Evidence map›Paper›PMID 25051062›Full record

ArticlePloS one2014

The association of uremic toxins and inflammation in hemodialysis patients.

Heng-Jung Hsu, Chiung-Hui Yen, I-Wen Wu, Kuang-Hung Hsu, Chih-Ken Chen, Chiao-Yin Sun, Chia-Chi Chou, Chun-Yu Chen, Chi-Jen Tsai, Mai-Szu Wu and 1 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.8field-weighted citation impact, top 17% 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

15 citing papers in PubMed, 35 citations in OpenAlex.

  1. Trial
  2. Review
  3. Article
  4. SerumDiagnostics (Basel, Switzerland) · 2025
    Article
  5. Review
  6. Review
  7. Article
  8. Article
  9. Review
  10. Article
  11. Article
  12. p-Cresyl Sulfate.Toxins · 2017
    Review
  13. Article
  14. Article
  15. Article
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

11 authors at 4 institutions in 1 country.

Heng-Jung HsuDivision of Nephrology, Chang Gung Memorial Hospital, Keelung, Taiwan; The Graduate Institute of Clinical Medical Sciences, Chang Gung University Medical College, Taoyuan School of Medicine, Taoyuan, Taiwan.
Chiung-Hui YenDepartment of Pediatrics, Taipei Medical University Hospital, Taipei, Taiwan.
I-Wen WuDivision of Nephrology, Chang Gung Memorial Hospital, Keelung, Taiwan.
Kuang-Hung HsuLaboratory of Epidemiology, Department of Health Care Management, Chang Gung University, Taoyuan, Taiwan.
Chih-Ken ChenDivision of Psychiatry, Chang Gung Memorial Hospital, Keelung, Taiwan.
Chiao-Yin SunDivision of Nephrology, Chang Gung Memorial Hospital, Keelung, Taiwan.
Chia-Chi ChouDivision of Nephrology, Chang Gung Memorial Hospital, Keelung, Taiwan.
Chun-Yu ChenDivision of Nephrology, Chang Gung Memorial Hospital, Keelung, Taiwan.
Chi-Jen TsaiDivision of Nephrology, Chang Gung Memorial Hospital, Keelung, Taiwan.
Mai-Szu WuDivision of Nephrology, Taipei Medical University Hospital, Taipei, Taiwan; Department of Internal Medicine, Taipei Medical University, Taipei, Taiwan.
Chin-Chan LeeDivision of Nephrology, Chang Gung Memorial Hospital, Keelung, Taiwan.
Keelung Chang Gung Memorial Hospital · TWChang Gung University · TWTaipei Medical University · TWTaipei Medical University Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCardiovascular disease is the leading cause of mortality in hemodialysis patients and is associated with chronic inflammation. Elevation of uremic toxins, particular protein-bound uremic toxins, is a possible cause of hyper-inflammation in hemodialysis patients. But the association between uremic toxins and inflammatory markers in hemodialysis is still unclear.

methodsWe conducted a cross-sectional study to evaluate the association of the serum uremic toxins and inflammatory markers in hemodialysis patients.

resultsThe uremic toxins were not associated with inflammatory markers--including high sensitivity C-reactive protein, IL(Interleukin) -1β, IL-6, tumor necrosis factor-α. In multiple linear regression, serum levels of total p-cresol sulfate (PCS) were independently significantly associated with serum total indoxyl sulfate (IS) (standardized coefficient: 0.274, p<0.001), and co-morbidity of diabetes mellitus (DM) (standardized coefficient: 0.342, p<0.001) and coronary artery disease (CAD) (standardized coefficient: 0.128, p = 0.043). The serum total PCS levels in hemodialysis with co-morbidity of DM and CAD were significantly higher than those without co-morbidity of DM and CAD (34.10±23.44 vs. 16.36±13.06 mg/L, p<0.001). Serum levels of total IS was independently significantly associated with serum creatinine (standardized coefficient: 0.285, p<0.001), total PCS (standardized coefficient: 0.239, p = 0.001), and synthetic membrane dialysis (standardized coefficient: 0.139, p = 0.046).

conclusionThe study showed that serum levels of total PCS and IS were not associated with pro-inflammatory markers in hemodialysis patients. Besides, serum levels of total PCS were independently positively significantly associated with co-morbidity of CAD and DM.

Indexed as

AgedComorbidityCoronary Artery DiseaseCreatinineCresolsCross-Sectional StudiesDiabetes Mellitus, Type 2FemaleHumansIndicanInflammationInflammation MediatorsKidney Failure, ChronicMaleMiddle AgedRenal Dialysis4-cresol sulfateCreatinineCresolsIndicanInflammation MediatorsSulfuric Acid Esters

Identifiers

PMID25051062
PMCPMC4106871
OpenAlexW2025904350

What OpenQuestion holds

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LicenceCC BY
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.