Evidence map›Paper›PMID 32949543›Full record

Observational studyThe Lancet. Neurology2020

Neurological disease in adults with Zika and chikungunya virus infection in Northeast Brazil: a prospective observational study.

Maria Lúcia Brito Ferreira, Maria de Fatima Pessoa Militão de Albuquerque, Carlos Alexandre Antunes de Brito, Rafael Freitas de Oliveira França, Álvaro José Porto Moreira, Maria Íris de Morais Machado, Roberta da Paz Melo, Raquel Medialdea-Carrera, Solange Dornelas Mesquita, Marcela Lopes Santos and 19 more

Open access · bronzeAbstract readObservational Study
In one paragraph

Observational study in The Lancet. Neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 74 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
74citing papers in PubMed, 3 pooled it
12.3field-weighted citation impact, top 1% 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

74 citing papers in PubMed, 3 syntheses or guidelines pooled it, 113 citations in OpenAlex.

  1. Pooled it
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  3. Miller Fisher syndrome associated with COVID-19: an up-to-date systematic review.Environmental science and pollution research international · 2021
    Pooled it
  4. Article
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  6. Autoantibodies neutralizing type I interferons underlie a third of cases of Chikungunya virus encephalitis or myelitis.Proceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  7. Article
  8. Review
  9. Review
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  12. [Spotlight on chikungunya-current diagnostics and treatment].Medizinische Klinik, Intensivmedizin und Notfallmedizin · 2026
    Article
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  18. Observational
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14 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

29 authors at 10 institutions in 4 countries.

Maria Lúcia Brito FerreiraDepartment of Neurology, Hospital da Restauração, Recife, Brazil.
Maria de Fatima Pessoa Militão de AlbuquerqueDepartment of Collective Health, Institute Aggeu Magalhães, Oswaldo Cruz Foundation, Recife, Brazil.
Carlos Alexandre Antunes de BritoDepartment of Clinical Medicine, Federal University of Pernambuco, Recife, Brazil.
Rafael Freitas de Oliveira FrançaDepartment of Virology, Institute Aggeu Magalhães, Oswaldo Cruz Foundation, Recife, Brazil.
Álvaro José Porto MoreiraDepartment of Neurology, Hospital da Restauração, Recife, Brazil.
Maria Íris de Morais MachadoDepartment of Neurology, Hospital da Restauração, Recife, Brazil.
Roberta da Paz MeloDepartment of Neurology, Hospital da Restauração, Recife, Brazil.
Raquel Medialdea-CarreraNational Institute for Health Research Health Protection Research Unit on Emerging and Zoonotic Infections, Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, UK.
Solange Dornelas MesquitaDepartment of Neurology, Hospital da Restauração, Recife, Brazil.
Marcela Lopes SantosDepartment of Collective Health, Institute Aggeu Magalhães, Oswaldo Cruz Foundation, Recife, Brazil.
Ravi MehtaNational Institute for Health Research Health Protection Research Unit on Emerging and Zoonotic Infections, Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, UK.
Rafael Ramos E SilvaDepartment of Neurology, Hospital da Restauração, Recife, Brazil.
Sonja E LeonhardDepartment of Neurology, Erasmus University Medical Center, Rotterdam, Netherlands.
Mark EllulNational Institute for Health Research Health Protection Research Unit on Emerging and Zoonotic Infections, Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, UK; The Walton Centre NHS Foundation Trust, Liverpool, UK.
Anna Rosala-HallasDepartment of Biostatistics, University of Liverpool, Liverpool, UK.
Girvan BurnsideDepartment of Biostatistics, University of Liverpool, Liverpool, UK.
Lance TurtleNational Institute for Health Research Health Protection Research Unit on Emerging and Zoonotic Infections, Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, UK; Royal Liverpool and Broadgreen University Hospitals NHS Trust, Liverpool, UK.
Michael J GriffithsNational Institute for Health Research Health Protection Research Unit on Emerging and Zoonotic Infections, Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, UK; Alder Hey Children's NHS Foundation Trust, Liverpool, UK.
Bart C JacobsDepartment of Neurology, Erasmus University Medical Center, Rotterdam, Netherlands; Department of Immunology, Erasmus University Medical Center, Rotterdam, Netherlands.
Maneesh BhojakThe Walton Centre NHS Foundation Trust, Liverpool, UK.
Hugh J WillisonDepartment of Neurology and Institute of Infection, Immunity and Inflammation, University of Glasgow, Glasgow, UK.
Lindomar José PenaDepartment of Virology, Institute Aggeu Magalhães, Oswaldo Cruz Foundation, Recife, Brazil.
Carlos A PardoDepartment of Neurology, Division of Neuroimmunology and Neuroinfectious Disorders, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Ricardo A A XimenesDepartment of Tropical Medicine, Federal University of Pernambuco, Recife, Brazil.
Celina Maria Turchi MartelliDepartment of Collective Health, Institute Aggeu Magalhães, Oswaldo Cruz Foundation, Recife, Brazil.
David W G BrownBlood Borne Virus Unit, Virus Reference Department, Public Health England, London, England; Flavivirus Reference Laboratory, Evandro Chagas National Infectious Disease Institute, Oswaldo Cruz Foundation, Rio de Janeiro, Brazil.
Marli Tenório CordeiroDepartment of Virology, Institute Aggeu Magalhães, Oswaldo Cruz Foundation, Recife, Brazil.
Suzannah LantNational Institute for Health Research Health Protection Research Unit on Emerging and Zoonotic Infections, Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, UK.
Tom SolomonNational Institute for Health Research Health Protection Research Unit on Emerging and Zoonotic Infections, Institute of Infection, Veterinary & Ecological Sciences, University of Liverpool, Liverpool, UK; The Walton Centre NHS Foundation Trust, Liverpool, UK; Royal Liverpool and Broadgreen University Hospitals NHS Trust, Liverpool, UK. Electronic address: tsolomon@liverpool.ac.uk.
Fundação Oswaldo Cruz · BRHospital da Restauração · BRUniversity of Liverpool · GBNational Institute for Health Research · GBErasmus MC · NLUniversidade Federal de Pernambuco · BRJohns Hopkins Medicine · USRoyal Liverpool and Broadgreen University Hospital NHS Trust · GBUniversity of Glasgow · GBWalton Centre · GB

Funding

Emerging Neuroviruses and Neurological Inflammatory DiseasesR01NS110122 · NINDS · JOHNS HOPKINS UNIVERSITY · PI PARDO-VILLAMIZAR, CARLOS A · 2019 to 2023
$1.7M
Department of Health IS-HPU-1112-10117Medical Research Council MC_PC_15096Medical Research Council MC_PC_15101NINDS NIH HHS R01 NS110122Wellcome Trust 205228/Z/16/ZWellcome Trust WT 202789/Z/16/Z
6 · The paper itself

Abstract

backgroundSince 2015, the arthropod-borne viruses (arboviruses) Zika and chikungunya have spread across the Americas causing outbreaks, accompanied by increases in immune-mediated and infectious neurological disease. The spectrum of neurological manifestations linked to these viruses, and the importance of dual infection, are not known fully. We aimed to investigate whether neurological presentations differed according to the infecting arbovirus, and whether patients with dual infection had a different disease spectrum or severity.

methodsWe report a prospective observational study done during epidemics of Zika and chikungunya viruses in Recife, Pernambuco, a dengue-endemic area of Brazil. We recruited adults aged 18 years or older referred to Hospital da Restauração, a secondary-level and tertiary-level hospital, with suspected acute neurological disease and a history of suspected arboviral infection. We looked for evidence of Zika, chikungunya, or dengue infection by viral RNA or specific IgM antibodies in serum or CSF. We grouped patients according to their arbovirus laboratory diagnosis and then compared demographic and clinical characteristics.

findingsBetween Dec 4, 2014, and Dec 4, 2016, 1410 patients were admitted to the hospital neurology service; 201 (14%) had symptoms consistent with arbovirus infection and sufficient samples for diagnostic testing and were included in the study. The median age was 48 years (IQR 34-60), and 106 (53%) were women. 148 (74%) of 201 patients had laboratory evidence of arboviral infection. 98 (49%) of them had a single viral infection (41 [20%] had Zika, 55 [27%] had chikungunya, and two [1%] had dengue infection), whereas 50 (25%) had evidence of dual infection, mostly with Zika and chikungunya viruses (46 [23%] patients). Patients positive for arbovirus infection presented with a broad range of CNS and peripheral nervous system (PNS) disease. Chikungunya infection was more often associated with CNS disease (26 [47%] of 55 patients with chikungunya infection vs six [15%] of 41 with Zika infection; p=0·0008), especially myelitis (12 [22%] patients). Zika infection was more often associated with PNS disease (26 [63%] of 41 patients with Zika infection vs nine [16%] of 55 with chikungunya infection; p≤0·0001), particularly Guillain-Barré syndrome (25 [61%] patients). Patients with Guillain-Barré syndrome who had Zika and chikungunya dual infection had more aggressive disease, requiring intensive care support and longer hospital stays, than those with mono-infection (median 24 days [IQR 20-30] vs 17 days [10-20]; p=0·0028). Eight (17%) of 46 patients with Zika and chikungunya dual infection had a stroke or transient ischaemic attack, compared with five (6%) of 96 patients with Zika or chikungunya mono-infection (p=0·047).

interpretationThere is a wide and overlapping spectrum of neurological manifestations caused by Zika or chikungunya mono-infection and by dual infections. The possible increased risk of acute cerebrovascular disease in patients with dual infection merits further investigation.

fundingFundação do Amparo a Ciência e Tecnologia de Pernambuco (FACEPE), EU's Horizon 2020 research and innovation programme, National Institute for Health Research. TRANSLATIONS: For the Portuguese and Spanish translations of the abstract see Supplementary Materials section.

Indexed as

AdultAgedBrazilChikungunya FeverFemaleHumansMaleMiddle AgedNervous System DiseasesProspective StudiesZika Virus Infection

Identifiers

PMID32949543
PMCPMC7494308
OpenAlexW3085417549

What OpenQuestion holds

Textmetadata
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.