Evidence map›Paper›PMID 37724591›Full record

ArticleKorean journal of radiology2023

Assessing Abdominal Aortic Aneurysm Progression by Using Perivascular Adipose Tissue Attenuation on Computed Tomography Angiography.

Shuai Zhang, Hui Gu, Na Chang, Sha Li, Tianqi Xu, Menghan Liu, Ximing Wang

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Korean journal of radiology, 2023. 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
2.1field-weighted citation impact, top 12% 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, 8 citations in OpenAlex.

  1. Article
  2. Article
  3. Emerging Mechanisms of Abdominal Aortic Aneurysm.Current atherosclerosis reports · 2026
    Review
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
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

7 authors at 2 institutions in 1 country.

Shuai Zhang *Department of Radiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Shandong University, Jinan, Shandong, China.ORCID https://orcid.org/0000-0002-9631-0411
Hui Gu *Department of Radiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Shandong University, Jinan, Shandong, China.ORCID https://orcid.org/0000-0002-5216-9436
Na ChangDepartment of Medical Technology, Jinan Nursing Vocational College, Jinan, Shandong, China.ORCID https://orcid.org/0009-0000-4106-1721
Sha LiDepartment of Clinical Medicine, Shandong Provincial Hospital, Shandong University, Jinan, Shandong, China.ORCID https://orcid.org/0000-0002-9415-1576
Tianqi XuDepartment of Clinical Medicine, Shandong Provincial Hospital, Shandong University, Jinan, Shandong, China.ORCID https://orcid.org/0009-0000-2533-0485
Menghan LiuDepertment of Health Management, The First Affiliated Hospital of Shandong First Medical University, Jinan, Shandong, China. lmh141216@163.com.ORCID https://orcid.org/0009-0001-6054-2472
Ximing WangDepartment of Radiology, Shandong Provincial Hospital Affiliated to Shandong First Medical University, Shandong University, Jinan, Shandong, China. wangximing369@yeah.net.ORCID https://orcid.org/0000-0001-5136-8057
Shandong Provincial Hospital · CNJinan Maternity And Care Hospital · CN

Funding

National Natural Science Foundation of China 81871354National Natural Science Foundation of China 82271993National Science Foundation for Scientists of China 81871354National Science Foundation for Scientists of China 82271993
6 · The paper itself

Abstract

objectiveRecent studies have highlighted the active and potential role of perivascular adipose tissue (PVAT) in atherosclerosis and aneurysm progression, respectively. This study explored the link between PVAT attenuation and abdominal aortic aneurysm (AAA) progression using computed tomography angiography (CTA). MATERIALS AND

methodsThis multicenter retrospective study analyzed patients with AAA who underwent CTA at baseline and follow-up between March 2015 and July 2022. The following parameters were obtained: maximum diameter and total volume of the AAA, presence or absence of intraluminal thrombus (ILT), maximum diameter and volume of the ILT, and PVAT attenuation of the aortic aneurysm at baseline CTA. PVAT attenuation was divided into high (> -73.4 Hounsfield units [HU]) and low (≤ -73.4 HU). Patients who had or did not have AAA progression during the follow-up, defined as an increase in the aneurysm volume > 10 mL from baseline, were identified. Kaplan-Meier and multivariable Cox regression analyses were used to investigate the association between PVAT attenuation and AAA progression.

resultsOur study included 167 participants (148 males; median age: 70.0 years; interquartile range: 63.0-76.0 years), of which 145 (86.8%) were diagnosed with AAA accompanied by ILT. Over a median period of 11.3 months (range: 6.0-85.0 months), AAA progression was observed in 67 patients (40.1%). Multivariable Cox regression analysis indicated that high baseline PVAT attenuation (adjusted hazard ratio [aHR] = 2.23; 95% confidence interval [CI], 1.16-4.32;

conclusionElevated PVAT attenuation is independently associated with AAA progression, including patients of AAA with ILT, suggesting the potential of PVAT attenuation as a predictive imaging marker for AAA expansion.

Indexed as

Adipose TissueAortic Aneurysm, AbdominalComputed Tomography AngiographyAgedAorta, AbdominalDisease ProgressionFemaleHumansMaleMiddle AgedRetrospective StudiesAbdominal aortic aneurysmAneurysm progressionCT angiopraphyIntraluminal thrombusPerivascular adipose tissue

Identifiers

PMID37724591
PMCPMC10550735
OpenAlexW4386852356

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.