This study utilized data from two cycles of the 2011–2014 NHANES surveys, recruiting a total of 1858 participants, aimed at exploring the association between grip strength in U.S. adults aged 20 years and older and concentrations of phenols and parabens in urine. Using generalized linear models, we found a significant relationship between BPA and decreased grip strength, while BP3 and BuP were closely associated with increased grip strength. In contrast, MeP, PrP, 24-DCB, and 25-DCB showed no statistically significant impact on grip strength. Further exploration with dose-response curves revealed varying degrees of compound-specific dose dependency on grip strength. Utilizing mixed-effects models such as WQS and qgcomp, we identified significant statistical differences between phenols and parabens mixtures and decreased grip strength, with BPA contributing most significantly; in the qgcomp model, BuP, BPA, and MeP exhibited positive weights, whereas BPA, 25-DCB, PrP, and 24-DCB showed negative weights, with BPA having the most pronounced negative weight. Additionally, comprehensive subgroup analyses were conducted based on age, gender, race/ethnicity, poverty status, diabetes, hypertension, smoking, and alcohol consumption habits. Subgroup analysis results highlighted significant differences across demographic indicators, underlying diseases, and lifestyle habits, with demographic factors such as age and gender exerting the most notable influence on the association between phenols and parabens and grip strength, followed by underlying diseases, while the impact of lifestyle habits such as smoking and alcohol consumption was comparatively minor.
BPA is a widely used endocrine-disrupting chemical employed primarily in the production of polycarbonate plastics, epoxy resins lining metal cans, and various plastic consumer goods. Findings from the Hartford County cohort16 indicate that impaired grip strength is associated with features of metabolic syndrome such as elevated fasting triglycerides, blood pressure, and waist circumference, as well as insulin resistance. Moreover, research by Oliana Carnevali et al.24 suggests that fish fed with BPA-contaminated feed exhibit decreased unsaturated fatty acids and increased triglycerides and saturated fatty acid chains, with alterations in protein content, affecting the composition and texture of skeletal muscle. Experimental studies by Kristina et al. 25using rodent models suggest that maternal exposure to BPA may induce insulin resistance in offspring rats, thereby impacting skeletal muscle function.
Additionally, it is noteworthy that we observed a positive correlation between elevated levels of BP3 and BuP with grip strength. Luo et al. 26analyzing 2013–2014 NHANES data, demonstrated that grip strength correlates with BMD in non-adjacent skeletal regions, highlighting hand grip strength as an indicator for assessing BMD across different genders and menopausal statuses. Concurrently, a study27indicated an association between hand grip strength and hand BMD in healthy individuals aged 19–50 years. Wang et al.17 based on NHANES data, reported an association between BP3 and paraben compounds with increased BMD, supported by further validation from Gu et al. 18. Thus, we hypothesize that the positive correlation between BP3 and BuP with grip strength may be related to BMD. Despite limited current research on the impact of BP3 and BuP on grip strength, their specific mechanisms remain unclear and warrant further investigation. Our study provides preliminary evidence of the association between BP3, BuP, and grip strength.
The impairment of grip strength is associated with characteristics of metabolic syndrome and insulin resistance. BPA a common endocrine disruptor, has garnered particular attention for its involvement in insulin resistance, obesity, and type 2 diabetes (T2D) development. A previous study demonstrated28 that exposure to BPA exacerbates insulin resistance during pregnancy, with reduced insulin-stimulated Akt phosphorylation observed in skeletal muscle and liver tissues of pregnant mice treated with bisphenol A. Concurrently, another study29 indicated that BPA exposure may exacerbate existing metabolic stress, leading to increased cellular senescence. Currently, the mechanisms through which phenols and parabens impact grip strength remain unclear, lacking direct evidence and necessitating further research for validation.
The association between environmental pollutants and grip strength has garnered increasing attention. Multiple studies have indicated a negative correlation between exposure to metal mixtures such as cadmium, copper, lead, strontium, and arsenic, and grip strength, while zinc shows a positive correlation21,30–32. Sun et al. found that phthalate exposure among American adults was inversely related to grip strength33. Additionally, glyphosate, a widely used herbicide globally, has been linked unfavorably with all grip strength measurements34. Both indoor and outdoor air pollution have also been reported to lower grip strength in adults35. Grip strength exhibits diverse associations with environmental pollutants. Phenols and parabens, prevalent pollutants in personal care and consumer products, are widely distributed in the environment. Therefore, it is imperative to conduct in-depth research into their relationship with grip strength.
A study on serum testosterone levels and urinary concentrations of BPA, BP-3, triclosan, and parabens has demonstrated differential results influenced by age and sex 36. Among adolescents, BPA shows a negative correlation with testosterone levels in boys but a positive correlation in girls, whereas BP-3 is significantly associated with decreased testosterone levels only in adolescent boys. Multiple studies17,18,37,38 on phenols and parabens have also indicated gender-specific associations. In this study, significant variations in the relationship between phenols and parabens with grip strength were observed across gender and age groups.
Our study has several strengths. Firstly, we utilized nationally representative NHANES data collected through standardized protocols and multiple measurement methods, ensuring high-quality data control. Additionally, we conducted subgroup analyses based on age, sex, economic status, race, underlying diseases, and lifestyle habits. Furthermore, we employed the qgcomp model to address the limitation of the WQS model, which assumes a single direction of effect. However, our study also has several limitations. Firstly, it is cross-sectional in design, thus precluding causal inference regarding the impact of mixed chemical exposures on cognitive function. Secondly, despite accounting for various covariates, residual and unmeasured confounding factors may still influence observational studies. Lastly, the rapid metabolism of phenols and parabens results in fluctuations in metabolite concentrations in urine over time.