Impaired peripheral microvascular reactivity in patients with nonobstructive coronary artery disease

Objective This study aimed to determine whether peripheral microvascular reactivity is impaired in patients with nonobstructive coronary artery disease (NOCAD). Methods Stable patients presenting with angina were recruited and, based on results from coronary angiography, were categorized into OCAD (...

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Published inMicrocirculation (New York, N.Y. 1994) Vol. 30; no. 4; pp. e12807 - n/a
Main Authors Sanip, Zulkefli, Pahimi, Nurnajwa, Bokti, Nur Adilah, Yusof, Zurkurnai, Mohamed, Mohd Sapawi, W. Isa, W. Yus Haniff, Rasool, Aida Hanum
Format Journal Article
LanguageEnglish
Published United States Wiley Subscription Services, Inc 01.05.2023
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Summary:Objective This study aimed to determine whether peripheral microvascular reactivity is impaired in patients with nonobstructive coronary artery disease (NOCAD). Methods Stable patients presenting with angina were recruited and, based on results from coronary angiography, were categorized into OCAD (coronary stenosis of ≥50%) and NOCAD (stenosis <50%) groups. A control group with no history of angina was also recruited. Forearm skin microvascular reactivity was measured using the laser Doppler blood perfusion monitor and the process of postocclusive skin reactive hyperemia (PORH). Results Patients were categorized into OCAD (n = 42), NOCAD (n = 40), and control (n = 39) groups. Compared with the control group, the PORH perfusion percent change (PORH% change) was significantly lower in the OCAD and NOCAD groups. No significant differences were noted between the OCAD and NOCAD groups. Additionally, the NOCAD group without any coronary obstruction takes a longer time to reach peak perfusion and had lower PORH% change compared with the nonangina control group. Conclusion Angina patients with NOCAD have microvascular dysfunction as demonstrated by reduced magnitude of reperfusion with an ischemic stimulus. NOCAD patients without coronary obstruction also displayed a slower response to reperfusion.
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ISSN:1073-9688
1549-8719
DOI:10.1111/micc.12807