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Clin Biochem ; 32(6): 429-37, Aug. 1999.
Artigo em Inglês | MedCarib | ID: med-738

RESUMO

OBJECTIVES: We hypothesized that common variation in the angiotensinogen (AGT), beta-3-adrenergic receptor. intestinal fatty acid-binding protein, serum paraoxonase, paraoxonase-2, hepatic lipase, apolipoprotein E (APOE), and Werner helicase (WRN) genes would be associated with variation in biochemical phenotypes in a previously unstudied neonatal sample. DESIGN AND METHODS: We examined associations of both nongenetic and genetic variables with plasma lipoprotein traits in neonates from Trinidad. RESULTS: Among nongenetic variables, we found significant associations between plasma concentrations of 1.) lipoprotein (a) [Lp(a)] and both ethnicity (p=0.037) and birth weight (p=0.001); 2)total cholesterol and gender (p=0.010); 3)triglyceride and birth weight (p=0.035); and 4)apolipoprotein A1 and gender (p=0.016). Among genetic variables, we found that: 1)common variation on chromosome 1q in AGT codon 235 was significantly associated with variation in plasma apolipoproteins Al (p<0.0001); and 3)common variation in APOE at codons 112 and 158 was significantly associated with variation in plasma triglycerides (p=0.013). CONCLUSIONS: The associations with AGT and WRN are novel and may have resulted either from direct influence of the genetic variants or through linkage disequilibrium with other functional loci, such as the familial combined hyperlipidemia locus on chromosome 1q in the case of AGT. Despite the fact that there are some limitations in making determinations from cord blood, the results suggest that there may be genetic determinants of plasma lipoproteins in neonates. (AU)


Assuntos
Lactente , Feminino , Humanos , Masculino , Lipoproteínas/sangue , Lipoproteínas/genética , África , Alelos , Angiotensinogênio/genética , Apolipoproteínas E/genética , Ásia , Proteínas de Transporte/genética , DNA Helicases/genética , Esterases/sangue , Esterases/genética , Frequência do Gene , Genética Populacional , Lipase/genética , Proteína P2 de Mielina/genética , Fenótipo , Receptores Adrenérgicos beta/genética , Trinidad e Tobago/etnologia , Variação Genética
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