Coronary microvascular dysfunction, left ventricular remodeling, and clinical outcomes in aortic stenosis.


Journal

Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology
ISSN: 1532-6551
Titre abrégé: J Nucl Cardiol
Pays: United States
ID NLM: 9423534

Informations de publication

Date de publication:
Apr 2021
Historique:
received: 12 02 2019
accepted: 25 03 2019
pubmed: 3 5 2019
medline: 1 2 2022
entrez: 3 5 2019
Statut: ppublish

Résumé

We investigated role of coronary microvascular disease (CMD) in maladaptive LV remodeling and prognosis in patients with aortic sclerosis or stenosis and no overt CAD. This was a retrospective cohort study of patients with aortic sclerosis or stenosis, normal myocardial perfusion and LV ejection fraction (EF) > 50% (n = 43) and matched controls without AS (n = 43). PET and echocardiograms were performed within 1 year of each other. Myocardial perfusion and myocardial flow reserve (MFR) were quantified using PET imaging. LV structure and function, including global longitudinal strain (GLS), were quantified by transthoracic echocardiography. Global MFR declined with increasing AS severity (P = 0.04). Probability of impaired MFR increased with severity of adverse LV remodeling (OR 1.88, CI 1.03 to 3.41, P =0.04). Reduced MFR associated with impaired GLS (r = - 0.29, P = 0.002) and associated with reduced MACE-free survival at 7.27 years median follow-up. Adjusted annualized rate of MACE was highest in those with impaired GLS and MFR and lowest in those with normal GLS and MFR (30.99% vs 1.86%, P =0.002). In patients with AS and no overt CAD, impaired MFR associates with adverse LV remodeling and subclinical LV mechanical dysfunction, and is a marker increased clinical risk.

Sections du résumé

BACKGROUND BACKGROUND
We investigated role of coronary microvascular disease (CMD) in maladaptive LV remodeling and prognosis in patients with aortic sclerosis or stenosis and no overt CAD.
METHODS METHODS
This was a retrospective cohort study of patients with aortic sclerosis or stenosis, normal myocardial perfusion and LV ejection fraction (EF) > 50% (n = 43) and matched controls without AS (n = 43). PET and echocardiograms were performed within 1 year of each other. Myocardial perfusion and myocardial flow reserve (MFR) were quantified using PET imaging. LV structure and function, including global longitudinal strain (GLS), were quantified by transthoracic echocardiography.
RESULTS RESULTS
Global MFR declined with increasing AS severity (P = 0.04). Probability of impaired MFR increased with severity of adverse LV remodeling (OR 1.88, CI 1.03 to 3.41, P =0.04). Reduced MFR associated with impaired GLS (r = - 0.29, P = 0.002) and associated with reduced MACE-free survival at 7.27 years median follow-up. Adjusted annualized rate of MACE was highest in those with impaired GLS and MFR and lowest in those with normal GLS and MFR (30.99% vs 1.86%, P =0.002).
CONCLUSION AND RELEVANCE CONCLUSIONS
In patients with AS and no overt CAD, impaired MFR associates with adverse LV remodeling and subclinical LV mechanical dysfunction, and is a marker increased clinical risk.

Identifiants

pubmed: 31044406
doi: 10.1007/s12350-019-01706-y
pii: 10.1007/s12350-019-01706-y
pmc: PMC6824970
mid: NIHMS1528353
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

579-588

Subventions

Organisme : NHLBI NIH HHS
ID : K23 HL135438
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL132021
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL094301
Pays : United States

Commentaires et corrections

Type : CommentIn

Références

Eur Heart J Cardiovasc Imaging. 2012 Oct;13(10):827-33
pubmed: 22736713
J Am Soc Echocardiogr. 2016 Apr;29(4):277-314
pubmed: 27037982
Circulation. 2009 Aug 18;120(7):577-84
pubmed: 19652094
J Am Coll Cardiol. 2014 Jul 15;64(2):144-54
pubmed: 25011718
J Am Coll Cardiol. 2012 Nov 6;60(19):1854-63
pubmed: 23062541
N Engl J Med. 2007 Feb 22;356(8):830-40
pubmed: 17314342
N Engl J Med. 1999 Jul 15;341(3):142-7
pubmed: 10403851
J Am Coll Cardiol. 2010 Jul 20;56(4):278-87
pubmed: 20633819
Nat Rev Cardiol. 2015 Jan;12(1):48-62
pubmed: 25311229
J Am Soc Echocardiogr. 2012 Aug;25(8):835-41
pubmed: 22742867
Circulation. 2005 Jun 21;111(24):3290-5
pubmed: 15956131
JACC Cardiovasc Imaging. 2010 Jun;3(6):623-40
pubmed: 20541718
Echocardiography. 2002 Nov;19(8):655-9
pubmed: 12487634
Eur Heart J. 2014 May;35(17):1101-11
pubmed: 24366916
J Am Coll Cardiol. 2009 Jul 7;54(2):150-6
pubmed: 19573732
Circ Cardiovasc Imaging. 2014 Nov;7(6):938-45
pubmed: 25320287
Heart. 2011 Feb;97(4):301-7
pubmed: 20720251
Circulation. 2014 Oct 21;130(17):1483-92
pubmed: 25205802
Circulation. 2012 Oct 16;126(16):2020-35
pubmed: 22923432
JAMA Cardiol. 2017 Apr 1;2(4):409-416
pubmed: 28146260
J Appl Physiol (1985). 2009 Jan;106(1):113-21
pubmed: 18974370
Eur J Nucl Med Mol Imaging. 2007 Nov;34(11):1765-74
pubmed: 17619189
Heart. 2006 Feb;92(2):208-12
pubmed: 15908482
JAMA Cardiol. 2018 Sep 1;3(9):839-847
pubmed: 30140889
Circulation. 2002 Jan 29;105(4):470-6
pubmed: 11815430
Circulation. 2011 Nov 15;124(20):2215-24
pubmed: 22007073
J Am Coll Cardiol. 2000 Mar 1;35(3):569-82
pubmed: 10716457
J Am Soc Echocardiogr. 2017 Apr;30(4):372-392
pubmed: 28385280
J Am Soc Echocardiogr. 2015 Jan;28(1):1-39.e14
pubmed: 25559473
J Am Coll Cardiol. 2018 Feb 27;71(8):860-871
pubmed: 29471937
Clin Cardiol. 1989 Dec;12(12 Suppl 4):IV34-5
pubmed: 2533528
Eur Heart J Cardiovasc Imaging. 2018 Aug 1;19(8):859-867
pubmed: 28950306
Lancet. 2006 Sep 16;368(9540):1005-11
pubmed: 16980116
J Nucl Med. 2009 Jul;50(7):1062-71
pubmed: 19525467
Eur Heart J. 2016 Apr 14;37(15):1196-207
pubmed: 26508168
Circ Cardiovasc Imaging. 2014 Jan;7(1):173-81
pubmed: 24214885
J Am Coll Cardiol. 2017 Jul 11;70(2):252-289
pubmed: 28315732

Auteurs

Wunan Zhou (W)

Cardiovascular Imaging Program, Departments of Medicine and Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Navkranbir Bajaj (N)

Cardiovascular Imaging Program, Departments of Medicine and Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Ankur Gupta (A)

Cardiovascular Imaging Program, Departments of Medicine and Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Yee-Ping Sun (YP)

Cardiovascular Imaging Program, Departments of Medicine and Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Brigham and Women's Hospital Heart and Vascular Center, Harvard Medical School, 75 Francis St, ASB-L1 037C, Boston, MA, USA.

Sanjay Divakaran (S)

Cardiovascular Imaging Program, Departments of Medicine and Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Courtney Bibbo (C)

Cardiovascular Imaging Program, Departments of Medicine and Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Jon Hainer (J)

Cardiovascular Imaging Program, Departments of Medicine and Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Viviany Taqueti (V)

Cardiovascular Imaging Program, Departments of Medicine and Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Brigham and Women's Hospital Heart and Vascular Center, Harvard Medical School, 75 Francis St, ASB-L1 037C, Boston, MA, USA.

Sharmila Dorbala (S)

Cardiovascular Imaging Program, Departments of Medicine and Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Brigham and Women's Hospital Heart and Vascular Center, Harvard Medical School, 75 Francis St, ASB-L1 037C, Boston, MA, USA.

Ron Blankstein (R)

Cardiovascular Imaging Program, Departments of Medicine and Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Brigham and Women's Hospital Heart and Vascular Center, Harvard Medical School, 75 Francis St, ASB-L1 037C, Boston, MA, USA.

Pinak Shah (P)

Brigham and Women's Hospital Heart and Vascular Center, Harvard Medical School, 75 Francis St, ASB-L1 037C, Boston, MA, USA.

Tsuyoshi Kaneko (T)

Division of Cardiac Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.

Dale Adler (D)

Brigham and Women's Hospital Heart and Vascular Center, Harvard Medical School, 75 Francis St, ASB-L1 037C, Boston, MA, USA.

Patrick O'Gara (P)

Brigham and Women's Hospital Heart and Vascular Center, Harvard Medical School, 75 Francis St, ASB-L1 037C, Boston, MA, USA.

Marcelo Di Carli (M)

Cardiovascular Imaging Program, Departments of Medicine and Radiology, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA. mdicarli@bwh.harvard.edu.
Brigham and Women's Hospital Heart and Vascular Center, Harvard Medical School, 75 Francis St, ASB-L1 037C, Boston, MA, USA. mdicarli@bwh.harvard.edu.

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