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Impact of steroid therapy on pediatric acute liver failure: prognostic implication and interplay between TNF-α and
Rania M El-Shanawany1, Eman A El-Maadawy2, Hanaa A El-Araby1
1Pediatric Hepatology, Gastroenterology, and Nutrition Department, National Liver Institute, Menoufia University, Menoufia, Shebin El-Koom, 32511, Egypt.
Insights
Lower miR-122 levels in children with acute liver failure treated with steroids correlate with better outcomes. This microRNA, along with increased TNF-α, plays a role in disease progression and may aid in prognosis.
Area of Science:
- Pediatric Gastroenterology
- Hepatology
- Molecular Biology
Background:
- Acute liver failure (ALF) presents a significant risk in children, with limited evidence on steroid efficacy.
- MicroRNA-122 (miR-122) is a key player in liver function and disease, showing altered expression in various liver conditions.
- miR-122 is explored as a potential biomarker for disease progression, prognosis, and therapeutic targeting in liver diseases.
Purpose of the Study:
- To evaluate miR-122 expression in pediatric ALF patients before and after steroid therapy.
- To investigate the relationship between miR-122, tumor necrosis factor-alpha (TNF-α), and treatment response in ALF.
- To assess miR-122's potential as a biomarker for predicting outcomes in pediatric ALF.
Main Methods:
- Serum samples from 24 children with ALF were analyzed.
- miR-122 levels were quantified using quantitative real-time RT-PCR (qRT-PCR).
- TNF-α levels were measured via enzyme-linked immunosorbent assay (ELISA).
Main Results:
- Surviving ALF children showed significantly decreased miR-122 levels post-steroid treatment compared to pre-treatment and deceased patients.
- TNF-α levels were significantly elevated in surviving patients post-steroid treatment compared to pre-treatment and deceased children.
- A negative correlation was found between TNF-α and miR-122 post-steroids (r=-0.46, p=0.04), and miR-122 showed 72% sensitivity and 67% specificity in distinguishing survivors.
Conclusions:
- Lower miR-122 levels in pediatric ALF patients treated with steroids are associated with improved outcomes.
- While not a standalone marker, miR-122 may be valuable as part of a biomarker panel for ALF.
- Elevated TNF-α and reduced miR-122 suggest their involvement in ALF pathophysiology, warranting further investigation.
Background:
Acute liver failure (ALF) is a rare illness marked by rapid deterioration of liver function, leading to high morbidity and mortality rates, particularly in children. While steroids have been observed to correlate with improved survival, evidence supporting their efficacy in ALF children remains limited. miR-122, a liver-specific microRNA, plays a pivotal role in liver pathology, with its expression significantly altered in various liver diseases. Thus, it is considered a potential biomarker for disease progression, aids in prognosis, and identifies therapeutic targets. Our study aims to assess the expression of miR-122 in 24 children with ALF, both before and after steroid therapy, alongside its relationship with tumor necrosis factor-α (TNF-α), to better understand its potential role in treatment response and disease outcomes. miR-122 levels were determined using quantitative real-time RT-PCR (qRT-PCR), while TNF-α levels were assessed using enzyme-linked immunosorbent assay (ELISA) in patient sera.
Results:
In ALF children who survived after steroid treatment, miR-122 was markedly decreased compared to both pre-treatment levels (p = 0.003) and levels in deceased patients (p = 0.01). In addition, TNF-α levels significantly increased in surviving patients compared to pre-treatment levels (p = 0.008) and levels in deceased children (p = 0.028). A negative correlation was observed between TNF-α and miR-122 following steroids (r=-0.46, p = 0.04). miR-122 demonstrated 72% sensitivity and 67% specificity in distinguishing survivors and non-survivors, as indicated by its receiver-operated characteristic curve. A positive correlation was found between miR-122 before steroid therapy and both aspartate aminotransferase (AST) and alanine aminotransferase (ALT) before (r = 0.641, p = 0.002 and r = 0.512, p = 0.02, respectively) and after (r = 0.492, p = 0.03 and r = 0.652, p = 0.003, respectively) steroids treatment.
Conclusion:
Our data implies that lower miR-122 levels in steroids-treated ALF children are associated with a better outcome. Although miR-122 is not a strong standalone marker, it could be valuable in a biomarker panel. The increased TNF-α levels and decreased miR-122 expression indicate their involvement in the disease's pathophysiology. More studies are needed to validate our results.
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