Functional Assessment of Long-Term Microvascular Cardiac Allograft Vasculopathy

BACKGROUND: Cardiac allograft vasculopathy (CAV) is a leading cause of death and retransplantation following heart transplantation (HTX). Surveillance angiography performed yearly is indicated for the early detection of the disease, but it remains of limited sensitivity.

METHODS: We performed bolus thermodilution-based coronary flow reserve (CFR) and index of microcirculatory resistance (IMR) and fractional flow reserve (FFR) measurements in HTX patients undergoing yearly surveillance coronary angiography without overt CAV.

RESULTS: In total, 27 HTX patients were included who had 52 CFR, IMR, and FFR measurements at a mean of 43 months after HTX. Only five measurements were performed in the first year. CFR decreased significantly by 0.13 every year (p = 0.04) and IMR tended to increase by 0.98 every year (p = 0.051), whereas FFR did not change (p = 0.161) and remained well above 0.80 over time. After one year, CFR decreased significantly (p = 0.022) and IMR increased significantly (p = 0.015), whereas FFR remained unchanged (p = 0.72).

CONCLUSIONS: The functional status of the epicardial coronary arteries of transplanted hearts did not deteriorate over time. On the contrary, a significant decrease in CFR was noted. In view of the increasing IMR, this is caused by the deterioration of the function of microvasculature. CFR and IMR measurements may provide an early opportunity to diagnose CAV.

Medienart:

E-Artikel

Erscheinungsjahr:

2023

Erschienen:

2023

Enthalten in:

Zur Gesamtaufnahme - volume:13

Enthalten in:

Journal of personalized medicine - 13(2023), 12 vom: 05. Dez.

Sprache:

Englisch

Beteiligte Personen:

Bora, Noemi [VerfasserIn]
Balogh, Orsolya [VerfasserIn]
Ferenci, Tamás [VerfasserIn]
Piroth, Zsolt [VerfasserIn]

Links:

Volltext

Themen:

Cardiac allograft vasculopathy
Coronary flow reserve
Heart transplantation
Index of microcirculatory resistance
Journal Article

Anmerkungen:

Date Revised 25.12.2023

published: Electronic

Citation Status PubMed-not-MEDLINE

doi:

10.3390/jpm13121686

funding:

Förderinstitution / Projekttitel:

PPN (Katalog-ID):

NLM366295772