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Dive into the research topics where Alexandre Silva de Mello is active.

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Featured researches published by Alexandre Silva de Mello.


American Journal of Medical Genetics Part A | 2005

Application of a comprehensive protocol for the identification of gaucher disease in Brazil

Kristiane Michelin; Alessandro Wajner; Fernanda Siqueira Souza; Alexandre Silva de Mello; Maira Graeff Burin; Maria Luiza Saraiva Pereira; Ricardo Flores Pires; Roberto Giugliani; Janice Carneiro Coelho

Gaucher disease (GD) is a sphingolipidosis caused by a genetic defect that leads to glucocerebrosidase (β‐glucosidase) deficiency. Between January 1982 and October 2003, 1,081 blood samples from patients suspected of having GD were referred for biochemical analysis. The activities of the enzymes β‐glucosidase (β‐glu) and chitotriosidase (CT) were measured in these samples. Among the 412 diagnosed cases of GD (38.1%), the great majority were GD type 1. The Brazilian regions with the greatest concentration of these patients were the Southeast, South, and Northeast. The mean age of patients at diagnosis was 19 years. The activity of β‐glu in patients with GD was, on average, 10.7% of that of normal individuals. CT was, on average, 269 times more elevated in this group of patients. Among the 669 cases with no confirmation of GD, there were patients with Niemann–Pick disease types A, B, or C (44 cases), possible heterozygotes for GD (59 cases), patients with other lysosomal storage diseases (LSDs) (19 cases) or with other inborn errors of metabolism (3 cases). In 508 cases, no metabolic disorder was found. This study shows that the biochemical protocol employed was effective for the detection of GD, a disease that is reasonably frequent in Brazil.


Gene | 2014

Determination of the lysosomal hydrolase activity in blood collected on filter paper, an alternative to screen high risk populations.

Cristina Dickie de Castilhos; Jamila Mezzalira; Mariana Pereira de Souza Goldim; Vanessa Vitcoski Daitx; Cristina da Silva Garcia; Carla Vieira Andrade; Ana Carolina Breier; Jaqueline Cé; Alexandre Silva de Mello; Janice Carneiro Coelho

This study aimed to determine the enzymatic activity in dried blood samples collected on filter paper (DBS) for the diagnosis of the following diseases: Fabry, Pompe, Mucopolysaccharidosis type I (MPS I) and Mucopolysaccharosis type VI (MPS VI). DBS was used for high risk patientscreening, according to clinical suspicion. Plasma, leukocytes and cultured fibroblasts were used to confirm the diagnosis when necessary. Among the 529 DBS samples sent to the laboratory, 164 had abnormal results. Confirmatory materials of 73 individuals were rerouted. The frequency of diagnosis for lysosomal storage disorders was 5.9%. DBS is an alternative screening technique used in high risk populations, which should lead to earlier diagnosis for lysosomal storage disorders (LSDs), help patients get treatment sooner and improve the outcome of the disease.


Gene | 2012

Screening of high-risk Gaucher disease patients in Brazil using miniaturized dried blood spots and leukocyte techniques.

Mariana Pereira de Souza Goldim; Cristina da Silva Garcia; Cristina Dickie de Castilhos; Vanessa Vitcoski Daitx; Jamila Mezzalira; Ana Carolina Breier; Jaqueline Cé; Alexandre Silva de Mello; Carla Vieira Andrade; Nicole Sartori; Janice Carneiro Coelho

This study investigates the miniaturization of the screening technique using dried blood spots on filter paper (DBS) to measure GBA and CT activities, and GBA and β-galactosidase activities in leukocytes. 274 DBS from individuals with suspected GD were screened for 1.5 years. Of these, we confirmed the diagnosis in 13.5%. The miniaturization of the DBS and leukocyte techniques afforded to reduce costs and sample size appropriate for a reliable diagnosis.


American Journal of Medical Genetics Part A | 2003

Application of a protocol for the detection of disorders of sialic acid metabolism to 124 high-risk Brazilian patients

Cristina Dickie de Castilhos; Alexandre Silva de Mello; Maira Graeff Burin; Regis Rolim Guidobono; Silvane Gotardo; Roberto Giugliani; Janice Carneiro Coelho

Lysosomal storage disorders (LSD) present great clinical variability. Included in this group are sialic acid metabolism disorders (SAMD). In the present study, we describe the application of a 3‐step protocol for the diagnosis of SAMD, including (1) oligosaccharide and sialyloligosaccharide chromatography; (2) quantitative determination of sialic acid; and (3) measurement of neuraminidase activity. Application of our protocol to 124 individuals at risk for SAMD led to the diagnosis of five affected patients, two with type I sialidosis, one with type II sialidosis, and two with galactosialidosis. Due to its simplicity and efficiency, we propose the use of this protocol for the diagnostic evaluation of patients with suspected SAMD, which could be specially useful to non‐specialized laboratories and to services located in developing countries.


Genetics and Molecular Biology | 2004

Effect of amikacin, cephalothin, clindamycin and vancomycin on in vitro fibroblast growth

Fernanda Timm Seabra Souza; Alexandre Silva de Mello; Kristiane Michelin; Janice Carneiro Coelho

The effect of four antibiotics (amikacin, clindamycin, cephalothin and vancomycin) was investigated considering that bacterial infection in fibroblasts cultures is a very frequent event. The investigation included the effect of the antibiotics on fibroblast growth and on the activity of the enzyme glucocerebrosidase. The antibiotics were added to the fibroblast cultures and cell growth was evaluated by counting the number of cells and their viability. After cell harvesting, the enzyme activity and content of protein were measured. The results allowed us to conclude that none of the antibiotics affected the cellular number nor the cellular viability. The content of protein decreased when cephalothin and clindamycin were added to the cultures, and glucocerebrosidase was affected in the presence of amikacin. Vancomycin did not interfere with any of the parameters analyzed, so it was chosen to be used in cell cultures to prevent the contamination by gram positive bacteria.


Neuroscience Letters | 2017

Maternal consumption of high-fat diet and grape juice modulates global histone H4 acetylation levels in offspring hippocampus: A preliminary study

Luciana Kneib Gonçalves; Ivy Reichert Vital da Silva; Laura Reck Cechinel; Marina Rocha Frusciante; Alexandre Silva de Mello; Viviane Rostirola Elsner; Cláudia Funchal; Caroline Dani

This study aimed to investigate the impact of maternal consumption of a hyperlipid diet and grape juice on global histone H4 acetylation levels in the offsprinǵs hippocampus at different stages of development. During pregnancy and lactation of offspring, dams were divided into 4 groups: control diet (CD), high-fat diet (HFD), control diet and purple grape juice (PGJCD) and purple grape juice and high-fat diet (PGJHFD). Male Wistar rats were euthanized at 21days of age (PN21, adolescents) and at 50days of age (PN50, adults). The maternal consumption of grape juice increased global histone H4 acetylation levels in hippocampus of adolescents pups (PN21), an indicative of enhanced transcriptional activity and increased gene expression. On the other hand, the maternal high-fat diet diminished significantly this epigenetic marker in the adult phase (PN50), suggesting gene silencing. These preliminary findings demonstrated that the maternal choices are able to induce changes on histone H4 acetylation status in hippocampus of the offspring, which may modulate the expression of specific genes. Interestingly, this response occurs in an age and stimuli-dependent manner and strongly reinforce the importance of maternal choices during gestation.


Clinica Chimica Acta | 2004

Biochemical study on β-glucosidase in individuals with Gaucher's disease and normal subjects

Kristiane Michelin; Alessandro Wajner; Laureci da Silva Goulart; Ângela Fachel; Maria Luiza Saraiva Pereira; Alexandre Silva de Mello; Fernanda Siqueira Souza; Ricardo Flores Pires; Roberto Giugliani; Janice Carneiro Coelho


Lipids | 2015

U18666A Treatment Results in Cholesterol Accumulation, Reduced Na+, K+-ATPase Activity, and Increased Oxidative Stress in Rat Cortical Astrocytes

Daniela Copetti-Santos; Vitória da Costa Moraes; Dácio Franco Weiler; Alexandre Silva de Mello; Fernanda de Souza Machado; Jéssica Pereira Marinho; Cassiana Siebert; Janaína Kolling; Cláudia Funchal; Angela Terezinha de Souza Wyse; Janice Carneiro Coelho


Molecular and Cellular Biochemistry | 2014

LAMP2 as a marker of EBV-mediated B lymphocyte transformation in the study of lysosomal storage diseases

Alexandre Silva de Mello; Mariana Pereira de Souza Goldim; Jamila Mezzalira; Cristina da Silva Garcia; Vanessa Vitcoski Daitx; Cristina Dickie de Castilhos; Michelle S. Viegas; Otilia V. Vieira; Janice Carneiro Coelho


Archive | 2014

Comparação dos níveis de citocinas entre indivíduos saudáveis e portadores de mucopolissacaridose I e VI

Alexandre Silva de Mello; Jaqueline Cé; Ana Carolina Breier; Gilson Pires Dorneles; Bruna Krieger; Alessandra Peres; Janice Carneiro Coelho

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Janice Carneiro Coelho

Universidade Federal do Rio Grande do Sul

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Cristina Dickie de Castilhos

Universidade Federal do Rio Grande do Sul

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Kristiane Michelin

Universidade Federal do Rio Grande do Sul

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Maria Luiza Saraiva Pereira

Universidade Federal do Rio Grande do Sul

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Alexandre Pastoris Müller

Universidade Federal do Rio Grande do Sul

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Ana Carolina Breier

Universidade Federal do Rio Grande do Sul

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Carla Vieira Andrade

Universidade Federal do Rio Grande do Sul

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Cristina da Silva Garcia

Universidade Federal do Rio Grande do Sul

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Diogo Onofre Gomes de Souza

Universidade Federal do Rio Grande do Sul

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Franciele Rachel Provin

Universidade Federal do Rio Grande do Sul

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