Methodological Issues Related to the Reported Association of A Body Shape Index With Abdominal Aortic Calcification in Patients With Hypertension

IF 2.8 3区 医学 Q2 CARDIAC & CARDIOVASCULAR SYSTEMS
Laiba Shahab, Syed Huzaifa Khan, Javeria Kashaf Zain
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Addressing these issues will help to better understand the significance of the obtained results.</p><p>First of all, it seems that there is some inconsistency related to the application of a specific regression model. Indeed, ABSI depends on BMI, waist circumference, and height of participants. Therefore, taking all of them as covariates when performing multiple regression analysis implies control for BMI and waist circumference. ABSI was designed to be mathematically independent of BMI and waist circumference and hence substitutable for them in regression analysis models, as shown by Krakauer and Krakauer [<span>2</span>]. In addition, Christakoudi et al. demonstrated that adjustment for BMI and waist circumference renders ABSI mathematically meaningless [<span>3</span>]. Furthermore, Midi et al. stated that the simultaneous inclusion of mathematically correlated covariates in regression models may bias and render unstable the estimates of their coefficients [<span>4</span>]. Consequently, conclusions about the independent predictive ability of ABSI cannot be drawn on the basis of such models, and the results should be reproduced using a properly constructed model.</p><p>Aside from the problem highlighted above, three further concerns render the results less reliable. To start with, the authors conclude that <i>p</i> &gt; 0.05 in their restricted cubic spline analysis confirms a linear relationship between ABSI and AAC. However, a non-significant result for nonlinearity simply indicates insufficient statistical power to detect a curved relationship, not confirmation of true linearity [<span>5</span>]. This is further contradicted by Yin et al. who, using the exact same NHANES 2013–2014 data set, reported a <i>U</i>-shaped relationship between ABSI and AAC [<span>6</span>], directly challenging the linear claim of the target article. Second, the authors describe an AUC of 0.625 as having moderate discriminatory ability; however, by established standards in clinical prediction research, this value falls within the poor discrimination range [<span>7</span>]. Furthermore, no formal statistical comparison of AUC values was conducted using the DeLong test, the recommended method for comparing correlated AUC values [<span>8</span>]. Third, the TRIPOD guidelines, the international standard for prediction model reporting, require internal validation and benchmarking against existing models, neither of which was performed in this study [<span>9</span>]. 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引用次数: 0

Abstract

We have read with much interest the paper by Qiu and Wang, which appeared in Clinical Cardiology [1]. The researchers suggested that ABSI could predict the risk of AAC development and serve for cardiovascular risk stratification in hypertensive patients. We concur with both the novelty of the studied population as well as the significance of identifying AAC biomarkers. Nevertheless, we feel compelled to bring to your attention some issues regarding multicollinearity during the computation of ABSI, misinterpretation of the results of dose-response modeling, and excessive importance attributed to ABSI as a predictor. Addressing these issues will help to better understand the significance of the obtained results.

First of all, it seems that there is some inconsistency related to the application of a specific regression model. Indeed, ABSI depends on BMI, waist circumference, and height of participants. Therefore, taking all of them as covariates when performing multiple regression analysis implies control for BMI and waist circumference. ABSI was designed to be mathematically independent of BMI and waist circumference and hence substitutable for them in regression analysis models, as shown by Krakauer and Krakauer [2]. In addition, Christakoudi et al. demonstrated that adjustment for BMI and waist circumference renders ABSI mathematically meaningless [3]. Furthermore, Midi et al. stated that the simultaneous inclusion of mathematically correlated covariates in regression models may bias and render unstable the estimates of their coefficients [4]. Consequently, conclusions about the independent predictive ability of ABSI cannot be drawn on the basis of such models, and the results should be reproduced using a properly constructed model.

Aside from the problem highlighted above, three further concerns render the results less reliable. To start with, the authors conclude that p > 0.05 in their restricted cubic spline analysis confirms a linear relationship between ABSI and AAC. However, a non-significant result for nonlinearity simply indicates insufficient statistical power to detect a curved relationship, not confirmation of true linearity [5]. This is further contradicted by Yin et al. who, using the exact same NHANES 2013–2014 data set, reported a U-shaped relationship between ABSI and AAC [6], directly challenging the linear claim of the target article. Second, the authors describe an AUC of 0.625 as having moderate discriminatory ability; however, by established standards in clinical prediction research, this value falls within the poor discrimination range [7]. Furthermore, no formal statistical comparison of AUC values was conducted using the DeLong test, the recommended method for comparing correlated AUC values [8]. Third, the TRIPOD guidelines, the international standard for prediction model reporting, require internal validation and benchmarking against existing models, neither of which was performed in this study [9]. Taken together, these concerns regarding collinearity, misinterpretation of dose-response modeling, and overstatement of discriminative performance collectively raise important questions about the validity of the reported independence claim and the proposed clinical utility of ABSI for AAC risk stratification in hypertensive patients.

We respectfully invite the authors to address these methodological concerns, as doing so would substantially strengthen the scientific contribution of this work to the growing literature on anthropometric predictors of vascular calcification in hypertensive populations.

All authors have read and approved the final manuscript.

The authors have nothing to report.

The authors have nothing to report.

The authors have nothing to report.

The authors declare no conflicts of interest.

The authors have nothing to report.

已报道的高血压患者形体指数与腹主动脉钙化相关的方法学问题
我们饶有兴趣地阅读了邱和王发表在《临床心脏病学b[1]》上的论文。研究人员认为,ABSI可以预测高血压患者发生AAC的风险,并可用于心血管风险分层。我们同意研究人群的新颖性以及确定AAC生物标志物的重要性。然而,我们觉得有必要提请您注意一些问题,如在ABSI计算过程中的多重共线性,对剂量-反应建模结果的误解,以及将ABSI作为预测器的过度重视。解决这些问题将有助于更好地理解所获得结果的意义。首先,似乎与特定回归模型的应用有一些不一致。事实上,ABSI取决于参与者的BMI、腰围和身高。因此,在进行多元回归分析时,将它们都作为协变量意味着对BMI和腰围进行控制。如Krakauer和Krakauer[2]所示,ABSI被设计成在数学上独立于BMI和腰围,因此可以在回归分析模型中替代它们。此外,Christakoudi等人证明,BMI和腰围的调整使得ABSI在数学上毫无意义。此外,Midi等人指出,在回归模型中同时包含数学上相关的协变量可能会对其系数[4]的估计产生偏差并使其不稳定。因此,不能在这些模型的基础上得出关于ABSI独立预测能力的结论,应该使用适当构建的模型来重现结果。除了上面强调的问题之外,还有三个问题使结果不那么可靠。首先,作者得出结论,他们的限制性三次样条分析中的p >; 0.05证实了ABSI和AAC之间的线性关系。然而,非线性的非显著结果仅仅表明没有足够的统计能力来检测曲线关系,而不是确认真正的线性[5]。Yin等人使用完全相同的NHANES 2013-2014数据集,报告了ABSI和AAC[6]之间的u形关系,直接挑战了目标文章的线性主张。其次,作者将AUC为0.625描述为具有中等区分能力;然而,根据临床预测研究的既定标准,该值属于差判别范围[7]。此外,没有使用DeLong检验(比较相关AUC值[8]的推荐方法)对AUC值进行正式的统计比较。第三,TRIPOD指南,预测模型报告的国际标准,需要内部验证和对现有模型进行基准测试,这在本研究中都没有进行。综上所述,这些关于共线性的担忧、对剂量反应模型的误读和对区别性表现的夸大,共同提出了关于报道的独立性声明的有效性和ABSI在高血压患者AAC风险分层中的临床应用的重要问题。我们恭敬地邀请作者解决这些方法上的问题,因为这样做将大大加强这项工作对高血压人群血管钙化的人体测量预测文献的科学贡献。所有作者都阅读并批准了最终稿件。作者没有什么可报告的。作者没有什么可报告的。作者没有什么可报告的。作者声明无利益冲突。作者没有什么可报告的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Clinical Cardiology
Clinical Cardiology 医学-心血管系统
CiteScore
5.10
自引率
3.70%
发文量
189
审稿时长
4-8 weeks
期刊介绍: Clinical Cardiology provides a fully Gold Open Access forum for the publication of original clinical research, as well as brief reviews of diagnostic and therapeutic issues in cardiovascular medicine and cardiovascular surgery. The journal includes Clinical Investigations, Reviews, free standing editorials and commentaries, and bonus online-only content. The journal also publishes supplements, Expert Panel Discussions, sponsored clinical Reviews, Trial Designs, and Quality and Outcomes.
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