Evidence map›Paper›PMID 27317162›Full record

Trial reportLipids in health and disease2016

Effects of L-carnitine supplementation on lipid profiles in patients with coronary artery disease.

Bor-Jen Lee, Jun-Shuo Lin, Yi-Chin Lin, Ping-Ting Lin

2 registry-linked trialsOpen access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Lipids in health and disease, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 18 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 4 pooled it
3.8field-weighted citation impact, top 7% 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.

NCT03696940 phase3unknown statusstarted 2018, after this paper: background citation

Estudio clínico Fase III Para Evaluar la Eficacia terapéutica en Pacientes Mexicanos Con Dislipidemia Mediante el Uso vía Oral de L-Carnitina + Atorvastatina Comparado Con Atorvastatina

Ran2018Enrolled120Registered outcomes6Posted comparisons0ConditionsCardiovascular Risk Factor, DyslipidemiasArmsAtorvastatin 10mg, L-Carnitine 500Mg Oral Tablet + Atorvastatin 10 mg
Open the trial in the graph
NCT01819701 phase2 / phase3completednot on this map

L-carnitine and Coenzyme Q10 in Relation to the Oxidative Stress, Antioxidant Enzymes Activities, Inflammation, and the Risk of Coronary Artery Disease

TypeinterventionalSponsorTaichung Veterans General HospitalRan2013 to 2014Enrolled47ConditionsCoronary Artery DiseaseArmsLC-1000, LC-2000, Q10-150, Q10-300, Placebo
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 4 syntheses or guidelines pooled it, 42 citations in OpenAlex.

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  12. l-carnitine: Nutrition, pathology, and health benefits.Saudi journal of biological sciences · 2023
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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

4 authors at 4 institutions in 1 country.

Bor-Jen LeeThe Intensive Care Unit, Taichung Veterans General Hospital, Taichung, 40705, Taiwan.
Jun-Shuo LinDepartment of Nutrition, Sinying Hospital, Ministry of Health and Welfare, Tainan, 73042, Taiwan.
Yi-Chin LinSchool of Nutrition, Chung Shan Medical University, Taichung, 40201, Taiwan.
Ping-Ting LinSchool of Nutrition, Chung Shan Medical University, Taichung, 40201, Taiwan. apt810@csmu.edu.tw.ORCID http://orcid.org/0000-0002-4271-3928
Chest Hospital, Ministry of Health and Welfare · TWChung Shan Medical University · TWChung Shan Medical University Hospital · TWTaichung Veterans General Hospital · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundL-carnitine (LC) plays an important physiologic role in lipid metabolism. To date, no clinical study has been performed to examine the effect of LC supplementation on the lipid status of coronary artery disease (CAD) patients. The aim of this study was to investigate the lipid lowering effects of LC supplementation (1000 mg/d) in CAD patients.

methodsCAD patients were identified by cardiac catheterization as having at least 50 % stenosis of one major coronary artery. Forty-seven subjects were recruited and randomly assigned to the placebo (n = 24) and to the LC (n = 23) groups. The intervention was administered for 12 weeks. The levels of LC, lipid profiles, and antioxidant enzyme activity (superoxide dismutase, SOD) were measured.

resultsThe subjects in the LC group had significantly higher SOD activity (20.7 ± 4.2 versus 13.1 ± 2.9 U/mg of protein, P < 0.01), high density lipoprotein-cholesterol (1.34 ± 0.42 vs. 1.16 ± 0.24 mmol/L, HDL-C, P = 0.03), and apolipoprotein-A1 (Apo-A1, 1.24 ± 0.18 vs. 1.12 ± 0.13 g/L, P = 0.02) than those in the placebo group at week 12. Triglyceride (TG) level was slightly significantly reduced (1.40 ± 0.74 vs. 1.35 ± 0.62 mmol/L, P = 0.06) and the level of LC was negatively correlated with TG and apolipoprotein-B (Apo-B), and positively correlated with HDL-C and Apo-A1 after LC supplementation. Additionally, SOD activity was significantly negatively correlated with lipid profiles (total cholesterol, TG, and Apo-B) after supplementation.

conclusionLC supplementation at a dose of 1000 mg/d showed significantly increased in HDL-C and Apo-A1 levels and a slight decrease in TG levels but no other changes in other lipids in CAD patients, and this lipid-lowering effect may be related to its antioxidant ability. Further studies should be conducted to define an optimal dose of LC for lipid-lowering in patients with CAD.

trial registrationClinical Trials.gov Identifier: NCT01819701.

Indexed as

Dietary SupplementsAgedAged, 80 and overApolipoprotein A-IApolipoproteins BCardiac CatheterizationCarnitineCholesterol, HDLCholesterol, LDLCoronary Artery DiseaseCoronary VesselsFemaleHumansLipid MetabolismMaleSingle-Blind MethodAPOA1 protein, humanApolipoprotein A-IApolipoproteins BCarnitineCholesterol, HDLCholesterol, LDLSuperoxide DismutaseTriglyceridesAntioxidantCoronary artery diseaseL-carnitine supplementLipid profiles

Identifiers

PMID27317162
PMCPMC4912751
OpenAlexW2429749249

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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.