Evidence map›Paper›PMID 26161663›Full record

ArticlePloS one2015

Low Serum Neutrophil Gelatinase-associated Lipocalin Level as a Marker of Malnutrition in Maintenance Hemodialysis Patients.

Hirotaka Imamaki, Akira Ishii, Hideki Yokoi, Masato Kasahara, Takashige Kuwabara, Keita P Mori, Yukiko Kato, Takashi Kuwahara, Masugi Satoh, Kimihiko Nakatani and 7 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.8field-weighted citation impact, top 27% 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

9 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Review
  3. Observational
  4. Potential Biomarkers in Diagnosis of Renal Acanthamoebiasis.International journal of molecular sciences · 2021
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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

17 authors at 5 institutions in 1 country.

Hirotaka ImamakiDepartment of Nephrology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Akira IshiiDepartment of Nephrology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Hideki YokoiDepartment of Nephrology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Masato KasaharaInstitute for Advancement of Clinical and Translational Science, Kyoto University Hospital, Kyoto, Japan.
Takashige KuwabaraDepartment of Nephrology, Kyoto University Graduate School of Medicine, Kyoto, Japan; Department of Nephrology, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan.
Keita P MoriDepartment of Nephrology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Yukiko KatoDepartment of Nephrology, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Takashi KuwaharaDepartment of Nephrology, Saiseikai Ibaraki Hospital, Osaka, Japan.
Masugi SatohMisugikai Satou Hospital, Osaka, Japan.
Kimihiko NakataniFirst Department of Internal Medicine, Nara Medical University, Nara, Japan.
Yoshihiko SaitoFirst Department of Internal Medicine, Nara Medical University, Nara, Japan.
Naohisa TomosugiDivision of Advanced Medicine, Medical Research Institute, Kanazawa Medical University, Kanazawa, Japan.
Akira SugawaraDepartment of Nephrology, Osaka Red Cross Hospital, Osaka, Japan.
Kazuwa NakaoTK Project, Medical Innovation Center, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Masashi MukoyamaDepartment of Nephrology, Kyoto University Graduate School of Medicine, Kyoto, Japan; Department of Nephrology, Kumamoto University Graduate School of Medical Sciences, Kumamoto, Japan.
Motoko YanagitaDepartment of Nephrology, Kyoto University Graduate School of Medicine, Kyoto, Japan; TMK Project, Medical Innovation Center, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Kiyoshi MoriTMK Project, Medical Innovation Center, Kyoto University Graduate School of Medicine, Kyoto, Japan.
Kyoto University · JPKanazawa Medical University · JPSatou Hospital · JPKyoto University Hospital · JPNara Medical University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNeutrophil gelatinase-associated lipocalin (NGAL or LCN2) is an iron-transporting factor which possesses various activities such as amelioration of kidney injury and host defense against pathogens. Its circulating concentrations are elevated in acute and chronic kidney diseases and show a positive correlation with poor renal outcome and mortality, but its clinical significance in maintenance hemodialysis (HD) patients remains elusive.

methodsSerum NGAL levels were determined by enzyme-linked immunosorbent assay in out-patient, Japanese HD subjects. Their correlation to laboratory findings and morbidity (as development of severe infection or serum albumin reduction) was investigated using linear regression analysis and χ2 test.

resultsPre-dialysis serum NGAL levels in HD patients were elevated by 13-fold compared to healthy subjects (n=8, P<0.001). In a cross-sectional study of 139 cases, serum NGAL concentrations were determined independently by % creatinine generation rate (an indicator of muscle mass, standardized coefficient β=0.40, P<0.001), peripheral blood neutrophil count (β=0.38, P<0.001) and anion gap (which likely reflects dietary protein intake, β=0.16, P<0.05). Iron administration to anemic HD patients caused marked elevation of peripheral blood hemoglobin, serum ferritin and iron-regulatory hormone hepcidin-25 levels, but NGAL levels were not affected. In a prospective study of 87 cases, increase in serum albumin levels a year later was positively associated to baseline NGAL levels by univariate analysis (r=0.36, P<0.01). Furthermore, within a year, patients with the lowest NGAL tertile showed significantly increased risk for marked decline in serum albumin levels (≥0.4 g/dl; odds ratio 5.5, 95% confidence interval 1.5-20.3, P<0.05) and tendency of increased occurrence of severe infection requiring admission (odds ratio 3.1, not significant) compared to the middle and highest tertiles.

conclusionLow serum NGAL levels appear to be associated with current malnutrition and also its progressive worsening in maintenance HD patients.

Indexed as

Renal DialysisAcute-Phase ProteinsAgedAge FactorsAortaBiomarkersDisease ProgressionFemaleFollow-Up StudiesHumansInflammationIronLinear ModelsLipocalin-2LipocalinsMaleAcute-Phase ProteinsBiomarkersIronLCN2 protein, humanLipocalin-2LipocalinsProto-Oncogene ProteinsSerum Albumin

Identifiers

PMID26161663
PMCPMC4498679
OpenAlexW2204158587

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LicenceCC BY
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Registered trials

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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.