Evidence map›Paper›PMID 33028763›Full record

ArticleJournal of atherosclerosis and thrombosis2021

Development and Clinical Application of an Enzyme-Linked Immunosorbent Assay for Oxidized High-Density Lipoprotein.

Takeshi Okada, Mizuki Sumida, Tohru Ohama, Yuki Katayama, Ayami Saga, Hiroyasu Inui, Kotaro Kanno, Daisaku Masuda, Masahiro Koseki, Makoto Nishida and 2 more

Open access · diamondAbstract read
In one paragraph

Article in Journal of atherosclerosis and thrombosis, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.6field-weighted citation impact, top 30% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. Trial
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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

12 authors at 1 institution in 2 countries.

Takeshi OkadaDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine.
Mizuki SumidaResearch Laboratories, Hitachi Chemical Diagnostics Systems Co., Ltd.
Tohru OhamaDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine.
Yuki KatayamaResearch Laboratories, Hitachi Chemical Diagnostics Systems Co., Ltd.
Ayami SagaDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine.
Hiroyasu InuiDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine.
Kotaro KannoDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine.
Daisaku MasudaDepartment of Cardiology, Rinku General Medical Center.
Masahiro KosekiDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine.
Makoto NishidaDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine.
Yasushi SakataDepartment of Cardiovascular Medicine, Osaka University Graduate School of Medicine.
Shizuya YamashitaDepartment of Cardiology, Rinku General Medical Center.
Osaka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimsHDL particles have various anti-atherogenic functions, whereas HDL from atherosclerotic patients was demonstrated to be dysfunctional. One possible mechanism for the formation of dysfunctional HDL is the oxidation of its components. However, oxidized HDLs (Ox-HDLs) remain to be well investigated due to lack of reliable assay systems.

methodsWe have developed a novel sandwich enzyme-linked immunosorbent assay (ELISA) for Ox-HDL by using the FOH1a/DLH3 antibody, which can specifically recognize oxidized phosphatidylcholine, a major component of HDL phospholipid (HDL-PL). We defined forced oxidation of 1 mg/L HDL-PL as 1 U/L Ox-HDL. We assessed serum Ox-HDL levels of normolipidemic healthy subjects ( n=94) and dyslipidemic patients (n=177).

resultsThe coefficients of variation of within-run and between-run assays were 12.5% and 13.5%. In healthy subjects, serum Ox-HDL levels were 28.5±5.0 (mean±SD) U/L. As Ox-HDL levels were moderately correlated with HDL-PL (r=0.59), we also evaluated the Ox-HDL/HDL-PL ratio, which represents the proportion of oxidized phospholipids in HDL particles. In dyslipidemic patients, Ox-HDL levels were highly variable and ranged from 7.2 to 62.1U/L, and were extremely high (50.4±13.3U/L) especially in patients with hyperalphalipoproteinemia due to cholesteryl ester transfer protein deficiency. Regarding patients with familial hypercholesterolemia, those treated with probucol, which is a potent anti-oxidative and anti-hyperlipidemic drug, showed significantly lower Ox-HDL (16.2±5.8 vs. 30.2±5.4, p<0.001) and Ox-HDL/HDL-PL ratios (0.200±0.035 vs. 0.229±0.031, p=0.015) than those without probucol.

conclusionWe have established a novel sandwich ELISA for Ox-HDL, which might be a useful and easy strategy to evaluate HDL functionality, although the comparison study between this Ox-HDL ELISA and the assay of HDL cholesterol efflux capacity remains to be done. Our results indicated that probucol treatment may be associated with lower Ox-HDL levels.

Indexed as

DyslipidemiasLipoproteins, HDLProbucolAdultAntioxidantsAtherosclerosisEnzyme-Linked Immunosorbent AssayFemaleHumansHyperlipoproteinemia Type IIHypolipidemic AgentsMaleOxidation-ReductionReproducibility of ResultsAntioxidantsHypolipidemic AgentsLipoproteins, HDLProbucolApolipoproteinsFamilial hypercholesterolemiaHDLOxidized lipidsPhospholipids

Identifiers

PMID33028763
PMCPMC8265427
OpenAlexW3091798476

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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.