Normal liver stiffness and influencing factors in healthy children: An individual participant data meta-analysis

Darrick K Li1, Muhammad Rehan Khan2, Zhen Wang3

  • 1Division of Gastroenterology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, USA.

Insights

Transient elastography (TE) establishes liver stiffness ranges in healthy children, defining normal as 2.45-5.56 kPa. Factors like age, sedation, and steatosis influence these measurements.

Area of Science:

  • Pediatric Gastroenterology
  • Hepatology
  • Medical Imaging

Background:

  • Transient elastography (TE) is crucial for assessing liver fibrosis, but normal liver stiffness ranges in children are not well-established.
  • Accurate reference ranges are needed for reliable pediatric liver health assessment.

Purpose of the Study:

  • To determine the normal range of liver stiffness in healthy children using TE.
  • To identify biological and procedural factors influencing liver stiffness measurements in pediatric populations.

Main Methods:

  • A systematic review and individual participant data (IPD) meta-analysis of 10 studies involving 1702 children.
  • Analysis of 652 children after excluding those with obesity, diabetes, or abnormal liver tests, divided into younger (<3 years) and older (≥3 years) groups.
  • Application of univariate and multivariate linear regression models to identify predictors of liver stiffness.

Main Results:

  • Established a reference range for normal liver stiffness in healthy children as 2.45-5.56 kPa.
  • In older children (≥3 years), mean liver stiffness was 4.45 kPa, influenced by age, sedation, and S probe use.
  • In younger children (<3 years), mean liver stiffness was 4.79 kPa, influenced by sedation and Caucasian race.
  • Hepatic steatosis on ultrasound was significantly associated with increased liver stiffness across groups.

Conclusions:

  • Defined TE-derived liver stiffness ranges for healthy children, proposing an upper limit of 5.56 kPa.
  • Identified key factors influencing liver stiffness measurements in children, including age, sedation, probe type, and hepatic steatosis.
  • Provides essential reference data for pediatric liver health evaluations using TE.
Abstract

Related Concept Videos

Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test01:22

Effect of Hepatic Disease on Pharmacokinetics: Pathophysiologic Assessment and Liver Function Test

In clinical practice, the direct measurement of hepatic blood flow to evaluate liver function presents significant challenges due to the intricate and specialized nature of the necessary techniques. Consequently, healthcare professionals often rely on empirical estimates derived from thorough patient examinations and liver function tests to gauge liver health. Among the tools at their disposal, the Child–Pugh and MELD scoring systems stand out for their ability to categorize and assess...
102
Liver Physiology01:30

Liver Physiology

The liver, an essential organ in the human body, performs over 200 vital functions that can be broadly categorized into metabolic, hematological, endocrine regulation, and bile production.
Metabolic Regulation:
The liver is the central organ involved in regulating blood composition. It stabilizes blood glucose levels, maintaining them within the range of  70–110 mg/dL. When these levels drop, the liver breaks down glycogen reserves and releases glucose into the bloodstream. It can...
3.2K
Pharmacokinetics in Pediatric Patients: Drug Metabolism01:24

Pharmacokinetics in Pediatric Patients: Drug Metabolism

In pediatric care, understanding the nuances of hepatic drug metabolism is crucial, as it significantly differs from that of adults. This divergence is primarily due to the developmental stage of drug-metabolizing enzymes, which affects how medications are processed in the body. In neonates, for instance, the activity of Phase I enzymes—critical for the initial breakdown of drugs—is markedly reduced, functioning at just 20–40% of the levels seen in adults. This reduction poses...
108
Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow01:26

Effect of Hepatic Disease on Pharmacokinetics: Drug Dosing and Hepatic Blood Flow

Chronic liver disease significantly impacts drug metabolism due to alterations in hepatic blood flow and enzyme accessibility. This disruption affects the body's pharmacokinetics—the movement and processing of drugs within the system. Key enzymes crucial for metabolizing medications become less accessible, changing how drugs are processed and utilized. Furthermore, liver disease influences the synthesis of plasma proteins, such as albumin and globulins, which play critical roles in drug...
127
Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment01:08

Effect of Hepatic Disease on Pharmacokinetics: Dose Adjustments Due to Hepatic Impairment

Hepatic impairment, characterized by decreased liver function, does not uniformly mandate adjustments in drug dosage. Whether dosage modifications are necessary depends on various factors related to the drug's metabolism and elimination pathways. If a drug is primarily excreted via the kidneys and bypasses significant hepatic processing, if it undergoes minimal metabolic transformation in the liver, or if it is volatile and primarily expelled through the lungs, dose adjustments may not be...
105
Therapeutic Drug Monitoring: Affecting Factors01:29

Therapeutic Drug Monitoring: Affecting Factors

Therapeutic Drug Monitoring (TDM) is the clinical practice of measuring specific drug levels in a patient's blood or body tissues to manage and optimize therapy. TDM is crucial for drugs with narrow therapeutic windows, like warfarin and phenytoin, where incorrect doses can lead to treatment failure or severe side effects. This monitoring ensures the dosage administered is within a safe and effective range. The factors affecting therapeutic drug monitoring include:Patient-Specific Factors:a.
107