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Microbiological Challenges in the Diagnosis of Chronic Q Fever
Authors:Linda M. Kampschreur  Jan Jelrik Oosterheert  Annemarie M. C. Koop  Marjolijn C. A. Wegdam-Blans  Corine E. Delsing  Chantal P. Bleeker-Rovers  Monique G. L. De Jager-Leclercq  Cornelis A. R. Groot  Tom Sprong  Marrigje H. Nabuurs-Franssen  Nicole H. M. Renders  Marjo E. van Kasteren  Yvonne Soethoudt  Sybrandus N. Blank  Marjolijn J. H. Pronk  Rolf H. H. Groenwold  Andy I. M. Hoepelman  Peter C. Wever
Abstract:Diagnosis of chronic Q fever is difficult. PCR and culture lack sensitivity; hence, diagnosis relies mainly on serologic tests using an immunofluorescence assay (IFA). Optimal phase I IgG cutoff titers are debated but are estimated to be between 1:800 and 1:1,600. In patients with proven, probable, or possible chronic Q fever, we studied phase I IgG antibody titers at the time of positive blood PCR, at diagnosis, and at peak levels during chronic Q fever. We evaluated 200 patients, of whom 93 (46.5%) had proven, 51 (25.5%) had probable, and 56 (28.0%) had possible chronic Q fever. Sixty-five percent of proven cases had positive Coxiella burnetii PCR results for blood, which was associated with high phase I IgG. Median phase I IgG titers at diagnosis and peak titers in patients with proven chronic Q fever were significantly higher than those for patients with probable and possible chronic Q fever. The positive predictive values for proven chronic Q fever, compared to possible chronic Q fever, at titers 1:1,024, 1:2,048, 1:4,096, and ≥1:8,192 were 62.2%, 66.7%, 76.5%, and ≥86.2%, respectively. However, sensitivity dropped to <60% when cutoff titers of ≥1:8,192 were used. Although our study demonstrated a strong association between high phase I IgG titers and proven chronic Q fever, increasing the current diagnostic phase I IgG cutoff to >1:1,024 is not recommended due to increased false-negative findings (sensitivity < 60%) and the high morbidity and mortality of untreated chronic Q fever. Our study emphasizes that serologic results are not diagnostic on their own but should always be interpreted in combination with clinical parameters.
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