Exploring Novel Biomarkers of ICU-AW in Mechanically Ventilated Children at the Molecular Level

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Total Enrollment

500 participants

Study Classification

OBSERVATIONAL

Study Start Date

2025-09-01

Study Completion Date

2028-09-30

Brief Summary

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Acquired weakness (AW) is a common complication among patients in the Intensive Care Unit (ICU). It is a systemic muscle weakness and dysfunction associated with critical illness, often related to prolonged bed rest, mechanical ventilation, systemic inflammatory response syndrome (SIRS), and multiple organ dysfunction syndrome (MODS). The primary clinical manifestations include weakness in limb and respiratory muscles, particularly diminished strength in distal muscle groups. As a result, the weaning process from mechanical ventilation becomes more challenging, leading to prolonged ICU stays, increased mortality, and a higher risk of long-term functional disability. The significance of AW lies not only in its substantial impediment to short-term recovery but also in its role as a core component of Post-Intensive Care Syndrome (PICS), profoundly affecting patients' long-term outcomes.

Mechanical ventilation is a vital life-support technology for critically ill children in the Pediatric Intensive Care Unit (PICU). However, complications associated with mechanical ventilation have garnered increasing attention, particularly Acquired Weakness in mechanically ventilated children. With improving survival rates in the PICU, a growing number of pediatric critical illness survivors are at risk of developing AW. Despite rapid advancements in pediatric critical care medicine in China, there is currently a lack of an early warning system for AW in children receiving mechanical ventilation, resulting in significantly delayed clinical interventions. This project aims to identify novel biomarkers for pediatric ICU-AW and develop an early warning model. It holds promise for transitioning from the traditional post-symptomatic diagnostic approach to subclinical prediction of AW in children, which is of great clinical value for reducing disability rates and optimizing critical care rehabilitation strategies.

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Detailed Description

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An electronic database was established to collect clinical data from mechanically ventilated children, including baseline clinical characteristics, laboratory test results, and imaging data. Each participating research center designated dedicated investigators to enroll study subjects starting on the same date (eligible patients already hospitalized on the start date were included). These investigators were responsible for data cleaning, organization, and standardization to ensure data quality. For all enrolled patients, data on demographic characteristics, clinical features, and laboratory test results were recorded using case report forms (CRFs) on the day of enrollment (D0), day 3 (D3), day 10 (D10), the day of discharge from the pediatric intensive care unit (Ddis), or the day of death (DD).

To investigate the pathophysiology of ICU-acquired weakness (ICU-AW) under the inflammation-metabolism-neuromuscular injury hypothesis, dynamic plasma biological sample collection was performed. Samples were collected at different time points during mechanical ventilation to establish a biobank. Proteomic and genomic multi-omics approaches were employed to screen for inflammatory cytokines, specific degradation biomarkers of muscle injury, and metabolism-related genes such as those involved in mitochondrial function. Levels of these biomarkers in biological samples from mechanically ventilated children were measured to analyze their association with the onset and progression of ICU-AW, thereby untangling the pathophysiology of ICU-AW at the molecular level.

The Pathophysiology of ICU-AW remains unclear, and there is a lack of research exploring its molecular mechanisms, making it difficult to identify effective early warning indicators. Currently, it is believed that the pathophysiology of ICU-AW is associated with persistent inflammation, immunosuppression, and catabolic syndrome (PICS), resulting from the interplay of multiple factors and pathways. Key mechanisms include: inflammatory response and immune dysregulation, mitochondrial dysfunction and abnormal energy metabolism, oxidative stress, and microvascular changes, which collectively lead to muscular and neurological dysfunction. The core of its pathophysiology lies in the imbalance between protein synthesis and muscle protein degradation, which occurs in response to various stimuli. Key mechanisms include: 1) The ubiquitin-proteasome system (UPS). Pro-inflammatory cytokines (e.g: NF-κB) upregulate muscle-specific E3 ubiquitin ligases (such as MuRF1 and Atrogin-1), accelerating muscle protein degradation and contributing to muscle atrophy. 2) The autophagy-lysosome system. Abnormal activation of this system leads to muscle fiber atrophy, though its specific regulatory mechanisms remain unclear. Although some progress has been made in mechanistic studies of ICU-AW, its pathophysiological mechanisms are complex and not yet fully elucidated. There is a lack of biomarkers for early clinical identification and insufficient translational molecular research.

In recent years, the discovery of multi-dimensional molecular markers has provided new directions for early identification and mechanistic analysis of ICU-AW:

1. Direct markers of muscle structural damage: Urinary Titin. As a core protein of the muscle cytoskeleton, its release in urine quantitatively reflects the extent of muscle fiber breakdown. The mechanism of its release is closely related to key pathological pathways of ICU-AW (UPS activation, inflammation-oxidative stress synergy, and dysregulated mechanical signaling). A multicenter prospective study found that urinary Titin levels in non-surgical ICU patients were 10 to 30 times higher than normal levels and were significantly negatively correlated with dynamic changes in rectus femoris cross-sectional area measured by ultrasound (p \< 0.01), suggesting its potential as a non-invasive biomarker for monitoring muscle atrophy.
2. Combined markers of neuromuscular interaction damage: Neurofilament light chain (NfL)-a major cytoskeletal protein of neuronal axons and a marker of axonal injury-was significantly elevated in the serum of ICU-AW patients with CIP/CIM early after admission (median 4 days); Glial fibrillary acidic protein (GFAP)-reflecting astrocyte activation-contributes to the onset and progression of ICU-AW by mediating neuroinflammation, motor neuron injury, and neuromuscular junction dysfunction. Their dynamic changes not only offer new tools for early diagnosis and prognosis assessment of ICU-AW but may also represent potential targets for future therapeutic interventions.
3. Epigenetic regulatory markers: Abnormal DNA methylation and muscle dysfunction. HIC1 regulates muscle regeneration and modulates the concentration of postsynaptic acetylcholine receptors, while NADK2 is involved in lipid metabolism and mitochondrial stimulation. Recent studies in adults have shown that, compared to controls, ICU patients exhibit reduced methylation in the epigenomic regions of HIC1 and NADK2. The HIC1 and NADK2 genes may theoretically provide a biological basis for ICU-AW.

Conditions

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ICU Acquired Weakness

Study Design

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Observational Model Type

CASE_CONTROL

Study Time Perspective

PROSPECTIVE

Study Groups

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ICU-AW

Children receiving mechanical ventilation who developed ICU-AW at the study endpoint.

ICU-AW

Intervention Type DIAGNOSTIC_TEST

The enrolled children receiving mechanical ventilation were grouped based on the occurrence of ICU-acquired weakness (ICU-AW) at the study endpoint.

without ICU-AW

Children receiving mechanical ventilation who did not developed ICU-AW at the study endpoint.

No interventions assigned to this group

Interventions

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ICU-AW

The enrolled children receiving mechanical ventilation were grouped based on the occurrence of ICU-acquired weakness (ICU-AW) at the study endpoint.

Intervention Type DIAGNOSTIC_TEST

Eligibility Criteria

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Inclusion Criteria

1. Age between 28 days and 18 years;
2. Patients continuously admitted to the PICU during the study period and subjected to invasive mechanical ventilation.

Exclusion Criteria

1. Mechanical ventilation duration \< 72 hours;
2. Presence of primary central or neuromuscular diseases that significantly affect central or peripheral respiratory failure, including: traumatic brain injury, cerebrovascular disease history (e.g., cerebral hemorrhage, cerebral infarction), intracranial tumors, central nervous system infections, spinal cord injury, Guillain-Barré syndrome, porphyria, paraneoplastic neuropathy, etc.;
3. Conditions requiring immobilization such as limb joint surgery or fractures.

Minimum Eligible Age

1 Month

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No