{"title":"Associations between exposure to OPEs and rheumatoid arthritis risk among adults in NHANES, 2011-2018","authors":"Sneha Singh, Elsa Pirouz, Amir Shahmoradi","doi":"arxiv-2409.00745","DOIUrl":null,"url":null,"abstract":"Rheumatoid arthritis (RA) has an intricate etiology that includes\nenvironmental factors as well as genetics. Organophosphate esters (OPEs) are\nfrequently used as chemical additives in many personal care products and\nhousehold items. However, there has been limited research on their potential\neffects on rheumatoid arthritis (RA). The specific associations between OPEs\nand RA remain largely unexplored. This study investigates any potential\nassociations between adult rheumatoid arthritis risk and exposure to OPEs. We\ninvestigated data from the National Health and Nutrition Examination Survey\n(NHANES) 2011-2018 among participants over 20 years old. In two models,\nmultivariable logistic regression was utilized to investigate the relationship\nbetween exposure to OPEs and RA. Furthermore, subgroup analyses stratified by\nage, gender, and dose exposure response were evaluated. Generalized additive\nmodels and smooth curve fits were used to characterize the nonlinear\nrelationship between RA and OPEs. In conclusion, 5490 individuals (RA: 319,\nNon-RA: 5171) were analyzed. Higher quantiles (Q4) of DPHP and DBUP showed a\nhigher prevalence of RA than the lowest quantiles. Our findings show that adult\nRA prevalence is higher in those who have been exposed to OPEs (DPHP, DBUP).\nThese correlations seem to be stronger among women, the elderly, those with\nhigher BMIs, and those who have diabetes. The dose-response curve for DPHP and\nDBUP demonstrated an upward-sloping trend. In contrast, BCEP and BCPP showed a\nU-shaped relationship and an inverted U-shaped relationship with the\nprobability of RA. BDCPP demonstrates a complex relationship with a peak at\nlower concentrations followed by a decrease. Our study concludes that exposure\nto OPEs plays a crucial role in the pathogenesis of RA.","PeriodicalId":501266,"journal":{"name":"arXiv - QuanBio - Quantitative Methods","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"arXiv - QuanBio - Quantitative Methods","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/arxiv-2409.00745","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Rheumatoid arthritis (RA) has an intricate etiology that includes
environmental factors as well as genetics. Organophosphate esters (OPEs) are
frequently used as chemical additives in many personal care products and
household items. However, there has been limited research on their potential
effects on rheumatoid arthritis (RA). The specific associations between OPEs
and RA remain largely unexplored. This study investigates any potential
associations between adult rheumatoid arthritis risk and exposure to OPEs. We
investigated data from the National Health and Nutrition Examination Survey
(NHANES) 2011-2018 among participants over 20 years old. In two models,
multivariable logistic regression was utilized to investigate the relationship
between exposure to OPEs and RA. Furthermore, subgroup analyses stratified by
age, gender, and dose exposure response were evaluated. Generalized additive
models and smooth curve fits were used to characterize the nonlinear
relationship between RA and OPEs. In conclusion, 5490 individuals (RA: 319,
Non-RA: 5171) were analyzed. Higher quantiles (Q4) of DPHP and DBUP showed a
higher prevalence of RA than the lowest quantiles. Our findings show that adult
RA prevalence is higher in those who have been exposed to OPEs (DPHP, DBUP).
These correlations seem to be stronger among women, the elderly, those with
higher BMIs, and those who have diabetes. The dose-response curve for DPHP and
DBUP demonstrated an upward-sloping trend. In contrast, BCEP and BCPP showed a
U-shaped relationship and an inverted U-shaped relationship with the
probability of RA. BDCPP demonstrates a complex relationship with a peak at
lower concentrations followed by a decrease. Our study concludes that exposure
to OPEs plays a crucial role in the pathogenesis of RA.