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Analysis of the associations among Helicobacter pylori infection adiponectin leptin and 10-year fracture risk using the fracture risk assessment tool: A cross-sectional community-based study

机译:使用骨折风险评估工具分析幽门螺杆菌感染脂联素瘦素和10年骨折风险之间的关联:一项基于社区的横断面研究

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摘要

Helicobacter pylori (H. pylori) infection may induce inflammatory cytokines or adipokines that influence bone turnover and bone fracture risk. This study aimed to evaluate the association among H. pylori infection, adipokines, and 10-year fracture risk using the Fracture Risk Assessment Tool scale. From August 2013 to February 2016, a community-based cohort was surveyed by Keelung Chang-Gung Memorial Hospital. Subjects were included if they were older than 40 years and not pregnant. All participants underwent a standardized questionnaire survey, physical examination, urea breath test, and blood tests. A total of 2,689 participants (1,792 women) were included in this cross-sectional study. In both sexes, participants with a high fracture risk were older and had higher adiponectin values than participants without a high fracture risk (mean age, female: 72.9 ± 5.6 vs. 55.8 ± 7.3 years, P < 0.0001; male: 78.9 ± 4.7 vs. 58.1 ± 8.9 years, P < 0.001) (adiponectin, female: 10.8 ± 6.3 vs. 8.7 ± 5.2 ng/ml, P < 0.001; male: 9.7 ± 6.1 vs. 5.5 ± 3.8 ng/ml, P < 0.001). Adiponectin was correlated with high fracture risk in both sexes, but H. pylori infection and leptin was not. In logistic regression analysis, adiponectin could not predict high fracture risk when adjusting the factor of body mass index (BMI) in men group. In conclusion, H. pylori infection and leptin could not predict 10-year fracture risk in either sex. Adiponectin was correlated with bone fracture risk in both sexes and the correlation might be from the influence of BMI.
机译:幽门螺杆菌(H. pylori)感染可能诱发炎症性细胞因子或脂肪因子,影响骨骼更新和骨折风险。本研究旨在使用骨折风险评估工具量表评估幽门螺杆菌感染,脂肪因子和10年骨折风险之间的关联。从2013年8月到2016年2月,基隆长庚纪念医院对一个社区队列进行了调查。如果受试者年龄大于40岁且未怀孕,则将其包括在内。所有参与者均接受了标准化问卷调查,身体检查,尿素呼气试验和血液检查。这项横断面研究总共包括2689名参与者(1792名女性)。在男女中,骨折风险高的参与者比没有骨折风险高的参与者年龄更大,脂联素值更高(平均年龄,女性:72.9±5.6 vs. 55.8±7.3岁,P <0.0001;男性:78.9±4.7 vs 58.1±8.9岁,P <0.001)(脂联素,女性:10.8±6.3 vs. 8.7±5.2 ng / ml,P <0.001;男性:9.7±6.1 vs. 5.5±3.8 ng / ml,P <0.001)。脂联素与高性别骨折风险相关,而幽门螺杆菌感染和瘦素则不相关。在逻辑回归分析中,当调整男性组的体重指数(BMI)因子时,脂联素不能预测高骨折风险。总之,幽门螺杆菌感染和瘦素不能预测任何性别的10年骨折风险。脂联素与两性骨折风险相关,可能与BMI的影响有关。

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