Cysteinyl leukotriene involvement in chronic lung disease in premature infants
Cysteinyl leukotriene involvement in chronic lung disease in premature infants
The pathopbysiology of chronic lung disease (CLD) in premature infants who require mechanical ventilation and prolonged oxygen supplementation has been well-described but the underlying mechanisms are not understood. Our aim was to test the hypothesis that excess cysteinyl leukotriene (LT) production was a contributing factor in CLD. We compared LT production and lung function, at 7 months of age, in nine premature infants with CLD and in eight control infants without CLD. None of the control infants developed any neonatal respiratory problems, but two subsequently required bronchodilator therapy. Respiratory function was assessed by the measurement of thoracic gas volume (TGV), airways resistance (Raw) and functional residual capacity (FRC). Total cysteinyl LT production was quantified by measurement of leukotriene E4 (LTE4) in a spot urine sample. Although all patients were asymptomatic at follow-up, there was evidence of significant lung function abnormalities in infants with CLD. The CLD infants had significantly elevated TGV, Raw and FRC values reflecting airway obstruction when compared to the controls. Urinary LTE4 levels were significantly higher in the CLD infants when compared to the controls (geometric mean: 741 and 337 pmol · mmol-1 creatinine, respectively). There was no direct correlation between urinary LTE4 levels in the CLD group and TGV, Raw or FRC values. Although this study is small and a direct correlation between lung function and urinary leukotriene E4 was not demonstrated, pathological lung function and an enhanced urinary leukotriene E4 production in infants with chronic lung disease would tend to suggest that the cysteinyl leukotrienes were involved in the sequelae of this disease.
Chronic lung disease, Lung function, Prematurity, Urinary leukotriene E
1907-1912
Cook, A. J.
44a62c6d-9d19-4dd0-ba23-18aeb2e6e6b8
Yuksel, B.
43b1edf1-50e1-45af-ac42-324d9a1bfed2
Sampson, A. P.
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Greenough, A.
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Price, J. F.
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1996
Cook, A. J.
44a62c6d-9d19-4dd0-ba23-18aeb2e6e6b8
Yuksel, B.
43b1edf1-50e1-45af-ac42-324d9a1bfed2
Sampson, A. P.
4ca76f6f-ff35-425d-a7e7-c2bd2ea2df60
Greenough, A.
75a1b8a8-773e-49bd-b038-f9e7bfae1b2a
Price, J. F.
bd1568a3-65bb-48a4-b197-d89be55301e4
Cook, A. J., Yuksel, B., Sampson, A. P., Greenough, A. and Price, J. F.
(1996)
Cysteinyl leukotriene involvement in chronic lung disease in premature infants.
European Respiratory Journal, 9 (9), .
(doi:10.1183/09031936.96.09091907).
Abstract
The pathopbysiology of chronic lung disease (CLD) in premature infants who require mechanical ventilation and prolonged oxygen supplementation has been well-described but the underlying mechanisms are not understood. Our aim was to test the hypothesis that excess cysteinyl leukotriene (LT) production was a contributing factor in CLD. We compared LT production and lung function, at 7 months of age, in nine premature infants with CLD and in eight control infants without CLD. None of the control infants developed any neonatal respiratory problems, but two subsequently required bronchodilator therapy. Respiratory function was assessed by the measurement of thoracic gas volume (TGV), airways resistance (Raw) and functional residual capacity (FRC). Total cysteinyl LT production was quantified by measurement of leukotriene E4 (LTE4) in a spot urine sample. Although all patients were asymptomatic at follow-up, there was evidence of significant lung function abnormalities in infants with CLD. The CLD infants had significantly elevated TGV, Raw and FRC values reflecting airway obstruction when compared to the controls. Urinary LTE4 levels were significantly higher in the CLD infants when compared to the controls (geometric mean: 741 and 337 pmol · mmol-1 creatinine, respectively). There was no direct correlation between urinary LTE4 levels in the CLD group and TGV, Raw or FRC values. Although this study is small and a direct correlation between lung function and urinary leukotriene E4 was not demonstrated, pathological lung function and an enhanced urinary leukotriene E4 production in infants with chronic lung disease would tend to suggest that the cysteinyl leukotrienes were involved in the sequelae of this disease.
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Published date: 1996
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Copyright 2018 Elsevier B.V., All rights reserved.
Keywords:
Chronic lung disease, Lung function, Prematurity, Urinary leukotriene E
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Local EPrints ID: 455208
URI: http://eprints.soton.ac.uk/id/eprint/455208
ISSN: 0903-1936
PURE UUID: e81a2fc1-a84e-4760-aed9-c943a80f80c2
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Date deposited: 15 Mar 2022 17:33
Last modified: 17 Mar 2024 02:43
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Author:
A. J. Cook
Author:
B. Yuksel
Author:
A. Greenough
Author:
J. F. Price
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