# Morbidity and Mortality Among People Living With HTLV‐1: A 30‐Year Retrospective Analysis in a Brazilian Cohort

**Authors:** Elizabeth Souza Neves, Otavio Melo Espíndola, Raquel de Vasconcelos Carvalhaes de Oliveira, Ana Claudia Celestino Bezerra Leite, Marco Antonio Sales Dantas Lima, Marcus Tulius Teixeira Silva, Rafael Osellame, Pedro Abrahão Pinheiro Guimarães, Ricardo Vezzani Batista, André Luiz Anjos Oliveira, Abelardo Queiroz Campos Araújo

PMC · DOI: 10.1002/jmv.70849 · Journal of Medical Virology · 2026-02-20

## TL;DR

A 30-year study of 508 HTLV-1-infected individuals in Brazil found that hospitalization and death are strongly linked to neurological complications and infections.

## Contribution

This study provides a long-term analysis of HTLV-1-related morbidity and mortality, emphasizing the role of HAM/TSP and secondary infections.

## Key findings

- HAM/TSP patients had higher mortality (15%) and hospitalization rates (40.2%) compared to the general HTLV-1 cohort.
- Infectious diseases were the leading cause of hospitalization (66.7%) and death (69%) in HTLV-1 patients.
- Motor impairment and higher HTLV-1 proviral load were associated with increased mortality.

## Abstract

HTLV‐1 infection is a chronic condition associated with the development of malignancies, inflammatory, and neurological disorders. In this study, the causes of hospitalization and mortality were assessed in a cohort of 508 individuals living with HTLV‐1 followed over a 30‐year period. Overall mortality was 8.5% in this population and increased to 15% among patients with HTLV‐1‐associated myelopathy/tropical spastic paraparesis (HAM/TSP), a major neurological syndrome characterized by motor, sensory, and urinary dysfunction. Hospitalization was required by 147 participants of the cohort (28.9%), and this increased to 40.2% (121 of 301) among those with HAM/TSP. Patients were admitted at least once, with a mean of two admissions per patient. Hospitalization was associated with HAM/TSP, particularly the degree of motor disability and HIV coinfection. Infectious diseases were the leading cause of both hospitalization (66.7%) and death (69%), most commonly urinary tract infections, pneumonia, and infected pressure ulcers. In addition, mortality was also directly related to the intensity of motor impairment and the number of hospitalizations. HAM/TSP was associated with an increased risk of hospitalization and readmission. Additionally, greater motor impairment was linked to higher risks of both hospitalization and mortality, while elevated HTLV‐1 PVL was found to contribute to an increased risk of death. In conclusion, these findings highlight the importance of prevention and timely management of secondary infections to reduce morbidity and mortality in individuals living with HTLV‐1, particularly those affected by HAM/TSP, which frequently present urinary dysfunction and pressure ulcers.

## Linked entities

- **Diseases:** HTLV-1-associated myelopathy/tropical spastic paraparesis (MONDO:0008039), pneumonia (MONDO:0005249)

## Full-text entities

- **Genes:** CNTN2 (contactin 2) [NCBI Gene 6900] {aka AXT, EPEO5, FAME5, TAG-1, TAX, TAX1}, HBB (hemoglobin subunit beta) [NCBI Gene 3043] {aka CD113t-C, ECYT6, beta-globin}
- **Diseases:** seborrheic dermatitis (MESH:D012628), Death (MESH:D003643), detrusor-sphincter dyssynergia (MESH:D001259), HAC (MESH:D015490), bronchiectasis (MESH:D001987), loss of mobility and (MESH:D014086), retroviral infection (MESH:D000071297), arthritis (MESH:D001168), infected pressure ulcers (MESH:D003668), UTIs (MESH:D014552), polymyositis (MESH:D017285), HAM/TSP (MESH:D015493), infection (MESH:D007239), pulmonary tuberculosis (MESH:D014397), Neurological disability (MESH:D009069), cognitive impairment (MESH:D003072), Infectious diseases (MESH:D003141), motor impairment (MESH:D000068079), sepsis (MESH:D018805), immune dysregulation (OMIM:614878), HIV co-infection (MESH:D015658), central nervous system infection (MESH:D002494), bronchiolitis (MESH:D001988), influenza (MESH:D007251), Skin disorders (MESH:D012871), mycobacteriosis (MESH:D009165), inflammation (MESH:D007249), respiratory infections (MESH:D012141), PVL (MESH:C536761), ATLL (MESH:D015459), peritoneal carcinomatosis (MESH:D010534), neurogenic bladder (MESH:D001750), malignancies (MESH:D009369), dysbiosis (MESH:D064806), polyneuropathy (MESH:D011115), chronic bronchitis (MESH:D029481), uveitis (MESH:D014605), infective dermatitis (MESH:D003872), pneumonia (MESH:D011014), HTLV-1 infection (MESH:D006800), respiratory (MESH:D012131), dysautonomia (MESH:D054969), NNM (MESH:D009461), myelopathy (MESH:D013118), spinal cord injury (MESH:D013119), motor, sensory, and urinary dysfunction (MESH:D001745)
- **Species:** Homo sapiens (human, species) [taxon 9606], Human T-cell leukemia virus type I (no rank) [taxon 11908], Human immunodeficiency virus 1 (no rank) [taxon 11676]

## Full text

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## References

34 references — full list in the complete paper: https://tomesphere.com/paper/PMC12921832/full.md

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Source: https://tomesphere.com/paper/PMC12921832