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1.
Eur J Neurol ; 20(4): 697-703, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23279712

RESUMO

BACKGROUND AND PURPOSE: Recent multiple sclerosis (MS) prevalence studies classify Italy as a high-risk area without intra-regional latitude effect. OBJECTIVES: To determine MS prevalence in Verona, Italy, and frequency of myelin oligodendrocyte glycoprotein (MOG) gene G511C polymorphism and HLA-DRB1*15 locus in a sample of cases and healthy controls. METHODS: The study area population on the prevalence date (31 December 2001) was 253208 (133508 women, 119700 men). Multiple case sources were examined. Patients fulfilling McDonald's criteria (2001) were included. Crude, age- and sex-specific prevalence rates were computed. MOG G511C polymorphism and HLA-DRB1*15 were determined by standard methods. RESULTS: We identified 270 cases of MS yielding a crude prevalence rate of 106.6/100000 (95% CI: 94-120). Prevalence was higher in women (140.8/100000) than in men (68.5/100000). The age-adjusted prevalence rate standardized to the European population was 96.0/100000. MOG G511C polymorphism did not differ between cases and controls. HLA-DRB1*15 frequency was 58/155 (37%) in cases and 24/157 (15%) in controls (P<0.001). There was no HLA-DRB1*15 influence on susceptibility to other autoimmune disorders. CONCLUSIONS: The high MS prevalence in Verona confirms Italy as a high-risk area with a homogenous distribution across the country. HLA-DRB1*15 is a relevant MS susceptibility locus in the Italian population, possibly with little influence on the occurrence of concomitant autoimmune disorders.


Assuntos
Esclerose Múltipla/epidemiologia , Esclerose Múltipla/genética , Adolescente , Adulto , Fatores Etários , Idoso , Estudos de Casos e Controles , Feminino , Frequência do Gene , Cadeias HLA-DRB1/genética , Humanos , Itália/epidemiologia , Masculino , Pessoa de Meia-Idade , Glicoproteína Mielina-Oligodendrócito/genética , Reação em Cadeia da Polimerase , Polimorfismo de Nucleotídeo Único , Prevalência , Fatores Sexuais , Adulto Jovem
2.
Eur J Vasc Endovasc Surg ; 41(3): 358-63, 2011 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-21236709

RESUMO

OBJECTIVES: An inflammatory process following stroke in human brains and systemic inflammatory responses after stroke in humans have been reported by numerous investigators. The aim of the study was to investigate if genes involved in the cyclooxygenase 2 (COX-2) pathway are upregulated at peripheral level in patients after transient ischaemic attack (TIA) and stroke. DESIGN OF STUDY: Blood samples were obtained from two groups of patients undergoing carotid endarterectomy. The first group included 25 patients who presented TIA or ischaemic stroke. The second group included 35 patients who had an asymptomatic internal carotid artery stenosis. Total RNA was isolated and the expression of Toll-like Receptor 4 (TLR4), COX-2, membrane-associated Prostaglandin E synthase (mPGES-1), Prostaglandin E2 receptors (EP3 and EP4) was analysed by real time RT-PCR. RESULTS: Expression of COX-2 and TLR4 were significantly increased in symptomatic patients (p < 0.001). Correlation analysis showed that TLR4 expression significantly correlated with COX-2 expression (R = 0.65; p < 0.01) in ischaemic stroke patients. This correlation was not observed in TIA and asymptomatic patients. CONCLUSIONS: Our results suggest that the peripheral mechanism of inflammatory injury after stroke may be mediated by TLR4 through a COX-2-dependent pathway.


Assuntos
Isquemia Encefálica/genética , Estenose das Carótidas/genética , Ciclo-Oxigenase 2/genética , RNA/sangue , Acidente Vascular Cerebral/genética , Receptor 4 Toll-Like/genética , Idoso , Idoso de 80 Anos ou mais , Isquemia Encefálica/enzimologia , Isquemia Encefálica/imunologia , Estenose das Carótidas/enzimologia , Estenose das Carótidas/imunologia , Estenose das Carótidas/cirurgia , Endarterectomia das Carótidas , Feminino , Humanos , Oxirredutases Intramoleculares/genética , Ataque Isquêmico Transitório/enzimologia , Ataque Isquêmico Transitório/genética , Ataque Isquêmico Transitório/imunologia , Itália , Masculino , Pessoa de Meia-Idade , Prostaglandina-E Sintases , Receptores de Prostaglandina E Subtipo EP3/genética , Receptores de Prostaglandina E Subtipo EP4/genética , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Acidente Vascular Cerebral/enzimologia , Acidente Vascular Cerebral/imunologia , Regulação para Cima
3.
Hum Mutat ; 16(3): 271, 2000 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-10980539

RESUMO

The study describes the mutations causing adrenoleukodystrophy in seven Italian families. Four missense mutations leading to amino acid substitutions, two frameshift mutations leading to a premature termination signal, and a splicing mutation were identified. Mutations 2014C>T (P543L), 2053A>G (Q556A), 673-674insCC, and 1874+1G>A are described for the first time in this report. Mutations 1638C>T (R418W), 1588G>A(R401Q), and 1801-1802delAG are already known to be link to ALD.


Assuntos
Transportadores de Cassetes de Ligação de ATP/genética , Adrenoleucodistrofia/genética , Proteínas de Membrana/genética , Mutação/genética , Proteínas Repressoras , Proteínas de Saccharomyces cerevisiae , Membro 1 da Subfamília D de Transportadores de Cassetes de Ligação de ATP , Adrenoleucodistrofia/enzimologia , Adulto , Substituição de Aminoácidos/genética , Criança , Coenzima A Ligases/genética , Éxons/genética , Feminino , Mutação da Fase de Leitura/genética , Humanos , Masculino , Mutação de Sentido Incorreto/genética , Linhagem , Análise de Sequência de DNA
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