CC BY 4.0 · Arq Neuropsiquiatr 2023; 81(03): 271-283
DOI: 10.1055/s-0043-1764417
Original Article

Impaired flexibility in patients with tropical spastic paraparesis/HTLV-associated myelopathy: evaluation via pendulum fleximeter

Flexibilidade prejudicada em pacientes com paraparesia espástica tropical/mielopatia associada ao HTLV: avaliação via flexímetro pendular
1   Escola Bahiana de Medicina e Saúde Pública, Salvador BA, Brazil.
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1   Escola Bahiana de Medicina e Saúde Pública, Salvador BA, Brazil.
,
1   Escola Bahiana de Medicina e Saúde Pública, Salvador BA, Brazil.
,
1   Escola Bahiana de Medicina e Saúde Pública, Salvador BA, Brazil.
,
1   Escola Bahiana de Medicina e Saúde Pública, Salvador BA, Brazil.
,
1   Escola Bahiana de Medicina e Saúde Pública, Salvador BA, Brazil.
,
1   Escola Bahiana de Medicina e Saúde Pública, Salvador BA, Brazil.
,
1   Escola Bahiana de Medicina e Saúde Pública, Salvador BA, Brazil.
,
1   Escola Bahiana de Medicina e Saúde Pública, Salvador BA, Brazil.
2   Universidade Federal da Bahia, Salvador BA, Brazil.
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1   Escola Bahiana de Medicina e Saúde Pública, Salvador BA, Brazil.
3   Fundação Oswaldo Cruz, Instituto Gonçalo Moniz, Laboratório Avançado de Saúde Pública, Salvador BA, Brazil.
› Author Affiliations

Abstract

Background Flexibility is crucial to the harmonious execution of joint movements. While skeletal muscle dysfunction in patients with HTLV-1 can interfere with mobility, it is unclear whether these patients experience reduced flexibility.

Objective To evaluate the differences in flexibility between HTLV-1-infected individuals with and without myelopathy compared with uninfected controls. We also investigated whether age, sex, body mass index (BMI), physical activity level, or lower back pain influence flexibility in HTLV-1-infected individuals.

Methods The sample consisted of 56 adults, of which 15 did not have HTLV-1, 15 had HTLV-1 without myelopathy, and 26 had TSP/HAM. Their flexibility was assessed using the sit-and-reach test and a pendulum fleximeter.

Results No differences in flexibility were observed between the groups with and without myelopathy and controls without HTLV-1 infection using the sit-and-reach test. The pendulum fleximeter results of individuals with TSP/HAM presented the lowest flexibility among the groups with respect to trunk flexion, hip flexion and extension, knee flexion, and ankle dorsiflexion, even after adjusting for age, sex, BMI, level of physical activity, and lower back pain using multiple linear regression models. Additionally, HTLV-1-infected individuals without myelopathy demonstrated reduced flexibility in movements: knee flexion, dorsiflexion, and ankle plantar flexion.

Conclusions Individuals with TSP/HAM demonstrated reduced flexibility in most of the movements evaluated by the pendulum fleximeter. Additionally, HTLV-1-infected individuals without myelopathy demonstrated reduced knee and ankle flexibility, potentially representing a marker of myelopathic development.

Resumo

Antecedentes A flexibilidade é fundamental para a execução harmoniosa dos movimentos articulares. Embora a disfunção do músculo esquelético em pacientes com HTLV-1 possa interferir na mobilidade, não está claro se esses pacientes apresentam flexibilidade reduzida.

Objetivo Avaliar as diferenças de flexibilidade entre os indivíduos infectados com e sem mielopatia e o grupo controle sem infecção HTLV-1. Também investigamos se idade, sexo, índice de massa corporal (IMC), nível de atividade física ou dor lombar influenciam a flexibilidade em indivíduos infectados pelo HTLV-1.

Métodos A amostra foi composta por 56 adultos, dos quais 15 não possuíam HTLV-1, 15 possuíam HTLV-1 sem mielopatia e 26 possuíam TSP/HAM. A flexibilidade foi avaliada por meio do teste de sentar e alcançar e do flexímetro de pêndulo.

Resultados Não foram observadas diferenças na flexibilidade entre os grupos com e sem mielopatia no teste de sentar e alcançar. Os resultados do flexímetro pendular dos indivíduos com TSP/HAM apresentaram a menor flexibilidade entre os grupos em relação à flexão do tronco, flexão e extensão do quadril, flexão do joelho e dorsiflexão do tornozelo, mesmo após ajuste para idade, sexo, IMC, nível de atividade física e dor lombar usando modelos de regressão múltipla linear. Além disso, os indivíduos infectados pelo HTLV-1 sem mielopatia demonstraram redução da flexibilidade nos movimentos de flexão do joelho, dorsiflexão e flexão plantar do tornozelo.

Conclusão Indivíduos com TSP/HAM demonstraram redução da flexibilidade na maioria dos movimentos avaliados pelo flexímetro pendular. Além disso, indivíduos infectados pelo HTLV-1 sem mielopatia demonstraram redução da flexibilidade do joelho e tornozelo, representando potencialmente um marcador de desenvolvimento mielopático.

Authors' Contributions

BGC: designed and supervised the work; CL, CA, AR, FO, TA: acquired the data; CL: wrote the first draft; CL, CD, ALG, NBS, BGC: critically revised the manuscript. All authors read and approved the final version of the manuscript, analyzed and interpreted the data, and drafted the manuscript.


Support

This work was supported by the National Council for Scientific and Technological Development (Conselho Nacional de Desenvolvimento Científico e Tecnológico—CNPq), Foundation for Research Support of Bahia (Fundação de Amparo à Pesquisa do Estado da Bahia—FAPESB). Bernardo Galvão-Castro, Christiane Dias (Pr n0 60133/2022) and Ney Boa-Sorte received a research grant from the National Foundation for the Development of Private Higher Education (Fundação Nacional de Desenvolvimento do Ensino Superior Particular (FUNADESP), Caroline Landim received a scholarship from the Coordination for the Improvement of Higher Education Personnel (Coordenação de Aperfeiçoamento de Pessoal de Nivel Superior (CAPES). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.




Publication History

Received: 02 June 2022

Accepted: 16 October 2022

Article published online:
14 April 2023

© 2023. Academia Brasileira de Neurologia. This is an open access article published by Thieme under the terms of the Creative Commons Attribution 4.0 International License, permitting copying and reproduction so long as the original work is given appropriate credit (https://creativecommons.org/licenses/by/4.0/)

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  • References

  • 1 Poiesz BJ, Ruscetti FW, Gazdar AF, Bunn PA, Minna JD, Gallo RC. Detection and isolation of type C retrovirus particles from fresh and cultured lymphocytes of a patient with cutaneous T-cell lymphoma. Proc Natl Acad Sci U S A 1980; 77 (12) 7415-7419
  • 2 Gessain A, Cassar O. Epidemiological Aspects and World Distribution of HTLV-1 Infection. Front Microbiol 2012; 3: 388
  • 3 Pereira FM, de Almeida MDCC, Santos FLN. et al. Evidence of New Endemic Clusters of Human T-Cell Leukemia Virus (HTLV) Infection in Bahia, Brazil. Front Microbiol 2019; 10: 1002
  • 4 Dourado I, Alcantara LCJ, Barreto ML, da Gloria Teixeira M, Galvão-Castro B. HTLV-I in the general population of Salvador, Brazil: a city with African ethnic and sociodemographic characteristics. J Acquir Immune Defic Syndr 2003; 34 (05) 527-531
  • 5 Nunes D, Boa-Sorte N, Grassi MFR. et al. HTLV-1 is predominantly sexually transmitted in Salvador, the city with the highest HTLV-1 prevalence in Brazil. PLoS One 2017; 12 (02) e0171303
  • 6 Yoshida M, Miyoshi I, Hinuma Y. Isolation and characterization of retrovirus from cell lines of human adult T-cell leukemia and its implication in the disease. Proc Natl Acad Sci U S A 1982; 79 (06) 2031-2035
  • 7 Gessain A, Barin F, Vernant JC. et al. Antibodies to human T-lymphotropic virus type-I in patients with tropical spastic paraparesis. Lancet 1985; 2 (8452): 407-410
  • 8 Osame M, Usuku K, Izumo S. et al. HTLV-I associated myelopathy, a new clinical entity. Lancet 1986; 1 (8488): 1031-1032 https://linkinghub.elsevier.com/retrieve/pii/S0140673686912985
  • 9 Mochizuki M, Yamaguchi K, Takatsuki K, Watanabe T, Mori S, Tajima K. HTLV-I and uveitis. Lancet 1992; 339 (8801): 1110
  • 10 LaGrenade L, Hanchard B, Fletcher V, Cranston B, Blattner W. Infective dermatitis of Jamaican children: a marker for HTLV-I infection. Lancet 1990; 336 (8727): 1345-1347
  • 11 Rathsam-Pinheiro RH, Boa-Sorte N, Grassi MFR. et al. Revisiting Keratoconjunctivitis sicca associated with Human T-Cell Lymphotropic Virus Type 1: prevalence, clinical aspects and proviral load. Braz J Infect Dis 2019; 23 (02) 95-101
  • 12 Schierhout G, McGregor S, Gessain A, Einsiedel L, Martinello M, Kaldor J. Association between HTLV-1 infection and adverse health outcomes: a systematic review and meta-analysis of epidemiological studies. Lancet Infect Dis 2020; 20 (01) 133-143 https://linkinghub.elsevier.com/retrieve/pii/S1473309919304025
  • 13 Araujo AQC, Wedemann D. HTLV-1 Associated Neurological Complex. What is Hidden below the Water?. AIDS Rev 2019; 21 (04) 211-217
  • 14 Kalil RS, Vasconcellos I, Rosadas C. et al. Association between high proviral load, cognitive impairment, and white matter brain lesions in HTLV-1-infected individuals. J Neurovirol 2021; 27 (06) 810-819
  • 15 Bangham CRM, Araujo A, Yamano Y, Taylor GP. HTLV-1-associated myelopathy/tropical spastic paraparesis. Nat Rev Dis Primers 2015; 1: 15012
  • 16 Macêdo MC, Baptista AF, Galvão-Castro B. et al. IMPACT OF POSTURAL DEVIATION ON QUALITY OF LIFE AMONG PATIENTS WITH HAM/TSP. Revista Brasileira de Neurologia e Psiquiatria. 2013; 7 (02) 54-67
  • 17 Coutinho Ide J, Galvão-Castro B, Lima J, Castello C, Eiter D, Grassi MFR. Impact of HTLV-associated myelopathy/T tropical spastic paraparesis (HAM/TSP) on activities of daily living (ADL) in HTLV-1 infected patients. Acta Fisiátrica 2011;18(01) Disponível em: https://www.revistas.usp.br/actafisiatrica/article/view/103458
  • 18 Rocha-Santos I, Boa-Sorte N, Rios Grassi MF, Couto de Sá C, Araújo TH, Galvão Castro B. Using a new tool to evaluate the functional capacity of patients with HTLV-1 associated myelopathy/Tropical spastic paraparesis (HAM/TSP). BJMHH 2017; 5 (04) 176-182 Disponível em: http://10.71.50.111/index.php/medicine/article/view/1694
  • 19 Fonseca EPD, Sá KN, Nunes RFR, Ribeiro Junior AC, Lira SFB, Pinto EB. Balance, functional mobility, and fall occurrence in patients with human T-cell lymphotropic virus type-1-associated myelopathy/tropical spastic paraparesis: a cross-sectional study. Rev Soc Bras Med Trop 2018; 51 (02) 162-167
  • 20 Santos IR, Grassi MF, Boa-Sorte N, Kruschewsky Rde A, Galvão-Castro B. Assessment of functional capacity and flexibility of patients infected with HTLV-1. Retrovirology 2015; 12: P39 S1, 1742–4690–12–S1-P397 Disponível em: https://retrovirology.biomedcentral.com/articles/10.1186/1742-4690-12-S1-P39
  • 21 Achour JA. ALONGAMENTO E FLEXIBILIDADE: DEFINIÇÕES E CONTRAPOSIÇÕES. Rev Bras Ativ Fís Saúde 2007;12(01) Disponível em: https://www.rbafs.org.br/RBAFS/article/view/806
  • 22 Wells KF, Dillon EK. The Sit and Reach—A Test of Back and Leg Flexibility. Research Quarterly American Association for Health. Physical Education and Recreation. 1952; 23 (01) 115-118 Disponível em: https://www.tandfonline.com/doi/full/10.1080/10671188.1952.10761965
  • 23 Petreça DR, Benedetti TRB, Silva DAS. Validação do teste de flexibilidade da AAHPERD para idosos brasileiros. Rev Bras Cineantropom Desempenho Hum 2011; 13 (06) 455-460 DOI: 10.5007/1980-0037.2011v13n6p455. . Disponível em: http://www.periodicos.ufsc.br/index.php/rbcdh/article/view/17165
  • 24 Gouveia Vde O, Araújo Ade F, Maciel Sdos S, Ferreira Jde A, Santos Hdos. Reliability of the measures inter and intra-evaluators with universal goniometer and fleximeter. Fisioter Pesqui 2014; 21 (03) 229-235
  • 25 Florêncio LL, Pereira PA, Silva ERT, Pegoretti KS, Gonçalves MC, Bevilaqua-Grossi D. Agreement and reliability of two non-invasive methods for assessing cervical range of motion among young adults. Rev Bras Fisioter 2010; 14 (02) 175-181
  • 26 DANTAS EH. Alongamento e flexionamento. 5° ed. Shape; 2005
  • 27 Boyd BS, Villa PS. Normal inter-limb differences during the straight leg raise neurodynamic test: a cross sectional study. BMC Musculoskelet Disord 2012; 13: 245
  • 28 Galvão-Castro B, Rios Grassi MF, Nunes A. et al. Challenges in establishing telehealth care during the COVID-19 pandemic in a neglected HTLV-1-infected population in northeastern Brazil. PLoS Negl Trop Dis 2020; 14 (12) e0008922
  • 29 De Castro-Costa CM, Araújo AQC, Barreto MM. et al. Proposal for diagnostic criteria of tropical spastic paraparesis/HTLV-I-associated myelopathy (TSP/HAM). AIDS Res Hum Retroviruses 2006; 22 (10) 931-935
  • 30 Kurtzke JF. Rating neurologic impairment in multiple sclerosis: an expanded disability status scale (EDSS). Neurology 1983; 33 (11) 1444-1452
  • 31 OSAME M. Review of WHO Kagoshima meeting and diagnostic guidelines for HAM/TSP. In Blattner W. (Ed). Human retrovirology: HTLV, 1st Ed. New York: Raven Press; 1990: 191-197
  • 32 Caskey MF, Morgan DJ, Porto AF. et al. Clinical manifestations associated with HTLV type I infection: a cross-sectional study. AIDS Res Hum Retroviruses 2007; 23 (03) 365-371
  • 33 Tan G, Jensen MP, Thornby JI, Shanti BF. Validation of the Brief Pain Inventory for chronic nonmalignant pain. J Pain 2004; 5 (02) 133-137
  • 34 Ferreira KA, Teixeira MJ, Mendonza TR, Cleeland CS. Validation of brief pain inventory to Brazilian patients with pain. Support Care Cancer 2011; 19 (04) 505-511
  • 35 Craig CL, Marshall AL, Sjöström M. et al. International physical activity questionnaire: 12-country reliability and validity. Med Sci Sports Exerc 2003; 35 (08) 1381-1395
  • 36 Frey M, Poynter A, Younge K, De Carvalho D. The relationship between lumbopelvic flexibility and sitting posture in adult women. J Biomech 2019; 84: 204-210
  • 37 Monteiro Gde A. Avaliação da Flexibilidade Utilizando o Flexímetro Sanny. 1° ed.. Sanny; 2000
  • 38 Franzoi AC, Araújo AQC. Disability and determinants of gait performance in tropical spastic paraparesis/HTLV-I associated myelopathy (HAM/TSP). Spinal Cord 2007; 45 (01) 64-68
  • 39 Caiafa RC, Orsini M, Felicio LR, Puccioni-Sohler M. Muscular weakness represents the main limiting factor of walk, functional independence and quality of life of myelopathy patients associated to HTLV-1. Arq Neuropsiquiatr 2016; 74 (04) 280-286
  • 40 Costa KHA, Silva TBDV, Souza GDS, Barbosa RFM. Influence of proprioceptive neuromuscular facilitation on the muscle tonus and amplitude of movement in HTLV-1-infected patients with HAM/TSP. Rev Soc Bras Med Trop 2018; 51 (04) 550-553 http://www.scielo.br/scielo.php?script=sci_arttext&pid=S0037-86822018000400550&lng=en&tlng=en
  • 41 Caron O. Effects of local fatigue of the lower limbs on postural control and postural stability in standing posture. Neurosci Lett 2003; 340 (02) 83-86 https://linkinghub.elsevier.com/retrieve/pii/S0304394002014556
  • 42 Melo Filho J, Eduardo FMC, Moser de ADL. Estabilização lombo-pélvica: evidências em avaliação e tratamento. 12 (06) 472-481
  • 43 Campbell WW, DeJong RN. DeJong's the neurologic examination: William W. Campbell. 7th ed.. Philadelphia, PA: Lippincott Williams & Wilkins; 2013: 819
  • 44 Tanajura D, Castro N, Oliveira P. et al. Neurological Manifestations in Human T-Cell Lymphotropic Virus Type 1 (HTLV-1)-Infected Individuals Without HTLV-1-Associated Myelopathy/Tropical Spastic Paraparesis: A Longitudinal Cohort Study. Clin Infect Dis 2015; 61 (01) 49-56
  • 45 Araújo Patrício N, Carvalho de Macêdo M, Carneiro Landim Machado C, De Sousa Mota R, Fontes Baptista A, Nunes Sá K. CORRELATION BETWEEN PAIN AND POSTURAL DEVIATION IN INDIVIDUALS WITH HTLV-1. RPF 2016;6(02) Disponível em: https://www5.bahiana.edu.br/index.php/fisioterapia/article/view/917
  • 46 Macêdo MC, Mota Rde S, Patrício NA. et al. Quality of life and pain multidimensional aspects in individuals with HTLV-1. Braz J Infect Dis 2016; 20 (05) 494-498 https://linkinghub.elsevier.com/retrieve/pii/S1413867016301155
  • 47 San-Martin DL, Santos DND, Baptista AF. Pain Study Group. Pain prevalence, characteristics and associated factors in human T-cell lymphotropic virus type 1 infected patients: a systematic review of the literature. Braz J Infect Dis 2016; 20 (06) 592-598
  • 48 Mota RS, Macêdo MC, Corradini S, Patrício NA, Baptista AF, Sá KN. The effect of home exercise on the posture and mobility of people with HAM/TSP: a randomized clinical trial. Arq Neuropsiquiatr 2020; 78 (03) 149-157