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CMV-DNA detection in patients with thrombocytopenia

Letter to Editor

CMV-DNA detection in patients with thrombocytopenia

Department of Clinical Medicine, Campinas State University, Campinas, Brazil

The production of platelet autoantibodies may have an idiopathic pathogenesis or may occur in conjunction with other autoimmune diseases, cancer, the use of certain drugs1 or infections such as human immunodeficiency virus (HIV) and cytomegalovirus (CMV), resulting in secondary autoimmune thrombocytopenia.1,2 Recently, we reported an unusual case of severe thrombocytopenia associated with CMV infection in a healthy person whose response to treatment with ganciclovir was followed by an improvement in the platelet count.3 Based on this finding, we have assessed the prevalence and possible clinical implications of CMV-DNA positive patients with thrombocytopenia attended at a university teaching hospital.

From June 1996 to January 1997 we studied 84 patients with chronic thrombocytopenia (63 females and 21 males). The median age of these individuals was 37.4 years (range: 3 to 82 years) and the median follow-up was 25 months (range: 2 to 140 months). Idiopathic thrombocytopenia purpura (ITP) was diagnosed in 61 out of the 84 patients (73%). In the remaining 23 patients, the cause of thrombocytopenia was a systemic autoimmune disease in 15 cases, drug consumption in four cases, related to HIV infection in two cases, and cancer in two cases. All patients were screened for the presence of CMV-DNA.

Genomic DNA was extracted from peripheral blood and the CMV-DNA was amplified by nested polymerase chain reaction (PCR) using the primers described by Demmler et al.4 Amplification of the b-globin gene was used as an internal control. CMV-DNA was detected in two out of the 84 patients. In both of these patients, there was a concomitant HIV infection.

Thrombocytopenia is a common hematological complication which affects almost half of HIV-infected patients.5 In one of the two CMV-positive patients with HIV, the platelet count returned to normal only after specific antiviral therapy with ganciclovir. The improvement in the platelet count only after treatment with ganciclovir suggests that the CMV infection was probably the cause of this thrombocytopenia.

The demonstration of CMV-DNA by nested-PCR is very useful in this situation because of the difficulty in detecting CMV-IgM antibody in immunosuppressed patients, particularly those with acquired immune deficiency syndrome (Aids).6 The absence of CMV-DNA in the other patients confirmed the rarity of thrombocytopenia occurrence caused by CMV infection among non-immunosuppressed individuals.3,7 The detection of CMV infection in patients with thrombocytopenia and an HIV infection should provide correct diagnosis of the primary cause of the platelet disorder and may allow the use of specific therapy. We suggest that screening for CMV-DNA among patients with thrombocytopenia associated with an HIV infection could be a useful addition to the general diagnostic guidelines already proposed.5

REFERENCES

1. Karpatkin S. Autoimmune thrombocytopenia purpura. Semin Hematol 1995;22:260-88.

2. Van Spronsen DJ, Breed WPM. Cytomegalovirus-induced thrombocytopenia and hemolysis in an immunocompetent adult. Br J Haematol 1996;92:218-20.

3. Arruda VR, Rossi CL, Nogueira E, et al. Cytomegalovirus infection as a cause of severe thrombocytopenia in a non-immunosuppressed patient. Acta Hematologica 1997;98:228-30.

4. Demmler GJ, Buffone GJ, Schimbor CM, May RA. Detection of cytomegalovirus in urine from newborn by using polymerase chain reaction DNA amplification. J Infect Dis 1988;158:1177-84.

5. Glatt AE, Anand A. Thrombocytopenia in patients infected with human immunodeficiency virus: treatment update. Clin Infec Dis 1995;21:415-23.

6. Lazzarotto T, Dal Monte P, Boccuni MC, Ripalti A, Landini NV. Lack of correlation between virus detection and serologic tests for diagnosis of active cytomegalovirus infection in patients with AIDS. J Clin Microbiol 1992;30:1027-9.

7. Chanarin I, Walford DM. Thrombocytopenia in cytomegalovirus mononucleosis. Lancet 1993;ii:238-9.

PUBLISHING INFORMATION

Valder Roberval Arruda, PhD. Department of Clinical Medicine, Campinas State University, Campinas, SP, Brazil.

Gislaine Borba Oliveira, MD. Department of Clinical Medicine, Campinas State University, Campinas, SP, Brazil.

Joyce Maria Annichino-Bizzacchi, PhD. Department of Clinical Medicine, Campinas State University, Campinas, SP, Brazil.

Paula Durante, PhD. Department of Clinical Medicine, Campinas State University, Campinas, SP, Brazil.

Fernando Ferreira Costa, PhD. Department of Clinical Medicine, Campinas State University, Campinas, SP, Brazil.

Sandra Cecília Botelho Costa, PhD. Department of Clinical Medicine, Campinas State University, Campinas, SP, Brazil.

Address for correspondence:

Fernando Ferreira Costa

Centro de Hematologia e Hemoterapia,

Universidade Estadual de Campinas

Caixa Postal, 6198

São Paulo/SP ¾ Brasil - CEP 13.081-970

Fax: (+55 19) 239-3511

E-mail: ferreira@unicamp.br

Publication Dates

  • Publication in this collection
    02 May 2002
  • Date of issue
    Mar 2002
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