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1.
Mult Scler ; 7(5): 340-4, 2001 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-11724451

RESUMO

This study deals with the assessment of quality of life and its main clinical and demographical determinants in a clinical series of 103 patients with multiple sclerosis (MS) (37 men; 66 women; mean age 44.89 years; mean disease duration 12.40 years; mean EDSS score 4.07). We used the MSQOL-54 inventory, a disease-specific instrument recently validated in an Italian population. Each patient underwent a complete clinical assessment, including that of disability status (Expanded Disability Status Scale), cognitive function (Mini Mental State Examination), depression (Hamilton Rating Scale for Depression) and fatigue (Fatigue Severity Scale). In terms of Pearson's correlations, there was a moderate inverse relationship between disability level and the MSQOL-54 physical composite score, and a moderate to strong inverse correlation between depression or fatigue severity and both the physical and mental composite scores. In a stepwise linear regression analysis, depression, fatigue and disability level were confirmed to be significant and independent predictors of quality of life. Quality of life instruments can help to provide a broader measure of the disease impact and to develop a care program tailored to the patient's needs.


Assuntos
Depressão/psicologia , Avaliação da Deficiência , Fadiga/psicologia , Esclerose Múltipla/psicologia , Qualidade de Vida , Adulto , Idoso , Depressão/etiologia , Pessoas com Deficiência/psicologia , Fadiga/etiologia , Feminino , Humanos , Modelos Lineares , Masculino , Pessoa de Meia-Idade , Esclerose Múltipla/complicações , Inquéritos e Questionários
2.
Blood ; 93(7): 2261-6, 1999 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-10090935

RESUMO

Combined factors V and VIII deficiency is an autosomal recessive bleeding disorder associated with plasma levels of coagulation factors V and VIII approximately 5% to 30% of normal. The disease gene was recently identified as the endoplasmic reticulum-Golgi intermediate compartment protein ERGIC-53 by positional cloning, with the detection of two founder mutations in 10 Jewish families. To identify mutations in additional families, the structure of the ERGIC-53 gene was determined by genomic polymerase chain reaction (PCR) and sequence analysis of bacterial artificial chromosome clones containing the ERGIC-53 gene. Nineteen additional families were analyzed by direct sequence analysis of the entire coding region and the intron/exon junctions. Seven novel mutations were identified in 10 families, with one additional family found to harbor one of the two previously described mutations. All of the identified mutations would be predicted to result in complete absence of functional ERGIC-53 protein. In 8 of 19 families, no mutation was identified. Genotyping data indicate that at least two of these families are not linked to the ERGIC-53 locus. Taken together, these results suggest that a significant subset of combined factors V and VIII deficiency is due to mutation in one or more additional genes.


Assuntos
Deficiência do Fator V/genética , Genes , Hemofilia A/genética , Lectinas de Ligação a Manose , Proteínas de Membrana/genética , Mutação , Substituição de Aminoácidos , Cromossomos Bacterianos , Clonagem Molecular , Análise Mutacional de DNA , Éxons/genética , Deficiência do Fator V/complicações , Deficiência do Fator V/etnologia , Feminino , Genes Recessivos , Heterogeneidade Genética , Ligação Genética , Genótipo , Haplótipos , Hemofilia A/complicações , Hemofilia A/etnologia , Humanos , Íntrons/genética , Judeus/genética , Masculino , Proteínas de Membrana/deficiência , Linhagem , Mutação Puntual , Reação em Cadeia da Polimerase , Deleção de Sequência
3.
J Lab Clin Med ; 129(4): 462-9, 1997 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-9104890

RESUMO

The aim of this study was to define the neurohumoral response associated with the renal hemodynamic perturbations induced by mental stress acting as an adrenergic stimulus. In 8 healthy women, the effects of mental stress were studied during four consecutive 30-minute periods (baseline, mental stress, recovery I, recovery II). Mental stress induced sympathetic activation as evidenced by increases in blood pressure, heart rate, and plasma norepinephrine level. Effective renal plasma flow (iodine 131-labeled hippurate clearance) decreased only during mental stress (-22%, p < 0.05 vs baseline); glomerular filtration rate (iodine 125-labeled iotalamate clearance) remained constant during the entire experiment; the filtration fraction increased significantly during mental stress and recovery I (+30% and +22%, respectively, p < 0.02 for both). Complex neuroendocrine responses were associated with the hemodynamic changes. Urinary excretion of endothelin-1 and 6-keto-PGF(1alpha) increased during mental stress (+53%, p < 0.01, and +20%, p < 0.01, respectively) and recovery I (+49% and +29%, respectively, p < 0.01 for both). Urinary cyclic guanosine monophosphate rose only during mental stress (+77%, p < 0.05), whereas excretion of PGE2 showed a stepwise increase throughout recovery I and II (+292%, p < 0.01, and +360%, p < 0.001, respectively). In conclusion, the present experiments demonstrate that renal hemodynamic response induced by mental stress is a complex reaction in which endothelin-1, prostaglandins, and presumably nitric oxide take part.


Assuntos
Adaptação Fisiológica , Endotelina-1/fisiologia , Rim/fisiopatologia , Prostaglandinas/fisiologia , Estresse Psicológico/fisiopatologia , Adulto , Feminino , Humanos
7.
Curr Genet ; 18(2): 167-8, 1990 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-1977527

RESUMO

We studied two polymorphic forms of mtDNA extracted from A. lixula eggs. In order to compare and to quantitate the variability, we sequenced specific regions of the two molecules. In this way, we obtained a precise measurement of the variability within two haplotypes. We also obtained a direct demonstration that some differences in nucleotide sequence can escape detection when restriction endonuclease analysis is used. Our results underline the unreliability of the use of restriction mapping to estimate divergence between relatively short and closely related DNA sequences.


Assuntos
Enzimas de Restrição do DNA/metabolismo , DNA Mitocondrial/genética , Variação Genética , Polimorfismo de Fragmento de Restrição , Ouriços-do-Mar/genética , Animais , Sequência de Bases , DNA Mitocondrial/metabolismo , Haplótipos , Mapeamento por Restrição
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