1.CXCL12 G801A polymorphism and cancer risk: An updated meta-analysis.
Dan MENG ; Yin-Xiang WU ; Vidhi HEERAH ; Shuang PENG ; Meng-di CHU ; Yong-Jian XU ; Wei-Ning XIONG ; Shu-Yun XU
Journal of Huazhong University of Science and Technology (Medical Sciences) 2015;35(3):319-326
Many studies have reported the relationship between CXCL12 G801A polymorphism and cancer risk, with conflicting results. In this study, we tried to clarify the possibility that this polymorphism may increase cancer risk by conducting an updated meta-analysis. PubMed and EMbase were searched for case-control studies regarding the association of the gene polymorphism and cancer risk. Data were extracted and odds ratios (ORs) with 95% confidence intervals (95% CIs) were used to assess the strength of the association. Heterogeneity among articles and publication bias was also assessed. Significantly increased risk for cancer was found (A vs. G: OR=1.26, 95% CI=1.13-1.40, P<0.01; AA+AG vs. GG: OR=1.33, 95% CI=1.16-1.52, P<0.01). In subgroup analysis, statistically elevated cancer risk was found in both Asian and Caucasian populations (for Asian, AA+AG vs. GG: OR=1.74, 95% CI=1.22-2.47, P<0.01; for Caucasian, AA+AG vs. GG: OR=1.24, 95% CI=1.09-1.42, P<0.01). Our result indicated that CXCL12 G801A polymorphism is a risk factor for cancer. To validate the finding, further large-size case-control studies are warranted.
Asian Continental Ancestry Group
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genetics
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Chemokine CXCL12
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genetics
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European Continental Ancestry Group
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genetics
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Genetic Predisposition to Disease
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Humans
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Neoplasms
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ethnology
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genetics
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pathology
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Odds Ratio
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Polymorphism, Single Nucleotide
2.Repeatability and Reproducibility of Quantitative Assessment of the Retinal Microvasculature Using Optical Coherence Tomography Angiography Based on Optical Microangiography.
Qi ZHAO ; Wen Li YANG ; Xiao Na WANG ; Ruikang K WANG ; Qi Sheng YOU ; Zhong Di CHU ; Chen XIN ; Meng Yu ZHANG ; Dong Jun LI ; Zi Yang WANG ; Wei CHEN ; Yi Feng LI ; Rui CUI ; Lin SHEN ; Wen Bin WEI
Biomedical and Environmental Sciences 2018;31(6):407-412
OBJECTIVEThe aim of this study was to determine the repeatability and reproducibility of optical coherence tomography angiography (OCTA) based on optical microangiography (OMAG) measurements of macular vessels in normal eyes.
METHODSIn this prospective cohort study, 40 eyes of 40 healthy volunteers underwent repeated OCTA (Cirrus HD-OCT 5000 angiography system, Carl Zeiss Meditec, Inc.) scans on two separate visit days. On each visit day, the eyes were scanned three times. The following parameters were used to quantitatively describe the OCTA images of the superficial vascular network: vessel area density (VAD), vessel skeleton density (VSD), vessel diameter index (VDI), vessel perimeter index (VPI), vessel complexity index (VCI), flux, and foveal avascular zone (FAZ). Coefficient of variation (CV) and intraclass correlation coefficient (ICC) were calculated for evaluating intravisit and intervisit repeatability, as well as interobserver reproducibility.
RESULTSThe measurements showed high repeatability [CVs ⪕ 4.2% (intravisit) and ⪕ 4.6% (intervisit)] and interobserver reproducibility (ICCs ⪖ 0.923) for all parameters.
CONCLUSIONThis study demonstrated good repeatability and reproducibility of OCTA based on OMAG for the measurement of superficial vessel parameters in normal eyes.
Adult ; Cohort Studies ; Evaluation Studies as Topic ; Female ; Fluorescein Angiography ; standards ; Healthy Volunteers ; Humans ; Image Processing, Computer-Assisted ; Male ; Microvessels ; diagnostic imaging ; Middle Aged ; Prospective Studies ; Reproducibility of Results ; Retina ; diagnostic imaging ; Retinal Vessels ; diagnostic imaging ; Tomography, Optical Coherence ; standards ; Young Adult