Evidence map›Paper›PMID 27899853›Full record

ArticleActa Cardiologica Sinica2016

Four Statin Benefit Groups Defined by The 2013 ACC/AHA New Cholesterol Guideline are Characterized by Increased Plasma Level of Electronegative Low-Density Lipoprotein.

Chih-Sheng Chu, Liang-Yin Ke, Hua-Chen Chan, Hsiu-Chua Chan, Chih-Chieh Chen, Kai-Hung Cheng, Hsiang-Chun Lee, Hsuan-Fu Kuo, Ching-Tang Chang, Kuan-Cheng Chang and 3 more

Open access · greenAbstract read
In one paragraph

Article in Acta Cardiologica Sinica, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.9field-weighted citation impact, top 21% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

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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

13 authors at 4 institutions in 4 countries.

Chih-Sheng ChuDivision of Cardiology, Department of Internal Medicine, Kaohsiung Medical University (KMU) Hospital; ; Faculty of Medicine, College of Medicine, KMU; ; Center for Lipid Biosciences, KMU Hospital, KMU; ; Center for Lipid and Glycomedicine Research.
Liang-Yin KeCenter for Lipid Biosciences, KMU Hospital, KMU; ; Center for Lipid and Glycomedicine Research; ; Department of Medical Laboratory Science and Biotechnology, College of Health Sciences.
Hua-Chen ChanCenter for Lipid Biosciences, KMU Hospital, KMU; ; Center for Lipid and Glycomedicine Research; ; Graduate Institute of Medicine, College of Medicine, KMU, Kaohsiung, Taiwan.
Hsiu-Chua ChanCenter for Lipid and Glycomedicine Research.
Chih-Chieh ChenCenter for Lipid Biosciences, KMU Hospital, KMU.
Kai-Hung ChengDivision of Cardiology, Department of Internal Medicine, Kaohsiung Medical University (KMU) Hospital; ; Faculty of Medicine, College of Medicine, KMU; ; Center for Lipid Biosciences, KMU Hospital, KMU; ; Graduate Institute of Medicine, College of Medicine, KMU, Kaohsiung, Taiwan.
Hsiang-Chun LeeDivision of Cardiology, Department of Internal Medicine, Kaohsiung Medical University (KMU) Hospital; ; Faculty of Medicine, College of Medicine, KMU; ; Center for Lipid Biosciences, KMU Hospital, KMU; ; Graduate Institute of Medicine, College of Medicine, KMU, Kaohsiung, Taiwan.
Hsuan-Fu KuoDivision of Cardiology, Department of Internal Medicine, Kaohsiung Medical University (KMU) Hospital; ; Faculty of Medicine, College of Medicine, KMU; ; Graduate Institute of Medicine, College of Medicine, KMU, Kaohsiung, Taiwan.
Ching-Tang ChangDivision of Cardiology, Department of Internal Medicine, Kaohsiung Medical University (KMU) Hospital; ; Faculty of Medicine, College of Medicine, KMU; ; Graduate Institute of Medicine, College of Medicine, KMU, Kaohsiung, Taiwan.
Kuan-Cheng ChangDivision of Cardiology.
Sheng-Hsiung SheuDivision of Cardiology, Department of Internal Medicine, Kaohsiung Medical University (KMU) Hospital; ; Faculty of Medicine, College of Medicine, KMU.
Chu-Huang ChenCenter for Lipid Biosciences, KMU Hospital, KMU; ; Vascular and Medicinal Research, Texas Heart Institute, Houston, TX, USA; ; L5 Research Center, China Medical University (CMU) Hospital, CMU, Taichung, Taiwan; ; Section of Cardiovascular Research, Department of Medicine, Baylor College of Medicine, Houston, TX, USA.
Wen-Ter LaiDivision of Cardiology, Department of Internal Medicine, Kaohsiung Medical University (KMU) Hospital; ; Faculty of Medicine, College of Medicine, KMU; ; Center for Lipid and Glycomedicine Research.
Kaohsiung Medical University · TWKawamura Hospital · JPCenter for Innovation · USTissue Dynamics (Israel) · IL

Funding

Oxidation of Apolipoprotein B-100 in LDLR01HL063364 · NHLBI · BAYLOR COLLEGE OF MEDICINE · PI YANG, CHAO-YUH · 2001 to 2004
$1.2M
NHLBI NIH HHS R01 HL063364
6 · The paper itself

Abstract

backgroundSignificantly higher cytotoxic and thrombogenic human electronegative low-density lipoprotein (LDL), or L5, has been found in patients with stable coronary artery disease and acute coronary syndrome. We hypothesized that the statin-benefit groups (SBGs) defined by the new cholesterol guideline were of higher electronegative L5.

methodsIn total, 62 hyperlipidemia patients (mean age 59.4 ± 10.5, M/F 40/22) were retrospectively divided into SBGs (n = 44) and N-SBGs (n = 18). The levels of complete basic lipid panel, biochemical profile and electronegative L5 of each individual were obtained before and after rosuvastatin 10 mg/day for 3 months.

resultsAfter 3 months' statin therapy, significant reduction of total cholesterol, LDL-C and triglyceride were demonstrated (all p-values < 0.05), with 38.4% LDL-C reduction. The percentage of L5 was significantly reduced by 40.9% (from 4.4% to 2.6%) after statin therapy (p = 0.001). Regarding absolute L5 concentration, derived from L5% multiplied by LDL-C, there was approximate 63.8% reduction (from 6.3 mg/dL to 2.3 mg/dL) of absolute L5 (p < 0.001) after statin treatment. Notably, while plasma LDL-C levels were similar between SBGs and N-SBGs (152.8 ± 48.6 vs. 146.9 ± 35.0 mg/dL), the SBGs had significantly elevated L5% (5.2 ± 7.4% vs. 2.6 ± 1.9%, p = 0.031) and higher absolute L5 concentration (7.4 ± 10.4 vs. 3.7 ± 3.1 mg/dL, p = 0.036). Linear regression showed the significantly positive correlation between the plasma L5 concentration and the 10-year cardiovascular risk by pooled cohort equation (r = 0.297, p < 0.05).

conclusionsThe four SBGs defined by the 2013 ACC/AHA new cholesterol guideline tend to have increased atherogenic electronegative L5. Statin therapy can effectively reduce the electronegative L5 of these four major SBGs.

Indexed as

Cardiovascular risksCholesterol guidelineElectronegative LDLStatin

Identifiers

PMID27899853
PMCPMC5126444
OpenAlexW2560351222

What OpenQuestion holds

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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.