Global Burden of Diseases Dataset, Methodology and Its Use in Rheumatic and Musculoskeletal Diseases

IF 2.4 4区 医学 Q2 RHEUMATOLOGY
Shi-Hang Chen, Yuan Tang, Harry Asena Musonye, Hai-Feng Pan
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The Global Health Data Exchange (GHDx) platform [<span>12</span>] provided a directory of the GBD study input data sources. A detailed methodological information for various diseases, injuries, and risk factors can be found in GBD 2021 Methods Appendices (Table 1) [<span>13</span>]. A principle of GBD study was the comparability of research results. To achieve this, the GBD study employed a series of methods during data processing, including quality rating of studies, independent disease coding, and standardized data modeling analysis, to enhance consistency and comparability across different countries and data sources.</p><p>Data input methods for diseases and injuries were categorized into causes of deaths [<span>7</span>] and nonfatal health outcomes [<span>6</span>]. For the causes of death category, data primarily came from vital registration (VR) sources, accessed mainly through the World Health Organization mortality database. In countries with high-quality VR systems (characterized by high completeness and low rates of garbage coding), VR data typically served as the primary source of cause-of-death information. For specific diseases and in countries lacking complete VR systems, statistics were supplemented by additional data types. The data underwent processing, cleaning, and auditing. It was mapped to a unified GBD cause list, while disease-specific misclassification issues were addressed, miscellaneous codes reassigned, and noise reduced before being stored in the cause-of-death (CoD) database. The CODEm modeling method, specifically designed for GBD, was primarily adapted to estimate uncorrected mortality rates. This approach was supported by additional modeling techniques such as negative binomial models, natural history models, sub-cause proportion models, and prevalence-based models. These models accounted for the influence of covariates to obtain initial mortality estimates. 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Uncorrected deaths were estimated by using these covariates in the CODEm modeling approach, and adjusted mortality was then calculated using the CoDCorrect process [<span>13</span>].</p><p>For nonfatal outcomes, the GBD 2021 nonfatal estimation process outlined eight essential steps: [<span>6</span>] (1) data identification and extraction to compile sources (e.g., systematic reviews, survey data preparation, disease registries, and case notifications); (2) data adjustments (e.g., crosswalking, bias adjustment, network analysis, and age-sex splitting); (3) prevalence and incidence estimation using DisMod-MR 2.1 or alternative modeling strategies (e.g., ST-GPR modeling and MR-BRT meta-regression modeling); (4) injury estimation; (5) severity distribution; (6) incorporation of disability weights; (7) comorbidity adjustments; and (8) calculation of Years Lived with Disability (YLD) by sequelae and cause. 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Harry Asena Musonye: software development, investigation, visualization, validation, and writing – review and editing. Hai-Feng Pan: methodology, project administration, supervision, resources, funding acquisition, and writing – review and editing.</p><p>The authors declare that there are no conflicts of interest regarding the publication of this article. 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引用次数: 0

Abstract

The Global Burden of Disease (GBD) study has strictly adhered to the Guidelines for Accurate and Transparent Health Estimates Reporting [1, 2], which aims to assess global mortality and disability rates caused by major diseases, injuries, and risk factors [3]. Established in 1991, the study published its first results in 1993 [4]. The most recent update, released in May 2024, provided data spanning 1990 to 2021. With nearly 12 000 researchers from 163 countries and territories involved, [5] it has become the largest and most detailed scientific project to quantify health levels and trends worldwide [3].

The GBD study comprehensively evaluated various causes of death, injuries, risk factors, and health conditions, providing a critical basis for analyzing global population health and trends [2, 6-9]. It also helped the health sector identify overlooked health issues, reveal inequalities, predict dynamic trends, and guide policy formulation.

The GBD study covered 204 countries and territories, divided into 7 super-regions, 21 regions, and multiple custom regions, with one widely used being a five-level classification based on the Sociodemographic Index (SDI). The SDI, [6, 7] a geometric mean of the total fertility rate under age 25, mean years of education for those aged 15 and older, and lag-distributed income per capita, ranged from 0 to 1. It is divided into five categories: 0–0.47 for low SDI, 0.47–0.62 for low-middle SDI, 0.62–072 for middle SDI, 0.72–0.81 for high-middle SDI, and 0.81–1.00 for high SDI [10]. In addition, subnational analyses were conducted in 21 countries [6, 7].

A key feature of the GBD study was detailed age stratification, covering 51 age groups from birth to 95 years and older [8]. Age-standardized rates (ASRs) [11] were used to remove the influence of differing age structures between populations, ensuring more accurate comparisons of disease or mortality rates across populations.

The GBD study's data was sourced from hospitals, government agencies, surveys, and other databases worldwide. The Global Health Data Exchange (GHDx) platform [12] provided a directory of the GBD study input data sources. A detailed methodological information for various diseases, injuries, and risk factors can be found in GBD 2021 Methods Appendices (Table 1) [13]. A principle of GBD study was the comparability of research results. To achieve this, the GBD study employed a series of methods during data processing, including quality rating of studies, independent disease coding, and standardized data modeling analysis, to enhance consistency and comparability across different countries and data sources.

Data input methods for diseases and injuries were categorized into causes of deaths [7] and nonfatal health outcomes [6]. For the causes of death category, data primarily came from vital registration (VR) sources, accessed mainly through the World Health Organization mortality database. In countries with high-quality VR systems (characterized by high completeness and low rates of garbage coding), VR data typically served as the primary source of cause-of-death information. For specific diseases and in countries lacking complete VR systems, statistics were supplemented by additional data types. The data underwent processing, cleaning, and auditing. It was mapped to a unified GBD cause list, while disease-specific misclassification issues were addressed, miscellaneous codes reassigned, and noise reduced before being stored in the cause-of-death (CoD) database. The CODEm modeling method, specifically designed for GBD, was primarily adapted to estimate uncorrected mortality rates. This approach was supported by additional modeling techniques such as negative binomial models, natural history models, sub-cause proportion models, and prevalence-based models. These models accounted for the influence of covariates to obtain initial mortality estimates. The CoDCorrect process was then applied to align cause-of-death estimates with all-cause mortality estimates, producing corrected mortality rates. Years of Life Lost (YLL) were calculated by multiplying the number of deaths for each cause-age-sex-location-year combination by the standard life expectancy at each age.

Rheumatoid arthritis (RA) data sources included vital registration, verbal autopsy, and surveillance data, which, after standardization, ICD mapping, age-sex splitting, garbage code removal, and noise reduction, were stored in the CoD database. Covariates for modeling rheumatoid arthritis mortality included factors such as smoking, milk intake, healthcare quality index, alcohol consumption, mean BMI, mean cholesterol, education level, income, and the SDI. Uncorrected deaths were estimated by using these covariates in the CODEm modeling approach, and adjusted mortality was then calculated using the CoDCorrect process [13].

For nonfatal outcomes, the GBD 2021 nonfatal estimation process outlined eight essential steps: [6] (1) data identification and extraction to compile sources (e.g., systematic reviews, survey data preparation, disease registries, and case notifications); (2) data adjustments (e.g., crosswalking, bias adjustment, network analysis, and age-sex splitting); (3) prevalence and incidence estimation using DisMod-MR 2.1 or alternative modeling strategies (e.g., ST-GPR modeling and MR-BRT meta-regression modeling); (4) injury estimation; (5) severity distribution; (6) incorporation of disability weights; (7) comorbidity adjustments; and (8) calculation of Years Lived with Disability (YLD) by sequelae and cause. This series of analyses provided incidence, prevalence, and YLD for disease and injury sequelae. Adding YLL and YLD produced the DALYs [6]. Table 1 described the data input methodology for three common rheumatic diseases.

Data visualization enhanced the effectiveness of information delivery and promoted action in the policy making process [14]. The GBD study offered 52 powerful visualization tools that helped users gain deep insights into global health data. The GBD Results Tool allowed users to view and download global health estimates as CSV files. GBD Compare provided comprehensive analyses of how disease patterns had changed over time. GBD Foresight evaluated and predicted future scenarios from 2022 to 2050. More detailed information regarding GBD data visuals can be found on the Health Data Research and Analysis website (https://www.healthdata.org/interactive-data-visuals).

The GBD study not only provides reliable data and a transparent methodology, but also offers a variety of visualization tools. Despite some limitations in data sources and knowledge translation, the GBD study provides detailed estimates of the global disease burden, helping policymakers identify major health challenges, compare health disparities across demographics levels, evaluate the cost-effectiveness of interventions and address global health challenges collectively. In the coming years, GBD research has the potential to assess the global burden of disease more accurately, comprehensively, and realistically.

Shi-Hang Chen: conceptualization, data curation, visualization, validation, and writing – original draft. Yuan Tang: formal analysis, validation, resources, and writing – review and editing. Harry Asena Musonye: software development, investigation, visualization, validation, and writing – review and editing. Hai-Feng Pan: methodology, project administration, supervision, resources, funding acquisition, and writing – review and editing.

The authors declare that there are no conflicts of interest regarding the publication of this article. None of the authors of this article directly participated in the GBD study.

全球疾病负担数据集,方法及其在风湿病和肌肉骨骼疾病中的应用。
全球疾病负担(GBD)研究严格遵循《准确透明的健康估计报告指南》[1,2],旨在评估全球主要疾病、损伤和危险因素bbb造成的死亡率和致残率。该研究成立于1991年,1993年发表了第一批研究结果。最近一次更新是在2024年5月发布的,提供了1990年至2021年的数据。b[3]0有来自163个国家和地区的近12 000名研究人员参与,它已成为量化全球健康水平和趋势的最大和最详细的科学项目。GBD研究全面评估了各种死因、伤害、危险因素和健康状况,为分析全球人口健康和趋势提供了重要基础[2,6 -9]。它还帮助卫生部门查明被忽视的卫生问题,揭示不平等现象,预测动态趋势,并指导政策制定。GBD研究涵盖了204个国家和地区,分为7个超级地区,21个地区和多个定制地区,其中一个被广泛使用的是基于社会人口指数(SDI)的五级分类。SDI[6,7]是25岁以下总生育率、15岁及以上人口平均受教育年限和人均滞后分配收入的几何平均值,其范围从0到1。低SDI为0-0.47,低-中SDI为0.47-0.62,中SDI为0.62-072,高-中SDI为0.72-0.81,高SDI为0.81-1.00。此外,还在21个国家进行了次国家级分析[6,7]。GBD研究的一个关键特征是详细的年龄分层,涵盖了从出生到95岁及以上的51个年龄组。使用年龄标准化率(ASRs)[11]来消除人群之间不同年龄结构的影响,确保更准确地比较人群之间的疾病或死亡率。GBD研究的数据来自世界各地的医院、政府机构、调查和其他数据库。全球健康数据交换(GHDx)平台[12]提供了GBD研究输入数据源目录。各种疾病、损伤和危险因素的详细方法学信息可在GBD 2021方法附录(表1)[13]中找到。GBD研究的一个原则是研究结果的可比性。为了实现这一目标,GBD研究在数据处理过程中采用了一系列方法,包括研究质量评级、独立疾病编码和标准化数据建模分析,以增强不同国家和数据源之间的一致性和可比性。疾病和伤害的数据输入方法分为死亡原因[7]和非致命性健康结果[6]。对于死亡原因类别,数据主要来自主要通过世界卫生组织死亡率数据库访问的生命登记(VR)来源。在拥有高质量虚拟现实系统(其特点是完整性高、垃圾编码率低)的国家,虚拟现实数据通常是死因信息的主要来源。对于特定疾病和缺乏完整虚拟现实系统的国家,统计数据得到了其他数据类型的补充。数据经过了处理、清理和审计。将其映射到统一的GBD原因列表,同时解决特定疾病的错误分类问题,重新分配杂项代码,并在将其存储在死因(CoD)数据库中之前减少噪声。专门为GBD设计的CODEm建模方法主要用于估计未校正的死亡率。该方法得到了其他建模技术的支持,如负二项模型、自然历史模型、子原因比例模型和基于患病率的模型。这些模型考虑了协变量的影响,以获得初步的死亡率估计。然后应用CoDCorrect过程将死因估计值与全因死亡率估计值对齐,产生校正后的死亡率。寿命损失年数(YLL)的计算方法是将每个死因-年龄-性别-地点-年份组合的死亡人数乘以每个年龄段的标准预期寿命。类风湿关节炎(RA)的数据来源包括生命登记、尸检和监测数据,这些数据经过标准化、ICD制图、年龄性别划分、垃圾代码去除和降噪后存储在CoD数据库中。类风湿关节炎死亡率建模的协变量包括吸烟、牛奶摄入量、医疗质量指数、饮酒、平均BMI、平均胆固醇、教育水平、收入和SDI等因素。在CODEm建模方法中使用这些协变量估计未校正死亡率,然后使用CoDCorrect过程[13]计算校正死亡率。 对于非致死性结果,GBD 2021非致死性估计过程概述了八个基本步骤:[6](1)数据识别和提取,以汇编来源(例如,系统评价、调查数据准备、疾病登记和病例通知);(2)数据调整(如人行横道、偏差调整、网络分析、年龄-性别划分等);(3)使用DisMod-MR 2.1或替代建模策略(例如ST-GPR建模和MR-BRT元回归建模)估算患病率和发病率;(4)损伤估计;(5)严重性分布;(6)纳入残疾权重;(7)共病调整;(8)按后遗症和病因计算伤残年数。这一系列的分析提供了发病率,患病率,以及疾病和损伤后遗症的YLD。添加YLL和YLD生成DALYs[6]。表1描述了三种常见风湿病的数据输入方法。数据可视化提高了信息传递的有效性,促进了政策制定过程中的行动[0]。GBD研究提供了52种强大的可视化工具,帮助用户深入了解全球健康数据。GBD结果工具允许用户以CSV文件的形式查看和下载全局运行状况估计。GBD比较提供了疾病模式如何随时间变化的全面分析。GBD Foresight评估和预测了2022年至2050年的未来情景。关于GBD数据可视化的更详细信息可以在健康数据研究和分析网站(https://www.healthdata.org/interactive-data-visuals).The)上找到GBD研究不仅提供可靠的数据和透明的方法,而且还提供各种可视化工具。尽管在数据来源和知识转化方面存在一些局限性,GBD研究提供了对全球疾病负担的详细估计,帮助决策者确定主要的卫生挑战,比较人口统计水平之间的卫生差距,评估干预措施的成本效益,并共同应对全球卫生挑战。在未来几年,GBD研究有可能更准确、全面和现实地评估全球疾病负担。陈世航:概念化、数据整理、可视化、验证、撰写原稿。元唐:形式分析,验证,资源,写作-审查和编辑。Harry Asena Musonye:软件开发,调查,可视化,验证和写作-审查和编辑。潘海峰:方法论,项目管理,监督,资源,资金获取,写作-审查和编辑。作者声明本文的发表不存在任何利益冲突。本文作者均未直接参与GBD研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.70
自引率
4.00%
发文量
362
审稿时长
1 months
期刊介绍: The International Journal of Rheumatic Diseases (formerly APLAR Journal of Rheumatology) is the official journal of the Asia Pacific League of Associations for Rheumatology. The Journal accepts original articles on clinical or experimental research pertinent to the rheumatic diseases, work on connective tissue diseases and other immune and allergic disorders. The acceptance criteria for all papers are the quality and originality of the research and its significance to our readership. Except where otherwise stated, manuscripts are peer reviewed by two anonymous reviewers and the Editor.
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