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P-26
ORAL CONTRACEPTIVES, HORMONE REPLACEMENT THERAPY AND
ANDROGEN SENSITIVE SKIN DISORDERS
I. Ali, RP Dawber Department of Dermatology,
Oxford Radcliffe Hospitals, UK.
Oral contraceptive pills (OCP) and hormone
replacement therapy (HRT) are amongst the most commonly used
drugs by women. Their effect on androgen sensitive skin disease
is paradoxical in that they can act as both exacerbating factors
and serve as therapeutic agents. These conflicting properties
can be related to the androgenicity of the progestogen contained
in the preparation. Progestogens have varying androgenic properties
depending on their chemical derivation. Older combined contraceptive
pills contained higher levels of oestrogen which was later
reduced to decrease the risk of thrombo-embolic disease. As
the oestrogen dose was reduced the androgenic properties of
the progestogen became more apparent and newer progestogens
were developed with less androgenic properties such as gestodene,
desogestrel and norgestimate.1 The anti androgenic progestogen,
cyproterone acetate has been available since the 1940’s and
is the most established progestogen in the treatment of androgen
sensitive skin disease. It is available as a combined oral
contraceptive pill, Dianette(r) and as a HRT preparation,
Climen(r). Recently a new progestogen with anti androgenic
properties has been released on to the market called drospirenone.
It has similar efficacy to cyproterone acetate in the treatment
of acne and has beneficial effects on hirsutism.2 The availability
of new drugs further expands the options of OCP preparations
available for the female patient. Improved understanding of
the components in OCPs and HRT can enable the dermatologist
to gain maximum benefits from these as pharmacotherapies and
suggest possible alternatives when faced with common side
effects.
References:
1. P D Darney.The androgenicity of progestins.
Am J Med 98 (1A):104-110
2. Van Vloten WA et al.The effect of 2 combined
oral contraceptives containing either drospirenone or cyproterone
acetate on acne and seborrhea. Cutis, 2002 (4 Suppl): S2-15.
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