ArticleFrontiers in neurology2025
Phenotypic aging mediates the association between neutrophil percentage-to-albumin ratio and muscular dystrophies: a population-based study.
Article in Frontiers in neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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1 citing paper in PubMed.
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Authors and funding
4 authors.
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Abstract
Background: Current research on Muscular Dystrophies (MD) suggests that its occurrence is closely related to several mechanisms, including gene mutations, dystrophin deficiency, and alterations in the Akt/mTOR/p70S6K signaling pathway. The development of MD is influenced by factors such as genetics, inflammation, age, and underlying conditions. However, few studies have explored the association between the Neutrophil Percentage-to-Albumin Ratio (NPAR), phenotypic age, and MD. This study investigates the relationship between NPAR and MD and evaluates whether phenotypic age influences this association. Methods: Subgroup analysis, restricted cubic splines (RCS), and multivariable logistic regression were employed to explore the relationship between NPAR and MD. Additionally, mediation analysis was conducted to investigate the potential role of phenotypic age in the relationship between NPAR and MD. Results: A total of 3,416 participants were included in this study, among whom 268 cases of MD were reported (6%, weighted). After adjusting for all variables using multivariable logistic regression, each unit increase in NPAR and phenotypic age was associated with a 29% (OR = 1.29, 95% CI: 1.19-1.39) and 7% (OR = 1.07, 95% CI: 1.03-1.12) increase in the odds of muscular dystrophies, respectively. Consistent results were obtained when NPAR and phenotypic age were categorized into tertiles, with a Conclusion: This study found a significant positive correlation between NPAR and MD, with phenotypic age acting as a partial mediator in this relationship. This finding underscores the potential of NPAR as a predictive marker for MD prevalence and highlights the importance of promoting healthy aging to reduce the risk of MD.
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