首页> 外文期刊>Population health management >A Comparison of Disease Burden Between Twins and Control Pairs in Medicare: Quantification of Heredity's Role in Human Health
【24h】

A Comparison of Disease Burden Between Twins and Control Pairs in Medicare: Quantification of Heredity's Role in Human Health

机译:在医疗保险中,双胞胎和对照组之间的疾病负担比较:遗传在人类健康中的作用的量化

获取原文
获取原文并翻译 | 示例
       

摘要

To quantify heredity's effects on the burden of illness in the Medicare population, this study linked information between participants in a research twin registry to a comprehensive set of Medicare claims. To calculate disease categories, the authors used the Centers for Medicare & Medicaid Services Hierarchical Conditions Categories (HCC) model that was developed to risk adjust Medicare's capitation payments to private health care plans based on the health expenditure risk of their enrollees. Using the Medicare database, 2 sets of unrelated but demographically matched control pairs (MCPs) were generated, one specific for the monozygotic twin population and the second specific for the dizygotic twin population. The concordance and correlation rates of the 70 HCC categories for the 2 twin populations, in comparison to their corresponding MCP, was then calculated using Medicare claims data from 1991 through 2011. When indicated, HCCs for which there was a statistically significant difference between the twin and corresponding MCP control group were analyzed by calculating concordance and correlation rates of the International Classification of Diseases, Ninth Revision codes that compose the HCC. Findings reveal that monozygotic twins share 6.5% more HCC disease categories than their MCP while dizygotic twins share 3.8% more HCC disease categories than their MCP. Atrial fibrillation is a highly heritable disease category, a finding consistent with prior literature describing the heritability of the cardiac arrhythmias. These findings are consistent with qualitative assessments of heredity's role found in previous models of population health, and provide both novel methods and quantitative evidence to support future model development. (Population Health Management 2015;18:383-391)
机译:为了量化遗传对Medicare人群疾病负担的影响,本研究将双生子登记册中参与者之间的信息与一组全面的Medicare索赔联系起来。为了计算疾病类别,作者使用了Medicare和Medicaid Services分层条件中心(HCC)模型,该模型用于根据参保者的健康支出风险对Medicare的人头费进行风险调整以适应私人医疗计划。使用Medicare数据库,生成了两组不相关但在人口统计学上匹配的对照对(MCP),一组对单卵双胞胎种群特异性,另一组对双卵双胞胎种群特异性。然后,使用1991年至2011年的Medicare索赔数据,计算了两个双胞胎人群的70个HCC类别与其相应的MCP的一致性和相关率。当指出时,双胞胎之间的HCC在统计学上有显着差异通过计算组成HCC的《国际疾病分类》第九修订版的一致性和相关率来分析相应的MCP对照组。研究结果表明,单卵双胞胎比MCP多患6.5%的HCC疾病,而双卵双胞胎比MCP多患3.8%的HCC疾病。心房颤动是一种高度可遗传的疾病,这一发现与先前描述心律不齐的遗传性的文献一致。这些发现与在先前的人口健康模型中发现的遗传作用的定性评估是一致的,并提供了新颖的方法和定量证据来支持未来的模型开发。 (人口健康管理2015; 18:383-391)

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号