Evidence map›Paper›PMID 17869259›Full record

ArticleAtherosclerosis2008

Histological topographical comparisons of atherosclerosis progression in juveniles and young adults.

Satoki Homma, Dana A Troxclair, Arthur W Zieske, Gray T Malcom, Jack P Strong, Pathobiological Determinants of Atherosclerosis in Youth (PDAY) Research Group

Open access · greenAbstract readComparative StudyMulticenter Study
In one paragraph

Article in Atherosclerosis, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 13% 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, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Regional heterogeneity within the aorta: relevance to aneurysm disease.The Journal of thoracic and cardiovascular surgery · 2008
    Review
  7. 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

6 authors at 1 institution in 1 country.

Satoki HommaLouisiana State University Health Sciences Center, Pathology, New Orleans, LA, USA. satoki.homma@nifty.com
Dana A Troxclair
Arthur W Zieske
Gray T Malcom
Jack P Strong
Pathobiological Determinants of Atherosclerosis in Youth (PDAY) Research Group
Louisiana State University Health Sciences Center New Orleans · US

Funding

PDAY CARDIOVASCULAR SPECIMEN AND DATA LIBRARYR24HL060808 · NHLBI · LSU HEALTH SCIENCES CENTER · PI ZIESKE, ARTHUR W · 1998 to 2010
$1.4M
NHLBI NIH HHS HL60808NHLBI NIH HHS R24 HL060808
6 · The paper itself

Abstract

backgroundThe histologically topographic comparisons on atherosclerosis progression among three anatomical sites, mid-thoracic and lower abdominal aorta and left anterior descending coronary artery (LAD) were performed using a young population (age 15-34 years) from the Pathobiological Determinants of Atherosclerosis in Youth (PDAY) study. METHODS AND

resultsThe histological classification based on the American Heart Association grading scheme showed that in the thoracic aorta type 2 lesions (numerous macrophage foam cells with fine particles but no pools of extracellular lipid) appeared in the first 10-year age group, with no significant change in prevalence in the next 10 years. Lesions greater than type 2 were rarely seen in the thoracic aorta. Although type 2 lesions appeared later in the LAD than in the aorta, the lesions within the LAD progressed rapidly to more advanced lesions (types 4 and 5) or atheroma. Lesion development in the abdominal aorta was intermediate to lesion development in the thoracic aorta and the LAD.

conclusionsThe most striking topographic difference on lesion progression among the three anatomical sites was the vulnerability of type 2 lesions to progress into advanced lesions. The histology study, including immunohistochemistry limited to the type 2 lesions suggested that lesion progression was related to the intimal thickness and the amount of collagen but not to the number of macrophage foam cells.

Indexed as

AdolescentAdultAorta, AbdominalAorta, ThoracicAtherosclerosisBlack or African AmericanCoronary Artery DiseaseFemaleHumansImmunohistochemistryMalePrevalenceSex FactorsTunica IntimaTunica MediaUnited States

Identifiers

PMID17869259
PMCPMC2696014
OpenAlexW2093844629

What OpenQuestion holds

Textmetadata
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.