Evidence map›Paper›PMID 19641724›Full record

ArticleExperimental and clinical cardiology2004

Assessment of right ventricular fibrosis in different forms of pulmonary atresia with ventricular septal defect.

Pieter C van de Woestijne, Lennart Klompe, Peter L de Jong, Theodorus Hf Peters, Arie P Kappetein, Hari S Sharma, Ad Jjc Bogers

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Article in Experimental and clinical cardiology, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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3 · Its place in the literature

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0 citing papers in PubMed, 1 citations in OpenAlex.

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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Pieter C van de WoestijneDepartments of Cardiothoracic Surgery and.
Lennart Klompe
Peter L de Jong
Theodorus Hf Peters
Arie P Kappetein
Hari S Sharma
Ad Jjc Bogers

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundIn pulmonary atresia with ventricular septal defect (PA-VSD), the corrective surgical strategy aims to reduce the right ventricular (RV) overload and restore physiological pulmonary perfusion before the characteristic RV hypertrophy and fibrosis become irreversible.

objectiveTo assess RV fibrosis in different forms of PA-VSD.

methodsRV biopsies were obtained at corrective surgery from PA-VSD patients (n=14, mean age 2.5+/-1.2 years) with patent arterial duct (PAD group, n=6; mean age 1.7+/-0.5 years) or systemic-pulmonary collateral arteries (SPCA group, n=8; mean age 3.2+/-1.2 years) and from age-matched controls (control group, n=6; mean age 2.5+/-1.8 years). Myocardial expression patterns (messenger RNA [mRNA] and protein levels) of the extracellular matrix proteins (eg, fibronectin and collagens [subtype I alpha and III) were quantitatively analyzed in relation to myocardial cell hypertrophy.

resultsComparing the age of PA-VSD patients at surgery, the SPCA group was older than the PAD group (P=0.01). Expression analysis by reverse transcriptase polymerase chain reaction showed significantly higher mRNA levels in patients with PA-VSD for collagen III (PA-VSD versus controls; 0.9+/-0.2 versus 0.6+/-0.1, P=0.03) than in controls, whereas collagen I alpha and fibronectin mRNA levels did not differ. No differences were found between the PAD and SPCA groups. The myocyte cross sectional surface area showed enhanced myocyte hypertrophy in patients with PA-VSD compared with the control group (P=0.015), with no significant difference between the PAD and SPCA groups. Video image analysis of immunohistochemical staining corrected for hypertrophy revealed unchanged interstitial collagens and fibronectin levels in all groups. However, perivascular staining corrected for the vessel lumen area showed significantly lower total collagen levels in patients with PA-VSD than in the control group (3.2+/-1.2 versus 7.2+/-2.8, respectively; P=0.004).

conclusionsThe results indicate that the extracellular matrix support for the coronary blood vessels appears to be suboptimal in patients with PA-VSD. The staged surgical approach in the SPCA group (with a higher age at correction) did not result in an excessive accumulation of fibrosis markers in the RV myocardium.

Indexed as

CollagenFibronectinHumanPulmonary atresiaRight ventricular hypertrophyVentricular septal defect

Identifiers

PMID19641724
PMCPMC2716745
OpenAlexW135779366

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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.