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DOI 10.1159/000339934

Медицинская библиотека · Gynecologic and obstetric investigation · 2012

Changes in serum levels of cartilage oligomeric matrix protein after estrogen and alendronate therapy in postmenopausal women.

Seo Seok Kyo, Yang Hyo In, Lim Kyung Jin, Jeon Young Eun, Choi Young Sik, Cho SiHyun, Lee Byung Seok

Контролируемое клиническое исследованиеСтатьяПеревод в очереди

Аннотация

BACKGROUND

Cartilage oligomeric matrix protein (COMP) is a biomarker for joint destruction and its serum levels are used for assessing therapeutic efficacy. This study aims to compare changes in serum COMP levels in postmenopausal women with osteopenia/osteoporosis receiving estrogen and alendronate.

METHODS

A total of 62 postmenopausal women diagnosed with osteopenia or osteoporosis were treated with either estrogen (17β-estradiol 1 mg, n = 30) or bisphosphonate (alendronate 5 mg, n = 32) for 6 months. The controls were healthy postmenopausal women (n = 30). Serum COMP and osteocalcin levels were measured at baseline and after 6 months of treatment.

RESULTS

Estrogen decreased levels of COMP at 6 months compared to baseline levels (–8.35 ± 19.38%), whereas the bisphosphonate and control groups resulted in no significant changes (–5.50 ± 18.69 and –1.49 ± 25.34%, respectively). Concentrations of osteocalcin decreased significantly in both treatment groups (estrogen –25.60 ± 24.42% and alendronate –13.76 ± 23.89%, respectively). There was a significant positive correlation between changes after 6 months in COMP and osteocalcin (R = 0.48, p = 0.002).

CONCLUSIONS

Postmenopausal women treated with estrogen showed significantly decreased levels of COMP after 6 months. Estrogen might provide a further treatment modality in the prevention of joint destruction.

Для цитирования: Seo Seok Kyo, Yang Hyo In, Lim Kyung Jin, Jeon Young Eun, Choi Young Sik, Cho SiHyun, Lee Byung Seok. Changes in serum levels of cartilage oligomeric matrix protein after estrogen and alendronate therapy in postmenopausal women.. Gynecologic and obstetric investigation. 2012. DOI: 10.1159/000339934.

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