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Primary versus iatrogenic (post-PCI) coronary microvascular dysfunction: a wire-based multimodal comparison
Hakan Hasdemir1, Ahmet Taş2,3, Erdem Cevik4
1Department of Cardiology, Acibadem Atakent Hospital, Istanbul, Turkey.
Background:
Although there are studies examining each one separately, there are no data in the literature comparing the magnitudes of the iatrogenic, percutaneous coronary intervention (PCI)-induced, microvascular dysfunction (Type-4 CMD) and coronary microvascular dysfunction (CMD) in the setting of ischaemia in non-obstructed coronary arteries (INOCA) (Type-1 CMD).
Objectives:
We aimed to compare the characteristics of Type-1 and Type-4 CMD subtypes using coronary haemodynamic (resistance and flow-related parameters), thermodynamic (wave energy-related parameters) and hyperemic ECG changes.
Methods:
Coronary flow reserve (CFR) value of <2.5 was defined as CMD in both groups. Wire-based multimodal perfusion markers were comparatively analysed in 35 patients (21 INOCA/CMD and 14 CCS/PCI) enrolled in NCT05471739 study.
Results:
Both groups had comparably blunted CFR values per definition (2.03±0.22 vs 2.11±0.37; p: 0.518) and similar hyperemic ST shift in intracoronary ECG (0.16±0.09 vs 0.18±0.07 mV; p: 0.537). While the Type-1 CMD was characterised with impaired hyperemic blood flow acceleration (46.52+12.83 vs 68.20+28.63 cm/s; p: 0.017) and attenuated diastolic microvascular decompression wave magnitudes (p=0.042) with higher hyperemic microvascular resistance (p<0.001), Type-4 CMD had blunted CFR mainly due to higher baseline flow velocity due to post-occlusive reactive hyperemia (33.6±13.7 vs 22.24±5.3 cm/s; p=0.003).
Conclusions:
The perturbations in the microvascular milieu seen in CMD in INOCA setting (Type-1 CMD) seem to be more prominent than that of seen following elective PCI (Type-4 CMD), although resulting reversible ischaemia is equally severe in the downstream myocardium.
Insights
Coronary microvascular dysfunction (CMD) in non-obstructed arteries (Type-1 CMD) shows more severe microvascular impairment than PCI-induced CMD (Type-4 CMD), despite similar ischemia severity.
Area of Science:
- Cardiology
- Vascular Biology
- Internal Medicine
Background:
- Coronary microvascular dysfunction (CMD) is increasingly recognized in various clinical settings.
- Distinguishing between different CMD subtypes, such as ischemia in non-obstructed coronary arteries (INOCA, Type-1 CMD) and percutaneous coronary intervention (PCI)-induced CMD (Type-4 CMD), is crucial.
- Limited data exist comparing the severity and characteristics of Type-1 and Type-4 CMD.
Purpose of the Study:
- To comparatively analyze the coronary hemodynamic, thermodynamic, and electrocardiographic characteristics of Type-1 CMD and Type-4 CMD.
- To elucidate the distinct pathophysiological mechanisms underlying these two CMD subtypes.
- To provide a comprehensive comparison of microvascular impairment in INOCA versus post-PCI settings.
Main Methods:
- A comparative analysis of wire-based multimodal perfusion markers was performed in 35 patients.
- Patients were categorized into INOCA/CMD (Type-1) and stented coronary artery/PCI (Type-4) groups.
- Coronary flow reserve (CFR) <2.5 defined CMD; intracoronary ECG, hemodynamic, and thermodynamic parameters were assessed.
Main Results:
- Both Type-1 and Type-4 CMD groups exhibited similarly blunted CFR values and hyperemic ST shifts.
- Type-1 CMD was associated with impaired hyperemic blood flow acceleration and attenuated diastolic microvascular decompression waves, alongside higher hyperemic microvascular resistance.
- Type-4 CMD showed blunted CFR primarily due to higher baseline flow velocity from post-occlusive reactive hyperemia.
Conclusions:
- Microvascular dysfunction in the INOCA setting (Type-1 CMD) appears more pronounced than that following elective PCI (Type-4 CMD).
- Despite differing microvascular characteristics, both CMD subtypes result in equally severe reversible ischemia in the downstream myocardium.
- These findings highlight distinct pathophysiological pathways for Type-1 and Type-4 CMD, impacting therapeutic strategies.
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