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1 Dept of Biostatistics, University of Franche-Comte, and 2 SERF (Santé et Environnement Rural, University of Franche-Comté) Group 3 Dept of Mycology and 5 Dept of Respiratory Diseases, CHU Besançon, Besançon 4 GERMOP, Dept of Respiratory Diseases, Hôpital Louis Pradel, Lyon, France.
CORRESPONDENCE: G. Reboux, Dept of Mycology, Jean Minjoz University Hospital, Boulevard Fleming, 25030 Besançon Cedex, France. Fax: 33 381668914. E-mail: Gabriel.reboux{at}ufc-chu.univ-fcomte.fr
Keywords: Diagnosis, hypersensitivity pneumonitis, precipitins, prospective study, serology
Received: January 4, 2006
Accepted December 12, 2006
Serum precipitins have a controversial diagnostic value in hypersensitivity pneumonitis (HP). The present authors objective was to assess their diagnostic value by developing scores from a panel of specific antigens tested by two techniques (electrosyneresis and double diffusion) to discriminate active HP from other interstitial lung diseases.
Consecutive patients presenting with a condition for which HP was considered in the differential diagnosis were included in the study. All patients underwent the same standardised diagnostic procedure, including precipitin tests performed in routine conditions. Clinical manifestations, bronchoalveolar lavage and high-resolution computed tomography defined the presence or absence of HP. Receiver-operating characteristic curves and logistic regression were used to develop the serological scores.
A total of 122 patients (including 31 cases of HP) were included in the study. Five antigens from the panel were selected for the serological scores (Absidia corymbifera, Eurotium amstelodami, Wallemia sebi, Saccharopolyspora rectivirgula and mesophilic Streptomyces sp.). Electrosyneresis was more discriminative than the double-diffusion technique. Predictive negative values varied 8188% and predictive positive values varied 7175% for prevalence of HP 2035%.
In conclusion, serological scores using a panel of relevant antigens may guide both biological and clinical practice in areas of high prevalence of hypersensitivity pneumonitis.
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