Literature DB >> 1587378

The effect of hormone replacement therapy on postmenopausal bone loss.

C Castelo-Branco1, M J Martínez de Osaba, F Pons, J González-Merlo.   

Abstract

Eighty-four postmenopausal women who were randomly allocated to one of four groups, completed a 1 year follow-up. The first group (n = 20) received 0.625 mg/day conjugated estrogens cyclically (CE; 25 days/month). The second (n = 23) received 0.625 mg/day of CE continuously, and the third (n = 17) received 50 micrograms/day of transdermal 17 beta-estradiol cyclically (24 days/month). All these groups also received 2.5 mg of medroxiprogesterone acetate sequentially for the last 12 days of hormone replacement therapy, while the fourth group (n = 24) constituted a treatment-free control group. Dual photon absorptiometry was carried out before therapy and was repeated after 1 year. Serum calcium, phosphate and osteocalcine levels, and the urinary calcium/creatinine and hydroxyproline/creatinine ratios, were measured prior to treatment and 6 and 12 months thereafter. All treatment groups showed an increase in bone mineral content. This increase was higher in the continuous CE treatment group (4.4%, P less than 0.05) and in transdermal group (7.1%, P less than 0.01). Concomitant biochemical effects at 6 and 12 months, reduction in urine calcium and hydroxyproline, reduction in blood calcium, phosphate and osteocalcine, were compatible with the observed effects on bone mineral.

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Year:  1992        PMID: 1587378     DOI: 10.1016/0028-2243(92)90058-7

Source DB:  PubMed          Journal:  Eur J Obstet Gynecol Reprod Biol        ISSN: 0301-2115            Impact factor:   2.435


  9 in total

Review 1.  Hormone replacement therapy: II. A pharmacoeconomic appraisal of its role in the prevention of postmenopausal osteoporosis and ischaemic heart disease.

Authors:  R Whittington; D Faulds
Journal:  Pharmacoeconomics       Date:  1994-06       Impact factor: 4.981

2.  Association of serum phosphorus with left ventricular mass in men and women with stable cardiovascular disease: data from the Heart and Soul Study.

Authors:  Georges Saab; Mary A Whooley; Nelson B Schiller; Joachim H Ix
Journal:  Am J Kidney Dis       Date:  2010-06-26       Impact factor: 8.860

3.  Estrogen directly and specifically downregulates NaPi-IIa through the activation of both estrogen receptor isoforms (ERα and ERβ) in rat kidney proximal tubule.

Authors:  Dara Burris; Rose Webster; Sulaiman Sheriff; Rashma Faroqui; Moshe Levi; John R Hawse; Hassane Amlal
Journal:  Am J Physiol Renal Physiol       Date:  2015-01-21

4.  Klotho/fibroblast growth factor 23- and PTH-independent estrogen receptor-α-mediated direct downregulation of NaPi-IIa by estrogen in the mouse kidney.

Authors:  Rose Webster; Sulaiman Sheriff; Rashma Faroqui; Faraaz Siddiqui; John R Hawse; Hassane Amlal
Journal:  Am J Physiol Renal Physiol       Date:  2016-05-18

Review 5.  Pharmacokinetic characterisation of transdermal delivery systems.

Authors:  B Berner; V A John
Journal:  Clin Pharmacokinet       Date:  1994-02       Impact factor: 6.447

Review 6.  Transdermal estradiol. A review of its pharmacological profile, and therapeutic potential in the prevention of postmenopausal osteoporosis.

Authors:  J A Balfour; D McTavish
Journal:  Drugs Aging       Date:  1992 Nov-Dec       Impact factor: 3.923

7.  Estrogen downregulates the proximal tubule type IIa sodium phosphate cotransporter causing phosphate wasting and hypophosphatemia.

Authors:  S Faroqui; M Levi; M Soleimani; H Amlal
Journal:  Kidney Int       Date:  2008-02-27       Impact factor: 10.612

Review 8.  Management of osteoporosis. An overview.

Authors:  C Castelo-Branco
Journal:  Drugs Aging       Date:  1998       Impact factor: 3.923

9.  Yield of diagnostic tests in unexplained renal hypophosphatemia: a case series.

Authors:  A P Bech; E J Hoorn; R Zietse; J F M Wetzels; T Nijenhuis
Journal:  BMC Nephrol       Date:  2018-09-04       Impact factor: 2.388

  9 in total

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