Effects of dietary sodium on metabolites: the Dietary Approaches to Stop Hypertension (DASH)-Sodium Feeding Study

被引:57
作者
Derkach, Andriy [1 ]
Sampson, Joshua [1 ]
Joseph, Justin [1 ,2 ]
Playdon, Mary C. [1 ]
Stolzenberg-Solomon, Rachael Z. [1 ]
机构
[1] NCI, Div Canc Epidemiol & Genet, NIH, Rockville, MD 20850 USA
[2] Virginia Commonwealth Univ, Dept Chem, Box 2006, Richmond, VA 23284 USA
关键词
metabolomics; epidemiology; sodium intake; trial; high and low sodium intake; feeding trial; African American; GAMMA-GLUTAMYL-TRANSFERASE; BLOOD-PRESSURE; CARDIOVASCULAR-DISEASE; MASS-SPECTROMETRY; SALT; IDENTIFICATION; METAANALYSIS; ASSOCIATION; PATHWAY; TRIAL;
D O I
10.3945/ajcn.116.150136
中图分类号
R15 [营养卫生、食品卫生]; TS201 [基础科学];
学科分类号
100403 ;
摘要
Background: High sodium intake is known to increase blood pressure and is difficult to measure in epidemiologic studies. Objective: We examined the effect of sodium intake on metabolites within the DASH (Dietary Approaches to Stop Hypertension Trial)Sodium Trial to further our understanding of the biological effects of sodium intake beyond blood pressure. Design: The DASH-Sodium Trial randomly assigned individuals to either the DASH diet (low in fat and high in protein, low-fat dairy, and fruits and vegetables) or a control diet for 12 wk. Participants within each diet arm received, in random order, diets containing high (150 nmol or 3450 mg), medium (100 nmol or 2300 mg), and low (50 nmol or 1150 mg) amounts of sodium for 30 d (crossover design). Fasting blood samples were collected at the end of each sodium intervention. We measured 531 identified plasma metabolites in 73 participants at the end of their high- and low-sodium interventions and in 46 participants at the end of their high-and medium-sodium interventions (N = 119). We used linear mixed-effects regression to model the relation between each log-transformed metabolite and sodium intake. We also combined the resulting P values with Fisher's method to estimate the association between sodium intake and 38 metabolic pathways or groups. Results: Six pathways were associated with sodium intake at a Bonferroni-corrected threshold of 0.0013 (e.g., fatty acid, food component or plant, benzoate, gamma-glutamyl amino acid, methionine, and tryptophan). Although 82 metabolites were associated with sodium intake at a false discovery rate <= 0.10, only 4-ethylphenylsufate, a xenobiotic related to benzoate metabolism, was significant at a Bonferroni-corrected threshold (P<10(-5)). Adjustment for co-inciding change in blood pressure did not substantively alter the association for the top-ranked metabolites. Conclusion: Sodium intake is associated with changes in circulating metabolites, including gut microbial, tryptophan, plant component, and gamma-glutamyl amino acid-related metabolites. This trial was registered at clinicaltrials.gov as NCT00000608.
引用
收藏
页码:1131 / 1141
页数:11
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共 43 条
  • [41] Analysis of metabolites in plasma reveals distinct metabolic features between Dahl salt-sensitive rats and consomic SS.13BN rats
    Wang, Le
    Hou, Entai
    Wang, Zhengjun
    Sun, Na
    He, Liqing
    Chen, Lan
    Liang, Mingyu
    Tian, Zhongmin
    [J]. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2014, 450 (01) : 863 - 869
  • [42] Comparative metabolomics in vegans and omnivores reveal constraints on diet-dependent gut microbiota metabolite production
    Wu, Gary D.
    Compher, Charlene
    Chen, Eric Z.
    Smith, Sarah A.
    Shah, Rachana D.
    Bittinger, Kyle
    Chehoud, Christel
    Albenberg, Lindsey G.
    Nessel, Lisa
    Gilroy, Erin
    Star, Julie
    Weljie, Aalim M.
    Flint, Harry J.
    Metz, David C.
    Bennett, Michael J.
    Li, Hongzhe
    Bushman, Frederic D.
    Lewis, James D.
    [J]. GUT, 2016, 65 (01) : 63 - 72
  • [43] Microbial metabolism of dietary components to bioactive metabolites: opportunities for new therapeutic interventions
    Zhang, Linda S.
    Davies, Sean S.
    [J]. GENOME MEDICINE, 2016, 8