The role of parvovirus B19 in the pathogenesis of giant cell arteritis: A preliminary evaluation
Open Access
- 1 June 1999
- journal article
- research article
- Published by Wiley in Arthritis & Rheumatism
- Vol. 42 (6) , 1255-1258
- https://doi.org/10.1002/1529-0131(199906)42:6<1255::aid-anr23>3.0.co;2-p
Abstract
Objective To determine whether parvovirus B19 DNA is more likely to be present in the temporal arteries of patients with giant cell arteritis (GCA) than in the temporal arteries of control subjects. Methods We prospectively examined temporal artery biopsy (TAB) tissue from 50 consecutive patients presenting for TAB for the presence of B19 DNA using the polymerase chain reaction (PCR). Clinical and demographic information was obtained from the patients' medical records. A separate PCR analysis of 30 original tissue specimens was conducted at the Centers for Disease Control and Prevention (CDC) using primers directed toward another target sequence in the nonstructural coding area of B19. Results The 50 patients had an average age of 70.8 years; 27 (54%) were female. Amplicons for human β‐globulin, but not for cytomegalovirus, were produced for all tissue samples. The PCR results for B19 agreed in 29 of 30 samples tested by our institution and by the CDC (97% agreement; κ = 0.9). A comparison of the B19 DNA analysis and the results of TAB indicated a statistically significant association between histologic evidence of GCA and the presence of B19 DNA in TAB tissue (χ2= 10.38, P = 0.0013). Conclusion These findings suggest that B19 may play a role in the pathogenesis of GCA.Keywords
This publication has 15 references indexed in Scilit:
- Association of Parvovirus B19 Infection with Giant Cell ArteritisClinical Infectious Diseases, 1996
- High frequency of parvovirus B19 in patients tested for rheumatoid factorBMJ, 1995
- 2 B19 parvovirusBailliere's Clinical Haematology, 1995
- Chronic parvovirus B19 infection and systemic necrotising vasculitis: opportunistic infection or aetiological agent?Published by Elsevier ,1994
- Multiple primer pairs for polymerase chain reaction (PCR) amplification of human parvovirus B19 DNAJournal of Virological Methods, 1993
- Erythrocyte P Antigen: Cellular Receptor for B19 ParvovirusScience, 1993
- Dependence of polymerase chain reaction product inactivation protocols on amplicon length and sequence compositionJournal of Clinical Microbiology, 1993
- Detection of HSV-specific DNA in biopsy tissue of patients with erythema multiforme by polymerase chain reactionBritish Journal of Dermatology, 1992
- Avoiding false positives with PCRNature, 1989
- Primer-Directed Enzymatic Amplification of DNA with a Thermostable DNA PolymeraseScience, 1988