Can plasma HHV8 viral load be used to differentiate multicentric Castleman disease from Kaposi sarcoma?

Author:

Sayer R12,Paul J3,Tuke P W4,Hargreaves S1,Noursadeghi M25,Tedder R S4,Grant P3,Edwards S G12,Miller R F1267

Affiliation:

1. Mortimer Market Centre, Camden Provider Services

2. T8, University College London Hospitals NHS Trust

3. Department of Virology, University College London Hospitals

4. Blood Borne Viruses Unit, Virus Reference Department, Centre for Infections, Health Protection Agency

5. Division of Infection and Immunity

6. Research Department of Infection and Population Health, Division of Population Health, University CollegeLondon

7. Department of Clinical Research, Faculty of Infections and Tropical Diseases, London School of Hygiene and Tropical Medicine, London, UK

Abstract

We measured plasma human herpesvirus 8 (HHV8) DNA load in consecutive patients presenting with HIV-associated multicentric Castleman disease (MCD) and in contemporaneous patients who had Kaposi sarcoma (KS), lymphoma or other diagnoses. All 11 patients with MCD had detectable plasma HHV8 DNA compared with 18 (72%) of 25 patients with KS, none with lymphoma and one of 38 patients with other diagnoses. Detectable plasma HHV8 DNA levels were higher among MCD patients, median (interquartile range [IQR]) = 43,500 (5200–150,000) copies/mL, when compared with those with KS, median (IQR) = 320 (167–822) copies/mL and those with lymphoma and other diagnoses (one-way analysis of variance; P = 0.0303). Using receiver operating characteristic analysis, a cut-off of >1000 copies HHV8 DNA/mL of plasma helped to discriminate between MCD and other diagnoses, with a specificity of 94.7% and a negative predictive value of 97.3%. The level of HHV8 viraemia, while not diagnostic, may aid discrimination between patients with MCD and those with KS and other systemic illnesses.

Publisher

SAGE Publications

Subject

Infectious Diseases,Pharmacology (medical),Public Health, Environmental and Occupational Health,Dermatology

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