, early nutrition support in neonates has been well established and discussed extensively. Some centers routinely use a “standardized” approach to nutrition support; we use a “tailored” approach that entails parenteral or …
- Research Article
53
- 10.1097/00005176-200004000-00003
- Apr 1, 2000
- Journal of Pediatric Gastroenterology and Nutrition
Nutritional aspects of chronic liver disease and liver transplantation in children.
- Ask R Discovery
- Chat PDF
AI summaries and top papers from 250M+ research sources.