The Relevance of Arterial Blood Pressure in the Management of Glaucoma Progression: A Systematic Review
- PMID: 37995334
- PMCID: PMC10906067
- DOI: 10.1093/ajh/hpad111
The Relevance of Arterial Blood Pressure in the Management of Glaucoma Progression: A Systematic Review
Abstract
Background: Glaucoma is one of the leading causes of global blindness and is expected to co-occur more frequently with vascular morbidities in the upcoming years, as both are aging-related diseases. Yet, the pathogenesis of glaucoma is not entirely elucidated and the interplay between intraocular pressure, arterial blood pressure (BP) and ocular perfusion pressure is poorly understood.
Objectives: This systematic review aims to provide clinicians with the latest literature regarding the management of arterial BP in glaucoma patients.
Methods: A systematic search was performed in Medline, Embase, Web of Science and Cochrane Library. Articles written in English assessing the influence of arterial BP and systemic antihypertensive treatment of glaucoma and its management were eligible for inclusion. Additional studies were identified by revising references included in selected articles.
Results: 80 Articles were included in this systemic review. A bimodal relation between BP and glaucoma progression was found. Both high and low BP increase the risk of glaucoma. Glaucoma progression was, possibly via ocular perfusion pressure variation, strongly associated with nocturnal dipping and high variability in the BP over 24 h.
Conclusions: We concluded that systemic BP level associates with glaucomatous damage and provided recommendations for the management and study of arterial BP in glaucoma. Prospective clinical trials are needed to further support these recommendations.
Keywords: 24-h ABPM; blood pressure; blood pressure variability; glaucoma; hypertension; nocturnal dipping.
© The Author(s) 2023. Published by Oxford University Press on behalf of American Journal of Hypertension, Ltd.
Conflict of interest statement
None regarding to this publication. The authors report no conflict of interest regarding the submitted work. Ingeborg Stalmans reports financial support for clinical trials from Aerie during the conduct of the study; and grants and personal fees from Omikron, Santen and Thea, personal fees from Allergan/AbbVie, Elios Vision, EyeD, Horus, Omikron, Santen, Théa, and personal fees and intellectual property from Mona outside the submitted work.
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