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。

IF 9.4 1区 医学 Q1 GERIATRICS & GERONTOLOGY
Jian Huang
{"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}
引用次数: 0

摘要

我怀着极大的兴趣阅读了Huang等人的文章《在日本社区居住的中老年人长期使用他汀类药物后肌肉减少症的风险》。虽然该研究涉及一个具有重要临床意义的主题,但我想对可能影响研究结果内部有效性的两个关键方法学方面表示关注。首先,文章报道,在倾向得分匹配后,包括年龄在内的几个变量的标准化平均差(SMD)恰好为0.00(见表1)。即使使用最先进的匹配技术,连续变量的这种完美平衡也是极不可能的,并且强烈表明可能存在数据或计算错误。先前的研究一致表明,在实践中,尽管仔细匹配b[2],但残余失衡几乎总是持续存在。例如,通过提供倾向得分分布(如Love图或密度图)的图形表示,在报告平衡诊断方面提高透明度,将允许读者彻底评估匹配过程的充分性,并验证匹配是否在组间达到了可接受的平衡。其次,采用风险集抽样法构建对照组;然而,文章没有提供关于所使用的具体算法或其潜在局限性的足够细节。风险集抽样是纵向研究中解决时间相关混淆的关键方法[b],但其实施可能会有很大差异,如果不仔细执行可能会引入偏差。该研究没有具体说明受试者是如何选择的,替代抽样时使用的精确匹配程序,也没有说明该方法背后的任何假设。对风险集抽样算法的详细描述,以及对其局限性和对研究结论的潜在影响的讨论,对于评估分析的稳健性和可重复性至关重要。这些要点值得进一步澄清,因为它们对研究结果的解释具有重要意义。作者声明无利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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.

The author declares no conflicts of interest.

求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Journal of Cachexia Sarcopenia and Muscle
Journal of Cachexia Sarcopenia and Muscle MEDICINE, GENERAL & INTERNAL-
CiteScore
13.30
自引率
12.40%
发文量
234
审稿时长
16 weeks
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.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信