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Background:
Patients with critical illness in the intensive care unit (ICU) experience marked skeletal muscle weakness, muscle atrophy and disability in physical function, commonly termed ICU-acquired weakness (ICU-AW). The pathophysiology of ICU-AW is complex, but a key feature of skeletal muscle wasting is disturbed protein metabolism reflected in both increased rate of muscle protein degradation and reduced synthesis. Treatment with 3-OHB seems a promising new anticatabolic treatment in patients with critical illness, preventing ICU-AW. To date, no data exist on the clinical and functional effects of ketone body modulation in patients with critical illness.
Objective:
The aim to investigate the effect of exogenous 3-OHB administration on muscle protein kinetics and lipolysis in patients with critical illness, aiming towards preventing ICU-AW.
Design:
A randomized double-blind isocaloric placebo-controlled cross-over study in 10 mechanically ventilated patients with critical illness in the ICU.
Methods:
Evaluation of whole-body and focal leg protein kinetics using labeled phenylalanine and tyrosine tracers. Assessment of free fatty acid (FFA) turnover using a labeled palmitate tracer. Femoral arterial blood flow (assessed with pulsed-wave Doppler ultrasound) is evaluated once per study period. Blood- and urinary samples are collected routinely throughout the study day. Whenever feasible, muscle and fat biopsies will be taken for analysis of protein and adipocyte metabolic signaling and mitochondrial function.
Perspectives: This investigation may grant essential knowledge on ketosis in critical illness. This may lead to larger clinical trials, and hopefully a new and better treatment strategy aimed at preserving muscle mass and function during and improving recovery after critical illness.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Ketone monoester (3-OHB) | Experimental | Weight-adjusted dose of 3-OHB Monoester (KetoneAID KE4, Virginia, US). Bolus of 300 mg/kg followed by a 2-hour continuous enteral infusion with a dosing of 100 mg/kg/hour (maximal total dose 50 grams). There is a 1-hour lag between the bolus and the continuous infusion. |
|
| Placebo Treatment | Placebo Comparator | Maltodextrin- and fatbased placebo in isocaloric, isovolemic dose to the experimental arm. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| KetoneAid KE4 Pro Monoester | Dietary Supplement | A dietary supplement containing ketone monoester. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Net leg phenylalanine release | As measured by rate of phenylalanine appearance in relation with the rate of disappearance. | 3 hours |
| Measure | Description | Time Frame |
|---|---|---|
| Change in rate of appearance of phenylalanine over the leg. | 3 hours. | |
| Change in rate of disappearance of phenylalanine over the leg. | 3 hours. | |
| Whole body palmitate flux |
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Inclusion Criteria:
Exclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Kristoffer Berg-Hansen, MD | Contact | 60540700 | krbhan@gmail.com | |
| Niels Møller, Prof. | Contact | niels.moeller@clin.au.dk |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Aarhus University Hospital | Aarhus | DK-8200 | Denmark |
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| ID | Term |
|---|---|
| D016638 | Critical Illness |
| ID | Term |
|---|---|
| D020969 | Disease Attributes |
| D010335 | Pathologic Processes |
| D013568 | Pathological Conditions, Signs and Symptoms |
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| ID | Term |
|---|---|
| C008315 | maltodextrin |
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A randomized double-blind isocaloric placebo-controlled cross-over study.
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| Maltodextrin and fat-based placebo | Dietary Supplement | Dosis isocaloric to the KetoneAid Arm |
|
As measured by rate of appearance of a palmitate-tracer |
| 3 hours. |
| Change in arterial pH. | 3 hours. |
| Changes in inflammatory cytokines (IL-1, IL-6, IL-18, TNFa) | 3 hours. |
| Changes in intramyocellular protein metabolic signalling pathways. | The Akt-, mTor-, and ubiquitin-proteasome pathways. | 3 hours. |