Key result
Coronary microvascular dysfunction shows no association with sublingual microvascular abnormalities in INOCA.
Why the study?
Coronary microvascular dysfunction is a mechanism of INOCA diagnosed invasively, but it is unknown whether it reflects a systemic microcirculatory disorder detectable noninvasively by sublingual sidestream darkfield microscopy.
Does coronary microvascular dysfunction correlate with sublingual microvascular abnormalities in patients with INOCA?
Cross-Sectional (n=135)
No
Does coronary microvascular dysfunction correlate with sublingual microvascular abnormalities in patients with INOCA?
Sublingual sidestream darkfield microscopy does not appear to be a useful noninvasive surrogate marker for diagnosing coronary microvascular dysfunction in patients with INOCA.
Answers are grounded in this paper and cite their sources.
Sublingual sidestream darkfield microscopy should not serve as a CMD surrogate in INOCA; leaves open whether alternative noninvasive markers exist.
BACKGROUND: Coronary microvascular dysfunction (CMD) is a mechanism of ischemia with nonobstructive coronary arteries (INOCA) diagnosed by invasive coronary function testing (CFT). It is unknown whether CMD reflects a systemic microcirculatory disorder. Sidestream darkfield (SDF) microscopy permits noninvasive imaging of red blood cells (RBCs) in the sublingual microcirculation. OBJECTIVES: We sought to evaluate whether SDF microscopy identifies sublingual microvascular abnormalities in patients with INOCA due to CMD. METHODS: Adults with INOCA underwent CFT for CMD, defined by abnormal coronary flow reserve <2.5 or index of microcirculatory resistance ≥25. Sublingual SDF microscopy was performed to determine the endothelial glycocalyx perfused boundary region (PBR), RBC filling percentage (%RBC), and perfused microvascular density (PMVD). RESULTS: A total of 135 participants with INOCA (mean age 59.3 ± 12.1 years, 80% female) underwent CFT and sublingual SDF microscopy. CMD was present in 63 participants (46.7%). The median PBR was 1.96 (IQR: 0.4), median %RBC was 72.6 (IQR: 8.0), and median PMVD was 406 (IQR: 141). No differences in sublingual PBR, %RBC, and PMVD were observed by CMD status. No correlations between sublingual parameters and continuous measures of coronary flow reserve or index of microcirculatory resistance were observed. CONCLUSIONS: Noninvasive SDF microscopy did not identify sublingual microvascular abnormalities in INOCA patients with CMD.
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SMILOWITZ et al. (2026) conducted a cross-sectional in Ischemia with nonobstructive coronary arteries (INOCA) (n=135). Coronary microvascular dysfunction (CMD) vs. INOCA without CMD was evaluated on Perfused boundary region (PBR) (p=0.506). Coronary microvascular dysfunction was not associated with sublingual microvascular abnormalities measured by noninvasive sidestream darkfield microscopy in patients with INOCA.
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