{"title":"233-OR: CGM指标数据缺失的发生和影响——1型糖尿病运动计划(T1DEXI)数据分析","authors":"DONGYING ZHAN, SIMON J. FISHER, XIAOHUA D. ZHANG","doi":"10.2337/db25-233-or","DOIUrl":null,"url":null,"abstract":"Introduction and Objective: Missing CGM data can confound clinical decision making. This study explores the impact of data missingness on CGM metrics from the T1DEXI study. Methods: Study 1: Gaps in CGM data were determined based on time intervals between consecutive readings. Study 2: To evaluate the effect of gap sizes on CGM parameters, a simulation study randomly introduced missing data with gap sizes of 1-10, 11-50, or >50 continuous missing data points while maintaining the same overall missing rate of 20.83% in all groups. CGM glucose metrics including mean, SD, CV, TAR, TIR, and TBR (see Figure B for abbreviations), were compared to a control group with no missing data. Results: In the T1DEXI CGM dataset, gaps of 1-10 account for 15.76% of all missingness but 68.47% of the frequency, gaps of 11-50 account for 41.06% of all missingness and 25.44% of the frequency, and gaps of >50 account for 43.18% of all missingness but only 6.09% of the frequency. The simulation study showed that, compared to smaller missing gaps, larger gaps resulted in higher Mean Absolute Percentage Error (Figure B). Conclusion: Small gaps in CGM data are frequent but cause minimal errors; whereas large data gaps, though less frequent are associated with large errors in CGM metrics particularly in TAR and TBR. These findings highlight the need for accurate prediction of large gaps to improve CGM data interpretation. Disclosure D. Zhan: None. S.J. Fisher: None. X.D. Zhang: None. Funding This research was supported by US National Institutes of Health (through Grants U01DK135111 and UL1TR001998), the DRC at Washington University (Grant No. P30DK020579), the University of Kentucky Diabetes and Obesity Research Priority Area and the Barnstable Brown Diabetes and Obesity Center. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH. This publication is based on the data from the Type 1 Diabetes EXercise Initiative (T1DEXI) Study that has been made available through Vivli, Inc. Vivli has not contributed to or approved, and is not in any way responsible for the contents of this publication.","PeriodicalId":11376,"journal":{"name":"Diabetes","volume":"8 1","pages":""},"PeriodicalIF":6.2000,"publicationDate":"2025-06-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"233-OR: Occurrence and Impact of Missing Data on CGM Metrics—Analysis of Data from Type 1 Diabetes Exercise Initiative (T1DEXI)\",\"authors\":\"DONGYING ZHAN, SIMON J. FISHER, XIAOHUA D. ZHANG\",\"doi\":\"10.2337/db25-233-or\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction and Objective: Missing CGM data can confound clinical decision making. This study explores the impact of data missingness on CGM metrics from the T1DEXI study. Methods: Study 1: Gaps in CGM data were determined based on time intervals between consecutive readings. Study 2: To evaluate the effect of gap sizes on CGM parameters, a simulation study randomly introduced missing data with gap sizes of 1-10, 11-50, or >50 continuous missing data points while maintaining the same overall missing rate of 20.83% in all groups. CGM glucose metrics including mean, SD, CV, TAR, TIR, and TBR (see Figure B for abbreviations), were compared to a control group with no missing data. Results: In the T1DEXI CGM dataset, gaps of 1-10 account for 15.76% of all missingness but 68.47% of the frequency, gaps of 11-50 account for 41.06% of all missingness and 25.44% of the frequency, and gaps of >50 account for 43.18% of all missingness but only 6.09% of the frequency. The simulation study showed that, compared to smaller missing gaps, larger gaps resulted in higher Mean Absolute Percentage Error (Figure B). Conclusion: Small gaps in CGM data are frequent but cause minimal errors; whereas large data gaps, though less frequent are associated with large errors in CGM metrics particularly in TAR and TBR. These findings highlight the need for accurate prediction of large gaps to improve CGM data interpretation. Disclosure D. Zhan: None. S.J. Fisher: None. X.D. Zhang: None. Funding This research was supported by US National Institutes of Health (through Grants U01DK135111 and UL1TR001998), the DRC at Washington University (Grant No. P30DK020579), the University of Kentucky Diabetes and Obesity Research Priority Area and the Barnstable Brown Diabetes and Obesity Center. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH. This publication is based on the data from the Type 1 Diabetes EXercise Initiative (T1DEXI) Study that has been made available through Vivli, Inc. Vivli has not contributed to or approved, and is not in any way responsible for the contents of this publication.\",\"PeriodicalId\":11376,\"journal\":{\"name\":\"Diabetes\",\"volume\":\"8 1\",\"pages\":\"\"},\"PeriodicalIF\":6.2000,\"publicationDate\":\"2025-06-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Diabetes\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.2337/db25-233-or\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"ENDOCRINOLOGY & METABOLISM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Diabetes","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.2337/db25-233-or","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ENDOCRINOLOGY & METABOLISM","Score":null,"Total":0}
233-OR: Occurrence and Impact of Missing Data on CGM Metrics—Analysis of Data from Type 1 Diabetes Exercise Initiative (T1DEXI)
Introduction and Objective: Missing CGM data can confound clinical decision making. This study explores the impact of data missingness on CGM metrics from the T1DEXI study. Methods: Study 1: Gaps in CGM data were determined based on time intervals between consecutive readings. Study 2: To evaluate the effect of gap sizes on CGM parameters, a simulation study randomly introduced missing data with gap sizes of 1-10, 11-50, or >50 continuous missing data points while maintaining the same overall missing rate of 20.83% in all groups. CGM glucose metrics including mean, SD, CV, TAR, TIR, and TBR (see Figure B for abbreviations), were compared to a control group with no missing data. Results: In the T1DEXI CGM dataset, gaps of 1-10 account for 15.76% of all missingness but 68.47% of the frequency, gaps of 11-50 account for 41.06% of all missingness and 25.44% of the frequency, and gaps of >50 account for 43.18% of all missingness but only 6.09% of the frequency. The simulation study showed that, compared to smaller missing gaps, larger gaps resulted in higher Mean Absolute Percentage Error (Figure B). Conclusion: Small gaps in CGM data are frequent but cause minimal errors; whereas large data gaps, though less frequent are associated with large errors in CGM metrics particularly in TAR and TBR. These findings highlight the need for accurate prediction of large gaps to improve CGM data interpretation. Disclosure D. Zhan: None. S.J. Fisher: None. X.D. Zhang: None. Funding This research was supported by US National Institutes of Health (through Grants U01DK135111 and UL1TR001998), the DRC at Washington University (Grant No. P30DK020579), the University of Kentucky Diabetes and Obesity Research Priority Area and the Barnstable Brown Diabetes and Obesity Center. The content is solely the responsibility of the authors and does not necessarily represent the official views of the NIH. This publication is based on the data from the Type 1 Diabetes EXercise Initiative (T1DEXI) Study that has been made available through Vivli, Inc. Vivli has not contributed to or approved, and is not in any way responsible for the contents of this publication.
期刊介绍:
Diabetes is a scientific journal that publishes original research exploring the physiological and pathophysiological aspects of diabetes mellitus. We encourage submissions of manuscripts pertaining to laboratory, animal, or human research, covering a wide range of topics. Our primary focus is on investigative reports investigating various aspects such as the development and progression of diabetes, along with its associated complications. We also welcome studies delving into normal and pathological pancreatic islet function and intermediary metabolism, as well as exploring the mechanisms of drug and hormone action from a pharmacological perspective. Additionally, we encourage submissions that delve into the biochemical and molecular aspects of both normal and abnormal biological processes.
However, it is important to note that we do not publish studies relating to diabetes education or the application of accepted therapeutic and diagnostic approaches to patients with diabetes mellitus. Our aim is to provide a platform for research that contributes to advancing our understanding of the underlying mechanisms and processes of diabetes.