Literature DB >> 12952369

Serum lipids and apolipoproteins in Greek postmenopausal women: association with estrogen, estrogen-progestin, tibolone and raloxifene therapy.

G Creatsas1, G Christodoulakos, I Lambrinoudaki, C Panoulis, C Chondros, P Patramanis.   

Abstract

The aim of this study was to assess lipid and apolipoprotein levels in postmenopausal women taking various regimens of replacement therapy or no therapy. Seven hundred forty-eight postmenopausal women followed in the Menopause Clinic of the 2nd Department of Obstetrics and Gynecology, University of Athens, Aretaieion Hospital, were studied in a cross-sectional design. Women were either non-users of replacement therapy (no. = 511) or users of one of the following regimens: conjugated equine estrogen 0.625 mg (CEE, no. = 34), CEE 0.625 mg plus medroxyprogesterone acetate 5 mg (CEE/MPA, no. = 60), 17beta-estradiol 2 mg plus norethisterone acetate 1 mg (E2/NETA, no. = 44), tibolone 2.5 mg (no. = 84), raloxifene HCI 60 mg (no. = 51). Total cholesterol (TC), LDL-cholesterol (LDL-C) and HDL-cholesterol (HDL-C), triglycerides (TG), apolipoprotein A1 (ApoA1) and apolipoprotein B (ApoB) levels were assessed. Women were grouped according to replacement regimen and mean levels of lipid and apolipoproteins were compared between groups. Women in the raloxifene group were older and longer menopaused. After adjustment for age and duration of menopause, TG levels were significantly lower in the tibolone and E2/NETA groups (75 and 89.9 mg/dl, respectively) compared to non-users. TC was lower in all therapy groups, but the difference acquired significance only in the E2/NETA (207.8 mg/dl), compared to non-users (231.5 mg/dl). LDL-C levels were significantly lower in the CEE (133.8 mg/dl), CEE/MPA (130.4 mg/dl) and raloxifene group (129.9 mg/dl) compared to non-users (151.9 mg/dl). There was no difference in HDL-C levels between users and non-users (58.9 mg/dl) except for the tibolone group where HDL-C was significantly lower (48.6 mg/dl). ApoA1 levels were significantly higher in the CEE/MPA group (194.4 mg/dl) and significantly lower in the tibolone group (141.6 mg/dl) compared to non-users (170.4 mg/dl). No difference was detected between groups concerning ApoB levels. In conclusion, tibolone therapy is associated with lower TG levels as well as lower HDL and ApoA1 levels. ERT, continuous combined estrogen-progestin therapy (HRT) and raloxifene are associated with lower LDL-C levels. Among continuous combined HRT users, CEE/MPA is associated with higher ApoA1 levels, while E2/NETA with lower TG levels. Large prospective randomized studies are required to validate these results.

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Year:  2003        PMID: 12952369     DOI: 10.1007/BF03345218

Source DB:  PubMed          Journal:  J Endocrinol Invest        ISSN: 0391-4097            Impact factor:   4.256


  35 in total

Review 1.  The protective effects of estrogen on the cardiovascular system.

Authors:  M E Mendelsohn; R H Karas
Journal:  N Engl J Med       Date:  1999-06-10       Impact factor: 91.245

Review 2.  Estrogen replacement therapy and cardiovascular protection: lipid mechanisms are the tip of an iceberg.

Authors:  A Nasr; M Breckwoldt
Journal:  Gynecol Endocrinol       Date:  1998-02       Impact factor: 2.260

3.  A cross-sectional study of the effects of hormon replacement therapy on the cardiovascular disease risk profile in healthy postmenopausal women.

Authors:  Gordana M Prelevic; Pandina Kwong; Dominic J Byrne; I Anita Jagroop; Jean Ginsburg; Dimitri P Mikhailidis
Journal:  Fertil Steril       Date:  2002-05       Impact factor: 7.329

Review 4.  Selective estrogen receptor modulator effects on serum lipoproteins and vascular function in postmenopausal women and in hypercholesterolemic men.

Authors:  A Blum; R O Cannon
Journal:  Ann N Y Acad Sci       Date:  2001-12       Impact factor: 5.691

Review 5.  Progestogens in hormonal replacement therapy: new molecules, risks, and benefits.

Authors:  Régine Sitruk-Ware
Journal:  Menopause       Date:  2002 Jan-Feb       Impact factor: 2.953

6.  Comparison of the antiatherosclerotic effect of tibolone with that of estradiol and ethinyl estradiol in cholesterol-fed, ovariectomized rabbits.

Authors:  P Zandberg; P N Demacker; E G de Reeder; M J Smit; D G Meuleman
Journal:  Menopause       Date:  2001       Impact factor: 2.953

7.  Effect of hormone replacement therapy on lipids in perimenopausal and early postmenopausal women.

Authors:  M E Ossewaarde; M L Bots; A A Bak; Y T Van Der Schouw; J C Witteman; J Planellas; H J Bennink; D E Grobbee
Journal:  Maturitas       Date:  2001-09-28       Impact factor: 4.342

8.  Two-year prospective and comparative study on the effects of tibolone on lipid pattern, behavior of apolipoproteins AI and B.

Authors:  C Castelo-Branco; E Casals; F Figueras; A Sanjuan; J J Vicente; J Balasch; J A Vanrell
Journal:  Menopause       Date:  1999       Impact factor: 2.953

9.  Effects of postmenopausal hormone replacement therapy on lipid, lipoprotein, and apolipoprotein (a) concentrations: analysis of studies published from 1974-2000.

Authors:  I F Godsland
Journal:  Fertil Steril       Date:  2001-05       Impact factor: 7.329

10.  Randomized trial of estrogen plus progestin for secondary prevention of coronary heart disease in postmenopausal women. Heart and Estrogen/progestin Replacement Study (HERS) Research Group.

Authors:  S Hulley; D Grady; T Bush; C Furberg; D Herrington; B Riggs; E Vittinghoff
Journal:  JAMA       Date:  1998-08-19       Impact factor: 56.272

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