Is there a role for menopausal hormone therapy in the management of postmenopausal osteoporosis?
Is there a role for menopausal hormone therapy in the management of postmenopausal osteoporosis?
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DOI:
10.1007/s00198-020-05497-8
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发表时间:
2020-12
期刊:
影响因子:
--
通讯作者:
Harvey NC
中科院分区:
文献类型:
--
作者:
Rozenberg S;Al-Daghri N;Aubertin-Leheudre M;Brandi ML;Cano A;Collins P;Cooper C;Genazzani AR;Hillard T;Kanis JA;Kaufman JM;Lambrinoudaki I;Laslop A;McCloskey E;Palacios S;Prieto-Alhambra D;Reginster JY;Rizzoli R;Rosano G;Trémollieres F;Harvey NC
We provide an evidence base and guidance for the use of menopausal hormone therapy (MHT) for the maintenance of skeletal health and prevention of future fractures in recently menopausal women. Despite controversy over associated side effects, which has limited its use in recent decades, the potential role for MHT soon after menopause in the management of postmenopausal osteoporosis is increasingly recognized. We present a narrative review of the benefits versus risks of using MHT in the management of postmenopausal osteoporosis. Current literature suggests robust anti-fracture efficacy of MHT in patients unselected for low BMD, regardless of concomitant use with progestogens, but with limited evidence of persisting skeletal benefits following cessation of therapy. Side effects include cardiovascular events, thromboembolic disease, stroke and breast cancer, but the benefit-risk profile differs according to the use of opposed versus unopposed oestrogens, type of oestrogen/progestogen, dose and route of delivery and, for cardiovascular events, timing of MHT use. Overall, the benefit-risk profile supports MHT treatment in women who have recently (< 10 years) become menopausal, who have menopausal symptoms and who are less than 60 years old, with a low baseline risk for adverse events. MHT should be considered as an option for the maintenance of skeletal health in women, specifically as an additional benefit in the context of treatment of menopausal symptoms, when commenced at the menopause, or shortly thereafter, in the context of a personalized benefit-risk evaluation.
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影响因子:
39.2
作者:
ALBRIGHT, F
通讯作者:
ALBRIGHT, F
影响因子:
4.9
作者:
Armeni, Eleni;Lambrinoudaki, Irene;Rees, Margaret
通讯作者:
Rees, Margaret
影响因子:
39.2
作者:
Harman, S. Mitchell;Black, Dennis M.;Hodis, Howard N.
通讯作者:
Hodis, Howard N.
DOI:
10.1097/gme.0000000000000956
发表时间:
2018-01
期刊:
Menopause (New York, N.Y.)
影响因子:
--
作者:
Crandall CJ;Hovey KM;Andrews CA;Chlebowski RT;Stefanick ML;Lane DS;Shifren J;Chen C;Kaunitz AM;Cauley JA;Manson JE
通讯作者:
Manson JE
影响因子:
8.7
作者:
Angerer, P;Störk, S;von Schacky, C
通讯作者:
von Schacky, C