Progestogen therapies: differences in clinical effects?

@article{Wiegratz2004ProgestogenTD,
  title={Progestogen therapies: differences in clinical effects?},
  author={Inka Wiegratz and Herbert Kuhl},
  journal={Trends in Endocrinology \& Metabolism},
  year={2004},
  volume={15},
  pages={277-285}
}
  • I. WiegratzH. Kuhl
  • Published 1 August 2004
  • Biology, Medicine
  • Trends in Endocrinology & Metabolism
View on Elsevier
doi.org
53 Citations
Highly Influential Citations
4
Background Citations
23
Methods Citations
1

53 Citations

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A variety of innovations have been developed since combined hormonal contraceptives were first available in the late 1950s, including changes in drug components, doses used, and the temporal sequencing of exposure to drugs.

Certain Progestins Prevent the Enhancing Effect of 17β-Estradiol on NO-Mediated Inhibition of Platelet Aggregation by Endothelial Cells

Certain progestins, including MPA, attenuate the 17β-E–induced NO-mediated inhibition of platelet aggregation by endothelial cells through preventing both eNOS and GTPCH I expression most likely via activation of glucocorticoid receptors.

Effects of estradiol with micronized progesterone or medroxyprogesterone acetate on risk markers for breast cancer in postmenopausal monkeys

Oral micronized progesterone has a more favorable effect on risk biomarkers for postmenopausal breast cancer than medroxyprogesterone acetate, and both progestogens significantly attenuated E2 effects on body weight, endometrium, and the TFF1 marker of estrogen receptor activity in the breast.

Human versus non-human sex steroid use in hormone replacement therapies part 1: Preclinical data

The effect of medroxyprogesterone acetate on estrogen-dependent risks and benefits – an attempt to interpret the Women's Health Initiative results

  • H. KuhlJ. Stevenson
  • Medicine, Biology
    Gynecological endocrinology : the official journal of the International Society of Gynecological Endocrinology
  • 2006
In contrast, CEE alone reduced non-significantly the risk of CHD in women aged 50–59 years, suggesting that primary prevention is possible if estrogen replacement therapy is initiated early.

Ethynilestradiol 20 mcg plus Levonorgestrel 100 mcg: Clinical Pharmacology

Overall, EE20/LNG100 combination is safe and well tolerated, and in several studies the incidence of adverse events in the treated group was comparable to that of the placebo group.

TREATMENT OF OSTEOPOROSIS

Differential effects of synthetic progestagens on neuron survival and estrogen neuroprotection in cultured neurons

...

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