Crook D, Cust M P, Gangar K F, Worthington M, Hillard T C, Stevenson J C, Whitehead M I, Wynn V
Institute for Metabolic Research, St John's Wood, London, England.
Am J Obstet Gynecol. 1992 Mar;166(3):950-5. doi: 10.1016/0002-9378(92)91370-p.
We attempted to ascertain whether transdermal postmenopausal estrogen-progestin therapy has the typical effects of oral therapy on serum lipoprotein risk markers for cardiovascular disease.
Sixty-one postmenopausal women were randomized to receive either transdermal continuous 17 beta-estradiol, 0.05 mg/day, with transdermal cyclic norethindrone acetate, 0.25 mg/day, or oral continuous conjugated equine estrogens, 0.625 mg/day, with oral cyclic dl-norgestrel, 0.15 mg/day. Twenty-nine untreated subjects served as controls. Lipoprotein profiles at 3 and 6 months were compared with baseline values by means of analysis of variance.
In the estrogen-alone phase both therapies reduced serum levels of total and low-density lipoprotein cholesterol; high-density lipoproteins were largely unchanged. Oral therapy increased triglycerides whereas this lipid fell with transdermal therapy. In the combined phase of the cycle both therapies reduced triglycerides, total cholesterol, low-density lipoprotein cholesterol, and high-density lipoprotein cholesterol.
Transdermal and oral therapies had similar effects on lipoprotein cholesterol but different effects on triglycerides.