Robert J Huang, Vidhya Balasubramanian, Miranda V Shum, Hanlee P Ji, Joo Ha Hwang
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Individual race and ethnicity were not available for this analysis.</p><p><strong>Findings: </strong>We analyzed data on 107,835 individuals and recorded 355,591 person-years (p-y) of follow-up. The crude overall incidence of NCGC was 98 per 100,000 p-y. In the fully-adjusted multivariable proportional hazards model, age ≥ 50 (HR 2.20, 95% CI 1.44-3.36), anemia (HR 5.09, 95% CI 3.46-7.50), former or current smoking (HR 1.42, 95% CI 1.11-1.81) and family history (HR 1.44, 95% CI 1.05-1.99) were individual-level factors associated with increased risk.</p><p><strong>Conclusions: </strong>We present one of the first estimates of NCGC risk following CAG diagnosis in an American population, and highlight risk factors for cancer progression. 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引用次数: 0
摘要
背景:慢性萎缩性胃炎(CAG)是一种易发生非贲门性胃癌(NCGC)的胃粘膜癌前病变。在美国,诊断为CAG后发生NCGC的风险尚未得到明确的描述。方法:我们使用商业索赔数据库(Marketscan, Merative LP),覆盖了超过1.5亿18-64岁的私人保险美国人,以创建诊断为CAG的个体队列。然后我们跟踪这些人的NCGC发展或他们最后一次临床就诊的时间。通过行政编码模式捕获人口统计学和临床特征,并将其与大都市统计区域的社会经济地位措施联系起来。个体种族和民族无法用于该分析。研究结果:我们分析了107,835人的数据,记录了355,591人年(p-y)的随访。NCGC的粗总发病率为98 / 100,000 p-y。在完全调整的多变量比例风险模型中,年龄≥50岁(HR 2.20, 95% CI 1.44-3.36)、贫血(HR 5.09, 95% CI 3.46-7.50)、曾经或现在吸烟(HR 1.42, 95% CI 1.11-1.81)和家族史(HR 1.44, 95% CI 1.05-1.99)是与风险增加相关的个人水平因素。结论:我们提出了美国人群中CAG诊断后NCGC风险的首次估计之一,并强调了癌症进展的危险因素。这些数据可能有助于指导美国未来的风险预防策略,如内窥镜监测。
Incidence of non-cardia gastric cancer among commercially-insured individuals aged 18-64 with chronic atrophic gastritis.
Background: Chronic atrophic gastritis (CAG) is a precancerous condition of the gastric mucosa which predisposes to non-cardia gastric cancer (NCGC). The risk for NCGC following diagnosis with CAG has not been described robustly in the United States.
Methods: We used a commercial claims database (Marketscan, Merative LP) covering over 150 million privately-insured Americans aged 18-64 to create a cohort of individuals diagnosed with CAG. We then followed these individuals for the development of NCGC or to the time of their last clinical encounter. Demographic and clinical characteristics were captured through administrative coding schema, and linked to metropolitan statistical area measures of socioeconomic status. Individual race and ethnicity were not available for this analysis.
Findings: We analyzed data on 107,835 individuals and recorded 355,591 person-years (p-y) of follow-up. The crude overall incidence of NCGC was 98 per 100,000 p-y. In the fully-adjusted multivariable proportional hazards model, age ≥ 50 (HR 2.20, 95% CI 1.44-3.36), anemia (HR 5.09, 95% CI 3.46-7.50), former or current smoking (HR 1.42, 95% CI 1.11-1.81) and family history (HR 1.44, 95% CI 1.05-1.99) were individual-level factors associated with increased risk.
Conclusions: We present one of the first estimates of NCGC risk following CAG diagnosis in an American population, and highlight risk factors for cancer progression. These data may help to guide future risk prevention strategies, such as endoscopic surveillance, in the United States.
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