Author(s): Dr Daniel Mazzoni, Basic Physician Trainee, Royal Brisbane and Women’s Hospital, Brisbane, Queensland, Australia; Nicolas Anning, Clinical Pharmacist, Royal Brisbane and Women’s Hospital, Brisbane, Queensland, Australia. Copy edited by Gus Mitchell. November 2020.
Beta-blockers are medications that antagonize the effects of adrenaline and noradrenaline by blocking adrenergic receptors.
Beta-blockers are used mainly for the treatment of cardiovascular diseases and glaucoma. Their use in dermatology is increasing for a variety of conditions.
How do beta-blockers work?
Two classes of beta-blocker are currently used in clinical practice: cardio-selective (beta-1 receptor-selective) and non-selective (beta-1, beta-2, and/or alpha-1 receptor) beta blockers.
Blockade of cardiac beta-1 adrenergic receptors results in decreased heart rate and blood pressure. Blockade of beta-2 adrenergic receptors causes the relaxation and dilatation of peripheralblood vessels, resulting in decreased blood pressure.
Commonly used examples of cardio-selective beta-blockers include:
Atenolol
Bisoprolol
Metoprolol
Nebivolol.
Non-selective beta-blockers include:
Propranolol
Carvedilol
Timolol
Labetalol.
What are the clinical uses for beta-blockers?
Beta-blockers may be administered orally (immediate or controlled release), intravenously, or topically as eye drops.
The current approved uses of beta-blockers in medicine are summarised below.
Small case series have demonstrated improvement in the flushing and persistenterythema of rosacea using oral carvedilol. Topical timolol seems to be less effective.
Infantile haemangioma
Rosacea
Rosacea
Pyogenic granuloma
Topical timolol has been reported to clear pyogenic granuloma in most, but not all, cases.
Kaposi sarcoma
A small number of cases have described successful treatment of Kaposi sarcoma using topical timolol in both HIV-positive and HIV-negative cases.
Chronic leg ulcer
Several case series using topical timolol have reported improved wound healing in chronic diabetic and venousleg ulcers.
Kaposi sarcoma
Leg ulcer
What are the adverse effects of beta-blockers?
The side effects of beta-blockers occur primarily due to their anti-adrenergic effect.
Common adverse effects of beta blockers include:
Bradycardia
Hypotension
Fatigue
Nausea
Dizziness.
Adverse effects may also occur if regular beta-blocker therapy is abruptly ceased. This is due to beta-blockers inducing up-regulation of beta-adrenergic receptors in the body.
Abrupt withdrawal of beta-blockers can induce:
Palpitations
Tremor
Sweating
Anxiety
Angina.
What are the cutaneous adverse effects of beta-blockers?
Psoriasis
Beta-blockers are a well-recognised trigger to exacerbate or precipitatepsoriasis.
Typical de novo drug-induced psoriasis may manifest as pustular psoriasis in the absence of joint or nail changes.
Studies suggest that exacerbations of psoriasis due to beta-blockers are more likely to occur in patients 50 years of age or older.
Beta-blockers may lead to treatment-resistant psoriasis in patients with pre-existing psoriasis.
Raynaud phenomenon
Exacerbation of Raynaud phenomenon is commonly reported in patients taking a beta-blocker.
Exacerbations are far more commonly implicated with non-selective beta blockers than beta-1 selective blockers.
Beta-blockers should be avoided or used cautiously in patients with severe Raynaud symptoms.
Alopecia
Alopecia due to beta-blockers is a telogeneffluvium, a reversible thinning of the hair.
Propranolol is commonly implicated in drug-induced alopecia.
Timolol eyedrops have also been reported to cause telogen effluvium.
Nail deformity
Psoriatic nail changes such as onycholysis, pitting, splitting, discolouration, and thickening can be induced by systemic beta-blockers.
Pincer nail deformity, a transverse nail curvature, has been reported in a very small number of cases, with resolution after cessation of the beta-blocker. It can be associated with psoriasis.
Abdelmaksoud A, Filoni A, Giudice G, Vestita M. Classic and HIV-related Kaposi sarcoma treated with 0.1% topical timolol gel. J Am Acad Dermatol. 2017;76(1):153–5. doi:10.1016/j.jaad.2016.08.041. PubMed
Australian Medicines Handbook 2020 (online). Beta-blockers. Australian Medicines Handbook Pty Ltd. Updated July 2020. Available at: https://amhonline.amh.net.au/ (accessed 26 July 2020).
Awad VM, Sakhamuru S, Kambampati S, Wasim S, Malik BH. Mechanisms of beta-blocker induced psoriasis, and psoriasis de novo at the cellular level. Cureus. 2020;12(7):e8964. doi:10.7759/cureus.8964. PubMed Central
Bostanci S, Ekmekci P, Akyol A, Peksari Y, Gürgey E. Pincer nail deformity: inherited and caused by a beta-blocker. Int J Dermatol. 2004;43(4):316–18. doi:10.1111/j.1365-4632.2004.01666.x. PubMed
Prabha N, Chhabra N, Arora R. Beta-blockers in dermatology. Indian J Dermatol Venereol Leprol. 2017;83(3):399–407. doi:10.4103/ijdvl.IJDVL_220_16. PubMed
Rai AK, Janani K, Rai R. Efficacy of topical timolol versus saline in chronic venous ulcers: a randomized controlled trial. J Cutan Aesthet Surg. 2020;13(1):18–23. doi:10.4103/JCAS.JCAS_13_19. PubMed Central
Tatu AL, Elisei AM, Chioncel V, Miulescu M, Nwabudike LC. Immunologic adverse reactions of β-blockers and the skin. Exp Ther Med. 2019;18(2):955–9. doi:10.3892/etm.2019.7504. PubMed Central