{"title":"对Huang等人发表的“日本社区中老年人长期使用他汀类药物后肌肉减少的风险”的评论。","authors":"Jian Huang","doi":"10.1002/jcsm.13801","DOIUrl":null,"url":null,"abstract":"<p>I read with great interest the article ‘Risk of Sarcopenia Following Long-Term Statin Use in Community-Dwelling Middle-Aged and Older Adults in Japan’ by Huang et al. [<span>1</span>]. Although the study addresses a topic of significant clinical relevance, I would like to express concerns regarding two critical methodological aspects that may affect the internal validity of the findings.</p><p>First, the article reported that after propensity score matching, several variables, including age, exhibit a standardized mean difference (SMD) of exactly 0.00 (see Table 1). Such a perfect balance for a continuous variable is highly unlikely, even with state-of-the-art matching techniques, and strongly suggests a potential data or calculation error. Previous research has consistently demonstrated that, in practice, residual imbalances almost invariably persist despite careful matching [<span>2</span>]. Greater transparency in reporting balance diagnostics, for example, by providing graphical representations of propensity score distributions such as Love plots or density plots, would allow readers to thoroughly assess the adequacy of the matching process and verify that the matching has achieved an acceptable balance between groups.</p><p>Second, the authors employed risk set sampling to construct the control group; however, the article did not provide sufficient details regarding the specific algorithm used or its potential limitations. Risk set sampling is a critical method for addressing time-dependent confounding in longitudinal studies [<span>3</span>], yet its implementation can vary considerably and may introduce biases if not carefully executed. The study did not specify how subjects were selected, the exact matching procedures used when sampling with replacement or any assumptions underlying the method. A detailed description of the risk set sampling algorithm, along with a discussion of its limitations and any potential impact on the study's conclusions, is essential for evaluating the robustness and reproducibility of the analysis.</p><p>These points warrant further clarification, as they have significant implications for the interpretation of the study's results.</p><p>The author declares no conflicts of interest.</p>","PeriodicalId":48911,"journal":{"name":"Journal of Cachexia Sarcopenia and Muscle","volume":"16 2","pages":""},"PeriodicalIF":9.4000,"publicationDate":"2025-04-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jcsm.13801","citationCount":"0","resultStr":"{\"title\":\"Comment on “Risk of Sarcopenia Following Long-Term Statin Use in Community-Dwelling Middle-Aged and Older Adults in Japan” by Huang et al.\",\"authors\":\"Jian Huang\",\"doi\":\"10.1002/jcsm.13801\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>I read with great interest the article ‘Risk of Sarcopenia Following Long-Term Statin Use in Community-Dwelling Middle-Aged and Older Adults in Japan’ by Huang et al. [<span>1</span>]. Although the study addresses a topic of significant clinical relevance, I would like to express concerns regarding two critical methodological aspects that may affect the internal validity of the findings.</p><p>First, the article reported that after propensity score matching, several variables, including age, exhibit a standardized mean difference (SMD) of exactly 0.00 (see Table 1). Such a perfect balance for a continuous variable is highly unlikely, even with state-of-the-art matching techniques, and strongly suggests a potential data or calculation error. Previous research has consistently demonstrated that, in practice, residual imbalances almost invariably persist despite careful matching [<span>2</span>]. Greater transparency in reporting balance diagnostics, for example, by providing graphical representations of propensity score distributions such as Love plots or density plots, would allow readers to thoroughly assess the adequacy of the matching process and verify that the matching has achieved an acceptable balance between groups.</p><p>Second, the authors employed risk set sampling to construct the control group; however, the article did not provide sufficient details regarding the specific algorithm used or its potential limitations. Risk set sampling is a critical method for addressing time-dependent confounding in longitudinal studies [<span>3</span>], yet its implementation can vary considerably and may introduce biases if not carefully executed. The study did not specify how subjects were selected, the exact matching procedures used when sampling with replacement or any assumptions underlying the method. A detailed description of the risk set sampling algorithm, along with a discussion of its limitations and any potential impact on the study's conclusions, is essential for evaluating the robustness and reproducibility of the analysis.</p><p>These points warrant further clarification, as they have significant implications for the interpretation of the study's results.</p><p>The author declares no conflicts of interest.</p>\",\"PeriodicalId\":48911,\"journal\":{\"name\":\"Journal of Cachexia Sarcopenia and Muscle\",\"volume\":\"16 2\",\"pages\":\"\"},\"PeriodicalIF\":9.4000,\"publicationDate\":\"2025-04-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1002/jcsm.13801\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Cachexia Sarcopenia and Muscle\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/jcsm.13801\",\"RegionNum\":1,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"GERIATRICS & GERONTOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Cachexia Sarcopenia and Muscle","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/jcsm.13801","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"GERIATRICS & GERONTOLOGY","Score":null,"Total":0}
Comment on “Risk of Sarcopenia Following Long-Term Statin Use in Community-Dwelling Middle-Aged and Older Adults in Japan” by Huang et al.
I read with great interest the article ‘Risk of Sarcopenia Following Long-Term Statin Use in Community-Dwelling Middle-Aged and Older Adults in Japan’ by Huang et al. [1]. Although the study addresses a topic of significant clinical relevance, I would like to express concerns regarding two critical methodological aspects that may affect the internal validity of the findings.
First, the article reported that after propensity score matching, several variables, including age, exhibit a standardized mean difference (SMD) of exactly 0.00 (see Table 1). Such a perfect balance for a continuous variable is highly unlikely, even with state-of-the-art matching techniques, and strongly suggests a potential data or calculation error. Previous research has consistently demonstrated that, in practice, residual imbalances almost invariably persist despite careful matching [2]. Greater transparency in reporting balance diagnostics, for example, by providing graphical representations of propensity score distributions such as Love plots or density plots, would allow readers to thoroughly assess the adequacy of the matching process and verify that the matching has achieved an acceptable balance between groups.
Second, the authors employed risk set sampling to construct the control group; however, the article did not provide sufficient details regarding the specific algorithm used or its potential limitations. Risk set sampling is a critical method for addressing time-dependent confounding in longitudinal studies [3], yet its implementation can vary considerably and may introduce biases if not carefully executed. The study did not specify how subjects were selected, the exact matching procedures used when sampling with replacement or any assumptions underlying the method. A detailed description of the risk set sampling algorithm, along with a discussion of its limitations and any potential impact on the study's conclusions, is essential for evaluating the robustness and reproducibility of the analysis.
These points warrant further clarification, as they have significant implications for the interpretation of the study's results.
期刊介绍:
The Journal of Cachexia, Sarcopenia and Muscle is a peer-reviewed international journal dedicated to publishing materials related to cachexia and sarcopenia, as well as body composition and its physiological and pathophysiological changes across the lifespan and in response to various illnesses from all fields of life sciences. The journal aims to provide a reliable resource for professionals interested in related research or involved in the clinical care of affected patients, such as those suffering from AIDS, cancer, chronic heart failure, chronic lung disease, liver cirrhosis, chronic kidney failure, rheumatoid arthritis, or sepsis.