Persistent Lung Inflammation After Clinical Resolution of Community-Acquired Pneumonia as Measured by
community-acquired pneumonia survivors
inflammation
pneumonia
pneumonia survivors
Journal
Chest
ISSN: 1931-3543
Titre abrégé: Chest
Pays: United States
ID NLM: 0231335
Informations de publication
Date de publication:
08 2021
08 2021
Historique:
received:
19
10
2020
revised:
17
02
2021
accepted:
19
02
2021
pubmed:
6
3
2021
medline:
4
1
2022
entrez:
5
3
2021
Statut:
ppublish
Résumé
Survivors of community-acquired pneumonia (CAP) are at increased risk of cardiovascular disease, cognitive and functional decline, and death, but the mechanisms remain unknown. Do CAP survivors have evidence of increased inflammatory activity in their lung parenchyma on 2-deoxy-2-[ We obtained Overall, 68% of CAP survivors (95% CI, 45%-85%) had distinct residual areas of increased An important proportion of CAP survivors have persistent pulmonary foci of increased inflammatory activity beyond resolution of their infection. As inflammation contributes to cardiovascular disease, cognitive decline, functional waning, and mortality risk in the general population, this finding provides a plausible mechanism for the increased morbidity and mortality that have been observed post-CAP.
Sections du résumé
BACKGROUND
Survivors of community-acquired pneumonia (CAP) are at increased risk of cardiovascular disease, cognitive and functional decline, and death, but the mechanisms remain unknown.
RESEARCH QUESTION
Do CAP survivors have evidence of increased inflammatory activity in their lung parenchyma on 2-deoxy-2-[
STUDY DESIGN AND METHODS
We obtained
RESULTS
Overall, 68% of CAP survivors (95% CI, 45%-85%) had distinct residual areas of increased
INTERPRETATION
An important proportion of CAP survivors have persistent pulmonary foci of increased inflammatory activity beyond resolution of their infection. As inflammation contributes to cardiovascular disease, cognitive decline, functional waning, and mortality risk in the general population, this finding provides a plausible mechanism for the increased morbidity and mortality that have been observed post-CAP.
Identifiants
pubmed: 33667494
pii: S0012-3692(21)00448-7
doi: 10.1016/j.chest.2021.02.048
pmc: PMC8727848
pii:
doi:
Substances chimiques
Radiopharmaceuticals
0
Fluorodeoxyglucose F18
0Z5B2CJX4D
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
446-453Subventions
Organisme : NHLBI NIH HHS
ID : P01 HL094307
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL104106
Pays : United States
Organisme : NHLBI NIH HHS
ID : R61 HL146390
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL121510
Pays : United States
Organisme : NHLBI NIH HHS
ID : R56 HL136730
Pays : United States
Organisme : NIA NIH HHS
ID : R01 AG058969
Pays : United States
Informations de copyright
Copyright © 2021 American College of Chest Physicians. All rights reserved.
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