Evidence map›Paper›PMID 31554669›Full record

Observational studyNeurology(R) neuroimmunology & neuroinflammation2019

Progressive multifocal leukoencephalopathy: A 25-year retrospective cohort study.

Pria Anand, Gladia C Hotan, Andre Vogel, Nagagopal Venna, Farrah J Mateen

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Neurology(R) neuroimmunology & neuroinflammation, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
4.5field-weighted citation impact, top 4% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

45 citing papers in PubMed, 81 citations in OpenAlex.

  1. Review
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  5. A first report of progressive multifocal leukoencephalopathy in childhood-onset NMOSD.Multiple sclerosis (Houndmills, Basingstoke, England) · 2025
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  10. Progressive multifocal leukoencephalopathy and spectrum of predisposing conditions: a 20-year retrospective cohort study in a tertiary center in São Paulo, Brazil.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2025
    Article
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  12. Review
  13. Ten Years ofNeurology(R) neuroimmunology & neuroinflammation · 2025
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors at 1 institution in 1 country.

Pria AnandFrom the Department of Neurology (P.A., A.V., N.V., F.J.M.), Massachusetts General Hospital, Boston; and Department of Brain and Cognitive Sciences (G.C.H.), Massachusetts Institute of Technology, Cambridge. pria.anand@gmail.com.
Gladia C HotanFrom the Department of Neurology (P.A., A.V., N.V., F.J.M.), Massachusetts General Hospital, Boston; and Department of Brain and Cognitive Sciences (G.C.H.), Massachusetts Institute of Technology, Cambridge.
Andre VogelFrom the Department of Neurology (P.A., A.V., N.V., F.J.M.), Massachusetts General Hospital, Boston; and Department of Brain and Cognitive Sciences (G.C.H.), Massachusetts Institute of Technology, Cambridge.
Nagagopal VennaFrom the Department of Neurology (P.A., A.V., N.V., F.J.M.), Massachusetts General Hospital, Boston; and Department of Brain and Cognitive Sciences (G.C.H.), Massachusetts Institute of Technology, Cambridge.
Farrah J MateenFrom the Department of Neurology (P.A., A.V., N.V., F.J.M.), Massachusetts General Hospital, Boston; and Department of Brain and Cognitive Sciences (G.C.H.), Massachusetts Institute of Technology, Cambridge.
Massachusetts General Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo characterize the risk factors, clinical course, and treatment of patients with progressive multifocal leukoencephalopathy (PML) diagnosed and followed over a 25-year epoch at 2 academic hospitals.

methodsPatients with a definite diagnosis of PML were identified by positive CSF PCR for JC virus or histopathology between January 1, 1994, and January 1, 2019. Demographic and PML-specific variables were recorded on symptomatic presentation and at follow-up, including risk factors, clinical outcome, neuroimaging findings, and modified Rankin Scale (mRS) score at last follow-up.

resultsThere were 91 patients with confirmed PML. HIV infection was the most common risk factor, identified in 49% (n = 45). Other frequent risk factors included lymphoma, leukemia, or myelodysplasia, identified in 31% of patients (n = 28); exposure to chemotherapeutic medications (30%, n = 27); and exposure to monoclonal antibody therapies (19%, n = 17). Thirty percent of the cohort was alive at the time of censoring, with a median mRS of 2 points, indicating slight disability at last follow-up. Median survival following PML diagnosis in HIV-infected patients was longer than in HIV-uninfected patients (1,992 vs 101 days,

conclusionsWe add to the limited literature on PML by reporting its epidemiology in a large observational cohort. These parameters may be useful for future clinical trials that measure survival and clinical outcomes.

Indexed as

RegistriesAdultAgedAged, 80 and overComorbidityFemaleFollow-Up StudiesHIV InfectionsHumansJC VirusLeukoencephalopathy, Progressive MultifocalMagnetic Resonance ImagingMaleMiddle AgedRetrospective StudiesRisk Factors

Identifiers

PMID31554669
PMCPMC6814409
OpenAlexW2976487454

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.