Evidence map›Paper›PMID 24944417›Full record

ArticleCurrent therapeutic research, clinical and experimental2003

Increased serum triglyceride clearance and elevated high-density lipoprotein 2 and 3 cholesterol during treatment of primary hypertriglyceridemia with bezafibrate.

Nagahiko Sakuma, Reiko Ikeuchi, Takeshi Hibino, Takayuki Yoshida, Seiji Mukai, Sachie Akita, Kazuhiro Yajima, Hiromichi Miyabe, Toshihiko Goto, Norio Takada and 3 more

Open access · greenAbstract read
In one paragraph

Article in Current therapeutic research, clinical and experimental, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.4field-weighted citation impact, top 37% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Review
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  3. Review
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 2 institutions in 1 country.

Nagahiko SakumaDepartment of Internal Medicine and Pathophysiology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Japan.
Reiko IkeuchiTakikawa Ikiiki Clinic, Nagoya, Japan.
Takeshi HibinoDepartment of Internal Medicine and Pathophysiology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Japan.
Takayuki YoshidaDepartment of Internal Medicine and Pathophysiology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Japan.
Seiji MukaiDepartment of Internal Medicine and Pathophysiology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Japan.
Sachie AkitaDepartment of Internal Medicine and Pathophysiology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Japan.
Kazuhiro YajimaDepartment of Internal Medicine and Pathophysiology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Japan.
Hiromichi MiyabeDepartment of Internal Medicine and Pathophysiology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Japan.
Toshihiko GotoDepartment of Internal Medicine and Pathophysiology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Japan.
Norio TakadaDepartment of Internal Medicine and Pathophysiology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Japan.
Nobuyuki OhteDepartment of Internal Medicine and Pathophysiology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Japan.
Mitoshi KunimatuDepartment of Biochemistry, Nagoya Women's University, Nagoya, Japan.
Genjiro KimuraDepartment of Internal Medicine and Pathophysiology, Nagoya City University, Graduate School of Medical Sciences, Nagoya, Japan.
Nagoya City University · JPNagoya Women's University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHypertriglyceridemia accompanied by low levels of high-density lipoprotein cholesterol (HDL-C) is a risk factor for coronary artery disease. High-density lipoprotein 2 (HDL2) and 3 (HDL3) are believed to suppress the progress of atherosclerosis through reverse cholesterol transport. As a result, peripheral tissues can be protected against excessive accumulation of cholesterol. Although bezafibrate is known to accelerate the increase of HDL-C, results are not standardized regarding increases of HDL3 and HDL2 subfractions.

objectiveThis study assessed the effects of bezafibrate on serum triglyceride (TG) fractional clearance rate (K2) and HDL2 and HDL3 cholesterol (HDL2-C and HDL3-C, respectively) levels in patients with primary hypertriglyceridemia (serum TG ≥150 mg/dL).

methodsOutpatients with primary hypertriglyceridemia were enrolled in this 8-week study conducted at the Third Department of Internal Medicine, Nagoya City University Hospital (Nagoya, Japan). Oral bezafibrate was administered at a dose of 400 mg/d (200-mg tablet BID, morning and evening) for 8 weeks. After 8 weeks, serum levels of total cholesterol (TC), TG, HDL-C, HDL2-C, and HDL3-C were measured. A fat emulsion tolerance test to assess K2 and measurements of plasma lipoprotein lipase (LPL) mass, LPL activity, and hepatic triglyceride lipase (HTGL) activity in postheparin plasma were performed before bezafibrate administration and after the course of treatment.

resultsSixteen patients (10 men, 6 women; mean [SD] age, 54 [12] years [range, 30-69 years]; mean [SD] body mass index, 23 [2] kg/m(2)) entered the study. The following findings were observed in male and female patients after 8 weeks of treatment. A statistically significant reduction was observed in mean serum TG level (P<0.01). Significant increases were seen in HDL-C, HDL2-C, and HDL3-C (all P<0.01), K2 (P<0.01), and in plasma LPL mass (P<0.01) and LPL activity (P<0.05). TC level and HTGL activity did not change significantly. No adverse effects related to the use of bezafibrate were documented.

conclusionsIn this study, bezafibrate treatment resulted in significant decreases in serum TG level and significant increases in HDL2-C and HDL3-C levels and plasma LPL mass and activity. We hypothesize that bezafibrate may increase HDL3-C by promoting TG-rich lipoprotein catabolism and may increase HDL2-C by promoting the conversion of HDL3 to HDL2.

Indexed as

bezafibratehepatic triglyceride lipasehigh-density lipoprotein 2high-density lipoprotein 3lipoprotein lipaseserum triglyceride clearance

Identifiers

PMID24944417
PMCPMC4053057
OpenAlexW1988426942

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.