Incidence, Clinical Presentation, and Outcome of Progressive Multifocal Leukoencephalopathy in HIV-Infected Patients during the Highly Active Antiretroviral Therapy Era: A Nationwide Cohort Study

被引:162
作者
Engsig, Frederik Neess [1 ]
Hansen, Ann-Brit Eg [1 ]
Omland, Lars Haukali [1 ]
Kronborg, Gitte [4 ]
Gerstoft, Jan [1 ]
Laursen, Alex Lund [5 ]
Pedersen, Court [2 ,3 ]
Mogensen, Christian Backer [6 ]
Nielsen, Lars [7 ]
Obel, Niels [1 ]
机构
[1] Univ Copenhagen Hosp, Rigshosp, Dept Infect Dis, DK-2100 Copenhagen, Denmark
[2] Odense Univ Hosp, DK-5000 Odense, Denmark
[3] Univ So Denmark, Odense, Denmark
[4] Copenhagen Univ Hosp, Hvidovre, Denmark
[5] Aarhus Univ Hosp, DK-8000 Aarhus, Denmark
[6] Kolding Cty Hosp, Kolding, Denmark
[7] Helsingborg Hosp, Helsingor, Denmark
关键词
HUMAN-IMMUNODEFICIENCY-VIRUS; SURVIVAL; DENMARK; RISK; DNA;
D O I
10.1086/595299
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Human immunodeficiency virus (HIV) infection predisposes to progressive multifocal leukoen-cephalopathy (PML). Here, we describe the incidence, presentation, and prognosis of PML in HIV-1-infected patients during the period before highly active antiretroviral therapy (HAART) (1995-1996) and during the early HAART (1997-1999) and late HAART (2000-2006) periods. Methods. Patients from a nationwide population-based cohort of adult HIV-1-infected individuals were included. We calculated incidence rates of PML and median survival times after diagnosis. We also described neurological symptoms at presentation and follow-up. Results. Among 4649 patients, we identified 47 patients with PML. The incidence rates were 3.3, 1.8, and 1.3 cases per 1000 person-years at risk in 1995-1996, 1997-1999, and 2000-2006, respectively. The risk of PML was significantly associated with low CD4(+) cell count, and 47% of cases were diagnosed by means of brain biopsy or polymerase chain reaction analysis for JC virus. The predominant neurological symptoms at presentation were coordination disturbance, cognitive defects, and limb paresis. Thirty-five patients died; the median survival time was 0.4 years (95% confidence interval [CI], 0.0-0.7) in 1995-1996 and 1.8 years ( 95% CI, 0.6-3.0) in both 1997-1999 and 2000-2006. CD4(+) cell count >50 cells/mu L at diagnosis of PML was significantly associated with reduced mortality. Conclusions. The incidence of PML in HIV-infected patients decreased after the introduction of HAART. Survival after PML remains poor. In the management of PML, the main focus should be on prophylactic measures to avoid immunodeficiency.
引用
收藏
页码:77 / 83
页数:7
相关论文
共 22 条
  • [1] Highly active antiretroviral therapy significantly improves the prognosis of patients with HIV-associated progressive multifocal leukoencephalopathy
    Albrecht, H
    Hoffmann, C
    Degen, O
    Stoehr, A
    Plettenberg, A
    Mertenskötter, T
    Eggers, C
    Stellbrink, HJ
    [J]. AIDS, 1998, 12 (10) : 1149 - 1154
  • [2] Clinical epidemiology and survival of progressive multifocal leukoencephalopathy in the era of highly active antiretroviral therapy: Data from the Italian Registry Investigative Neuro AIDS (IRINA)
    Antinori, A
    Cingolani, A
    Lorenzini, P
    Giancola, ML
    Uccella, I
    Bossolasco, S
    Grisetti, S
    Moretti, F
    Vigo, B
    Bongiovanni, M
    Del Grosso, B
    Arcidiacono, MI
    Fibbia, GC
    Mena, M
    Finazzi, MG
    Guaraldi, G
    Ammassari, A
    Monforte, AD
    Cinque, P
    De Luca, A
    [J]. JOURNAL OF NEUROVIROLOGY, 2003, 9 (Suppl 1) : 47 - 53
  • [3] PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY - A HITHERTO UNRECOGNIZED COMPLICATION OF CHRONIC LYMPHATIC LEUKAEMIA AND HODGKINS DISEASE
    ASTROM, KE
    MANCALL, EL
    RICHARDSON, EP
    [J]. BRAIN, 1958, 81 (01) : 93 - &
  • [4] Clinical course and prognostic factors of progressive multifocal leukoencephalopathy in patients treated with highly active antiretroviral therapy
    Berenguer, J
    Miralles, P
    Arrizabalaga, J
    Ribera, E
    Dronda, F
    Baraia-Etxaburu, J
    Domingo, P
    Márquez, M
    Rodriguez-Arrondo, FJ
    Laguna, F
    Rubio, R
    Rodrigo, JL
    Mallolas, J
    de Miguel, V
    [J]. CLINICAL INFECTIOUS DISEASES, 2003, 36 (08) : 1047 - 1052
  • [5] PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY ASSOCIATED WITH HUMAN IMMUNODEFICIENCY VIRUS-INFECTION - A REVIEW OF THE LITERATURE WITH A REPORT OF 16 CASES
    BERGER, JR
    KASZOVITZ, B
    POST, MJD
    DICKINSON, G
    [J]. ANNALS OF INTERNAL MEDICINE, 1987, 107 (01) : 78 - 87
  • [6] PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY
    BROOKS, BR
    WALKER, DL
    [J]. NEUROLOGIC CLINICS, 1984, 2 (02) : 299 - 313
  • [7] Cinque P, 2001, J NEUROVIROL, V7, P358
  • [8] DE LA, 2000, J INFECT DIS, V182, P1077
  • [9] Inflammatory reaction in progressive multifocal leukoencephalopathy: Harmful or beneficial?
    Du Pasquier, RA
    Koralnik, IJ
    [J]. JOURNAL OF NEUROVIROLOGY, 2003, 9 (Suppl 1) : 25 - 31
  • [10] DIAGNOSTIC-VALUE OF DETECTING JC VIRUS-DNA IN CEREBROSPINAL-FLUID OF PATIENTS WITH PROGRESSIVE MULTIFOCAL LEUKOENCEPHALOPATHY
    FONG, IW
    BRITTON, CB
    LUINSTRA, KE
    TOMA, E
    MAHONY, JB
    [J]. JOURNAL OF CLINICAL MICROBIOLOGY, 1995, 33 (02) : 484 - 486