Investigation of pre-diagnostic virological markers for progressive multifocal leukoencephalopathy in human immunodeficiency virus-infected patients. 2009

Mary K Grabowski, and Raphael P Viscidi, and Joseph B Margolick, and Lisa P Jacobson, and Keerti V Shah
Johns Hopkins Bloomberg School of Public Health, Baltimore, Maryland 21205, USA. mgrabows@jhsph.edu

Progressive multifocal leukoencephalopathy (PML) is a severe neurological disorder due to JC virus (JCV) infection. Pre-diagnostic biological markers and risk factors for PML are not well understood. We conducted a case-control study nested within the Multicenter AIDS Cohort Study to examine the association between JCV viruria and viremia and serum antibody to JCV capsids, in relation to subsequent PML diagnoses, 5 months to 12 years later. Other demographic and immunologic factors were also examined. The study population included 28 incident cases of PML, 26 matched HIV-positive controls, and 50 HIV-negative controls. Prevalence of JCV viruria was 37% in cases, 42% in HIV-positive controls, and 28% in HIV-negative controls (P = 0.43). Among persons with JCV viruria, persistent viruria was more common in cases (89%) than in HIV-positive controls (33%) (P = 0.02). Presence of JCV viruria was not related to the time to PML diagnosis (OR: 1.03, 95% CI: 0.8-1.4); however, the urinary concentration of JCV DNA increased with proximity to the date of PML diagnosis in cases. JCV seropositivity did not differ between cases or controls (P = 0.42). Four cases tested JCV seronegative, including one case only 5 months prior to diagnosis with PML. JCV DNA was detected in the serum of one HIV-positive control. Smoking was the only demographic variable analyzed associated with an increased risk for PML (MOR: 9.0, 95% CI: 1.2-394.5). The results suggest that persistent JCV viruria and increasing urinary concentration of JCV DNA may be predictive of PML for some patients.

UI MeSH Term Description Entries
D007577 JC Virus A species of POLYOMAVIRUS, originally isolated from the brain of a patient with progressive multifocal leukoencephalopathy. The patient's initials J.C. gave the virus its name. Infection is not accompanied by any apparent illness but serious demyelinating disease can appear later, probably following reactivation of latent virus. Human Polyomavirus JC,JC polyomavirus,Polyomavirus, JC,John Cunningham Virus,Polyomavirus hominis 2,Polyomavirus JC, Human,Virus, John Cunningham
D007968 Leukoencephalopathy, Progressive Multifocal An opportunistic viral infection of the central nervous system associated with conditions that impair cell-mediated immunity (e.g., ACQUIRED IMMUNODEFICIENCY SYNDROME and other IMMUNOLOGIC DEFICIENCY SYNDROMES; HEMATOLOGIC NEOPLASMS; IMMUNOSUPPRESSION; and COLLAGEN DISEASES). The causative organism is JC Polyomavirus (JC VIRUS) which primarily affects oligodendrocytes, resulting in multiple areas of demyelination. Clinical manifestations include DEMENTIA; ATAXIA; visual disturbances; and other focal neurologic deficits, generally progressing to a vegetative state within 6 months. (From Joynt, Clinical Neurology, 1996, Ch26, pp36-7) Encephalitis, JC Polyomavirus,Progressive Multifocal Leukoencephalopathy,JC Polyomavirus Encephalopathy,Encephalopathies, JC Polyomavirus,Encephalopathy, JC Polyomavirus,JC Polyomavirus Encephalitis,Leukoencephalopathies, Progressive Multifocal,Multifocal Leukoencephalopathies, Progressive,Multifocal Leukoencephalopathy, Progressive,Progressive Multifocal Leukoencephalopathies
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D001769 Blood The body fluid that circulates in the vascular system (BLOOD VESSELS). Whole blood includes PLASMA and BLOOD CELLS.
D004279 DNA, Viral Deoxyribonucleic acid that makes up the genetic material of viruses. Viral DNA
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults
D000368 Aged A person 65 years of age or older. For a person older than 79 years, AGED, 80 AND OVER is available. Elderly
D000914 Antibodies, Viral Immunoglobulins produced in response to VIRAL ANTIGENS. Viral Antibodies

Related Publications

Mary K Grabowski, and Raphael P Viscidi, and Joseph B Margolick, and Lisa P Jacobson, and Keerti V Shah
February 2009, Archives of neurology,
Mary K Grabowski, and Raphael P Viscidi, and Joseph B Margolick, and Lisa P Jacobson, and Keerti V Shah
June 1992, Human pathology,
Mary K Grabowski, and Raphael P Viscidi, and Joseph B Margolick, and Lisa P Jacobson, and Keerti V Shah
July 2007, Annals of neurology,
Mary K Grabowski, and Raphael P Viscidi, and Joseph B Margolick, and Lisa P Jacobson, and Keerti V Shah
March 1995, Annals of neurology,
Mary K Grabowski, and Raphael P Viscidi, and Joseph B Margolick, and Lisa P Jacobson, and Keerti V Shah
September 1999, The Journal of infectious diseases,
Mary K Grabowski, and Raphael P Viscidi, and Joseph B Margolick, and Lisa P Jacobson, and Keerti V Shah
October 1991, Annals of neurology,
Mary K Grabowski, and Raphael P Viscidi, and Joseph B Margolick, and Lisa P Jacobson, and Keerti V Shah
March 2012, American journal of health-system pharmacy : AJHP : official journal of the American Society of Health-System Pharmacists,
Mary K Grabowski, and Raphael P Viscidi, and Joseph B Margolick, and Lisa P Jacobson, and Keerti V Shah
September 1999, Medicina clinica,
Mary K Grabowski, and Raphael P Viscidi, and Joseph B Margolick, and Lisa P Jacobson, and Keerti V Shah
July 2000, Medicina clinica,
Mary K Grabowski, and Raphael P Viscidi, and Joseph B Margolick, and Lisa P Jacobson, and Keerti V Shah
October 2011, Clinical infectious diseases : an official publication of the Infectious Diseases Society of America,
Copied contents to your clipboard!