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1.
Neurocase ; 26(6): 364-367, 2020 12.
Artigo em Inglês | MEDLINE | ID: mdl-33125299

RESUMO

Frontotemporal dementia (FTD) is a heterogeneous syndrome characterized by the progressive damage of frontal and temporal brain regions. These networks largely overlap with those involved in pain and temperature processing. Although the impaired perception of pain and temperature has been previously described to be relatively common in patients with FTD, these symptoms are often not consistently assessed by Neurologists. We present the case of a patient with a probable behavioral variant FTD who died due to scalding with hot water in the shower. Impairments in the perception of pain and temperature might have played a fundamental role in this accident.


Assuntos
Queimaduras/etiologia , Demência Frontotemporal/complicações , Percepção da Dor , Transtornos da Percepção/etiologia , Sensação Térmica , Idoso , Evolução Fatal , Humanos , Masculino , Percepção da Dor/fisiologia , Transtornos da Percepção/complicações , Sensação Térmica/fisiologia
2.
Rev. esp. med. nucl. imagen mol. (Ed. impr.) ; 37(2): 87-93, mar.-abr. 2018. tab, ilus
Artigo em Espanhol | IBECS | ID: ibc-171452

RESUMO

Objetivo. El depósito cortical de amiloide, una seña de identidad de la enfermedad de Alzheimer, se ha observado en la hidrocefalia a presión normal (HPN). Nuestro objetivo fue comparar el patrón de retención de 11C-PIB PET/TC en pacientes con HPN y sujetos sanos. Material y métodos. Hemos comparado el patrón de retención de 11C-PIB en 13 casos de HPN seleccionados para cirugía derivativa con una población control normal. Las imágenes se analizaron visualmente y puntuaron de 1-4 (de ligera a muy alta retención de PIB) tanto en la sustancia gris como en la sustancia blanca (SB). La puntuación se analizó por separado en las regiones infra y supratentoriales de ambos grupos. Se emitió un informe clínico en términos de positivo, negativo o dudoso/equívoco. Resultados. Ocho 11C-PIB PET/TC se informaron como negativos, 3 positivos y 2 dudosos. Cinco de 13 pacientes mostraron al menos una región cortical con retención de PIB de intensidad mayor que la observada en el grupo control. En general, la retención de PIB en la SB de los pacientes con HPN tuvo puntuaciones menores que en el grupo control, mostrando una diferencia estadísticamente significativa en la SB infratentorial (92/104 vs. 54/56, p<0,05) y una tendencia a ser menor en las regiones supratentoriales (70/84 vs. 122/156; p=0,327), en particular en la región periventricular superior (25/28 vs. 40/52; p=0,134). Conclusiones. Los patrones de retención de 11C-PIB parecen ser diferentes en los pacientes con HPN comparados con sujetos normales. La retención de PIB en la SB de la HPN aparece menos intensa que en sujetos sanos y estos muestran un mayor grado de retención de PIB en las regiones corticales. Esto merece ser tomado en consideración (AU)


Objective. Cortical cerebral amyloid disease, a hallmark of Alzheimer's disease, has also been observed in idiopathic normal pressure hydrocephalus (iNPH). The aim of this study was to compare the 11C-PIB PET/CT retention pattern in iNPH patients and healthy subjects. Material and methods. A comparison was made of the 11C-PIB PET/CT retention pattern in 13 iNPH patients selected for surgical deviation, compared to a normal control population. Images were visually analyzed and scored for gray matter and white matter (WM) from 1 to 4 (slight to very high PIB retention). The scoring was analyzed in both groups separately for infra- and supra-tentorial regions. A comprehensive clinical report was presented in terms of positive, negative, or equivocal. Results. 11C-PIB PET/CT scan were reported as negative in 8, positive in 3, and equivocal in 2. Five of 13 patients showed at least one cortical area with PIB retention with an intensity higher than that observed in the control group. Overall, white matter (WM) PIB retention of iNPH scored lower than in the control group, showing a statistically significant difference in the infratentorial WM (92/104 vs 54/56; p<.05) and a tendency to be lower in the supratentorial regions (70/84 vs 122/156, p=.327), in particular in the upper periventricular region (25/28 vs 40/52; p=.134). Conclusions. The PIB retention pattern seems to be different in NPH, compared to normal subjects. PIB retention in WM of NPH appears less intense than in healthy subjects, and they show a higher degree of PIB retention in cortical regions. This deserves to be taken it into account (AU)


Assuntos
Humanos , Substância Cinzenta , Substância Branca , Hidrocefalia de Pressão Normal/diagnóstico por imagem , Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada/métodos , Doença de Alzheimer/diagnóstico por imagem , Amiloidose/diagnóstico por imagem
3.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-28869176

RESUMO

OBJECTIVE: Cortical cerebral amyloid disease, a hallmark of Alzheimer's disease, has also been observed in idiopathic normal pressure hydrocephalus (iNPH). The aim of this study was to compare the 11C-PIB PET/CT retention pattern in iNPH patients and healthy subjects. MATERIAL AND METHODS: A comparison was made of the 11C-PIB PET/CT retention pattern in 13 iNPH patients selected for surgical deviation, compared to a normal control population. Images were visually analyzed and scored for gray matter and white matter (WM) from 1 to 4 (slight to very high PIB retention). The scoring was analyzed in both groups separately for infra- and supra-tentorial regions. A comprehensive clinical report was presented in terms of positive, negative, or equivocal. RESULTS: 11C-PIB PET/CT scan were reported as negative in 8, positive in 3, and equivocal in 2. Five of 13 patients showed at least one cortical area with PIB retention with an intensity higher than that observed in the control group. Overall, white matter (WM) PIB retention of iNPH scored lower than in the control group, showing a statistically significant difference in the infratentorial WM (92/104 vs 54/56; p<.05) and a tendency to be lower in the supratentorial regions (70/84 vs 122/156, p=.327), in particular in the upper periventricular region (25/28 vs 40/52; p=.134). CONCLUSIONS: The PIB retention pattern seems to be different in NPH, compared to normal subjects. PIB retention in WM of NPH appears less intense than in healthy subjects, and they show a higher degree of PIB retention in cortical regions. This deserves to be taken it into account.


Assuntos
Compostos de Anilina/farmacocinética , Radioisótopos de Carbono/farmacocinética , Córtex Cerebral/diagnóstico por imagem , Substância Cinzenta/diagnóstico por imagem , Hidrocefalia de Pressão Normal/diagnóstico por imagem , Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada , Compostos Radiofarmacêuticos/farmacocinética , Tiazóis/farmacocinética , Substância Branca/diagnóstico por imagem , Idoso , Idoso de 80 Anos ou mais , Amiloide/análise , Córtex Cerebral/química , Córtex Cerebral/patologia , Feminino , Humanos , Hidrocefalia de Pressão Normal/patologia , Masculino , Pessoa de Meia-Idade , Especificidade de Órgãos
4.
Eur J Neurol ; 20(12): 1571-3, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-23398167

RESUMO

BACKGROUND AND PURPOSE: Common genetic variants (rs5848 and rs646776) have been reported as regulators of blood progranulin (GRN) levels in healthy individuals. METHODS: To assess the influence of rs5848 and rs646776 polymorphisms in both serum GRN level and risk for common neurodegenerative diseases, we studied 304 patients with Parkinson's disease (PD), 217 individuals with Alzheimer's disease, 131 subjects with mild cognitive impairment, and 126 controls. RESULTS: The mean concentration of GRN in the serum of patients with PD (319.6 ng/ml) was significantly lower than that of controls (371.5 ng/ml; P = 0.009), whereas there were no significant differences between other groups. Rs646776 minor allele carriers had lower serum GRN levels in each of the four subgroups. There was no correlation between rs5848 genotypes and serum GRN concentrations. Genotype frequencies of both polymorphisms did not differ between groups. CONCLUSION: Reduced circulating GRN levels might be associated with PD risk by pathogenic factors different from rs5848 and rs646776 polymorphisms.


Assuntos
Peptídeos e Proteínas de Sinalização Intercelular/sangue , Doença de Parkinson/sangue , Idoso , Idoso de 80 Anos ou mais , Feminino , Predisposição Genética para Doença , Genótipo , Humanos , Peptídeos e Proteínas de Sinalização Intercelular/genética , Masculino , Doença de Parkinson/genética , Polimorfismo de Nucleotídeo Único , Progranulinas
5.
J Neural Transm (Vienna) ; 120(5): 807-12, 2013 May.
Artigo em Inglês | MEDLINE | ID: mdl-23180304

RESUMO

Aside from APOE, the genetic factors that influence the progression from mild cognitive impairment (MCI) to Alzheimer's disease (AD) remain largely unknown. We assessed whether a genetic risk score (GRS), based on eight non-APOE genetic variants previously associated with AD risk in genome-wide association studies, is associated with either risk of conversion or with rapid progression from MCI to AD. Among 288 subjects with MCI, follow-up (mean 26.3 months) identified 118 MCI-converters to AD and 170 MCI-nonconverters. We genotyped ABCA7 rs3764650, BIN1 rs744373, CD2AP rs9296559, CLU rs1113600, CR1 rs1408077, MS4A4E rs670139, MS4A6A rs610932, and PICALM rs3851179. For each subject we calculated a cumulative GRS, defined as the number of risk alleles (range 0-16) with each allele weighted by the AD risk odds ratio. GRS was not associated with risk of conversion from MCI to AD. However, MCI-converters to AD harboring six or more risk alleles (second and third GRS tertiles) progressed twofold more rapidly to AD when compared with those with less than six risk alleles (first GRS tertile). Our GRS is a first step toward development of prediction models for conversion from MCI to AD that incorporate aggregate genetic factors.


Assuntos
Doença de Alzheimer/genética , Disfunção Cognitiva/genética , Predisposição Genética para Doença , Transportadores de Cassetes de Ligação de ATP/genética , Proteínas Adaptadoras de Transdução de Sinal/genética , Idoso , Idoso de 80 Anos ou mais , Doença de Alzheimer/complicações , Apolipoproteínas E/genética , Clusterina/genética , Disfunção Cognitiva/complicações , Progressão da Doença , Feminino , Seguimentos , Frequência do Gene , Estudos de Associação Genética , Estudo de Associação Genômica Ampla , Genótipo , Humanos , Masculino , Proteínas de Membrana/genética , Pessoa de Meia-Idade , Proteínas Monoméricas de Montagem de Clatrina/genética , Receptores de Complemento 3b/genética , Risco
13.
Med Cutan Ibero Lat Am ; 16(1): 43-9, 1988.
Artigo em Espanhol | MEDLINE | ID: mdl-2967409

RESUMO

We present herein our experience concerning the use of etretinate and methotrexate as concurrent therapies in three patients with severe psoriasis. On this regimen, rapid clearing of the psoriatic lesions has been achieved in all patients. The efficacy, safety, indications and dosage schedules for this combination therapy are discussed. No significant side effects have been observed in our patients. However, caution must be exercised in the use of this experimental combination regimen, which should only be used in severe psoriasis.


Assuntos
Dermatite Esfoliativa/tratamento farmacológico , Metotrexato/uso terapêutico , Psoríase/tratamento farmacológico , Adulto , Quimioterapia Combinada , Etretinato/uso terapêutico , Humanos , Masculino , Pessoa de Meia-Idade , Dermatopatias Vesiculobolhosas/tratamento farmacológico
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