Key result
Type IV collagen 7s levels significantly correlated with central venous pressure in patients with congenital heart disease older than one year (r = 0.28 to 0.51).
Why the study?
While liver fibrosis markers are known to reflect central venous pressure in adults, this relationship is not well-understood in children with congenital heart disease.
Does the measurement of liver fibrosis markers correlate with central venous pressure in patients with congenital heart disease?
Observational (n=160)
No
Does the measurement of liver fibrosis markers correlate with central venous pressure in patients with congenital heart disease?
Effect estimate: r = 0.28 to 0.51 (for 4COL7s in patients >1 year)
p-value: p=<0.05
Type IV collagen 7s is a useful non-invasive biomarker that correlates with central venous pressure in patients with congenital heart disease older than one year, potentially aiding in the early detection of hepatic congestion.
Background Central venous pressure (CVP) is one of the most important hemodynamic parameters in patients with congenital heart disease (CHD). In adults, it is well-known that liver fibrosis markers reflect CVP, but this is not well-understood in children. We investigated the liver fibrosis markers in pediatric CHD patients and their ability to predict CVP. Methods We studied 160 patients who underwent cardiac catheterization in our hospital between January 2017 and December 2020. The levels of the fibrotic markers, including type IV collagen 7s, procollagen type III peptide, and hyaluronic acid, were measured. Results Procollagen type III peptide was markedly elevated in infants younger than one year of age. From one to 15 years of age, it was slightly lower than in the infant group, with a peak at around 10 years of age. In the age group of 16 years and older, most of its values were generally high. Type IV collagen 7s and hyaluronic acid levels were high in infants, with no significant differences at later ages. Procollagen type III peptide and hyaluronic acid showed no significant correlation with CVP in any of the age groups, whereas type IV collagen 7s significantly correlated with CVP in the age group above one year old. Conclusions We found that elevated liver fibrosis markers, particularly type IV collagen 7s, correlated with central venous pressure in CHD patients older than one year. Measurement of liver fibrosis markers may allow the early detection of changes in CVP and liver function in patients with CHD.
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Oka et al. (2023) conducted an observational in Congenital heart disease (n=160). Liver fibrosis markers (type IV collagen 7s, procollagen type III peptide, hyaluronic acid) was evaluated on Correlation between central venous pressure (CVP) and liver fibrosis markers (r = 0.28 to 0.51 (for 4COL7s in patients >1 year), p=<0.05). Type IV collagen 7s levels significantly correlated with central venous pressure in patients with congenital heart disease older than one year (r = 0.28 to 0.51).
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