Sex Differences in Therapies for Heart Failure.
Adrenergic beta-Antagonists
/ pharmacology
Angiotensin Receptor Antagonists
/ pharmacology
Angiotensin-Converting Enzyme Inhibitors
/ pharmacology
Digoxin
/ pharmacology
Female
Heart Failure
/ drug therapy
Humans
Male
Mineralocorticoid Receptor Antagonists
/ therapeutic use
Sex Characteristics
Stroke Volume
HFpEF
Heart failure
angiotensin receptor blockers
angiotensin-converting enzyme inhibitors
digoxin
randomized controlled trial
sex differences
women
Journal
Current pharmaceutical design
ISSN: 1873-4286
Titre abrégé: Curr Pharm Des
Pays: United Arab Emirates
ID NLM: 9602487
Informations de publication
Date de publication:
2022
2022
Historique:
received:
19
04
2021
accepted:
27
09
2021
pubmed:
3
3
2022
medline:
19
8
2022
entrez:
2
3
2022
Statut:
ppublish
Résumé
Heart failure (HF) is a common cause of morbimortality with different etiopathogenesis and prognosis between men and women. This review provides a brief overview of gender-based differences in response to pharmacological therapies of heart failure with or without reduced ejection fraction (EF). It focuses on the differences in therapy outcomes with angiotensin-converting enzyme inhibitors (ACEi), angiotensin receptor blockers (ARBs), angiotensin neprilysin inhibitors (ARNI), beta-adrenergic blockers, mineralocorticoid/ aldosterone receptor antagonists, diuretics, ivabradine and digoxin. The baseline data originate from randomised controlled trials (RCTs) and large registries. We conclude that current guidelines recommending similar therapeutic approaches for both men and women are appropriate, while additional consideration should be given to different approaches regarding the use of ARBs, ACEi, and digoxin. Based on the available data, the ARBs might be considered a first-line therapy of HR for women instead of ACEi. Moreover, female patients should have stricter digoxin monitoring due to higher sensitivity and increased risk of complications. Finally, women are underrepresented in current clinical trials, and therefore future trials should aim to balance the gender recruitment disparity allowing sub-group analysis and comparisons between genders to guide individualised therapeutic strategies and appropriately targeted preventative steps.
Identifiants
pubmed: 35232346
pii: CPD-EPUB-121206
doi: 10.2174/1381612828666220301125514
doi:
Substances chimiques
Adrenergic beta-Antagonists
0
Angiotensin Receptor Antagonists
0
Angiotensin-Converting Enzyme Inhibitors
0
Mineralocorticoid Receptor Antagonists
0
Digoxin
73K4184T59
Types de publication
Journal Article
Review
Langues
eng
Sous-ensembles de citation
IM
Pagination
1295-1303Informations de copyright
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