The ASTERS Study: Assessing the Role of Sphingolipids in AcuTE Respiratory Distress Syndrome (ARDS)
| Status: | Not yet recruiting |
|---|---|
| Conditions: | Hospital, Pulmonary, Pulmonary |
| Therapuetic Areas: | Pulmonary / Respiratory Diseases, Other |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 2/7/2019 |
| Start Date: | June 1, 2019 |
| End Date: | December 31, 2019 |
| Contact: | Jamie L Sturgill, PhD |
| Email: | jlstur0@uky.edu |
| Phone: | 859-323-7277 |
Assessing the Role of Sphingolipids in AcuTE Respiratory Distress Syndrome
Acute lung injury (ALI) and the more severe manifestation, acute respiratory distress
syndrome (ARDS) describe syndromes of acute onset, bilateral, inflammatory pulmonary
infiltrates and impaired oxygenation. ARDS/ALI are a continuum of disease which results in a
life threatening, rapidly progressive illness and occurs in critically ill patients. Recent
reports in the Journal of the American Medical Association (JAMA) highlight the significant
public health impact ARDS/ALI has on the critically ill population in that despite robust
research efforts, these illnesses continue to be under diagnosed, under treated, and continue
to have a high mortality rate (≥ 40% of all confirmed diagnoses). The estimates for ARDS/ALI
incidence vary due to inconsistencies with proper diagnosis and lack of valid biomarkers of
disease; however, it is expected that anywhere from 20-50% of patients on mechanical
ventilation will develop this disease. Previous work by our group has shown that
sphingolipids play a multifaceted role in lung inflammation. Sphingolipid are a class of
bioactive lipids that play a role in cellular processes such as apoptosis, cell migration,
and adhesion. Ceramide is one species of sphingolipid the investigators have examined in both
man and mouse. Our laboratory has shown that ceramide is up-regulated in pulmonary
inflammation in mouse models of pneumonitis and is elevated in the exhaled breath condensate
of mechanically ventilated patients at risk for ARDS/ALI. Our work coupled with the work of
others highlighting a role for ceramide in chronic obstructive pulmonary disease (COPD),
surfactant dysfunction, and infectious disease make ceramide a logical candidate biomarker
that warrants further investigation. To our knowledge, there are no studies examining the
role of ceramide as a biomarker in ARDS/ALI. Thus, our overarching hypothesis is that
ceramide is elevated in the lungs of patients who develop ARDS/ALI. This lipid dysregulation
accounts for the pathophysiology seen in this disease and may be a potential pharmacologic
target for clinical treatment. Thus the purpose of this exploratory research is to maximize
existing specimens to further evaluate ceramide as a biomarker for acute lung injury.
syndrome (ARDS) describe syndromes of acute onset, bilateral, inflammatory pulmonary
infiltrates and impaired oxygenation. ARDS/ALI are a continuum of disease which results in a
life threatening, rapidly progressive illness and occurs in critically ill patients. Recent
reports in the Journal of the American Medical Association (JAMA) highlight the significant
public health impact ARDS/ALI has on the critically ill population in that despite robust
research efforts, these illnesses continue to be under diagnosed, under treated, and continue
to have a high mortality rate (≥ 40% of all confirmed diagnoses). The estimates for ARDS/ALI
incidence vary due to inconsistencies with proper diagnosis and lack of valid biomarkers of
disease; however, it is expected that anywhere from 20-50% of patients on mechanical
ventilation will develop this disease. Previous work by our group has shown that
sphingolipids play a multifaceted role in lung inflammation. Sphingolipid are a class of
bioactive lipids that play a role in cellular processes such as apoptosis, cell migration,
and adhesion. Ceramide is one species of sphingolipid the investigators have examined in both
man and mouse. Our laboratory has shown that ceramide is up-regulated in pulmonary
inflammation in mouse models of pneumonitis and is elevated in the exhaled breath condensate
of mechanically ventilated patients at risk for ARDS/ALI. Our work coupled with the work of
others highlighting a role for ceramide in chronic obstructive pulmonary disease (COPD),
surfactant dysfunction, and infectious disease make ceramide a logical candidate biomarker
that warrants further investigation. To our knowledge, there are no studies examining the
role of ceramide as a biomarker in ARDS/ALI. Thus, our overarching hypothesis is that
ceramide is elevated in the lungs of patients who develop ARDS/ALI. This lipid dysregulation
accounts for the pathophysiology seen in this disease and may be a potential pharmacologic
target for clinical treatment. Thus the purpose of this exploratory research is to maximize
existing specimens to further evaluate ceramide as a biomarker for acute lung injury.
Since it was first described in 1967 by Ashbaugh et al, ARDS/ALI remains a global clinical
problem resulting in high morbidity and mortality. These lung syndromes are life threatening,
rapidly progressive disease occurring in critically ill patients characterized by hypoxemia,
alterations in lung mechanics, and edema. Recent reports in the Journal of the American
Medical Association (JAMA) highlight the significant public health impact ARDS/ALI has on the
critically ill population in that despite robust research efforts, ARDS continues to be under
diagnosed, under treated, and continues to have a high mortality rate (= 40% of all confirmed
diagnoses). The estimates for ARDS/ALI incidence vary due to inconsistencies with proper
diagnosis and lack of valid biomarkers of disease; however, it is expected that anywhere from
20-50% of patients on long term mechanical ventilation will develop this disease. Despite
this robust effort to better improve patient care, clinicians are still lacking biomarkers of
disease and a strong understanding of the underlying pathophysiology of ARDS/ALI. Thus,
research is warranted in this area. Many research efforts have been aimed at unifying
diagnoses of the disease with clinical criteria, thus the ARDS Task force implemented the
Berlin definition of disease in 2012 but despite this, recent data from the Lung SAFE trial
showed that clinical recognition of disease was only 34.1% on initial presentation, again
emphasizing the need for objective measures of disease.
The oxygenation threshold set forth by the Berlin definition are critical for understanding
of ARDS/ALI disease severity and progression. Oxygenation is calculated by the PaO2/FiO2
ratio (P/F) which is the the ratio of arterial oxygen partial pressure (PaO2) as determined
by arterial blood gas to fractional inspired oxygen setting on the mechanical ventilator
(FiO2). This P/F ratio is also important to distinguish both diagnosis of ARDS but disease
severity. A normal healthy P/F ratio is between 400-500 whereas ALI is below 300 (aka Mild
ARDS by Berlin definition), ARDS is below 200, and severe ARDS is below 100. These are the
same clinical parameters used by our medical intensive care unit (MICU). The current
treatment modalities for ARDS/ALI are primarily supportive care in the form of lung
protective ventilator management, fluid management, prone positioning, and neuromuscular
blockage in severe ARDS. Clinical studies have examined potential pharmacologic therapies
including the use of albuterol, anti-platelet therapies, statins, aspirin, and steroids -
none of which had any significant benefit on clinical outcomes. Our data in mouse models and
preliminary data in a small cohort of patients at risk for ARDS/ALI highlight a novel role
for ceramide in the pathophysiology of this disease. Our preliminary data indicate that
ceramide may not only be a key player in the underlying pathology of ARDS/ALI, but may also
serve as a useful biomarker. Additionally, as there is a currently FDA approved drug that
targets ceramide formation and actions as the investigators have demonstrated, the work
outlined herein has significant translational potential. Thus, this proposal will examine the
premise that ceramide is a new critical player in ARDS/ALI and identify ceramide as a
biomarker for individualized medicine to optimize diagnosis and improve treatments. Given the
large numbers of individuals affected by ARDS/ALI, the outcomes of this research have the
potential to change the paradigm of how clinicians and researchers perceive inflammatory
airway disease and may then translate into better, targeted approaches for the management for
millions worldwide. This pilot study will be conducted as a prospective descriptive,
cross-sectional study with a single data collection. This design allows for greater control
over the measurements and maximization of data completeness. While a cross-sectional study
design does not allow us to examine causality, it does allow us to examine associations among
the variables/domains of interest, which align with the aim of the study. This design is
appropriate and scientifically rigorous while meeting the budgetary and time constraints of
the grant mechanism. The investigators have developed a state of the science, non-invasive
technique which can be utilized to assess sphingolipid levels in the breath of mechanically
ventilated subjects. Exhaled breath condensate (EBC) is collected using a commercially
available device, RTubeVent™ (Respiratory Research Inc., Austin, TX). The RTubeVent™, covered
by a frozen aluminum sleeve and fabric cloth sleeve, allows for the cooling of exhaled breath
into a condensed liquid form and is a safe, easy, relatively inexpensive, repeatable,
non-invasive approach to collect a biological fluid that is hypothesized to be more specific
to pulmonary biology changes compared to systemically collected biological fluids such as
serum or plasma. The RTubeVENT™ breath condensate collection device is designed for ease of
use in the ICU. It can be placed in-line in the expiratory limb of the breathing circuit or
at the ventilator exhaust port. This non-invasive device is fully self-contained and
disposable. As the subject is ventilated, the RTubeVENT™ gathers breath condensate in a
special cartridge designed exclusively for ventilator use. EBC has been identified by the
National Institutes of Health as an emerging source for biomarker research thus highlighting
another innovative aspect of this proposal. Once patients are enrolled in the study, the
investigators will collect EBC from the ventilator for approximately 20 minutes under the
guidance of respiratory therapy and take a 5cc blood draw for plasma isolation. Samples will
be immediately taken to the laboratory for processing where both EBC and plasma will be
aliquoted, and stored at -80°C until analysis. Liquid chromatography electrospray
ionization-tandem mass spectrometry (LC-ESI-MS/MS) will be used to detect sphingolipid levels
and samples will be batch processed to minimize variability. The investigators predict that
patients in the ARDS/ALI group will have significantly elevated ceramide levels as compared
to those in the control group.
problem resulting in high morbidity and mortality. These lung syndromes are life threatening,
rapidly progressive disease occurring in critically ill patients characterized by hypoxemia,
alterations in lung mechanics, and edema. Recent reports in the Journal of the American
Medical Association (JAMA) highlight the significant public health impact ARDS/ALI has on the
critically ill population in that despite robust research efforts, ARDS continues to be under
diagnosed, under treated, and continues to have a high mortality rate (= 40% of all confirmed
diagnoses). The estimates for ARDS/ALI incidence vary due to inconsistencies with proper
diagnosis and lack of valid biomarkers of disease; however, it is expected that anywhere from
20-50% of patients on long term mechanical ventilation will develop this disease. Despite
this robust effort to better improve patient care, clinicians are still lacking biomarkers of
disease and a strong understanding of the underlying pathophysiology of ARDS/ALI. Thus,
research is warranted in this area. Many research efforts have been aimed at unifying
diagnoses of the disease with clinical criteria, thus the ARDS Task force implemented the
Berlin definition of disease in 2012 but despite this, recent data from the Lung SAFE trial
showed that clinical recognition of disease was only 34.1% on initial presentation, again
emphasizing the need for objective measures of disease.
The oxygenation threshold set forth by the Berlin definition are critical for understanding
of ARDS/ALI disease severity and progression. Oxygenation is calculated by the PaO2/FiO2
ratio (P/F) which is the the ratio of arterial oxygen partial pressure (PaO2) as determined
by arterial blood gas to fractional inspired oxygen setting on the mechanical ventilator
(FiO2). This P/F ratio is also important to distinguish both diagnosis of ARDS but disease
severity. A normal healthy P/F ratio is between 400-500 whereas ALI is below 300 (aka Mild
ARDS by Berlin definition), ARDS is below 200, and severe ARDS is below 100. These are the
same clinical parameters used by our medical intensive care unit (MICU). The current
treatment modalities for ARDS/ALI are primarily supportive care in the form of lung
protective ventilator management, fluid management, prone positioning, and neuromuscular
blockage in severe ARDS. Clinical studies have examined potential pharmacologic therapies
including the use of albuterol, anti-platelet therapies, statins, aspirin, and steroids -
none of which had any significant benefit on clinical outcomes. Our data in mouse models and
preliminary data in a small cohort of patients at risk for ARDS/ALI highlight a novel role
for ceramide in the pathophysiology of this disease. Our preliminary data indicate that
ceramide may not only be a key player in the underlying pathology of ARDS/ALI, but may also
serve as a useful biomarker. Additionally, as there is a currently FDA approved drug that
targets ceramide formation and actions as the investigators have demonstrated, the work
outlined herein has significant translational potential. Thus, this proposal will examine the
premise that ceramide is a new critical player in ARDS/ALI and identify ceramide as a
biomarker for individualized medicine to optimize diagnosis and improve treatments. Given the
large numbers of individuals affected by ARDS/ALI, the outcomes of this research have the
potential to change the paradigm of how clinicians and researchers perceive inflammatory
airway disease and may then translate into better, targeted approaches for the management for
millions worldwide. This pilot study will be conducted as a prospective descriptive,
cross-sectional study with a single data collection. This design allows for greater control
over the measurements and maximization of data completeness. While a cross-sectional study
design does not allow us to examine causality, it does allow us to examine associations among
the variables/domains of interest, which align with the aim of the study. This design is
appropriate and scientifically rigorous while meeting the budgetary and time constraints of
the grant mechanism. The investigators have developed a state of the science, non-invasive
technique which can be utilized to assess sphingolipid levels in the breath of mechanically
ventilated subjects. Exhaled breath condensate (EBC) is collected using a commercially
available device, RTubeVent™ (Respiratory Research Inc., Austin, TX). The RTubeVent™, covered
by a frozen aluminum sleeve and fabric cloth sleeve, allows for the cooling of exhaled breath
into a condensed liquid form and is a safe, easy, relatively inexpensive, repeatable,
non-invasive approach to collect a biological fluid that is hypothesized to be more specific
to pulmonary biology changes compared to systemically collected biological fluids such as
serum or plasma. The RTubeVENT™ breath condensate collection device is designed for ease of
use in the ICU. It can be placed in-line in the expiratory limb of the breathing circuit or
at the ventilator exhaust port. This non-invasive device is fully self-contained and
disposable. As the subject is ventilated, the RTubeVENT™ gathers breath condensate in a
special cartridge designed exclusively for ventilator use. EBC has been identified by the
National Institutes of Health as an emerging source for biomarker research thus highlighting
another innovative aspect of this proposal. Once patients are enrolled in the study, the
investigators will collect EBC from the ventilator for approximately 20 minutes under the
guidance of respiratory therapy and take a 5cc blood draw for plasma isolation. Samples will
be immediately taken to the laboratory for processing where both EBC and plasma will be
aliquoted, and stored at -80°C until analysis. Liquid chromatography electrospray
ionization-tandem mass spectrometry (LC-ESI-MS/MS) will be used to detect sphingolipid levels
and samples will be batch processed to minimize variability. The investigators predict that
patients in the ARDS/ALI group will have significantly elevated ceramide levels as compared
to those in the control group.
Inclusion Criteria:
Admission to the medical intensive care unit Mechanically ventilated for less than 48 hours
Able to consent in English. -
Exclusion Criteria:
Unable to obtain consent Mechanically ventilated for more than 48 hours Moribund Prisoner
or ward of the state Pregnant Less than 18 years old, Metastatic lung cancer.
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