Evidence map›Paper›PMID 36643601›Full record

ArticleAtherosclerosis plus2022

Identification of the atherosclerosis phenotype

Lingyun Jia, Yuan Li, Yang Hua, Yumei Liu, Nan Zhang, Mingjie Gao, Ke Zhang, Jingzhi Li, Jidong Mi, Jianqi Zhang and 1 more

Open access · goldAbstract read
In one paragraph

Article in Atherosclerosis plus, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.2field-weighted citation impact, top 52% 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

2 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Dog models of human atherosclerotic cardiovascular diseases.Mammalian genome : official journal of the International Mammalian Genome Society · 2023
    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

11 authors at 1 institution in 1 country.

Lingyun JiaDepartment of Vascular Ultrasonography, Xuanwu Hospital, Capital Medical University, China.
Yuan LiBeijing Sinogene Biotechnology Co. Ltd, Beijing, 102200, China.
Yang HuaDepartment of Vascular Ultrasonography, Xuanwu Hospital, Capital Medical University, China.
Yumei LiuDepartment of Vascular Ultrasonography, Xuanwu Hospital, Capital Medical University, China.
Nan ZhangDepartment of Vascular Ultrasonography, Xuanwu Hospital, Capital Medical University, China.
Mingjie GaoDepartment of Vascular Ultrasonography, Xuanwu Hospital, Capital Medical University, China.
Ke ZhangDepartment of Vascular Ultrasonography, Xuanwu Hospital, Capital Medical University, China.
Jingzhi LiDepartment of Vascular Ultrasonography, Xuanwu Hospital, Capital Medical University, China.
Jidong MiBeijing Sinogene Biotechnology Co. Ltd, Beijing, 102200, China.
Jianqi ZhangBeijing Sinogene Biotechnology Co. Ltd, Beijing, 102200, China.
Shiyu JiaoDepartment of Physiology and Pathophysiology, School of Basic Medical Science, Capital Medical University, Beijing, 100069, China.
Capital Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and aims: This study evaluated the atherosclerosis phenotype by vascular duplex ultrasonography (VDU) in ApoE-deficient dogs. Methods: A total of 108 beagle dogs were examined by VDU, which included 32 wild-type, 68 heterozygous (ApoE-/+) mutant and 8 homozygous (ApoE-/-) mutant dogs. According to age, wild-type and ApoE-/+ dogs were divided into two subgroups: young (6-15 months) and adult dogs (18-29 months). All homozygous dogs were young dogs. Dogs were feed with normal diet. The plasma lipid levels were tested. The diameter of the common carotid artery (CCA), internal carotid artery (ICA), external carotid artery (ECA), abdominal aorta and common iliac artery (CIA) and the intima-media thickness (IMT) of the CCA and abdominal aorta were measured by VDU. The artery sections of ApoE-/- and control dogs were analyzed by histological analysis. Results: The plasma triglycerides (2.5-3 fold), total cholesterol (4-5 fold) and LDL levels (35-40 fold) of ApoE-/- dogs were higher than those of the wild-type and ApoE-/+ dogs. Compared with the wild-type and young ApoE-/+ dogs, the IMT of CCA and aorta in ApoE-/- dogs were increased ( Conclusions: The ApoE-deficient dogs were a reliable animal model of atherosclerosis. VDU is an optimal

Indexed as

Animal modelApoE-deficient dogsAtherosclerosisUltrasound

Identifiers

PMID36643601
PMCPMC9833219
OpenAlexW4200038768

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.