Objective: Intravaginal estriol (E3) effectively improves postmenopaus
al genito-urinary disturbances, without stimulating endometrial prolif
eration. The aim of the present study was to evaluate the effect of in
travaginal estriol (E3) plus nasal spray salmon calcitonin (sCT), to i
mprove neurovegetative symptoms and to prevent the decline of bone min
eral density (BMD) of postmenopausal women. Methods: Two hundred and f
ourteen (214) healthy postmenopausal women were treated for 12 months
with: (1) E3 (0.5 mg every other day) + Ca (0.5 g/day); (2) E3 + Ca sCT (50 IU x 2/day); (3) sCT + Ca; (4) Ca. Climacteric complaints, suc
h as hot flushes and sweating, BMD at the distal 1/10 of the radius, a
nalyzed by dual photon absorptiometry, urinary excretion of hydroxypro
line and serum alkaline phosphatase were evaluated at baseline and eve
ry 6 months. At the same time, patient compliance and drug tolerabilit
y were evaluated. Results: E3 but not sCT, improved hot flushes and sw
eating. E3 blunted but not completely counteracted the BMD decline obs
erved in women treated with only Ca, and reduced urinary hydroxyprolin
e excretion. sCT markedly increased BMD Values and reduced both urinar
y hydroxyproline excretion and serum alkaline phosphatase. These effec
ts were not potentiated by E3 coadministration. All treatments were we
ll tolerated. Conclusions: Present data indicate that the combined adm
inistration of intravaginal E3 and sCT may represent an alternative th
erapeutic regimen for those postmenopausal women who do not accept or
have contraindications to classical hormone replacement therapy.