Phospholipid levels in blood during community-acquired pneumonia.

Phospholipids, major constituents of bilayer cell membranes, are present in large amounts in pulmonary surfactant and play key roles in cell signaling. Here, we aim at finding clinically useful disease markers in community-acquired pneumonia (CAP) using comprehensive phospholipid profiling in blood...

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Main Authors: Daniel C Müller, Anna Kauppi, Alicia Edin, Åsa Gylfe, Anders B Sjöstedt, Anders Johansson
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0216379
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spelling doaj-6d30f9edb0a946c69143ee83668fb7b02021-03-03T20:41:51ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-01145e021637910.1371/journal.pone.0216379Phospholipid levels in blood during community-acquired pneumonia.Daniel C MüllerAnna KauppiAlicia EdinÅsa GylfeAnders B SjöstedtAnders JohanssonPhospholipids, major constituents of bilayer cell membranes, are present in large amounts in pulmonary surfactant and play key roles in cell signaling. Here, we aim at finding clinically useful disease markers in community-acquired pneumonia (CAP) using comprehensive phospholipid profiling in blood and modeling of changes between sampling time points. Serum samples from 33 patients hospitalized with CAP were collected at admission, three hours after the start of intravenous antibiotics, Day 1 (at 12-24 h), Day 2 (at 36-48 h), and several weeks after recovery. A profile of 75 phospholipid species including quantification of the bioactive lysophosphatidylcholines (LPCs) was determined using liquid chromatography coupled to time-of-flight mass spectrometry. To control for possible enzymatic degradation of LPCs, serum autotaxin levels were examined. Twenty-two of the 33 patients with a clinical diagnosis of CAP received a laboratory-verified CAP diagnosis by microbial culture or microbial DNA detection by qPCR. All major phospholipid species, especially the LPCs, were pronouncedly decreased in the acute stage of illness. Total and individual LPC concentrations increased shortly after the initiation of antibiotic treatment, concentrations were at their lowest 3h after the initiation, and increased after Day 1. The total LPC concentration increased by a change ratio of 1.6-1.7 between acute illness and Day 2, and by a ratio of 3.7 between acute illness and full disease resolution. Autotaxin levels were low in acute illness and showed little changes over time, contradicting a hypothesis of enzymatic degradation causing the low levels of LPCs. In this sample of patients with CAP, the results demonstrate that LPC concentration changes in serum of patients with CAP closely mirrored the early transition from acute illness to recovery after the initiation of antibiotics. LPCs should be further explored as potential disease stage biomarkers in CAP and for their potential physiological role during recovery.https://doi.org/10.1371/journal.pone.0216379
collection DOAJ
language English
format Article
sources DOAJ
author Daniel C Müller
Anna Kauppi
Alicia Edin
Åsa Gylfe
Anders B Sjöstedt
Anders Johansson
spellingShingle Daniel C Müller
Anna Kauppi
Alicia Edin
Åsa Gylfe
Anders B Sjöstedt
Anders Johansson
Phospholipid levels in blood during community-acquired pneumonia.
PLoS ONE
author_facet Daniel C Müller
Anna Kauppi
Alicia Edin
Åsa Gylfe
Anders B Sjöstedt
Anders Johansson
author_sort Daniel C Müller
title Phospholipid levels in blood during community-acquired pneumonia.
title_short Phospholipid levels in blood during community-acquired pneumonia.
title_full Phospholipid levels in blood during community-acquired pneumonia.
title_fullStr Phospholipid levels in blood during community-acquired pneumonia.
title_full_unstemmed Phospholipid levels in blood during community-acquired pneumonia.
title_sort phospholipid levels in blood during community-acquired pneumonia.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description Phospholipids, major constituents of bilayer cell membranes, are present in large amounts in pulmonary surfactant and play key roles in cell signaling. Here, we aim at finding clinically useful disease markers in community-acquired pneumonia (CAP) using comprehensive phospholipid profiling in blood and modeling of changes between sampling time points. Serum samples from 33 patients hospitalized with CAP were collected at admission, three hours after the start of intravenous antibiotics, Day 1 (at 12-24 h), Day 2 (at 36-48 h), and several weeks after recovery. A profile of 75 phospholipid species including quantification of the bioactive lysophosphatidylcholines (LPCs) was determined using liquid chromatography coupled to time-of-flight mass spectrometry. To control for possible enzymatic degradation of LPCs, serum autotaxin levels were examined. Twenty-two of the 33 patients with a clinical diagnosis of CAP received a laboratory-verified CAP diagnosis by microbial culture or microbial DNA detection by qPCR. All major phospholipid species, especially the LPCs, were pronouncedly decreased in the acute stage of illness. Total and individual LPC concentrations increased shortly after the initiation of antibiotic treatment, concentrations were at their lowest 3h after the initiation, and increased after Day 1. The total LPC concentration increased by a change ratio of 1.6-1.7 between acute illness and Day 2, and by a ratio of 3.7 between acute illness and full disease resolution. Autotaxin levels were low in acute illness and showed little changes over time, contradicting a hypothesis of enzymatic degradation causing the low levels of LPCs. In this sample of patients with CAP, the results demonstrate that LPC concentration changes in serum of patients with CAP closely mirrored the early transition from acute illness to recovery after the initiation of antibiotics. LPCs should be further explored as potential disease stage biomarkers in CAP and for their potential physiological role during recovery.
url https://doi.org/10.1371/journal.pone.0216379
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