Rural Environment as a Risk Factor for the Age at Onset of Machado-Joseph Disease

被引:0
|
作者
Martins, Ana Carolina [1 ,2 ]
Furtado, Gabriel Vasata [2 ]
Pinheiro, Jordania Dos Santos [2 ,3 ]
Saraiva-Pereira, Maria Luiza [1 ,2 ,4 ,5 ]
Jardim, Laura Bannach [1 ,2 ,4 ,6 ]
机构
[1] Univ Fed Rio Grande do Sul, Programa Posgrad Genet & Biol Mol, Porto Alegre, Brazil
[2] Hosp Clin Porto Alegre, Ctr Pesquisa Clin & Expt, Porto Alegre, Brazil
[3] Univ Fed Rio Grande do Sul, Fac Farm, Porto Alegre, Brazil
[4] Hosp Clin Porto Alegre, Med Genet Serv, Rua Ramiro Barcelos 2350, BR-90035003 Porto Alegre, Brazil
[5] Univ Fed Rio Grande do Sul, Dept Bioquim, Porto Alegre, Brazil
[6] Univ Fed Rio Grande do Sul, Dept Med Interna, Porto Alegre, Brazil
来源
MOVEMENT DISORDERS CLINICAL PRACTICE | 2025年
关键词
Machado-Joseph disease; rural environment; demographic density; rural population; untreated well water; AMYOTROPHIC-LATERAL-SCLEROSIS;
D O I
10.1002/mdc3.14338
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Machado-Joseph disease (SCA3/MJD) is a neurodegenerative condition caused by a dominant expansion of a CAG repeat (CAGexp). Most of the variability in the age at onset of symptoms (AO) remains unexplained, and environmental influences were scarcely studied. Objective: The objective was to test if AO of SCA3/MJD carriers can be associated with markers of the rural environment, such as demographic density (DeD), proportion of rural population (PRP), and the consumption of untreated well water (CWW). Methods: Symptomatic subjects from Rio Grande do Sul, Brazil, diagnosed between 1999 and 2017, and living in the same municipalities where they were born, were included, provided their CAGexp and AO were available, and the residual AO (RAO) could be estimated. DeD, PRP, and CWW were obtained from the Brazilian Census of 2010. Participants were stratified in high versus low DeD, PRP, and CWW groups, and their RAOs were compared for a P < 0.05. Results: A total of 188 subjects were studied. The mean (SD) RAOs of subjects from low and high DeD groups were -1.90 (6.98) and -0.11 (6.20) (P = 0.046); from low and high PRP groups were -0.12 (6.20) and -1.90 (6.99) (P = 0.046); and from low and high CWW groups were -0.11 (6.04) and -1.89 (7.11) (P = 0.034). Conclusions: AO of SCA3/MJD carriers was earlier in groups related to rural life. Our evidence suggests the presence of a risk factor in the rural environment, for earlier onset of symptoms in SCA3/MJD.
引用
收藏
页数:7
相关论文
共 50 条
  • [31] Akathisia: An unusual movement disorder in Machado-Joseph disease
    Pedroso, Jose Luiz
    Braga-Neto, Pedro
    Felicio, Andre C.
    Barsottini, Orlando G. P.
    Jardim, Laura B.
    Saraiva-Pereira, Maria Luiza
    PARKINSONISM & RELATED DISORDERS, 2011, 17 (09) : 712 - 713
  • [32] Positron emission tomography (PET) in Machado-Joseph disease
    Taniwaki, T
    Sakai, T
    Kobayashi, T
    Kuwabara, Y
    Otsuka, M
    Ichiya, Y
    Masuda, K
    Goto, I
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 1997, 145 (01) : 63 - 67
  • [33] PROSPECTIVE STUDY OF PERIPHERAL NEUROPATHY IN MACHADO-JOSEPH DISEASE
    Franca, Marcondes C., Jr.
    D'Abreu, Anelyssa
    Nucci, Anamarli
    Cendes, Fernando
    Lopes-Cendes, Iscia
    MUSCLE & NERVE, 2009, 40 (06) : 1012 - 1018
  • [34] Cutaneous Sympathetic Dysfunction in Patients with Machado-Joseph Disease
    Yamanaka, Yoshitaka
    Asahina, Masato
    Akaogi, Yuichi
    Fujinuma, Yoshikatsu
    Katagiri, Akira
    Kanai, Kazuaki
    Kuwabara, Satoshi
    CEREBELLUM, 2012, 11 (04): : 1057 - 1060
  • [35] A Variant in Genes of the NPY System as Modifier Factor of Machado-Joseph Disease in the Chinese Population
    Ding, Dongxue
    Chen, Zhao
    Wang, Chunrong
    Tang, Xiang
    Zhang, Lulu
    Fang, Qi
    Qiu, Rong
    Jiang, Hong
    FRONTIERS IN AGING NEUROSCIENCE, 2022, 14
  • [36] Variation in DNA Repair System Gene as an Additional Modifier of Age at Onset in Spinocerebellar Ataxia Type 3/Machado-Joseph Disease
    Mergener, Rafaella
    Furtado, Gabriel Vasata
    de Mattos, Eduardo Preusser
    Leotti, Vanessa Bielefeldt
    Jardim, Laura Bannach
    Saraiva-Pereira, Maria Luiza
    NEUROMOLECULAR MEDICINE, 2020, 22 (01) : 133 - 138
  • [37] Compromised mitochondrial complex II in models of Machado-Joseph disease
    Laco, Mario N.
    Oliveira, Catarina R.
    Paulson, Henry L.
    Rego, A. Cristina
    BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE, 2012, 1822 (02): : 139 - 149
  • [38] Association between Machado-Joseph disease and oxidative stress biomarkers
    Pacheco, Laura Segabinazzi
    da Silveira, Aron Ferreira
    Trott, Alexis
    Houenou, Lucien J.
    Algarve, Thais Doeler
    Bello, Caroline
    Lenz, Adriano Flesch
    Manica-Cattani, Maria Fernanda
    Manica da Cruz, Ivana Beatrice
    MUTATION RESEARCH-GENETIC TOXICOLOGY AND ENVIRONMENTAL MUTAGENESIS, 2013, 757 (02) : 99 - 103
  • [39] Trehalose alleviates the phenotype of Machado-Joseph disease mouse models
    Santana, Magda M.
    Paixao, Susana
    Cunha-Santos, Janete
    Silva, Teresa Pereira
    Trevino-Garcia, Allyson
    Gaspar, Laetitia S.
    Nobrega, Clevio
    Nobre, Rui Jorge
    Cavadas, Claudia
    Greif, Hagar
    de Almeida, Luis Pereira
    JOURNAL OF TRANSLATIONAL MEDICINE, 2020, 18 (01)
  • [40] Beneficial effects of tandospirone on ataxia of a patient with Machado-Joseph disease
    Takei, A
    Honma, S
    Kawashima, A
    Yabe, I
    Fukazawa, T
    Hamada, K
    Hamada, T
    Tashiro, K
    PSYCHIATRY AND CLINICAL NEUROSCIENCES, 2002, 56 (02) : 181 - 185