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1.
PLoS Negl Trop Dis ; 14(12): e0008032, 2020 12.
Artigo em Inglês | MEDLINE | ID: mdl-33332366

RESUMO

Background Zika, dengue and chikungunya viruses (ZIKV, CHIKV and DENV) are temporally associated with neurological diseases, such as Guillain-Barré syndrome (GBS). Because these three arboviruses coexist in Mexico, the frequency and severity of GBS could theoretically increase. This study aims to determine the association between these arboviruses and GBS in a Mexican population and to establish the clinical characteristics of the patients, including the severity of the infection. A case-control study was conducted (2016/07/01-2018/06/30) in Instituto Mexicano del Seguro Social (Mexican Social Security Institute) hospitals, using serum and urine samples that were collected to determine exposure to ZIKV, DENV, CHIKV by RT-qPCR and serology (IgM). For the categorical variables analysis, Pearson's χ2 or Fisher exact tests were used, and the Mann-Whitney U test for continuous variables. To determine the association of GBS and viral infection diagnosis through laboratory and symptomatology before admission, we calculated the odds ratio (OR) and 95% confidence intervals (95%CI) using a 2x2 contingency table. A p-value ≤ 0.05 was considered as significant. Ninety-seven GBS cases and 184 controls were included. The association of GBS with ZIKV acute infection (OR, 8.04; 95% CI, 0.89-73.01, p = 0.047), as well as laboratory evidence of ZIKV infection (OR, 16.45; 95% CI, 2.03-133.56; p = 0.001) or Flavivirus (ZIKV and DENV) infection (OR, 6.35; 95% CI, 1.99-20.28; p = 0.001) was observed. Cases of GBS associated with ZIKV demonstrated a greater impairment of functional status and a higher percentage of mechanical ventilation. According to laboratory results, an association between ZIKV or ZIKV and DENV infection in patients with GBS was found. Cases of GBS associated with ZIKV exhibited a more severe clinical picture. Cases with co-infection were not found.


Assuntos
Febre de Chikungunya/complicações , Dengue/complicações , Síndrome de Guillain-Barré/etiologia , Infecção por Zika virus/complicações , Adulto , Estudos de Casos e Controles , Feminino , Síndrome de Guillain-Barré/epidemiologia , Humanos , Masculino , México/epidemiologia , Pessoa de Meia-Idade , Fatores de Risco , Adulto Jovem
2.
PLoS One ; 15(3): e0230132, 2020.
Artigo em Inglês | MEDLINE | ID: mdl-32214354

RESUMO

BACKGROUND: Beginning August 2017, we conducted a prospective case-control investigation in Monterrey, Mexico to assess the association between Zika virus (ZIKV) and Guillain-Barré syndrome (GBS). METHODS: For each of 50 GBS case-patients, we enrolled 2-3 afebrile controls (141 controls in total) matched by sex, age group, and presentation to same hospital within 7 days. RESULTS: PCR results for ZIKV in blood and/or urine were available on all subjects; serum ZIKV IgM antibody for 52% of case-patients and 80% of controls. Subjects were asked about antecedent illness in the two months prior to neurological onset (for case-patients) or interview (for controls). Laboratory evidence of ZIKV infection alone (PCR+ or IgM+) was not significantly different between case-patients and controls (OR: 1.26, 95% CI: 0.45-3.54) but antecedent symptomatic ZIKV infection [a typical ZIKV symptom (rash, joint pain, or conjunctivitis) plus laboratory evidence of ZIKV infection] was higher among case-patients (OR: 12.45, 95% CI: 1.45-106.64). GBS case-patients with laboratory evidence of ZIKV infection were significantly more likely to have had typical ZIKV symptoms than controls with laboratory evidence of ZIKV infection (OR: 17.5, 95% CI: 3.2-96.6). This association remained significant even when only GBS case-patients who were afebrile for 5 days before onset were included in the analysis, (OR 9.57 (95% CI: 1.07 to 85.35). CONCLUSIONS: During ZIKV epidemics, this study indicates that increases in GBS will occur primarily among those with antecedent symptomatic ZIKV.


Assuntos
Síndrome de Guillain-Barré , Infecção por Zika virus , Zika virus , Adolescente , Adulto , Idoso , Estudos de Casos e Controles , Criança , Pré-Escolar , Surtos de Doenças , Feminino , Síndrome de Guillain-Barré/complicações , Síndrome de Guillain-Barré/epidemiologia , Humanos , Masculino , México/epidemiologia , Pessoa de Meia-Idade , Estudos Prospectivos , Adulto Jovem , Infecção por Zika virus/sangue , Infecção por Zika virus/complicações , Infecção por Zika virus/epidemiologia , Infecção por Zika virus/urina
3.
Rev. invest. clín ; 47(5): 387-92, sept.-oct. 1995. tab
Artigo em Espanhol | LILACS | ID: lil-164472

RESUMO

La leucodistrofia metacromática (LDM) es una enfermedad degenerativa causada por la deficiencia de la enzima aril sulfatasa A (ASA), que puede cursar con síntomas psiquiátricos. El propósito de esta investigación fue determinar la prevalencia de la deficiencia de ASA en un grupo de 23 pacientes con esquizofrenia. El valor de la mediana del ASA sérica en ellos fue 53.2 nmol/mL/h (rango 3.3-152-5). Seis (26 por ciento) presentaban actividades baja del ASA sérica (< 27.5 nmol/mL/h que es el límite inferior observado en 29 controles normales). Cinco de ellos tenían historia clínica de delirio de grandez, alucinaciones auditivas, hospitalizaciones múltiples, respuesta pobre a los neurolépticos y potenciales evocados anormales. Es probable que los síntomas esquizofrénicos fueran secundarios a la deficiencia de la enzima. Los hallazgos de este estudio son de utilidad en la clínica ya que ASA puede ayudar a identificar casos de LDM en pacientes presumiblemente esquizofrénicos


Assuntos
Criança , Adulto , Pessoa de Meia-Idade , Humanos , Masculino , Feminino , Cerebrosídeo Sulfatase , Cerebrosídeo Sulfatase/sangue , Cerebrosídeo Sulfatase/urina , Leucodistrofia Metacromática/diagnóstico , Leucodistrofia Metacromática/fisiopatologia , Esquizofrenia/enzimologia
4.
Rev. méd. IMSS ; 33(4): 387-90, jul.-ago. 1995.
Artigo em Espanhol | LILACS | ID: lil-174164

RESUMO

La homocistinuria debida a la deficiencia de la cisatianina -ß-sintetasa es un error del metabolismo, el cual se trasmite en forma autosómica recesiva. Esta enfermedad se presenta con una frecuencia de uno por cada 160,000 a uno por cada 200,000 recién nacidos. Se asocia frecuentemente a enfermedades vasculares y raras veces a demencia. En este trabajo se presenta el caso clínico de un hombre de 27 años de edad. Así mismo se discute la relación de trastornos psiquiátricos


Assuntos
Adulto , Humanos , Masculino , Osteoporose/fisiopatologia , Paresia/fisiopatologia , Tomografia , Cistationina beta-Sintase/deficiência , Demência/complicações , Demência/diagnóstico , Homocistinúria/genética , Deficiências da Aprendizagem/fisiopatologia , Deficiência Intelectual/fisiopatologia , Erros Inatos do Metabolismo/fisiopatologia , Eletroencefalografia/métodos , Transtornos Psicóticos/fisiopatologia
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