sábado, 9 de enero de 2016

Screening of intracerebral hemorrhage associated allele combinations at different loci using a novel association analysis.

2015 Dec 24. pii: S0378-1119(15)01527-9. doi: 10.1016/j.gene.2015.12.031. [Epub ahead of print]

Screening of intracerebral hemorrhage associated allele combinations at different loci using a novel association analysis.
Liping Gai, et al. Gene 2015 12 (From HuGE Literature Finder)

Screening of intracerebral hemorrhage associated allele combinations at different loci using a novel association analysis.

Author information

Abstract

BACKGROUND:

Genetic research has progressed along with scientific and technological developments. However, it is difficult to identify frequency differences in the allele combination at cross-loci.

OBJECTIVE:

The purpose of this study was to examine the relationship between the presence of specific allele combinations of short tandem repeat (STR) loci and the onset of intracerebral hemorrhage (ICH) using a novel methodology.

METHODS:

DNA samples were collected from patients with ICH, who were adult population. There were a total of 51 Chinese patients (102 chromosomes), comprising 30 males and 21 females. Alleles from short tandem repeat (STR) loci were determined using the STR Profiler Plus PCR amplification kit (15 STR loci). Statistically significant differences between observed and expected frequencies of allele combinations were identified. To further determine allele combinations related to the disease, analyses of patient age at disease onset for those carrying a specific allele combination were conducted. Finally, cross-validation of the two sets of analytical results was carried out.

RESULTS:

A total of 1550 pairwise combinations were obtained by computer counting, of which eight pairs of alleles showed significant differences between the observed and expected frequencies (p< 0.05, from 0.006 to 0.042). The p value for the cross-validation analysis was less than 0.05 for two pairs of alleles (D13S317-11 and vWA-17, p=0.021; D7S820-13 and D2S1338-18, p=0.023).

CONCLUSIONS:

The study identified each population had a unique gene distribution and that distribution followed certain rules. ICH onset may be associated with this allele combinations (D13S317-11 and vWA-17; D7S820-13 and D2S1338-18). The new methodology used in this study could enable additional discoveries pertaining to the relationship between specific ICH allele combinations at different loci and the onset of complex diseases.