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First published online May 15, 2007
J Nucl Med 2007, doi:10.2967/jnumed.106.039313
© 2007 by Society of Nuclear Medicine
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Diagnostic Performance and Prognostic Value of Extravascular Retention of 123I-Labeled Serum Amyloid P Component in Systemic Amyloidosis

Bouke P.C. Hazenberg 1*, Martin H. van Rijswijk 1, Marjolijn N. Lub-de Hooge 2, Edo Vellenga 3, Elizabeth B. Haagsma 4, Marcel D. Posthumus 1, and Pieter L. Jager 2

1 Department of Rheumatology and Clinical Immunology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
2 Department of Nuclear Medicine, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
3 Department of Hematology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands
4 Department of Gastroenterology and Hepatology, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands

* To whom correspondence should be addressed. E-mail: b.p.c.hazenberg{at}int.umcg.nl.


   Abstract

Serum amyloid P component (SAP) binds to amyloid. 123I-SAP scintigraphy is used to evaluate the extent and distribution of amyloid in systemic amyloidosis and has great clinical value in the detection of systemic amyloidosis. The aim of the study was to assess during scintigraphy the diagnostic performance and prognostic value of a simple parameter describing extravascular 123I-SAP retention in systemic amyloidosis. Methods: Two hundred megabecquerels of 123I-labeled human SAP was injected intravenously for scintigraphy in 20 controls and in 189 consecutive patients with systemic and localized amyloidosis. Extravascular retention of 123I-SAP was quantified from serum and urine measurements after 24 h (EVR24) and 48 h. Sensitivity and specificity were assessed, and retention was correlated with kidney, heart, liver, and nerve involvement and with survival. Results: The cutoff value representing a desired specificity of 90% of EVR24 was 50%. The associated sensitivity of EVR24 for detecting reactive systemic, immunocyte-derived (AL), and hereditary amyloidosis was 65%, 61%, and 22%, respectively, using a cutoff point of 50%. In AL amyloidosis, the EVR24 increased with the number of organs involved (from a mean of 43% for 1 organ to a mean of 81% for 4 organs). The EVR24 correlated with serum alkaline phosphatase (r = 0.63) and with creatinine clearance (r = -0.36). In AL amyloidosis, both cardiac involvement (hazard ratio, 3.9; 95% CI, 2.0-7.8) and EVR24 (hazard ratio, 2.0; 95% CI, 1.1-3.9) were independent predictors of survival. Conclusion: In AL amyloidosis, the EVR24 is strongly associated with organ involvement and with prognosis and might serve as an indicator of the body amyloid load. Quantification of SAP retention using the EVR24 has no additional value over 123I-SAP scintigraphy in the detection of systemic amyloidosis.

Key Words: diagnostic accuracy, prognostic factor, serum amyloid P component, systemic amyloidosis







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