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Plasma Proteomic Patterns Show Sex Differences in Early Concentric Left Ventricular Remodeling.

Authors :
van Ommen AM
Diez Benavente E
Onland-Moret NC
Valstar GB
Cramer MJ
Rutten FH
Teske AJ
Menken R
Hofstra L
Tulevski II
Sweitzer N
Somsen GA
den Ruijter HM
Source :
Circulation. Heart failure [Circ Heart Fail] 2023 Jul; Vol. 16 (7), pp. e010255. Date of Electronic Publication: 2023 Jun 29.
Publication Year :
2023

Abstract

Background: Concentric remodeling (cRM) can precede heart failure with preserved ejection fraction (HFpEF), a condition prevalent in women.<br />Methods: Patients (n=60 593, 54.2% women) visiting outpatient clinics of Cardiology Centers of the Netherlands were analyzed for cRM, HFpEF development, and mortality risk. We studied risk factors for relative wall thickness both sex-stratified and in women and men combined. Biomarker profiling was performed (4534 plasma proteins) in a substudy involving 557 patients (65.4% women) to identify pathways involved in cRM.<br />Results: cRM was present in 23.5% of women and 27.6% of men and associated with developing HFpEF (HR, 2.15 [95% CI, 1.51-2.99]) and mortality risk (HR, 1.09 [95% CI, 1.00-1.19]) in both sexes. Age, heart rate, and hypertension were statistically significantly stronger risk factors for relative wall thickness in women than men. Higher circulating levels of IFNA5 (interferon alpha-5) were associated with higher relative wall thickness in women only. Pathway analysis revealed differential pathway activation by sex and increased expression of inflammatory pathways in women.<br />Conclusions: cRM is prevalent in approximately 1 in 4 women and men visiting outpatient cardiology clinics and associated with HFpEF development and mortality risk in both sexes. Known risk factors for cRM were more strongly associated in women than men. Proteomic analysis revealed inflammatory pathway activation in women, with a central role for IFNA5. Differential biologic pathway activation by sex in cRM may contribute to the female predominance of HFpEF and holds promise for identification of new therapeutic avenues for prevention and treatment of HFpEF.<br />Registration: URL: https://www.<br />Clinicaltrials: gov; Unique identifier: NCT001747.<br />Competing Interests: Disclosures None.

Details

Language :
English
ISSN :
1941-3297
Volume :
16
Issue :
7
Database :
MEDLINE
Journal :
Circulation. Heart failure
Publication Type :
Academic Journal
Accession number :
37381923
Full Text :
https://doi.org/10.1161/CIRCHEARTFAILURE.122.010255