链接水平对健康和医学研究中大数据分析推论的影响:一项实证研究。

IF 3.3 3区 医学 Q2 MEDICAL INFORMATICS
Bora Lee, Young-Kyun Lee, Sung Han Kim, HyunJin Oh, Sungho Won, Suk-Yong Jang, Ye Jin Jeon, Bit-Na Yoo, Jean-Kyung Bak
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引用次数: 0

摘要

背景:根据关联级别出现的关联错误会对分析结果的准确性和可靠性产生不利影响。本研究旨在通过实证分析,找出个人身份信息关联水平、样本量和分析方法不同所导致的结果差异:方法:将直接可识别信息(DII)和间接可识别信息(III)的链接结果差异设定为:III 链接基于姓名、出生日期和性别,DII 链接基于居民身份证号码。各层次链接的数据集分别命名为数据库 III(DBIII)和数据库 DII(DBDII)。以 DII 链接数据集的分析结果为金标准,对描述性统计、分组比较、发病率估计、治疗效果和调节效果分析结果进行评估:DBDII和DBIII的关联率分别为71.1%和99.7%。在描述性统计和分组比较分析方面,大多数情况下的效果差异为 "无 "至 "极小"。关于样本量相对较小的宫颈癌,DBIII 的分析结果是低估了对照组的发病率,高估了治疗组的发病率(DBIII 的危险比 [HR] = 2.62 [95% 置信区间 (CI):1.63-4.23] 与 DBDII 的 1.80 [95% CI:1.18-2.73])。关于前列腺癌,根据监测、流行病学和最终结果总结分期,治疗效果有被高估或低估的矛盾趋势(HR = 2.对于局部分期,DBIII 的 HR = 2.27 [95% CI: 1.91-2.70] vs. DBDII 的 HR = 1.92 [95% CI: 1.70-2.17]; 对于区域分期,DBIII 的 HR = 1.80 [95% CI: 1.37-2.36] vs. DBDII 的 HR = 2.05 [95% CI: 1.67-2.52]):为防止健康和医学研究中的分析结果失真,在使用 DBDII 链接不同数据时,必须检查每个相关因素 (FOI) 的患者人群和样本量是否足够。在涉及罕见疾病或 FOI 样本规模较小的情况下,DBDII 连接很有可能不可避免。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Impact of linkage level on inferences from big data analyses in health and medical research: an empirical study.

Background: Linkage errors that occur according to linkage levels can adversely affect the accuracy and reliability of analysis results. This study aimed to identify the differences in results according to personally identifiable information linkage level, sample size, and analysis methods through empirical analysis.

Methods: The difference between the results of linkage in directly identifiable information (DII) and indirectly identifiable information (III) linkage levels was set as III linkage based on name, date of birth, and sex and DII linkage based on resident registration number. The datasets linked at each level were named as databaseIII (DBIII) and databaseDII (DBDII), respectively. Considering the analysis results of the DII-linked dataset as the gold standard, descriptive statistics, group comparison, incidence estimation, treatment effect, and moderation effect analysis results were assessed.

Results: The linkage rates for DBDII and DBIII were 71.1% and 99.7%, respectively. Regarding descriptive statistics and group comparison analysis, the difference in effect in most cases was "none" to "very little." With respect to cervical cancer that had a relatively small sample size, analysis of DBIII resulted in an underestimation of the incidence in the control group and an overestimation of the incidence in the treatment group (hazard ratio [HR] = 2.62 [95% confidence interval (CI): 1.63-4.23] in DBIII vs. 1.80 [95% CI: 1.18-2.73] in DBDII). Regarding prostate cancer, there was a conflicting tendency with the treatment effect being over or underestimated according to the surveillance, epidemiology, and end results summary staging (HR = 2.27 [95% CI: 1.91-2.70] in DBIII vs. 1.92 [95% CI: 1.70-2.17] in DBDII for the localized stage; HR = 1.80 [95% CI: 1.37-2.36] in DBIII vs. 2.05 [95% CI: 1.67-2.52] in DBDII for the regional stage).

Conclusions: To prevent distortion of the analyses results in health and medical research, it is important to check that the patient population and sample size by each factor of interest (FOI) are sufficient when different data are linked using DBDII. In cases involving a rare disease or with a small sample size for FOI, there is a high likelihood that a DII linkage is unavoidable.

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来源期刊
CiteScore
7.20
自引率
5.70%
发文量
297
审稿时长
1 months
期刊介绍: BMC Medical Informatics and Decision Making is an open access journal publishing original peer-reviewed research articles in relation to the design, development, implementation, use, and evaluation of health information technologies and decision-making for human health.
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