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Alcohol use is not a significant contributor to myelodysplastic syndromes

机译:酒精使用不是肌小肌骨质增强症的重要贡献者

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Purpose Myelodysplastic syndromes (MDS) are a class of clonal neoplastic disorders of largely unknown etiology, and published data remain inconclusive regarding the association between lifetime alcohol consumption and MDS risk. In these analyses, data from a population-based case-control study were used to investigate this association. Methods Eligible cases of MDS were identified through the Minnesota Cancer Reporting System; controls were matched by sex and age-decile. A central review process was used to confirm MDS diagnosis and classify subtypes. Unconditional and polytomous logistic regression were used to calculate odds ratios (OR) and 95% confidence intervals (CI). Kaplan-Meier curves were used to compare survival by category of lifetime alcohol consumption. Results In total, 398 cases of MDS and 698 controls were included. Alcohol consumption at 23-30, 31-49, and 50-65 years of age, recent consumption 1 year before diagnosis/interview, and lifetime consumption were not found to be significantly associated with MDS in males (OR range 0.63-0.99) or females (OR range 0.58-1.70). Analysis by MDS subtype further suggested there was not a significant association between recent alcohol consumption and odds of disease by subtype (OR range 0.39-1.13). Lifetime alcohol consumption was not significantly associated with survival after diagnosis of MDS Conclusions Previously reported associations between alcohol consumption and MDS risk were inconsistent. Results from our analyses by sex and disease subtype do not support alcohol as a significant contributor to risk of MDS.
机译:目的骨髓增生综合征(MDS)是一类基本上未知病因的克隆肿瘤障碍,并且公布的数据对于终身饮酒和MDS风险之间的关联仍然不确定。在这些分析中,来自群体的案例对照研究的数据用于调查该协会。方法通过明尼苏达癌症报告系统确定符合条件的MDS病例;对照对性和年龄减铁符合。中央审查过程用于确认MDS诊断和分类亚型。无条件和多种物质逻辑回归用于计算大量比率(或)和95%置信区间(CI)。 Kaplan-Meier曲线用于通过终身饮酒类别进行比较生存。结果总计398例MDS和698例控件。 23-30,31-49和50-65岁的酒精消费,近期消费1年诊断/面试前1年,并没有发现终身消费与男性中的MDS显着相关(或0.63-0.99)或女性(或0.58-1.70的范围)。 MDS亚型的分析进一步建议通过亚型(或0.39-1.13的疾病疾病的几率之间没有显着关联。终身酒精消耗与MDS结论之前报告的饮酒和MDS风险之间的关联术后的生存没有显着相关。通过性和疾病的分析结果,亚型不支持酒精作为MDS风险的重要贡献者。

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