High level of selenium exposure in the Strong Heart Study: a cause for incident cardiovascular disease?. (Record no. 593)

MARC details
000 -LEADER
fixed length control field 02502nam a22003137a 4500
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fixed length control field 220511s20222022 xxu||||| |||| 00| 0 eng d
022 ## - INTERNATIONAL STANDARD SERIAL NUMBER
International Standard Serial Number 1523-0864
024 ## - OTHER STANDARD IDENTIFIER
Standard number or code 10.1089/ars.2022.0029 [doi]
040 ## - CATALOGING SOURCE
Original cataloging agency Ovid MEDLINE(R)
099 ## - LOCAL FREE-TEXT CALL NUMBER (OCLC)
PMID 35350849
245 ## - TITLE STATEMENT
Title High level of selenium exposure in the Strong Heart Study: a cause for incident cardiovascular disease?.
251 ## - Source
Source Antioxidants & Redox Signaling. 2022 Mar 30
252 ## - Abbreviated Source
Abbreviated source Antioxid Redox Signal. 2022 Mar 30
253 ## - Journal Name
Journal name Antioxidants & redox signaling
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Year 2022
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Manufacturer FY2022
260 ## - PUBLICATION, DISTRIBUTION, ETC.
Publication date 2022 Mar 30
265 ## - SOURCE FOR ACQUISITION/SUBSCRIPTION ADDRESS [OBSOLETE]
Publication status aheadofprint
266 ## - Date added to catalog
Date added to catalog 2022-05-11
520 ## - SUMMARY, ETC.
Abstract Increasing evidence suggests that high selenium (Se) exposure is associated with adverse health effects. However, limited evidence exists on the association of Se exposure with cardiovascular disease (CVD), especially in communities affected by high naturally occurring Se in environmental media. We evaluated the prospective association between urinary Se levels and CVD incidence and mortality for 2,727 American Indian adults who participated in the Strong Heart Study, with urinary Se levels measured at baseline (1989-1991) and CVD outcomes ascertained through 2017. The median (interquartile range) of urinary Se was 49.0 (36.7, 67.4) microg/g creatinine. The multivariable adjusted hazard ratios (95%CI) of incident CVD, coronary heart disease, and stroke comparing the 75th vs. 25th percentile of urinary Se distributions were 1.11 (1.01, 1.22), 1.05 (0.94, 1.17), and 1.08 (0.88, 1.33), respectively. In flexible dose-response models, increased risk for CVD incidence was only observed when urinary Se level exceeded 60 microg/g creatinine. For CVD mortality, a non-statistically significant U-shaped relationship was found across urinary Se levels. There was no evidence of effect modification by other urinary metal/metalloid levels. Our observation leads to the hypothesis that elevated Se exposure is a risk factor for CVD, especially in Se-replete populations.
546 ## - LANGUAGE NOTE
Language note English
650 ## - SUBJECT ADDED ENTRY--TOPICAL TERM
Topical term or geographic name entry element IN PROCESS -- NOT YET INDEXED
651 ## - SUBJECT ADDED ENTRY--GEOGRAPHIC NAME
Institution MedStar Health Research Institute
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Medline publication type Journal Article
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Local Authors Umans, Jason G
790 ## - Authors
All authors Ali T, Best LG, Cole SA, Domingo-Relloso A, Fretts A, Goessler W, Moon KA, Navas-Acien A, Nigra AE, Tellez-Plaza M, Umans JG, Valeri L, Zhao D
856 ## - ELECTRONIC LOCATION AND ACCESS
DOI <a href="https://dx.doi.org/10.1089/ars.2022.0029">https://dx.doi.org/10.1089/ars.2022.0029</a>
Public note https://dx.doi.org/10.1089/ars.2022.0029
942 ## - ADDED ENTRY ELEMENTS (KOHA)
Koha item type Journal Article
Item type description Article
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Withdrawn status Lost status Damaged status Not for loan Collection Home library Current library Date acquired Total Checkouts Full call number Barcode Date last seen Price effective from Koha item type
          MedStar Authors Catalog MedStar Authors Catalog 05/11/2022   35350849 35350849 05/11/2022 05/11/2022 Journal Article

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