Evidence map›Paper›PMID 38787255›Full record

ArticlePathogens (Basel, Switzerland)2024

HTLV-1-Associated Myelopathy (HAM) Incidence in Asymptomatic Carriers and Intermediate Syndrome (IS) Patients.

Rosa Maria do Nascimento Marcusso, Tatiane Assone, Michel E Haziot, Jerusa Smid, Victor A Folgosi, Carolina Rosadas, Jorge Casseb, Augusto C Penalva de Oliveira, The Htlv-Clinical Definition Working Group

Abstract read
In one paragraph

Article in Pathogens (Basel, Switzerland), 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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

7 citing papers in PubMed.

  1. Article
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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

9 authors.

Rosa Maria do Nascimento MarcussoInstituto de Infectologia Emílio Ribas, São Paulo 01246-000, Brazil.ORCID 0000-0002-8396-0263
Tatiane AssoneDepartamento de Medicina Legal, Bioética, Medicina do Trabalho e Medicina Física e Reabilitação, Faculdade de Medicina, Universidade de São Paulo, São Paulo 01246-000, Brazil.ORCID 0000-0003-0993-4523
Michel E HaziotInstituto de Infectologia Emílio Ribas, São Paulo 01246-000, Brazil.ORCID 0000-0002-3549-1992
Jerusa SmidInstituto de Infectologia Emílio Ribas, São Paulo 01246-000, Brazil.
Victor A FolgosiDepartamento de Dermatologia, Faculdade de Medicina, Universidade de São Paulo, São Paulo 01246-000, Brazil.ORCID 0000-0002-0114-7587
Carolina RosadasSection of Virology, Department of Infectious Disease, Imperial College London, London SW7 2BX, UK.ORCID 0000-0002-3922-5667
Jorge CassebDepartamento de Dermatologia, Faculdade de Medicina, Universidade de São Paulo, São Paulo 01246-000, Brazil.ORCID 0000-0002-4553-2559
Augusto C Penalva de OliveiraInstituto de Infectologia Emílio Ribas, São Paulo 01246-000, Brazil.
The Htlv-Clinical Definition Working Group

Funding

FapespMRC MR/X0223358/1
6 · The paper itself

Abstract

Several studies suggest that HTLV-1 infection may be associated with a wider spectrum of neurological and clinical manifestations that do not meet diagnostic criteria for HAM. These conditions may later progress to HAM or constitute an intermediate clinical form: intermediate syndrome (IS), a mid-point between asymptomatic HTLV-1 carriers and those with full myelopathy. Thus, we determined the incidence of HAM cases in the HTLV-1-asymptomatic and IS patients, and the clinical/laboratory associated markers. A total of 204 HTLV-1-positive patients were included in this study, divided into two groups: Group 1, including 145 asymptomatic HTLV-1 subjects (ASY), and Group 2, including 59 patients with inflammatory clinical symptoms in more than three systems and a high proviral load (PVL). During a 60-month follow-up time, with the age ranging from 47 to 79 years, ten patients of the fifty-nine initially diagnosed as IS developed HAM (iHAM), and two patients of the initial 145 ASY developed HAM directly. Women were more prevalent in all groups. For the iHAM patients, the age ranged from 20 to 72 years, with a mean of 53 (±15 SD). Older age was associated with the development of HAM, higher PVL and IS; however, there was no any specific symptom or clinical sign, that was associated with risk for iHAM. In conclusion, IS cases could be an early phase of development of HAM. These findings show the presence of higher incidence probabilities in our cohort than previously reported.

Indexed as

Human T-lymphotropic virus 1AdultAgedCarrier StateFemaleHTLV-I InfectionsHumansIncidenceMaleMiddle AgedParaparesis, Tropical SpasticSpinal Cord DiseasesViral LoadYoung AdultBrazilearly stageHTLV-1-associated myelopathyincidencesurrogate markers

Identifiers

PMID38787255
PMCPMC11124065

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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 Socratic graph.