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Am. J. Respir. Crit. Care Med., Volume 156, Number 4, October 1997, 1217-1229

Surfactant Proteins-A and -B Are Elevated in Plasma of Patients with Acute Respiratory Failure

IAN R. DOYLE, ANDREW D. BERSTEN, and TERENCE E. NICHOLAS

Departments of Human Physiology and Critical Care Medicine, School of Medicine, Flinders Medical Centre, Adelaide, Australia

Surfactant protein-A (SP-A) leaks into the circulation of patients with acute respiratory distress syndrome (ARDS) or acute cardiogenic pulmonary edema (APE) in a manner inversely related to lung function. Since surfactant protein-B (SP-B) is synthesized as a precursor considerably smaller than alveolar SP-A, we investigated whether it enters the circulation more readily. Reactivities consistent with SP-B proprotein (~ 42 to ~ 45 kD) and the ~ 25 kD processing intermediate were detected in plasma. Plasma immunoreactive SP-B levels were significantly higher in ARDS (8,007 ± 1,654 ng/ml [mean ± SEM], n = 22) and APE (3,646 ± 635 ng/ml, n = 10) patients compared with normal subjects (1,685 ± 58 ng/ml, n = 33) and ventilated patients with no cardiorespiratory disease (1,829 ± 184 ng/ml, n = 7). All groups had plasma SP-B/SP-A ratios ~ 6- to ~ 8-fold higher than in normal lavage or ARDS tracheal aspirate fluid, consistent with protein sieving. During admission, both plasma SP-B and the SP-B/SP-A ratio were inversely related to blood oxygenation (PaO2/FIO2) (p < 0.0001 and p < 0.025, n = 260 from 39 patients; Spearman) and static respiratory system compliance (Delta V/Delta P) (p < 0.0001 and p < 0.01, n = 168 from 25 patients). We describe in detail three patients and conclude that immunoreactive SP-B enters more readily than SP-A, is cleared acutely, and provides a better indicator of lung trauma.




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