Evidence map›Paper›PMID 26302066›Full record

ArticleNutrition & diabetes2015

Effects of low-fat diet and aging on metabolic profiles of Creb3l4 knockout mice.

T-H Kim, J-M Park, S-H Jo, M-Y Kim, H Nojima, Y-H Ahn

Open access · goldAbstract read
In one paragraph

Article in Nutrition & diabetes, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

7 citing papers in PubMed, 13 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

6 authors at 2 institutions in 2 countries.

T-H KimDepartment of Biochemistry and Molecular Biology, Yonsei University College of Medicine, Seoul, Republic of Korea.
J-M ParkDepartment of Biochemistry and Molecular Biology, Yonsei University College of Medicine, Seoul, Republic of Korea.
S-H JoDepartment of Biochemistry and Molecular Biology, Yonsei University College of Medicine, Seoul, Republic of Korea.
M-Y KimDepartment of Biochemistry and Molecular Biology, Yonsei University College of Medicine, Seoul, Republic of Korea.
H NojimaDepartment of Molecular Genetics, Research Institute for Microbial Diseases, Osaka University, Osaka, Japan.
Y-H AhnDepartment of Biochemistry and Molecular Biology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Yonsei University · KROsaka University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesIncreased adipose tissue mass closely associates with the development of insulin resistance and type 2 diabetes mellitus. Previously, we reported that CREB3L4 expressed in adipose tissue negatively regulates adipogenesis, and Creb3l4 knockout mice fed a high-fat diet for 16 weeks showed fat cell hyperplasia, with improved glucose tolerance and insulin sensitivity. These mice did not show significant weight gain and fat mass. Because fat diet or aging is known to be associated with the development of obesity, we examined the effects of Creb3l4 gene subjected to low-fat diet (LFD) or aging process on body composition and obesity risk. SUBJECTS/

methodsWe fed Creb3l4 knockout mice a low-fat diet for 16 weeks (LFD group) or chow diet for over 1 year (aged group) and observed various metabolic parameters in the LFD-fed and aged Creb3l4 knockout mice.

resultsLFD-fed and aged Creb3l4 knockout mice showed significant weight gain and adiposity, impaired glucose tolerance and decreased insulin sensitivity, compared with wild-type mice.

conclusionsCreb3l4 has a critical role in metabolic phenotypes and a better understanding of its function may provide improved insight into the etiology of diabetes and other metabolic disorders.

Identifiers

PMID26302066
PMCPMC4558560
OpenAlexW2209087484

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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.