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10.3390/ijms23031583

http://scihub22266oqcxt.onion/10.3390/ijms23031583
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35163504!8835897!35163504
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suck abstract from ncbi


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pmid35163504      Int+J+Mol+Sci 2022 ; 23 (3): ä
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  • Time-Dependent Molecular Motifs of Pulmonary Fibrogenesis in COVID-19 #MMPMID35163504
  • Kamp JC; Neubert L; Ackermann M; Stark H; Werlein C; Fuge J; Haverich A; Tzankov A; Steinestel K; Friemann J; Boor P; Junker K; Hoeper MM; Welte T; Laenger F; Kuehnel MP; Jonigk DD
  • Int J Mol Sci 2022[Jan]; 23 (3): ä PMID35163504show ga
  • (1) Background: In COVID-19 survivors there is an increased prevalence of pulmonary fibrosis of which the underlying molecular mechanisms are poorly understood; (2) Methods: In this multicentric study, n = 12 patients who succumbed to COVID-19 due to progressive respiratory failure were assigned to an early and late group (death within 7 days of hospitalization, respectively) and compared to n = 11 healthy controls; mRNA and protein expression as well as biological pathway analysis were performed to gain insights into the evolution of pulmonary fibrogenesis in COVID-19; (3) Results: Median duration of hospitalization until death was 3 (IQR25-75, 3-3.75) and 14 (12.5-14) days in the early and late group, respectively. Fifty-eight out of 770 analyzed genes showed a significantly altered expression signature in COVID-19 compared to controls in a time-dependent manner. The entire study group showed an increased expression of BST2 and IL1R1, independent of hospitalization time. In the early group there was increased activity of inflammation-related genes and pathways, while fibrosis-related genes (particularly PDGFRB) and pathways dominated in the late group; (4) Conclusions: After the first week of hospitalization, there is a shift from pro-inflammatory to fibrogenic activity in severe COVID-19. IL1R1 and PDGFRB may serve as potential therapeutic targets in future studies.
  • |Aged[MESH]
  • |COVID-19/*genetics/*metabolism/mortality[MESH]
  • |Female[MESH]
  • |Hospital Mortality/trends[MESH]
  • |Hospitalization[MESH]
  • |Humans[MESH]
  • |Lung/pathology[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |Pulmonary Fibrosis/metabolism/*pathology[MESH]
  • |Respiratory Insufficiency/pathology[MESH]


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