TY - JOUR
T1 - Dietary B vitamin intake is associated with lower urinary monomethyl arsenic and oxidative stress marker 15-F2t-isoprostane among New Hampshire adults
AU - Howe, Caitlin G.
AU - Li, Zhigang
AU - Zens, Michael S.
AU - Palys, Thomas
AU - Chen, Yu
AU - Channon, Jacqueline Y.
AU - Karagas, Margaret R.
AU - Farzan, Shohreh F.
N1 - Funding Information:
Supported in part by NIH grants R00ES024144, T32ES013678, and R01CA057494 and National Institute of General Medical Sciences grant P20GM104416. The multiplex cytokine assays were carried out at the DartLab, the Immune Monitoring and Flow Cytometry Shared Resource, supported by National Cancer Institute Cancer Center support grant P30CA023108-37 to the Norris Cotton Cancer Center and by National Institute of General Medical Sciences Immunology COBRE grant P30GM103415-15. Author disclosures: CGH, ZL, MSZ, TP, YC, JYC, MRK, and SFF, no conflicts of interest. Supplemental Tables 1–22 and Supplemental Figure 1 are available from the ‘‘Online Supporting Material’’ link in the online posting of the article and from the same link in the online table of contents at http://jn.nutrition.org. Address correspondence to CGH (e-mail: caitligh@usc.edu). Abbreviations used: CVD, cardiovascular disease; DFE, dietary folate equivalent; DMA, dimethyl arsenic species; ICAM1, intercellular adhesion molecule 1; MMA, monomethyl arsenic species; MMP9, matrix metalloproteinase 9; PAI1, plasminogen activator inhibitor 1; PC, principal component; PCA, principal component analysis; SG, specific gravity; uDMA, dimethyl arsenic species in urine; UL, Tolerable Upper Intake Level; uMMA, monomethyl arsenic species in urine; VCAM1, vascular cell adhesion molecule 1; WQS, weighted quantile sum; 15-F2t-IsoP, 15-F2t-isoprostane.
Publisher Copyright:
© 2017 American Society for Nutrition.
PY - 2017/12/1
Y1 - 2017/12/1
N2 - Background: Arsenic exposure has been associated with an increased risk of cardiovascular disease (CVD). Growing evidence suggests that B vitamins facilitate arsenic metabolism and may protect against arsenic toxicity. However, to our knowledge, few studies have evaluated this in US populations. Objective: Our objective was to examine whether higher B vitamin intake is associated with enhanced arsenic metabolism and lower concentrations of preclinical markers of CVD among New Hampshire adults. Methods: We used weighted quantile sum (WQS) regression to evaluate the collective impact of 6 dietary B vitamins (thiamin, riboflavin, folate, niacin, and vitamins B-6 and B-12) on 1) the proportion of arsenic metabolites in urine and 2) 6 CVD-related markers [including urinary 15-F2t-isoprostane (15-F2t-IsoP)] among 418 participants (26-75 y of age) from the New Hampshire Health Study. Contributions of arsenic metabolites to B vitamin-CVD marker associations were also explored in structural equation models. Results: In WQS models, the weighted sum of B vitamin intakes from food sources was inversely associated with the proportion of monomethyl arsenic species in urine (uMMA) (β: -1.03; 95% CI: 21.91, 20.15; P = 0.02). Thiamin and vitamins B-6 and B-12 contributed the most to this association, whereas riboflavin had a negligible effect. Higher overall B vitamin intake was also inversely associated with 15-F2t-IsoP (β: -0.21; 95% CI: -0.32, -0.11; P < 0.01), with equal contributions from the 6 B vitamins, which was partially explained by differences in the proportion of uMMA (indirect effect β: -0.01; 95% CI: -0.04, -0.00). Conclusions: Among New Hampshire adults, higher intakes of certain B vitamins (particularly thiamin and vitamins B-6 and B-12 from food sources) may reduce the proportion of uMMA, an intermediate of arsenic metabolism that has been associated with an increased risk of CVD. Higher overall B vitamin intake may also reduce urinary 15-F2t-IsoP, a marker of oxidative stress and potential risk factor for CVD, in part by reducing the proportion of uMMA.
AB - Background: Arsenic exposure has been associated with an increased risk of cardiovascular disease (CVD). Growing evidence suggests that B vitamins facilitate arsenic metabolism and may protect against arsenic toxicity. However, to our knowledge, few studies have evaluated this in US populations. Objective: Our objective was to examine whether higher B vitamin intake is associated with enhanced arsenic metabolism and lower concentrations of preclinical markers of CVD among New Hampshire adults. Methods: We used weighted quantile sum (WQS) regression to evaluate the collective impact of 6 dietary B vitamins (thiamin, riboflavin, folate, niacin, and vitamins B-6 and B-12) on 1) the proportion of arsenic metabolites in urine and 2) 6 CVD-related markers [including urinary 15-F2t-isoprostane (15-F2t-IsoP)] among 418 participants (26-75 y of age) from the New Hampshire Health Study. Contributions of arsenic metabolites to B vitamin-CVD marker associations were also explored in structural equation models. Results: In WQS models, the weighted sum of B vitamin intakes from food sources was inversely associated with the proportion of monomethyl arsenic species in urine (uMMA) (β: -1.03; 95% CI: 21.91, 20.15; P = 0.02). Thiamin and vitamins B-6 and B-12 contributed the most to this association, whereas riboflavin had a negligible effect. Higher overall B vitamin intake was also inversely associated with 15-F2t-IsoP (β: -0.21; 95% CI: -0.32, -0.11; P < 0.01), with equal contributions from the 6 B vitamins, which was partially explained by differences in the proportion of uMMA (indirect effect β: -0.01; 95% CI: -0.04, -0.00). Conclusions: Among New Hampshire adults, higher intakes of certain B vitamins (particularly thiamin and vitamins B-6 and B-12 from food sources) may reduce the proportion of uMMA, an intermediate of arsenic metabolism that has been associated with an increased risk of CVD. Higher overall B vitamin intake may also reduce urinary 15-F2t-IsoP, a marker of oxidative stress and potential risk factor for CVD, in part by reducing the proportion of uMMA.
KW - 15-F-isoprostane
KW - Arsenic metabolism
KW - B vitamins
KW - Cardiovascular disease
KW - New Hampshire adults
UR - http://www.scopus.com/inward/record.url?scp=85036557192&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85036557192&partnerID=8YFLogxK
U2 - 10.3945/jn.117.253419
DO - 10.3945/jn.117.253419
M3 - Article
C2 - 29070711
AN - SCOPUS:85036557192
SN - 0022-3166
VL - 147
SP - 2289
EP - 2296
JO - Journal of Nutrition
JF - Journal of Nutrition
IS - 12
ER -