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1.
Pharmacogenomics J ; 16(4): 352-6, 2016 08.
Artigo em Inglês | MEDLINE | ID: mdl-26323598

RESUMO

Antipsychotic-induced weight gain (AIWG) is a common side effect with a high genetic contribution. We reanalyzed genome-wide association study (GWAS) data from the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) selecting a refined subset of patients most suitable for AIWG studies. The final GWAS was conducted in N=189 individuals. The top polymorphisms were analyzed in a second cohort of N=86 patients. None of the single-nucleotide polymorphisms was significant at the genome-wide threshold of 5x10(-8). We observed interesting trends for rs9346455 (P=6.49x10(-6)) upstream of OGFRL1, the intergenic variants rs7336345 (P=1.31 × 10(-5)) and rs1012650 (P=1.47 × 10(-5)), and rs1059778 (P=1.49x10(-5)) in IBA57. In the second cohort, rs9346455 showed significant association with AIWG (P=0.005). The combined meta-analysis P-value for rs9346455 was 1.09 × 10(-7). Our reanalysis of the CATIE GWAS data revealed interesting new variants associated with AIWG. As the functional relevance of these polymorphisms is yet to be determined, further studies are needed.The Pharmacogenomics Journal advance online publication, 1 September 2015; doi:10.1038/tpj.2015.59.


Assuntos
Antipsicóticos/efeitos adversos , Variantes Farmacogenômicos/efeitos dos fármacos , Polimorfismo de Nucleotídeo Único , Esquizofrenia/tratamento farmacológico , Aumento de Peso/efeitos dos fármacos , Aumento de Peso/genética , Adulto , Proteínas de Transporte/genética , Europa (Continente) , Feminino , Estudo de Associação Genômica Ampla , Genótipo , Humanos , Masculino , Pessoa de Meia-Idade , Testes Farmacogenômicos , Fenótipo , Ensaios Clínicos Controlados Aleatórios como Assunto , Medição de Risco , Fatores de Risco , Estados Unidos
2.
Braz J Biol ; 75(2): 300-4, 2015 May.
Artigo em Inglês | MEDLINE | ID: mdl-26132011

RESUMO

Siparuna guianensis is a neotropical tree species, found both on edge and interior of forest fragments, mainly on understory and regeneration areas. The fruit are zoochorous with a sweet aril. This work aims to determine the bird species that eat the fruits of S. guianensis in a semi deciduous forest fragment in Brazilian Cerrado and measure which species have the highest potential as seed dispersers. Seven individuals of S. guianensis were sampled, totaling 69 hours. A hundred and fifty four visits were registered by seven species of birds. Antilophia galeata had the biggest potential as seed dispersal agent. Antilophia galeata, Lanio penicillatus and Dacnis cayana can be important seed dispersers, since they have a high consumption and visitation rate. The consumption of S. guianensis by species of different feeding guilds can be an important strategy for dispersal of plant species in regeneration habitats, raising the chances of an effective dispersal.


Assuntos
Aves/fisiologia , Comportamento Alimentar/fisiologia , Monimiaceae/crescimento & desenvolvimento , Dispersão de Sementes/fisiologia , Animais , Aves/classificação , Brasil , Monimiaceae/classificação
3.
Mol Psychiatry ; 18(4): 443-50, 2013 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-23459466

RESUMO

We examined the influence of the genome-wide significant schizophrenia risk variant rs1625579 near the microRNA (miRNA)-137 (MIR137) gene on well-established sources of phenotypic variability in schizophrenia: age-at-onset of psychosis and brain structure. We found that the MIR137 risk genotype strongly predicts an earlier age-at-onset of psychosis across four independently collected samples of patients with schizophrenia (n=510; F1,506=17.7, P=3.1 × 10(-5)). In an imaging-genetics subsample that included additional matched controls (n=213), patients with schizophrenia who had the MIR137 risk genotype had reduced white matter integrity (F3,209=13.6, P=3.88 × 10(-8)) throughout the brain as well as smaller hippocampi and larger lateral ventricles; the brain structure of patients who were carriers of the protective allele was no different from healthy control subjects on these neuroimaging measures. Our findings suggest that MIR137 substantially influences variation in phenotypes that are thought to have an important role in clinical outcome and treatment response. Finally, the possible consequences of genetic risk factors may be distinct in patients with schizophrenia compared with healthy controls.


Assuntos
Predisposição Genética para Doença/genética , MicroRNAs/genética , Esquizofrenia/genética , Psicologia do Esquizofrênico , Adulto , Idade de Início , Atrofia , Estudos de Casos e Controles , Feminino , Estudo de Associação Genômica Ampla , Hipocampo/patologia , Humanos , Hipertrofia , Ventrículos Laterais/patologia , Masculino , Fibras Nervosas Mielinizadas/patologia , Fenótipo , Polimorfismo de Nucleotídeo Único/genética , Transtornos Psicóticos/genética , Esquizofrenia/diagnóstico
4.
Genet Mol Res ; 6(2): 256-61, 2007 May 09.
Artigo em Inglês | MEDLINE | ID: mdl-17573655

RESUMO

We have previously shown evidence of strong sex-biased genetic blending in the founding and ongoing history of the Brazilian population, with the African and Amerindian contribution being highest from maternal lineages (as measured by mitochondrial DNA) and the European contribution foremost from paternal lineages (estimated from Y-chromosome haplogroups). The same phenomenon has been observed in several other Latin American countries, suggesting that it might constitute a universal characteristic of the Iberian colonization of the Americas. However, it has also recently been detected in the Black population of the United States. We thus wondered if the same could be observed in American Caucasians. To answer that question, we retrieved 1387 hypervariable I Caucasian mitochondrial DNA sequences from the FBI population database and established their haplogroups and continental geographical sources. In sharp contrast with the situation of the Caucasian population of Latin American countries, only 3.1% of the American Caucasian sequences had African and/or Amerindian origin. To explain this discrepancy we propose that the finding of elevated genomic contributions from European males and Amerindian or African females depends not only on the occurrence of directional mating, but also on the "racial" categorization of the children born from these relations. In this respect, social practices in Latin America and in the United States diverge considerably; in the former socially significant "races" are normally designated according to physical appearance, while in the latter descent appears to be the most important factor.


Assuntos
Negro ou Afro-Americano/genética , Fluxo Gênico , Caracteres Sexuais , População Branca/genética , Algoritmos , Brasil , Cromossomos Humanos Y , DNA Mitocondrial/genética , Bases de Dados de Ácidos Nucleicos , Feminino , Humanos , Masculino , Estados Unidos
5.
Genet. mol. res. (Online) ; 6(2): 256-261, 2007.
Artigo em Inglês | LILACS | ID: lil-482045

RESUMO

We have previously shown evidence of strong sex-biased genetic blending in the founding and ongoing history of the Brazilian population, with the African and Amerindian contribution being highest from maternal lineages (as measured by mitochondrial DNA) and the European contribution foremost from paternal lineages (estimated from Y-chromosome haplogroups). The same phenomenon has been observed in several other Latin American countries, suggesting that it might constitute a universal characteristic of the Iberian colonization of the Americas. However, it has also recently been detected in the Black population of the United States. We thus wondered if the same could be observed in American Caucasians. To answer that question, we retrieved 1387 hypervariable I Caucasian mitochondrial DNA sequences from the FBI population database and established their haplogroups and continental geographical sources. In sharp contrast with the situation of the Caucasian population of Latin American countries, only 3.1% of the American Caucasian sequences had African and/or Amerindian origin. To explain this discrepancy we propose that the finding of elevated genomic contributions from European males and Amerindian or African females depends not only on the occurrence of directional mating, but also on the [quot ]racial[quot ] categorization of the children born from these relations. In this respect, social practices in Latin America and in the United States diverge considerably; in the former socially significant [quot ]races[quot ] are normally designated according to physical appearance, while in the latter descent appears to be the most important factor.


Assuntos
Humanos , Masculino , Feminino , Negro ou Afro-Americano/genética , Caracteres Sexuais , Fluxo Gênico , População Branca/genética , Bases de Dados de Ácidos Nucleicos , Algoritmos , Brasil , Cromossomos Humanos Y , DNA Mitocondrial/genética , Estados Unidos
6.
J Pediatr (Rio J) ; 74(6): 467-72, 1998.
Artigo em Português | MEDLINE | ID: mdl-14685590

RESUMO

OBJECTIVES: To identify rubella prevalence in different ages and population groups and rubella susceptibility of pregnant and postpartum women according to age, number of children and spontaneous abortion. METHODS: Cross-sectional study of sero-survey type. Children and students were selected in day-care centers and schools distributed by health districts of Fortaleza. Pregnant and postpartum healthy women were recruited in two large maternity units and three antenatal clinics; individuals previously vaccinated and presenting chronic or acute diseases where excluded. Written consent was obtained from participants or their caretakers. Anti-rubella IgG qualitative detection was performed with an Elisa-sandwich assay. RESULTS: Mean age-specific sero-prevalence rates of 999 samples were: 2 to 5 years= 59% (136/231); 6 to 9 years= 47% (95/204); 10 to 19 years= 56% (243/432) and 20 to 39 years= 80% (106/132). The mean age of 187 pregnant and postpartum women was 23 years (10-39) with a sero-prevalence of 76% (142/187), where 62% sero-positives aged 15 to 19 and 83% aged 26 to 39 years. A higher sero-prevalence was related to womens age (p<0.001), history of spontaneous abortion (p= 0.03), and two or more children (p=0.01). CONCLUSIONS: The high sero-prevalence of rubella in preschool age children reflects the intense viral transmission in child-care centers. The high susceptibility in adolescents (45%), among whom pregnancy is common, emphasizes the need to introduce rubella vaccine early and keep high immunization coverages in youngsters in order to eradicate congenital rubella syndrome. Also, postpartum routine immunization against rubella in this age group is of particular benefit.

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