Correlation between Genetic Variants and Polymorphism of Caveolin and Sudden Unexplained Death / 法医学杂志
Journal of Forensic Medicine
;
(6): 114-119, 2017.
Artículo
en Chino
| WPRIM
| ID: wpr-984912
ABSTRACT
OBJECTIVES@#To explore the genetic variation sites of caveolin (CAV) and their correlation with sudden unexplained death (SUD).@*METHODS@#The blood samples were collected from SUD group (71 cases), coronary artery disease (CAD) group (62 cases) and control group (60 cases), respectively. The genome DNA were extracted and sequencing was performed directly by amplifying gene coding region and exon-intron splicing region of CAV1 and CAV3 using PCR. The type of heritable variation of CVA was confirmed and statistical analysis was performed.@*RESULTS@#A total of 4 variation sites that maybe significative were identified in SUD group, and two were newfound which were CAV1: c.45C>T (T15T) and CAV1:c.512G>A (R171H), and two were SNP loci which were CAV1:c.246C>T (rs35242077) and CAV3:c.99C>T (rs1008642) and had significant difference (P<0.05) in allele and genotype frequencies between SUD and control groups. Forementioned variation sites were not found in CAD group.@*CONCLUSIONS@#The variants of CAV1 and CAV3 may be correlated with a part of SUD group.
Texto completo:
Disponible
Índice:
WPRIM (Pacífico Occidental)
Asunto principal:
Enfermedad de la Arteria Coronaria
/
Reacción en Cadena de la Polimerasa
/
Exones
/
Polimorfismo de Nucleótido Simple
/
Caveolinas
/
Muerte Súbita
/
Genotipo
Límite:
Humanos
/
Masculino
Idioma:
Chino
Revista:
Journal of Forensic Medicine
Año:
2017
Tipo del documento:
Artículo
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