Pin-Wei Chen, Erica C Jansen, Christopher M Cielo, Ariel A Williamson, Margaret Banker, Michael Kaye, Peter X K Song, Karen E Peterson, Alejandra Cantoral, Martha María Téllez-Rojo, Cathy Goldstein, Khadija Zanna, Akane Sano, Jennette P Moreno, Heidi Kalkwarf, Babette S Zemel, Jonathan A Mitchell
{"title":"儿童和青少年活动记录仪数据的自动睡眠评分方法的性能。","authors":"Pin-Wei Chen, Erica C Jansen, Christopher M Cielo, Ariel A Williamson, Margaret Banker, Michael Kaye, Peter X K Song, Karen E Peterson, Alejandra Cantoral, Martha María Téllez-Rojo, Cathy Goldstein, Khadija Zanna, Akane Sano, Jennette P Moreno, Heidi Kalkwarf, Babette S Zemel, Jonathan A Mitchell","doi":"10.1093/sleep/zsaf282","DOIUrl":null,"url":null,"abstract":"<p><strong>Study objectives: </strong>GGIR is an R package for processing raw acceleration data to estimate sleep health parameters. We aimed to 1) assess the performance of three sleep algorithms within GGIR against PSG for detecting sleep/wake in clinically referred, typically-developing children (criterion validity); and 2) describe GGIR-derived sleep estimates from typically developing children enrolled in multiple cohort studies (face validity).</p><p><strong>Methods: </strong>For criterion evaluation, children (8-16y, N=30) wore an actigraphy device for one night during in-lab polysomnography with performance assessed using epoch-by-epoch analyses. For face validity evaluation, four community/free living datasets were used: 1) BMAYC (3-5y, N=310), 2) SSS (5-8y, N=118), 3) S-Grow2 (12-13y; N=291) and 4) ELEMENT (9-18y; N=543). All raw acceleration data were processed using GGIR (v.3.0-0) with the Cole-Kripke (CK), Sadeh (S), and van Hees (vH) algorithm settings.</p><p><strong>Results: </strong>Following the in-lab test, 60% of children were diagnosed with mild to severe obstructive sleep apnea (OSA). For criterion evaluation, the 30-s epoch-by-epoch analyses revealed that average balanced accuracies were 0.80 (Sensitivity=0.80; Specificity=0.79), 0.76 (Sensitivity=0.86; Specificity=0.65), and 0.67 (Sensitivity=0.95, Specificity=0.39) for GGIR-CK, GGIR-vH, and GGIR-S, respectively. For face validity evaluation, sleep estimates mirrored the in-lab performance metrics (e.g., sleep duration estimates were similar when using GGIR-CK and GGIR-VH but approximately one hour longer when using GGIR-S).</p><p><strong>Conclusions: </strong>The in-lab performance metrics, from typically-developing children with and without OSA, and cohort-based descriptive statistics from samples of typically-developing children, provide benchmark data to guide investigators on the suitability of GGIR for automated processing of raw acceleration data for pediatric sleep estimation.</p>","PeriodicalId":22018,"journal":{"name":"Sleep","volume":" ","pages":""},"PeriodicalIF":4.9000,"publicationDate":"2025-09-19","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12494141/pdf/","citationCount":"0","resultStr":"{\"title\":\"Performance of an Automated Sleep Scoring Approach for Actigraphy Data in Children and Adolescents.\",\"authors\":\"Pin-Wei Chen, Erica C Jansen, Christopher M Cielo, Ariel A Williamson, Margaret Banker, Michael Kaye, Peter X K Song, Karen E Peterson, Alejandra Cantoral, Martha María Téllez-Rojo, Cathy Goldstein, Khadija Zanna, Akane Sano, Jennette P Moreno, Heidi Kalkwarf, Babette S Zemel, Jonathan A Mitchell\",\"doi\":\"10.1093/sleep/zsaf282\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Study objectives: </strong>GGIR is an R package for processing raw acceleration data to estimate sleep health parameters. We aimed to 1) assess the performance of three sleep algorithms within GGIR against PSG for detecting sleep/wake in clinically referred, typically-developing children (criterion validity); and 2) describe GGIR-derived sleep estimates from typically developing children enrolled in multiple cohort studies (face validity).</p><p><strong>Methods: </strong>For criterion evaluation, children (8-16y, N=30) wore an actigraphy device for one night during in-lab polysomnography with performance assessed using epoch-by-epoch analyses. For face validity evaluation, four community/free living datasets were used: 1) BMAYC (3-5y, N=310), 2) SSS (5-8y, N=118), 3) S-Grow2 (12-13y; N=291) and 4) ELEMENT (9-18y; N=543). All raw acceleration data were processed using GGIR (v.3.0-0) with the Cole-Kripke (CK), Sadeh (S), and van Hees (vH) algorithm settings.</p><p><strong>Results: </strong>Following the in-lab test, 60% of children were diagnosed with mild to severe obstructive sleep apnea (OSA). For criterion evaluation, the 30-s epoch-by-epoch analyses revealed that average balanced accuracies were 0.80 (Sensitivity=0.80; Specificity=0.79), 0.76 (Sensitivity=0.86; Specificity=0.65), and 0.67 (Sensitivity=0.95, Specificity=0.39) for GGIR-CK, GGIR-vH, and GGIR-S, respectively. For face validity evaluation, sleep estimates mirrored the in-lab performance metrics (e.g., sleep duration estimates were similar when using GGIR-CK and GGIR-VH but approximately one hour longer when using GGIR-S).</p><p><strong>Conclusions: </strong>The in-lab performance metrics, from typically-developing children with and without OSA, and cohort-based descriptive statistics from samples of typically-developing children, provide benchmark data to guide investigators on the suitability of GGIR for automated processing of raw acceleration data for pediatric sleep estimation.</p>\",\"PeriodicalId\":22018,\"journal\":{\"name\":\"Sleep\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":4.9000,\"publicationDate\":\"2025-09-19\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12494141/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Sleep\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1093/sleep/zsaf282\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Sleep","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/sleep/zsaf282","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"Medicine","Score":null,"Total":0}
Performance of an Automated Sleep Scoring Approach for Actigraphy Data in Children and Adolescents.
Study objectives: GGIR is an R package for processing raw acceleration data to estimate sleep health parameters. We aimed to 1) assess the performance of three sleep algorithms within GGIR against PSG for detecting sleep/wake in clinically referred, typically-developing children (criterion validity); and 2) describe GGIR-derived sleep estimates from typically developing children enrolled in multiple cohort studies (face validity).
Methods: For criterion evaluation, children (8-16y, N=30) wore an actigraphy device for one night during in-lab polysomnography with performance assessed using epoch-by-epoch analyses. For face validity evaluation, four community/free living datasets were used: 1) BMAYC (3-5y, N=310), 2) SSS (5-8y, N=118), 3) S-Grow2 (12-13y; N=291) and 4) ELEMENT (9-18y; N=543). All raw acceleration data were processed using GGIR (v.3.0-0) with the Cole-Kripke (CK), Sadeh (S), and van Hees (vH) algorithm settings.
Results: Following the in-lab test, 60% of children were diagnosed with mild to severe obstructive sleep apnea (OSA). For criterion evaluation, the 30-s epoch-by-epoch analyses revealed that average balanced accuracies were 0.80 (Sensitivity=0.80; Specificity=0.79), 0.76 (Sensitivity=0.86; Specificity=0.65), and 0.67 (Sensitivity=0.95, Specificity=0.39) for GGIR-CK, GGIR-vH, and GGIR-S, respectively. For face validity evaluation, sleep estimates mirrored the in-lab performance metrics (e.g., sleep duration estimates were similar when using GGIR-CK and GGIR-VH but approximately one hour longer when using GGIR-S).
Conclusions: The in-lab performance metrics, from typically-developing children with and without OSA, and cohort-based descriptive statistics from samples of typically-developing children, provide benchmark data to guide investigators on the suitability of GGIR for automated processing of raw acceleration data for pediatric sleep estimation.
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