Evidence map›Paper›PMID 14577659›Full record

Trial reportLipids2003

Vitamin E supplementation increases circulating vitamin E metabolites tenfold in end-stage renal disease patients.

Kylie Sherée Smith, Chia-Lin Lee, James W Ridlington, Scott W Leonard, Sridevi Devaraj, Maret G Traber

Abstract readClinical Trial
PubMed Publisher
In one paragraph

Trial report in Lipids, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
2.1field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 50 citations in OpenAlex.

  1. Pooled it
  2. Systemic Redox Imbalance in Chronic Kidney Disease: A Systematic Review.Oxidative medicine and cellular longevity · 2016
    Pooled it
  3. Trial
  4. Provision of antioxidant therapy in hemodialysis (PATH): a randomized clinical trial.Journal of the American Society of Nephrology : JASN · 2014
    Trial
  5. Low plasma α-tocopherol concentrations and adverse clinical outcomes in diabetic hemodialysis patients.Clinical journal of the American Society of Nephrology : CJASN · 2013
    Trial
  6. Article
  7. Article
  8. Review
  9. Review
  10. Oxidative Stress in Hemodialysis Patients: A Review of the Literature.Oxidative medicine and cellular longevity · 2017
    Review
  11. Review
  12. Review
  13. Review
  14. Vitamin E in renal therapeutic regiments.Pediatric nephrology (Berlin, Germany) · 2006
    Review
  15. Article
  16. Review
  17. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Kylie Sherée SmithDepartment of Nutrition and Food Management, Oregon State University, Corvallis, Oregon 97331, USA.
Chia-Lin Lee
James W Ridlington
Scott W Leonard
Sridevi Devaraj
Maret G Traber
Oregon State University · USUniversity of California Davis Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Vitamin E supplementation could elevate circulating vitamin E metabolites while modulating oxidative and inflammatory status in end-stage renal failure patients undergoing hemodialysis. Plasma concentrations of carboxyethyl-hydroxychromanols (alpha- and gamma-CEHC), ascorbic acid, alpha- and gamma-tocopherols, F2-isoprostanes, and inflammatory biomarkers [tumor necrosis factor-alpha (TNF-alpha), interleukin-6 (IL-6), ferritin, and C-reactive protein (CRP)] were measured in blood samples obtained from patients (n = 11) before and after dialysis on two occasions prior to, and at 1 and 2 mon of daily vitamin E supplementation (400 IU RRR-alpha-tocopherol). Supplementation nearly doubled plasma alpha-tocopherol concentrations (from 18 +/- 0.5 to 31 +/- 1.7 microM, P < 0.0001), whereas gamma-tocopherol concentrations decreased (from 2.8 +/- 0.3 to 1.7 +/- 0.2 microM, P = 0.001). Serum alpha-CEHC increased 10-fold from 68 +/- 3 to 771 +/- 175 nM (P < 0.0001), and gamma-CEHC increased from 837 +/- 164 to 1136 +/- 230 nM (P = 0.008). Vitamin E supplementation also increased postdialysis hematocrits from 38 +/- 1% to 41 +/- 1% (P < 0.001). Dietary antioxidant intakes (vitamins E and C) were low in most subjects; plasma ascorbic acid levels (88 +/- 27 microM) decreased significantly with dialysis (33 +/- 11 microM, P = 0.01). Plasma IL-6, CRP, TNF-alpha, and free F2-isoprostane concentrations were elevated throughout the study. There is a complex relationship between chronic inflammation and oxidative stress that is not mitigated by short-term vitamin E supplementation. Importantly, serum vitamin E metabolite concentrations that increased 10-fold within 30 d of supplementation did not increase further, suggesting routes other than urine for removal of metabolites.

Indexed as

AgedAntioxidantsAscorbic AcidBiological AvailabilityC-Reactive ProteinDietary SupplementsErythropoietinFemaleFerritinsHumansIronKidney Failure, ChronicMaleMiddle AgedRenal DialysisSolubilityAntioxidantsAscorbic AcidC-Reactive ProteinErythropoietinFerritinsIronVitamin E

Identifiers

PMID14577659
OpenAlexW1980860122

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.