The Impact of Obesity, Cardiovascular Diseases and Diabetes on Labor Market Participation and Productivity

肥胖、心血管疾病和糖尿病对劳动力市场参与度和生产力的影响

基本信息

项目摘要

Worldwide obesity has nearly tripled since 1975. Although estimates suggest heritability of obesity of more than 60 percent, the evolving human phenotype cannot be explained by a changing genotype because it occurred too rapidly. The prevailing explanation for the obesity epidemic is thus gene-environment interaction. While genotypes are exogenously determined and fixed in the medium run, the individual response to a changing obesogenic environment (labor saving technology, price, availability, and energy content of food) is largely genetic. These observations are the inspiration for our study.The proposed research project consists of three work packages. The first work package focuses on empirically estimating the causal effect of obesity, diabetes, CVDs, and hypertension on employment, wages, and other labor market outcomes. We use genetic markers as instruments for the diseases and take gene-environment interaction into account by controlling for the duration of exposure to an increasingly obesogenic environment. We use genotyped data and labor market outcomes from a large panel of US American adults born between 1900 and 1958 obtained from the Health and Retirement Study (HRS) and combine it with genetic information obtained from genome-wide association studies.In work package 2, we investigate the association between obesity and the development of other health deficits in the course of human aging. We measure individual health by constructing a frailty index, which captures in one number the biological aging process defined as the intrinsic, cumulative, progressive, and deleterious loss of function. We use the same data sources and instrumental variable strategy as WP 1 to determine the impact of obesity on physiological aging. We then test whether and to which extent the impact of obesity on labor market outcomes is mediated through increasing frailty. In work package 3 we use the empirical findings to develop a new economic theory of obesity, which explains the evolution of body weight and its impact on health, aging, productivity, and labor supply. Specifically, we further develop the health deficit model, which uses the frailty index as measure of human health and aging. We also investigate the role of bounded rational behavior in form of imperfect self-control and time inconsistent decision making. We calibrate numerical versions of the model with the HRS data and the results from WP 1 and 2 and use these models for inferences on the behavioral changes that are elicited by changing food prices, medical progress, and policy interventions to curb the obesity epidemic.
自1975年以来,全球肥胖人数几乎增加了两倍。虽然估计表明肥胖的遗传率超过60%,但人类表型的演变不能用基因型的变化来解释,因为它发生得太快了。因此,对肥胖流行病的普遍解释是基因-环境相互作用。虽然基因型是外源性决定的,并在中期运行中固定,但个体对不断变化的致胖环境(节省劳动力的技术,价格,可用性和食物的能量含量)的反应在很大程度上是遗传的。这些观察是我们研究的灵感。拟议的研究项目包括三个工作包。第一个工作包的重点是经验估计肥胖,糖尿病,心血管疾病和高血压对就业,工资和其他劳动力市场结果的因果关系。我们使用遗传标记作为疾病的工具,并通过控制暴露于日益肥胖的环境的持续时间来考虑基因-环境相互作用。我们使用健康与退休研究(HRS)中出生于1900年至1958年的美国成年人的基因型数据和劳动力市场结果,并将其与全基因组关联研究中获得的遗传信息联合收割机结合起来,在工作包2中,我们调查了肥胖与人类衰老过程中其他健康缺陷发展之间的关联。我们通过构建一个脆弱指数来衡量个人健康,该指数将生物衰老过程定义为内在的,累积的,渐进的和有害的功能丧失。我们使用与WP 1相同的数据源和工具变量策略来确定肥胖对生理衰老的影响。然后,我们测试肥胖对劳动力市场结果的影响是否以及在多大程度上是通过增加虚弱来介导的。在工作包3中,我们使用实证研究结果开发了一种新的肥胖经济理论,该理论解释了体重的演变及其对健康,老龄化,生产力和劳动力供应的影响。具体来说,我们进一步发展的健康赤字模型,它使用的脆弱指数作为衡量人类健康和老龄化。我们还研究了有限理性行为在不完美自我控制和时间不一致决策中的作用。我们用HRS数据和WP 1和WP 2的结果校准了模型的数值版本,并使用这些模型来推断食品价格变化、医疗进步和政策干预引起的行为变化,以遏制肥胖流行。

项目成果

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Professor Dr. Holger Strulik其他文献

Professor Dr. Holger Strulik的其他文献

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{{ truncateString('Professor Dr. Holger Strulik', 18)}}的其他基金

The Socioeconomic Health Gradient and Rising Old-Age Inequality
社会经济健康梯度和日益加剧的老年不平等
  • 批准号:
    391587678
  • 财政年份:
    2018
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Optimal Health and Retirement Policy Under Biologically Founded Human Ageing
生物学上的人类衰老下的最佳健康和退休政策
  • 批准号:
    246097153
  • 财政年份:
    2014
  • 资助金额:
    --
  • 项目类别:
    Research Grants
Je ne regrette rien? Present-Bias and Time-Inconsistent Health and Retirement Decisions
我不后悔吗?
  • 批准号:
    470615848
  • 财政年份:
  • 资助金额:
    --
  • 项目类别:
    Research Grants

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GPR75 in obesity-driven cardiovascular and metabolic complications
GPR75 在肥胖引起的心血管和代谢并发症中的作用
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    2023
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Bayesian machine learning for complex missing data and causal inference with a focus on cardiovascular and obesity studies
用于复杂缺失数据和因果推理的贝叶斯机器学习,重点关注心血管和肥胖研究
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Maternal Obesity During Pregnancy: Translatable Programmed Cardiovascular Dysfunction in Offspring
孕期母亲肥胖:后代可转化的程序性心血管功能障碍
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    MR/V03362X/1
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    2022
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    --
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Development and validation of cardiovascular MRI techniques on a low-field, ultra-wide bore system to assess patients with severe obesity
在低场、超宽口径系统上开发和验证心血管 MRI 技术,以评估严重肥胖患者
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    10569549
  • 财政年份:
    2022
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    --
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Development and validation of cardiovascular MRI techniques on a low-field, ultra-wide bore system to assess patients with severe obesity
在低场、超宽孔径系统上开发和验证心血管 MRI 技术,以评估严重肥胖患者
  • 批准号:
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A novel role for endothelial mineralocorticoid receptors in obesity-associated cardiovascular disease in females
内皮盐皮质激素受体在女性肥胖相关心血管疾病中的新作用
  • 批准号:
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  • 财政年份:
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A novel role for endothelial mineralocorticoid receptors in obesity-associated cardiovascular disease in females
内皮盐皮质激素受体在女性肥胖相关心血管疾病中的新作用
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A novel role for endothelial mineralocorticoid receptors in obesity-associated cardiovascular disease in females
内皮盐皮质激素受体在女性肥胖相关心血管疾病中的新作用
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    10654762
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Obesity Prevention in Postpartum Women at High-Risk of Cardiovascular Disease
心血管疾病高危产后妇女的肥胖预防
  • 批准号:
    10676792
  • 财政年份:
    2020
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    --
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Aldosterone, the Mineralocorticoid Receptor, and Cardiovascular Disease in Obesity
醛固酮、盐皮质激素受体与肥胖症中的心血管疾病
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