Novel Method for Noninvasive Sampling of the Distal Airspace in Acute Respiratory Distress Syndrome
A major barrier to a more complete understanding of acute respiratory distress syndrome (ARDS) pathophysiology is the inability to sample the distal airspace of patients with ARDS. The heat moisture exchanger (HME) filter is an inline bacteriostatic sponge that collects exhaled moisture from the lun...
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Published in | American journal of respiratory and critical care medicine Vol. 197; no. 8; pp. 1027 - 1035 |
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Main Authors | , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Thoracic Society
15.04.2018
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Subjects | |
Online Access | Get full text |
ISSN | 1073-449X 1535-4970 1535-4970 |
DOI | 10.1164/rccm.201707-1474OC |
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Abstract | A major barrier to a more complete understanding of acute respiratory distress syndrome (ARDS) pathophysiology is the inability to sample the distal airspace of patients with ARDS. The heat moisture exchanger (HME) filter is an inline bacteriostatic sponge that collects exhaled moisture from the lungs of mechanically ventilated patients.
To test the hypothesis that HME filter fluid (HMEF) represents the distal airspace fluid in patients with ARDS.
Samples of HMEF were collected from 37 patients with acute pulmonary edema (either from ARDS or hydrostatic causes [HYDRO; control subjects]). Concurrent undiluted pulmonary edema fluid (EF) and HMEF were collected from six patients. HMEF from 11 patients (8 ARDS and 3 HYDRO) were analyzed by liquid chromatography-coupled tandem mass spectometry. Total protein (bicinchoninic acid assay), MMP-9 (matrix metalloproteinase-9), and MPO (myeloperoxidase) (ELISA) were measured in 29 subjects with ARDS and 5 subjects with HYDRO. SP-D (surfactant protein-D), RAGE (receptor for advanced glycation end-products) (ELISA), and cytokines (IL-1β, IL-6, IL-8, and tumor necrosis factor-α) (electrochemiluminescent assays) were measured in six concurrent HMEF and EF samples.
Liquid chromatography-coupled tandem mass spectrometry on concurrent EF and HMEF samples from four patients revealed similar base peak intensities and m/z values indicating similar protein composition. There were 21 significantly elevated proteins in HMEF from patients with ARDS versus HYDRO. Eight proteins measured in concurrent EF and HMEF from six patients were highly correlated. In HMEF, total protein and MMP-9 were significantly higher in ARDS than in HYDRO.
These data suggest that HMEF is a novel, noninvasive method to accurately sample the distal airspace in patients with ARDS. |
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AbstractList | Rationale: A major barrier to a more complete understanding of acute respiratory distress syndrome (ARDS) pathophysiology is the inability to sample the distal airspace of patients with ARDS. The heat moisture exchanger (HME) filter is an inline bacteriostatic sponge that collects exhaled moisture from the lungs of mechanically ventilated patients. Objectives: To test the hypothesis that HME filter fluid (HMEF) represents the distal airspace fluid in patients with ARDS. Methods: Samples of HMEF were collected from 37 patients with acute pulmonary edema (either from ARDS or hydrostatic causes [HYDRO; control subjects]). Concurrent undiluted pulmonary edema fluid (EF) and HMEF were collected from six patients. HMEF from 11 patients (8 ARDS and 3 HYDRO) were analyzed by liquid chromatography–coupled tandem mass spectometry. Total protein (bicinchoninic acid assay), MMP-9 (matrix metalloproteinase-9), and MPO (myeloperoxidase) (ELISA) were measured in 29 subjects with ARDS and 5 subjects with HYDRO. SP-D (surfactant protein-D), RAGE (receptor for advanced glycation end-products) (ELISA), and cytokines (IL-1β, IL-6, IL-8, and tumor necrosis factor-α) (electrochemiluminescent assays) were measured in six concurrent HMEF and EF samples. Measurements and Main Results: Liquid chromatography–coupled tandem mass spectrometry on concurrent EF and HMEF samples from four patients revealed similar base peak intensities and m/z values indicating similar protein composition. There were 21 significantly elevated proteins in HMEF from patients with ARDS versus HYDRO. Eight proteins measured in concurrent EF and HMEF from six patients were highly correlated. In HMEF, total protein and MMP-9 were significantly higher in ARDS than in HYDRO. Conclusions: These data suggest that HMEF is a novel, noninvasive method to accurately sample the distal airspace in patients with ARDS. Keywords: acute respiratory distress syndrome; airspace fluid; biomarkers; heat moisture exchanger filter; pulmonary edema fluid A major barrier to a more complete understanding of acute respiratory distress syndrome (ARDS) pathophysiology is the inability to sample the distal airspace of patients with ARDS. The heat moisture exchanger (HME) filter is an inline bacteriostatic sponge that collects exhaled moisture from the lungs of mechanically ventilated patients.RATIONALEA major barrier to a more complete understanding of acute respiratory distress syndrome (ARDS) pathophysiology is the inability to sample the distal airspace of patients with ARDS. The heat moisture exchanger (HME) filter is an inline bacteriostatic sponge that collects exhaled moisture from the lungs of mechanically ventilated patients.To test the hypothesis that HME filter fluid (HMEF) represents the distal airspace fluid in patients with ARDS.OBJECTIVESTo test the hypothesis that HME filter fluid (HMEF) represents the distal airspace fluid in patients with ARDS.Samples of HMEF were collected from 37 patients with acute pulmonary edema (either from ARDS or hydrostatic causes [HYDRO; control subjects]). Concurrent undiluted pulmonary edema fluid (EF) and HMEF were collected from six patients. HMEF from 11 patients (8 ARDS and 3 HYDRO) were analyzed by liquid chromatography-coupled tandem mass spectometry. Total protein (bicinchoninic acid assay), MMP-9 (matrix metalloproteinase-9), and MPO (myeloperoxidase) (ELISA) were measured in 29 subjects with ARDS and 5 subjects with HYDRO. SP-D (surfactant protein-D), RAGE (receptor for advanced glycation end-products) (ELISA), and cytokines (IL-1β, IL-6, IL-8, and tumor necrosis factor-α) (electrochemiluminescent assays) were measured in six concurrent HMEF and EF samples.METHODSSamples of HMEF were collected from 37 patients with acute pulmonary edema (either from ARDS or hydrostatic causes [HYDRO; control subjects]). Concurrent undiluted pulmonary edema fluid (EF) and HMEF were collected from six patients. HMEF from 11 patients (8 ARDS and 3 HYDRO) were analyzed by liquid chromatography-coupled tandem mass spectometry. Total protein (bicinchoninic acid assay), MMP-9 (matrix metalloproteinase-9), and MPO (myeloperoxidase) (ELISA) were measured in 29 subjects with ARDS and 5 subjects with HYDRO. SP-D (surfactant protein-D), RAGE (receptor for advanced glycation end-products) (ELISA), and cytokines (IL-1β, IL-6, IL-8, and tumor necrosis factor-α) (electrochemiluminescent assays) were measured in six concurrent HMEF and EF samples.Liquid chromatography-coupled tandem mass spectrometry on concurrent EF and HMEF samples from four patients revealed similar base peak intensities and m/z values indicating similar protein composition. There were 21 significantly elevated proteins in HMEF from patients with ARDS versus HYDRO. Eight proteins measured in concurrent EF and HMEF from six patients were highly correlated. In HMEF, total protein and MMP-9 were significantly higher in ARDS than in HYDRO.MEASUREMENTS AND MAIN RESULTSLiquid chromatography-coupled tandem mass spectrometry on concurrent EF and HMEF samples from four patients revealed similar base peak intensities and m/z values indicating similar protein composition. There were 21 significantly elevated proteins in HMEF from patients with ARDS versus HYDRO. Eight proteins measured in concurrent EF and HMEF from six patients were highly correlated. In HMEF, total protein and MMP-9 were significantly higher in ARDS than in HYDRO.These data suggest that HMEF is a novel, noninvasive method to accurately sample the distal airspace in patients with ARDS.CONCLUSIONSThese data suggest that HMEF is a novel, noninvasive method to accurately sample the distal airspace in patients with ARDS. [...]to explore the utility of HMEF as a platform for discovery, we compared HMEF mass spectroscopy (MS) between ARDS and HYDRO and analyzed differentially expressed proteins in the context of both biological pathways and protein-protein interaction networks. Twentyone proteins, including MPO and MMP-9, were significantly elevated in ARDS versus HYDRO (P < 0.008) when adjusted for multiple comparisons with a BenjaminiHochberg (false discovery rate) procedure (Table 2). Because some proteins are expressed at very low concentrations in HMEF and thus could lead to a false positive result by Fisher's exact test, we used a quasiPoisson generalized linear model for each analyte as a more stringent test (Table 2). [...]serial HMEF analysis may help to define the natural history of ARDS by providing a window into the airspace during acute injury, progression, resolution, and repair. [...]this pilot study has a relatively small sample size. A major barrier to a more complete understanding of acute respiratory distress syndrome (ARDS) pathophysiology is the inability to sample the distal airspace of patients with ARDS. The heat moisture exchanger (HME) filter is an inline bacteriostatic sponge that collects exhaled moisture from the lungs of mechanically ventilated patients. To test the hypothesis that HME filter fluid (HMEF) represents the distal airspace fluid in patients with ARDS. Samples of HMEF were collected from 37 patients with acute pulmonary edema (either from ARDS or hydrostatic causes [HYDRO; control subjects]). Concurrent undiluted pulmonary edema fluid (EF) and HMEF were collected from six patients. HMEF from 11 patients (8 ARDS and 3 HYDRO) were analyzed by liquid chromatography-coupled tandem mass spectometry. Total protein (bicinchoninic acid assay), MMP-9 (matrix metalloproteinase-9), and MPO (myeloperoxidase) (ELISA) were measured in 29 subjects with ARDS and 5 subjects with HYDRO. SP-D (surfactant protein-D), RAGE (receptor for advanced glycation end-products) (ELISA), and cytokines (IL-1β, IL-6, IL-8, and tumor necrosis factor-α) (electrochemiluminescent assays) were measured in six concurrent HMEF and EF samples. Liquid chromatography-coupled tandem mass spectrometry on concurrent EF and HMEF samples from four patients revealed similar base peak intensities and m/z values indicating similar protein composition. There were 21 significantly elevated proteins in HMEF from patients with ARDS versus HYDRO. Eight proteins measured in concurrent EF and HMEF from six patients were highly correlated. In HMEF, total protein and MMP-9 were significantly higher in ARDS than in HYDRO. These data suggest that HMEF is a novel, noninvasive method to accurately sample the distal airspace in patients with ARDS. |
Author | Warren, Melissa A. Russell, Derek W. Grove, Brandon S. Ware, Lorraine B. Kerchberger, V. Eric Bastarache, Julie A. McDonald, W. Hayes Wickersham, Nancy E. McNeil, J. Brennan Shaver, Ciara M. |
Author_xml | – sequence: 1 givenname: J. Brennan surname: McNeil fullname: McNeil, J. Brennan organization: Division of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, and – sequence: 2 givenname: Ciara M. surname: Shaver fullname: Shaver, Ciara M. organization: Division of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, and – sequence: 3 givenname: V. Eric surname: Kerchberger fullname: Kerchberger, V. Eric organization: Division of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, and – sequence: 4 givenname: Derek W. surname: Russell fullname: Russell, Derek W. organization: Division of Allergy, Pulmonary, and Critical Care Medicine, University of Alabama at Birmingham Medical Center, Birmingham, Alabama; and – sequence: 5 givenname: Brandon S. surname: Grove fullname: Grove, Brandon S. organization: Division of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, and – sequence: 6 givenname: Melissa A. surname: Warren fullname: Warren, Melissa A. organization: Division of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, and – sequence: 7 givenname: Nancy E. surname: Wickersham fullname: Wickersham, Nancy E. organization: Division of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, and – sequence: 8 givenname: Lorraine B. surname: Ware fullname: Ware, Lorraine B. organization: Division of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, and, Department of Pathology, Microbiology, and Immunology, Vanderbilt University Medical Center, Nashville, Tennessee – sequence: 9 givenname: W. Hayes surname: McDonald fullname: McDonald, W. Hayes organization: Department of Biochemistry, Vanderbilt University, Nashville, Tennessee – sequence: 10 givenname: Julie A. surname: Bastarache fullname: Bastarache, Julie A. organization: Division of Allergy, Pulmonary, and Critical Care Medicine, Department of Medicine, and |
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Keywords | acute respiratory distress syndrome; airspace fluid; biomarkers; heat moisture exchanger filter; pulmonary edema fluid |
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References | bib14 bib15 bib12 bib13 bib10 bib32 bib30 bib31 Isaacs RJ (bib11) 2012; 4 bib29 bib28 bib25 bib26 bib23 bib24 bib21 bib22 Weiland JE (bib27) 1986; 133 bib20 bib9 bib7 bib8 bib5 bib18 bib6 bib19 bib3 bib16 bib4 bib17 bib1 bib2 29324185 - Am J Respir Crit Care Med. 2018 Apr 15;197(8):979-980 |
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Snippet | A major barrier to a more complete understanding of acute respiratory distress syndrome (ARDS) pathophysiology is the inability to sample the distal airspace... [...]to explore the utility of HMEF as a platform for discovery, we compared HMEF mass spectroscopy (MS) between ARDS and HYDRO and analyzed differentially... Rationale: A major barrier to a more complete understanding of acute respiratory distress syndrome (ARDS) pathophysiology is the inability to sample the distal... |
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SubjectTerms | Aged Bioinformatics Biomarkers Chromatography Diagnostic Techniques, Respiratory System Edema Female Gelatin Sponge, Absorbable Gene expression Humans Hypotheses Male Mass spectrometry Middle Aged Minimally Invasive Surgical Procedures - instrumentation Minimally Invasive Surgical Procedures - methods Original Patients Proteins Proteomics Pulmonary Alveoli - physiopathology Respiration, Artificial - methods Respiratory distress syndrome Respiratory Distress Syndrome, Adult - diagnosis Respiratory Distress Syndrome, Adult - physiopathology Respiratory therapy Scientific imaging Ventilators |
Title | Novel Method for Noninvasive Sampling of the Distal Airspace in Acute Respiratory Distress Syndrome |
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