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Medical Journal of Cairo University [The]. 2004; 72 (4 Suppl.): 1-20
in English | IMEMR | ID: emr-204493

ABSTRACT

Objective: To evaluate the effects of tissue-specific tibolone and continuous combined hormone replacement therapy [ccHRT] on mammographic parenchymal density and plasma lipoprotein profile in healthy postmenopausal women


Design and Setting: This was a prospective double-blind, randomised placebo-controlled study conducted at Al-Azhar University Hospitals in Damietta and Cairo


Subjects and Methods: 90 healthy postmenopausal women aged 48 to 55 years with a normal mammogram and lipid profile at baseline were equally randomized to receive one of three treatment arms: [1] tibolone 2.5 mg [group I. n=30]; [2] continuous combined 17-beta estradiol 2 mg plus norethisterone acetate 1 mg [E2/NETA] [group II, n=30]; [3] placebo [group III, n=30]. Mammograms were performed at baseline and after 12 months of treatment. Mammographic density was quantified according to the Wolfe classification and by the percentage area of the breast that had a dense pattern. Plasma levels of total cholesterol, low-density lipoprotein [LDL-C], high- density lipoprotein [HDL-C] cholesterol; triglycerides [TG]; lipoprotein [a] [Lp[a]]; apolipoprotein A [apoLpA] and apolipoprotein B [apoLpB] were determined on four occasions [i.e., baseline. 3-, 6- and 12-month visits]


Results: An increase in mammographic density was much more common among women receiving continuous combined hormone replacement therapy [43% - 50%] than among those receiving tibolone [3% - 6%] and placebo [0%] treatment. The difference between E2 /NETA and placebo was highly significant [p[c]<0.001]. Treatment with tibolone did not differ from that with placebo. In the tibolone group, 6% 13% of the women showed an involutionary change in breast density in the 12-month reevaluation. In contrast, none of the women receiving E2/NETA or placebo showed an involutionary changes in breast density. Considering the effects of treatment regimens on lipids profile, it was found that tibolone therapy was associated with a statistically significant reduction in serum triglycerides, HDL-C, apolipoprotein A and lipoprotein [a] by [22%, 20%. 10%. 20%, respectively] [p[a] <0.05], whilst no significant changes were seen in LDL-C and apolipoprotein B levels. In E2/NETA-group, there was a significant reduction of total cholesterol, LDL-C ,apolipoprotein B. HDL-C and lipoprotein [a] by [9%. 11%. 10.7%. 7.4%. 18%. respectively] [p[a] <0.05], whilst no significant changes were seen in triglycerides levels [p[a] >0.05]. Decrements were observed within 3 months of active treatments and maintained thereafter. Group I showed a more pronounced reduction of HDL-C, apolipoprotein A and triglycerides than Group II and Group III. The levels of LDL-C and apolipoprotein B declined significantly only in Group II [P[a] <0.05], while LDL-C/HDL-C ratio increased significantly in Group I by 23% when compared with GII [2.3%] and GIII [10.2%] after 12 months of treatment [P[b] and P[c]<0.05]


Conclusion: An increase in mammographic parenchymal density should be regarded as an unwanted side effect of HRT. In contrast to conventional estrogen/progestogen treatment, tissue-specific tibolone seems to exert little stimulation of breast tissue with no impairment of mammogram interpretation. Both tibolone and continuous combined HRT induced a favorable plasma lipid response. These therapeutic effects may contribute to the reduction or prevention of atherogenesis in postmenopausal women. Larger longterm studies are needed to confirm the impact of prolonged tibolone or continuous combined HRT administration on mammography and plasma lipoproteins

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