{"title":"Beverage Consumption and Facial Skin Aging: Evidence From Mendelian Randomization Analysis: Comment From Liu et al","authors":"Hainan Li, Ao He, Xian Zhao","doi":"10.1111/jocd.16597","DOIUrl":null,"url":null,"abstract":"<p>This article examines the connection between beverage consumption and facial aging, and evaluates the potential causal relationship between the two using Mendelian randomization (MR) analysis. This provides a new research direction for studying the potential causes of facial aging. But there are still some serious problems with the article.</p><p>First, the exposure and outcome data utilized in the author's study were sourced from the same database, UK Biobank, leading to a significant overlap in samples. This overlap is a widely recognized factor that can influence MR bias, including issues like winner's curse and weak instrumental variables [<span>1</span>]. Such a wide overlap would increase the incidence of Class I errors, leading to an overestimation of the causal effect [<span>2</span>]. Therefore, we believe that it is necessary for the authors to perform additional sensitivity analyses or use non-overlapping cohorts. Recently, a new approach called MRLap, which addresses sample overlap by correcting using regression intercepts for cross-trait linkage imbalance scores, has demonstrated a good fit in simulations with 5% to 95% overlap [<span>1</span>].</p><p>In the selection of instrumental variables, the authors did not disclose the specific information of each instrumental variable, especially the P-value related to the outcome phenotype. The study did not correct for reverse causality by using the Steiger test [<span>3, 4</span>]. In addition, the authors do not appear to have conducted a leave-one-out test. This omission makes it impossible for the reader to determine whether the authors have excluded a single or multiple instrumental variables that could influence this causal relationship [<span>5</span>]. Such exclusions could significantly impact the overall MR estimate, casting doubt on the adherence to the exclusion limitation hypothesis. In light of these significant deficiencies, it is recommended that the results be reanalyzed and reevaluated.</p><p>We appreciate the authors' use of replication analysis to validate their findings. However, the replication cohort database source chosen should have minimal or no sample overlap with the exposure database used for the initial study. It is essential to ensure that the same diagnostic criteria are used as in the discovery cohort database. To ensure the reliability of the results [<span>6</span>].</p><p>The final major problem with this study is the omission of power calculations. Statistical power is considered one of the major challenges in MR studies because most genetic variants only predict a small fraction of phenotypic variation. A recent study emphasizes the importance of being cautious when excluding single nucleotide polymorphisms (SNPs) to address horizontal pleiotropy. If the SNPs linked to confounding factors are crucial to the phenotype being studied, excluding them might inadvertently lead to “blindly reducing the noise,” which could weaken the ability to detect signals and raise the likelihood of Type I errors [<span>7</span>]. While we applaud the authors' efforts to address the assumption of independence, it is also important to recognize the significance of statistical efficacy [<span>8</span>].</p><p>In conclusion, our reassessment presents a more nuanced position by utilizing precise definitions of phenotypes and expanded analytical techniques. This includes a thorough evaluation of instrumental variables and power analysis. We commend the authors for exploring the causal relationship between the two, which is instructive for the clinical in-depth investigation of the etiology of facial rejuvenation. However, further improvement of the research process is still essential for establishing a strong causal relationship. In addition, triangulation, including large-scale prospective cohort studies and randomized controlled trials, should be considered to strengthen the evidence.</p><p>Hainan Li and Ao He are responsible for manuscript writing and topic selection; Xian Zhao is responsible for theoretical guidance and coordination.</p><p>The authors have nothing to report.</p><p>The authors declare no conflicts of interest.</p>","PeriodicalId":15546,"journal":{"name":"Journal of Cosmetic Dermatology","volume":"24 1","pages":""},"PeriodicalIF":2.3000,"publicationDate":"2024-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11743224/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Cosmetic Dermatology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/jocd.16597","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"DERMATOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
This article examines the connection between beverage consumption and facial aging, and evaluates the potential causal relationship between the two using Mendelian randomization (MR) analysis. This provides a new research direction for studying the potential causes of facial aging. But there are still some serious problems with the article.
First, the exposure and outcome data utilized in the author's study were sourced from the same database, UK Biobank, leading to a significant overlap in samples. This overlap is a widely recognized factor that can influence MR bias, including issues like winner's curse and weak instrumental variables [1]. Such a wide overlap would increase the incidence of Class I errors, leading to an overestimation of the causal effect [2]. Therefore, we believe that it is necessary for the authors to perform additional sensitivity analyses or use non-overlapping cohorts. Recently, a new approach called MRLap, which addresses sample overlap by correcting using regression intercepts for cross-trait linkage imbalance scores, has demonstrated a good fit in simulations with 5% to 95% overlap [1].
In the selection of instrumental variables, the authors did not disclose the specific information of each instrumental variable, especially the P-value related to the outcome phenotype. The study did not correct for reverse causality by using the Steiger test [3, 4]. In addition, the authors do not appear to have conducted a leave-one-out test. This omission makes it impossible for the reader to determine whether the authors have excluded a single or multiple instrumental variables that could influence this causal relationship [5]. Such exclusions could significantly impact the overall MR estimate, casting doubt on the adherence to the exclusion limitation hypothesis. In light of these significant deficiencies, it is recommended that the results be reanalyzed and reevaluated.
We appreciate the authors' use of replication analysis to validate their findings. However, the replication cohort database source chosen should have minimal or no sample overlap with the exposure database used for the initial study. It is essential to ensure that the same diagnostic criteria are used as in the discovery cohort database. To ensure the reliability of the results [6].
The final major problem with this study is the omission of power calculations. Statistical power is considered one of the major challenges in MR studies because most genetic variants only predict a small fraction of phenotypic variation. A recent study emphasizes the importance of being cautious when excluding single nucleotide polymorphisms (SNPs) to address horizontal pleiotropy. If the SNPs linked to confounding factors are crucial to the phenotype being studied, excluding them might inadvertently lead to “blindly reducing the noise,” which could weaken the ability to detect signals and raise the likelihood of Type I errors [7]. While we applaud the authors' efforts to address the assumption of independence, it is also important to recognize the significance of statistical efficacy [8].
In conclusion, our reassessment presents a more nuanced position by utilizing precise definitions of phenotypes and expanded analytical techniques. This includes a thorough evaluation of instrumental variables and power analysis. We commend the authors for exploring the causal relationship between the two, which is instructive for the clinical in-depth investigation of the etiology of facial rejuvenation. However, further improvement of the research process is still essential for establishing a strong causal relationship. In addition, triangulation, including large-scale prospective cohort studies and randomized controlled trials, should be considered to strengthen the evidence.
Hainan Li and Ao He are responsible for manuscript writing and topic selection; Xian Zhao is responsible for theoretical guidance and coordination.
期刊介绍:
The Journal of Cosmetic Dermatology publishes high quality, peer-reviewed articles on all aspects of cosmetic dermatology with the aim to foster the highest standards of patient care in cosmetic dermatology. Published quarterly, the Journal of Cosmetic Dermatology facilitates continuing professional development and provides a forum for the exchange of scientific research and innovative techniques.
The scope of coverage includes, but will not be limited to: healthy skin; skin maintenance; ageing skin; photodamage and photoprotection; rejuvenation; biochemistry, endocrinology and neuroimmunology of healthy skin; imaging; skin measurement; quality of life; skin types; sensitive skin; rosacea and acne; sebum; sweat; fat; phlebology; hair conservation, restoration and removal; nails and nail surgery; pigment; psychological and medicolegal issues; retinoids; cosmetic chemistry; dermopharmacy; cosmeceuticals; toiletries; striae; cellulite; cosmetic dermatological surgery; blepharoplasty; liposuction; surgical complications; botulinum; fillers, peels and dermabrasion; local and tumescent anaesthesia; electrosurgery; lasers, including laser physics, laser research and safety, vascular lasers, pigment lasers, hair removal lasers, tattoo removal lasers, resurfacing lasers, dermal remodelling lasers and laser complications.