Evidence map›Paper›PMID 35694826›Full record

ArticleEuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology2022

Prognostic value of structural and functional coronary microvascular dysfunction in patients with non-obstructive coronary artery disease; from the multicentre international ILIAS registry.

Coen K M Boerhout, Guus A de Waard, Joo Myung Lee, Hernan Mejia-Renteria, Seung Hun Lee, Ji-Hyun Jung, Masahiro Hoshino, Mauro Echavarria-Pinto, Martijn Meuwissen, Hitoshi Matsuo and 21 more

Registry-linked trialOpen access · greenAbstract readMulticenter Study
In one paragraph

Article in EuroIntervention : journal of EuroPCR in collaboration with the Working Group on Interventional Cardiology of the European Society of Cardiology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT04485234 (Inclusive Invasive Physiological Assessment in Angina Syndromes Registry), which is not on this map. Cited by 58 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
58citing papers in PubMed, 2 pooled it
14.4field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT04485234 completednot on this map

Inclusive Invasive Physiological Assessment in Angina Syndromes Registry (ILIAS Registry)

Typeobservational_patient_registrySponsorAcademisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)Ran2019 to 2021Enrolled2,322ConditionsCoronary Artery Disease, Microvascular Coronary Artery DiseaseArmsResting distal coronary to aortic pressure ratio, Fractional flow reserve, Coronary Flow Reserve, Microvascular resistance
3 · Its place in the literature

Who cites it

58 citing papers in PubMed, 2 syntheses or guidelines pooled it, 110 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Review
  6. Review
  7. Observational
  8. Coronary microvascular dysfunction: a narrative review.Cardiovascular diagnosis and therapy · 2026
    Review
  9. Review
  10. Article
  11. Article
  12. Chronic ischemic heart disease: A nonuniform syndrome.American heart journal plus : cardiology research and practice · 2026
    Review
  13. Microvascular Resistance Reserve (MRR): a new concept to understand the coronary microcirculation.Netherlands heart journal : monthly journal of the Netherlands Society of Cardiology and the Netherlands Heart Foundation · 2026
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Review
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

31 authors at 19 institutions in 8 countries.

Coen K M BoerhoutDepartment of Cardiology, Amsterdam UMC - location AMC, Amsterdam, the Netherlands.
Guus A de WaardDepartment of Cardiology, Amsterdam UMC - location VUmc, Amsterdam, the Netherlands.
Joo Myung LeeDivision of Cardiology, Department of Medicine, Heart Vascular Stroke Institute, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, Republic of Korea.
Hernan Mejia-RenteriaHospital Clínico San Carlos, IDISSC, and Universidad Complutense de Madrid, Madrid, Spain.
Seung Hun LeeDivision of Cardiology, Department of Internal Medicine, Chonnam National University Hospital, Gwangju, Republic of Korea.
Ji-Hyun JungSejong General Hospital, Sejong Heart Institute, Bucheon, Republic of Korea.
Masahiro HoshinoGifu Heart Center, Department of Cardiovascular Medicine, Gifu, Japan.
Mauro Echavarria-PintoHospital General ISSSTE Querétaro - Facultad de Medicina, Universidad Autónoma de Querétaro, Querétaro, Mexico.
Martijn MeuwissenDepartment of Cardiology, Amphia Hospital, Breda, the Netherlands.
Hitoshi MatsuoGifu Heart Center, Department of Cardiovascular Medicine, Gifu, Japan.
Maribel Madera-CamberoTergooi Hospital, Department of Cardiology, Blaricum, the Netherlands.
Ashkan EftekhariDepartment of Cardiology, Aarhus University Hospital, Aarhus, Denmark.
Mohamed A EffatDivision of Cardiovascular Health and Diseases, Department of Internal Medicine, University of Cincinnati, Cincinnati, Ohio, USA.
Tadashi MuraiTsuchiura Kyodo General Hospital, Department of Cardiology, Tsuchiura City, Japan.
Koen MarquesDepartment of Cardiology, Amsterdam UMC - location VUmc, Amsterdam, the Netherlands.
Yolande AppelmanDepartment of Cardiology, Amsterdam UMC - location VUmc, Amsterdam, the Netherlands.
Joon-Hyung DohDepartment of Medicine, Keimyung University Dongsan Medical Center, Daegu, Republic of Korea.
Evald Høj ChristiansenDepartment of Cardiology, Aarhus University Hospital, Aarhus, Denmark.
Rupak BanerjeeMechanical and Materials Engineering Department, University of Cincinnati, Cincinnati, OH, USA; and Research Services, Veteran Affairs Medical Center, Cincinnati, OH, USA.
Chang-Wook NamDepartment of Medicine, Inje University Ilsan Paik Hospital, Goyang, Republic of Korea.
Giampaolo NiccoliDepartment of Cardiovascular Medicine, Catholic University of the Sacred Heart, Institute of Cardiology, Rome, Italy.
Masafumi NakayamaGifu Heart Center, Department of Cardiovascular Medicine, Gifu, Japan.
Nobuhiro TanakaDepartment of Cardiology, Tokyo Medical University, Hachioji Medical Center, Tokyo, Japan.
Eun-Seok ShinDepartment of Cardiology, Ulsan University Hospital, University of Ulsan College of Medicine, Ulsan, Republic of Korea.
Marcel A M BeijkDepartment of Cardiology, Amsterdam UMC - location AMC, Amsterdam, the Netherlands.
Paul KnaapenDepartment of Cardiology, Amsterdam UMC - location VUmc, Amsterdam, the Netherlands.
Javier EscanedHospital Clínico San Carlos, IDISSC, and Universidad Complutense de Madrid, Madrid, Spain.
Tsunekazu KakutaTsuchiura Kyodo General Hospital, Department of Cardiology, Tsuchiura City, Japan.
Bon-Kwon KooDepartment of Internal Medicine, Seoul National University Hospital, Cardiovascular Center, Seoul, Republic of Korea.
Jan J PiekDepartment of Cardiology, Amsterdam UMC - location AMC, Amsterdam, the Netherlands.
Tim P van de HoefDepartment of Cardiology, Amsterdam UMC - location AMC, Amsterdam, the Netherlands.
Aarhus University Hospital · DKGifu Heart Center · JPTsuchiura Kyodo General Hospital · JPAmphia Ziekenhuis · NLAutonomous University of Queretaro · MXChonnam National University Hospital · KRHospital Clínico San Carlos · ESInje University Ilsan Paik Hospital · KRKeimyung University Dongsan Medical Center · KRSejong General Hospital · KRSeoul National University Hospital · KRSungkyunkwan University · KRTergooi · NLTokyo Medical University Hachioji Medical Center · JPTowada City Hospital · JPUlsan College · KRUniversidad Complutense de Madrid · ESUniversità Cattolica del Sacro Cuore · ITUniversity of Cincinnati · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoronary microvascular dysfunction (CMD) is an important contributor to angina syndromes. Recently, two distinct endotypes were identified using combined assessment of coronary flow reserve (CFR) and minimal microvascular resistance (MR), termed structural and functional CMD.

aimsWe aimed to assess the relevance of the combined assessment of CFR and MR in patients with angina and no obstructive coronary arteries.

methodsPatients with chronic coronary syndromes (CCS) and non-obstructive coronary artery disease (fractional flow reserve [FFR] ≥0.80) were selected (N=1,102). Functional CMD was defined as abnormal CFR in combination with normal MR and structural CMD as abnormal CFR with abnormal MR. Clinical endpoints were the incidence of major adverse cardiac events (MACE) and target vessel failure (TVF) at 5-year follow-up.

resultsAbnormal CFR was associated with an increased risk of MACE and TVF at 5-year follow-up. Microvascular resistance parameters were not associated with MACE or TVF at 5-year follow-up. The risk of MACE and TVF at 5-year follow-up was similarly increased for patients with structural or functional CMD compared with patients with normal microvascular function. There were no differences between both endotypes (p=0.88 for MACE, and p=0.55 for TVF).

conclusionsCoronary microvascular dysfunction, identified by an impaired CFR, was unequivocally associated with increased MACE and TVF rates over a 5-year follow-up period. In contrast, impaired MR was not associated with 5-year adverse clinical events. Moreover, there was no significant difference in the risk of MACE and TVF between a low CFR accompanied by pathologically increased MR (structural CMD) or not (functional CMD). CLINICALTRIALS: gov: NCT04485234.

Indexed as

Coronary Artery DiseaseFractional Flow Reserve, MyocardialMyocardial IschemiaCoronary AngiographyHumansMicrocirculationPrognosisRegistries

Identifiers

PMID35694826
PMCPMC10241297
OpenAlexW4282939789

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.