Article Text

Angiogenic cytokines in patients with idiopathic interstitial pneumonia
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  1. N R Simler1,
  2. P E Brenchley2,
  3. A W Horrocks3,
  4. S M Greaves3,
  5. P S Hasleton4,
  6. J J Egan5
  1. 1North West Lung Research Centre, South Manchester University NHS Hospitals Trust, Wythenshawe Hospital, Manchester M23 9LT, UK
  2. 2Renal Research Laboratory, Manchester Royal Infirmary, Manchester M13 9WL, UK
  3. 3Department of Radiology, South Manchester University NHS Hospitals Trust, Wythenshawe Hospital, Manchester M23 9LT, UK
  4. 4Department of Pathology, South Manchester University NHS Hospitals Trust, Wythenshawe Hospital, Manchester M23 9LT, UK
  5. 5Department of Respiratory Medicine, Mater Misericordiae Hospital, University College Dublin, Dublin 7, Ireland
  1. Correspondence to:
    Dr J J Egan
    The Mater Misericordiae Hospital and St Vincent’s University Hospital, University College Dublin, Eccles Street, Dublin 7, Ireland; jeganmater.ie

Abstract

Background: Angiogenesis has been implicated in the pathogenesis of idiopathic interstitial pneumonia (IIP). The aim of this study was to examine the relationship between plasma concentrations of the angiogenic cytokines interleukin 8 (IL-8), vascular endothelial growth factor (VEGF), and endothelin-1 (ET-1) and clinical parameters of disease progression over a 6 month period to identify potential aetiological mediators and prognostic markers of disease activity in patients with IIP.

Methods: Forty nine patients with IIP (40 men) were recruited to the study. Plasma cytokine measurements, pulmonary function tests, and high resolution computed tomography (HRCT) scans were performed on recruitment and after 6 months. Plasma cytokine measurements were also performed in 15 healthy volunteers for control purposes.

Results: Patients with IIP had significantly higher median (IQR) baseline concentrations of IL-8 and ET-1 than controls (155 (77–303) pg/ml v 31 (0–100) pg/ml, p<0.001) and (1.21 (0.91–1.88) pg/ml v 0.84 (0.67–1.13) pg/ml, p<0.01), respectively. Baseline concentrations of IL-8, ET-1, and VEGF were significantly related to the baseline HRCT fibrosis score (r = 0.42, p<0.005; r = 0.39, p<0.01; and r = 0.42, p<0.005, respectively). Patients with IIP who developed progressive disease had significantly higher baseline levels of IL-8 (345 (270–497) pg/ml v 121 (73–266) pg/ml, p = 0.001) and VEGF (1048 (666–2149) pg/ml v 658 (438–837) pg/ml, p = 0.019). Over 6 months the change in VEGF was significantly related to the change in HRCT fibrosis score (r = 0.565, p = 0.035) and negatively related to the change in forced vital capacity (r = −0.353, p = 0.035).

  • DIP, desquamative interstitial pneumonia
  • ET-1, endothelin-1
  • FEV1, forced expiratory volume in 1 second
  • FVC, forced vital capacity
  • IIP, idiopathic interstitial pneumonia
  • IL-8, interleukin 8
  • IPF, idiopathic pulmonary fibrosis
  • NSIP, non-specific interstitial pneumonia
  • TLC, total lung capacity
  • Tlco, carbon monoxide transfer factor
  • VEGF, vascular endothelial growth factor
  • idiopathic interstitial pneumonia
  • pulmonary fibrosis
  • angiogenesis
  • cytokines
  • prognostic markers

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Supplementary materials

  • Publisher Correction

    Please note that the Conclusions are missing from the abstract of this article.

    The missing text is shown below:
    Conclusions: These results support a role for angiogenesis in the pathogenesis of IIP, and IL-8 and VEGF deserve further evaluation as prognostic markers.

    The complete abstract is provided as a PDF here.

    The error is much regretted.

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