Dustin J Oranchuk, Katie L Boncella, Daniella Gonzalez-Rivera, Michael O Harris-Love
{"title":"与传统的回波特性相比,肌肉组织模拟材料的超声图像纹理特征减少了探针角度和增益设置带来的变异性。","authors":"Dustin J Oranchuk, Katie L Boncella, Daniella Gonzalez-Rivera, Michael O Harris-Love","doi":"10.4081/ejtm.2025.13511","DOIUrl":null,"url":null,"abstract":"<p><p>Cost-effective and portable ultrasonography offers a promising approach for monitoring skeletal muscle damage and quality in many contexts. However, echogenicity analysis relies on precise transducer orientations and machine parameters, posing challenges for data pooling across different raters and settings. Muscle texture analysis offers a potential means of reducing inter-rater and machine-setting variability. Scans were assessed at nine angles, controlled using a custom transducer shell and software. Scans were performed three times, and different gains were applied. All scans were performed on a muscle tissue-mimicking phantom to eliminate biological variability. Intra-angle and intra-gain variability and internal consistency were assessed via coefficient of variation (CV%) and Cronbach's alpha (αc). Spearman's (ρ) correlations were employed to determine the relationship between echogenicity and each texture feature. Entropy (angle: CV=2.7-7.6%; gain: CV=10.5%; αc=0.86), and inverse difference moment (angle: CV=3.7-9.8%; gain: CV=16.5%; αc=0.87) were less variable than echogenicity (angle: CV=6.4-19.4%; gain: CV=39.0%; αc=0.82). Angular second moment (angle: CV=17.9-116.6%; gain: CV=71.6%; αc=0.68), contrast (angle: CV=7.8-14.7%; gain: CV=41.8%;αc=0.75), and correlation (angle: CV=9.0-13.5%; gain: CV=28.6%; αc=0.49) features were generally more variable. Entropy (ρ=0.82-0.98, p≤0.011) and inverse difference moment (ρ=-0.98--0.83, p≤0.008), were more strongly correlated with echogenicity than angular second moment (ρ=-0.98--0.77, p≤0.016), contrast (ρ=0.53-0.98, p≤0.15), and correlation (ρ=-0.25--0.19, p=0.520-0.631). Entropy and inverse difference moment features may allow data sharing between laboratory and clinical settings with ultrasound machine parameters and raters of varying skill levels. Clinical and mechanistic studies are required to determine if texture features can replace echogenicity assessments.</p>","PeriodicalId":46459,"journal":{"name":"European Journal of Translational Myology","volume":" ","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2025-04-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sonographic image texture features in muscle tissue-mimicking material reduce variability introduced by probe angle and gain settings compared to traditional echogenicity.\",\"authors\":\"Dustin J Oranchuk, Katie L Boncella, Daniella Gonzalez-Rivera, Michael O Harris-Love\",\"doi\":\"10.4081/ejtm.2025.13511\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Cost-effective and portable ultrasonography offers a promising approach for monitoring skeletal muscle damage and quality in many contexts. However, echogenicity analysis relies on precise transducer orientations and machine parameters, posing challenges for data pooling across different raters and settings. Muscle texture analysis offers a potential means of reducing inter-rater and machine-setting variability. Scans were assessed at nine angles, controlled using a custom transducer shell and software. Scans were performed three times, and different gains were applied. All scans were performed on a muscle tissue-mimicking phantom to eliminate biological variability. Intra-angle and intra-gain variability and internal consistency were assessed via coefficient of variation (CV%) and Cronbach's alpha (αc). Spearman's (ρ) correlations were employed to determine the relationship between echogenicity and each texture feature. Entropy (angle: CV=2.7-7.6%; gain: CV=10.5%; αc=0.86), and inverse difference moment (angle: CV=3.7-9.8%; gain: CV=16.5%; αc=0.87) were less variable than echogenicity (angle: CV=6.4-19.4%; gain: CV=39.0%; αc=0.82). Angular second moment (angle: CV=17.9-116.6%; gain: CV=71.6%; αc=0.68), contrast (angle: CV=7.8-14.7%; gain: CV=41.8%;αc=0.75), and correlation (angle: CV=9.0-13.5%; gain: CV=28.6%; αc=0.49) features were generally more variable. Entropy (ρ=0.82-0.98, p≤0.011) and inverse difference moment (ρ=-0.98--0.83, p≤0.008), were more strongly correlated with echogenicity than angular second moment (ρ=-0.98--0.77, p≤0.016), contrast (ρ=0.53-0.98, p≤0.15), and correlation (ρ=-0.25--0.19, p=0.520-0.631). Entropy and inverse difference moment features may allow data sharing between laboratory and clinical settings with ultrasound machine parameters and raters of varying skill levels. Clinical and mechanistic studies are required to determine if texture features can replace echogenicity assessments.</p>\",\"PeriodicalId\":46459,\"journal\":{\"name\":\"European Journal of Translational Myology\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2025-04-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Translational Myology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4081/ejtm.2025.13511\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MEDICINE, RESEARCH & EXPERIMENTAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Translational Myology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4081/ejtm.2025.13511","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, RESEARCH & EXPERIMENTAL","Score":null,"Total":0}
Sonographic image texture features in muscle tissue-mimicking material reduce variability introduced by probe angle and gain settings compared to traditional echogenicity.
Cost-effective and portable ultrasonography offers a promising approach for monitoring skeletal muscle damage and quality in many contexts. However, echogenicity analysis relies on precise transducer orientations and machine parameters, posing challenges for data pooling across different raters and settings. Muscle texture analysis offers a potential means of reducing inter-rater and machine-setting variability. Scans were assessed at nine angles, controlled using a custom transducer shell and software. Scans were performed three times, and different gains were applied. All scans were performed on a muscle tissue-mimicking phantom to eliminate biological variability. Intra-angle and intra-gain variability and internal consistency were assessed via coefficient of variation (CV%) and Cronbach's alpha (αc). Spearman's (ρ) correlations were employed to determine the relationship between echogenicity and each texture feature. Entropy (angle: CV=2.7-7.6%; gain: CV=10.5%; αc=0.86), and inverse difference moment (angle: CV=3.7-9.8%; gain: CV=16.5%; αc=0.87) were less variable than echogenicity (angle: CV=6.4-19.4%; gain: CV=39.0%; αc=0.82). Angular second moment (angle: CV=17.9-116.6%; gain: CV=71.6%; αc=0.68), contrast (angle: CV=7.8-14.7%; gain: CV=41.8%;αc=0.75), and correlation (angle: CV=9.0-13.5%; gain: CV=28.6%; αc=0.49) features were generally more variable. Entropy (ρ=0.82-0.98, p≤0.011) and inverse difference moment (ρ=-0.98--0.83, p≤0.008), were more strongly correlated with echogenicity than angular second moment (ρ=-0.98--0.77, p≤0.016), contrast (ρ=0.53-0.98, p≤0.15), and correlation (ρ=-0.25--0.19, p=0.520-0.631). Entropy and inverse difference moment features may allow data sharing between laboratory and clinical settings with ultrasound machine parameters and raters of varying skill levels. Clinical and mechanistic studies are required to determine if texture features can replace echogenicity assessments.