Abstract

While oxidant stress is elevated in adult forms of pulmonary hypertension (PH), levels of oxidant stress in pediatric PH are unknown. The objective of this study is to measure F2-isoprostanes, a marker of oxidant stress, in children with idiopathic pulmonary hypertension (IPH) and PH due to bronchopulmonary dysplasia (BPD). We hypothesized that F2-isoprostanes in pediatric IPH and PH associated with BPD will be higher than in controls. Plasma F2-isoprostanes were measured in pediatric PH patients during clinically indicated cardiac catheterization and compared with controls. F2-Isoprostane levels were compared between IPH, PH due to BD, and controls. Five patients with IPH, 12 with PH due to BPD, and 20 control subjects were studied. Patients with IPH had statistically higher isoprostanes than controls 62 pg/mL (37–210) versus 20 pg/mL (16–27), P < 0.01). The patients with PH and BPD had significantly lower isoprostanes than controls 15 pg/mL (8–17) versus 20 pg/ml (16–27), P < 0.02. F2-isoprostanes are elevated in children with IPH compared to both controls and patients with PH secondary to BPD. Furthermore, F2-isoprostanes in PH secondary to BPD are lower than control levels. These findings suggest that IPH and PH secondary to BPD have distinct mechanisms of disease pathogenesis.

Highlights

  • It has long been recognized that patients with pediatric idiopathic pulmonary hypertension (IPH) have poor longterm survival

  • Multiple studies measuring F2isoprostanes, a stable marker of oxidant stress resulting from the oxidation of cell-membrane arachidonic acid, have shown adult IPH patients, have higher F2-isoprostane levels than do control patients [3, 4]

  • We hypothesize that children with IPH and PH due to bronchopulmonary dysplasia (BPD) will have F2isoprostane levels higher than those measured in healthy control subjects

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Summary

Introduction

It has long been recognized that patients with pediatric idiopathic pulmonary hypertension (IPH) have poor longterm survival. Oxidant stress appears to play a role in the molecular mechanism of adult IPH. Multiple studies measuring F2isoprostanes, a stable marker of oxidant stress resulting from the oxidation of cell-membrane arachidonic acid, have shown adult IPH patients, have higher F2-isoprostane levels than do control patients [3, 4]. There are no published data on oxidant stress or F2isoprostane levels in pediatric patients with PH secondary to BPD or IPH. The objective of this study is to measure F2isoprostanes in children with IPH and PH due to BPD and to compare them to normal controls to assess the role of oxidant stress in pediatric populations with PH. We hypothesize that children with IPH and PH due to BPD will have F2isoprostane levels higher than those measured in healthy control subjects. Evidence supporting similar biochemical mechanisms between these pediatric populations with PH would support the practice of utilizing similar therapeutic strategies in these children

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