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2016 ; 9
(ä): 5451-9
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Association between insulin-like growth factor-binding protein-3 polymorphism-202
A/C and the risk of prostate cancer: a meta-analysis
#MMPMID27660462
Qin Z
; Li X
; Tang J
; Jiang X
; Yu Y
; Wang C
; Xu W
; Hua Y
; Yu B
; Zhang W
Onco Targets Ther
2016[]; 9
(ä): 5451-9
PMID27660462
show ga
BACKGROUND: Some previous studies have investigated the relationship between
insulin-like growth factor-binding protein-3 polymorphism and prostate cancer
(PCa) susceptibility; however, the findings from those studies remain
inconsistent. Hence, the aim of this meta-analysis was to provide a more reliable
conclusion about such associations. METHODS: A meta-analysis based on twelve
studies was conducted, and 8,341 PCa cases and 7,734 controls were included in
this analysis. All relevant studies published till February 1, 2016, were
identified by searching the databases such as PubMed, EMBASE, and Web of Science.
Data were pooled by odds ratios (ORs) with 95% confidence intervals (CIs) in
order to assess the strength of such associations. Publication bias was evaluated
using Begg's funnel plots and Egger's regression test. RESULTS: Several articles
provided data only for particular genotypes; therefore, only dominant model
analyses were carried out for all of these studies. Initially, the results from
this analysis indicated that rs2854744 was not associated with PCa susceptibility
(OR=1.12, 95% CI=0.996-1.2). However, after excluding one study due to its
heterogeneity and publication bias, a significant relationship was detected
between rs2854744 and PCa risk (OR=1.10, 95% CI=1.03-1.17). When stratified by
genotyping method, significant results were detected only in the Sequenom method
group (OR=1.13, 95% CI=1.04-1.22). Moreover, the results from a subgroup analysis
that was conducted by using source of controls were significant only in the
population-based control group. CONCLUSION: This meta-analysis suggested that the
insulin-like growth factor-binding protein-3 polymorphism-202 A/C was associated
with PCa susceptibility.