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1.
Artigo em Inglês | IMSEAR | ID: sea-158369

RESUMO

Background & objectives: Schizophrenia, the debilitating neuropsychiatric disorder, is known to be heritable, involving complex genetic mechanisms. Several chromosomal regions associated with schizophrenia have been identified during the past; putative gene (s) in question, to be called the global signature for the pathophysiology of the disease, however, seems to evade us. The results obtained from the several population-wise association-non association studies have been diverse. we therefore, undertook the present study on Tamil speaking population in south India to examine the association between the single nucleotide polymorphisms (SNPs) at the serotonin receptor gene (5HT2A) and the occurrence of the disease. Methods: Blood samples collected from 266 cases and 272 controls were subjected to genotyping (PCR amplification of candidate SNPs, RFLP and sequencing). The data on the SNPs were subjected to statistical analysis for assessing the gene frequencies in both the cases and the controls. Results: The study revealed significant association between the genotypic frequencies of the serotonin receptor polymorphism and schizophrenia. SNP analysis revealed that the frequencies of GG (30%, rs6311) and CC genotypes (32%, rs6313), were higher in patients (P<0.05) than in controls. The study also showed presence of G and C alleles in patients. significant levels of linkage disequilibrium (LD) were found to exist between the genotype frequencies of rs6311 and rs6313. Interpretation & conclusions: This study indicated an association between the SNPs (rs6311 and rs6313) of the serotonin receptor 5HT2A and schizophrenia. HapMap analysis revealed that in its genotype distribution, the Tamil speaking population was different from several other populations across the world, signifying the importance of such ethnicity-based studies to improve our understanding of this complex disease.


Assuntos
Adulto , Feminino , Frequência do Gene , Estudos de Associação Genética , Predisposição Genética para Doença , Humanos , Índia , Desequilíbrio de Ligação , Masculino , Pessoa de Meia-Idade , Polimorfismo de Nucleotídeo Único , Receptor 5-HT2A de Serotonina/genética , Esquizofrenia/genética , Esquizofrenia/patologia , Serotonina/genética
2.
Artigo em Inglês | IMSEAR | ID: sea-125192

RESUMO

Tropical pancreatitis and fibrocalculous pancreatitic diabetes are usually considered two ends of the same disease although some studies suggest the likelihood of distinct entities. We report the occurrence of these two diseases in two siblings. The literature comparing the similarities and differences between them is briefly reviewed.


Assuntos
Adulto , Calcinose/complicações , Complicações do Diabetes/complicações , Humanos , Masculino , Pancreatite/etiologia
3.
Artigo em Inglês | IMSEAR | ID: sea-64545

RESUMO

Isolated cases and small series of acute pancreatitis complicating viral infections have been reported. However, data on the natural history of such patients are sparse. We report a series of five patients of acute pancreatitis complicating diverse viral infections. During follow-up ranging from 6 to 36 months, two of these five patients developed evidence of chronic pancreatitis.


Assuntos
Dor Abdominal/sangue , Doença Aguda , Adolescente , Adulto , Amilases/sangue , Doença Crônica , Progressão da Doença , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Pancreatite/sangue , Ultrassonografia , Viroses/complicações
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