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Incidence, clinical factors, and endotype characterization of coronary microvascular dysfunction in patients with nonobstructive coronary artery disease undergoing 13N-ammonia positron emission tomography

Incidence, clinical factors, and endotype characterization of coronary microvascular dysfunction in patients with nonobstructive coronary artery disease undergoing 13N-ammonia positron emission tomography - Incidence, clinical factors, and endotype characterization of coronary microvascular dysfunction in patients with nonobstructive coronary artery disease undergoing 13N-ammonia positron emission tomography

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000056324
Enrollment
400
Registered
2024-12-01
Start date
2017-02-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

patients with suspected or known coronary artery disease

Interventions

None listed

Sponsors

Shiro Miura, Department of Cardiology, Sapporo Kojinkai Memorial Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Consecutive individuals with clinical signs or symptoms of ischemic heart disease who underwent myocardial perfusion PET, between January 2017 and April 2024, at our institution.

Exclusion criteria

Exclusion criteria: We excluded 536 patients owing to prior documented myocardial infarction and/or coronary revascularization (n=434) [myocardial infarction (n=210), percutaneous coronary intervention (n=378), or coronary artery bypass grafting (n=93)], known cardiomyopathy (n=46), previous hospitalization for heart failure (n=22), left ventricular ejection fraction <30% (n=15), congenital heart disease (n=9), significant valvular heart disease (n=8), and missing data (n=2). Of the remaining 777 patients, 683 patients underwent anatomical coronary assessments via coronary computed tomography angiography (CCTA), invasive CAG, or both within 6 months of the PET examination; and we excluded 84 patients who did not undergo CCTA or CAG within the 6 months, and 10 patients with inadequate imaging qualities

Design outcomes

Primary

MeasureTime frame
Incidence of CMD and identified clinical factors and PET-related parameters that were associated with a decrease in myocardial flow reserve (MFR).

Countries

Japan

Contacts

Public ContactSHIRO MIURA

Sapporo Kojinkai Memorial Hospital Department of Cardiology,

shirotan1027m@yahoo.co.jp08017135544

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026